This document describes a study examining a synthetic small molecule analogue (SMA-12b) of an immunomodulatory parasitic worm product (ES-62) and its ability to treat experimental arthritis. The key findings are:
1) SMA-12b prevents and treats collagen-induced arthritis in mice by modifying the expression of inflammatory genes, particularly inhibiting IL-1β production.
2) SMA-12b increases the expression of antioxidant response genes regulated by the transcription factor NRF2.
3) SMA-12b is unable to inhibit IL-1β expression in macrophages derived from NRF2-deficient mice, suggesting it acts through NRF2-mediated mechanisms.
Ameliorative effect of salicin against gamma irradiation inducedRam Sahu
This document summarizes a study that investigated the radioprotective effects of salicin against gamma irradiation-induced changes in the brain tissue of male rats. The study found that salicin administration reduced lipid peroxidation and minimized changes to protein patterns caused by irradiation. Specifically, salicin showed the highest protective effect against irradiation in rats that received salicin treatment after irradiation. However, salicin was not able to fully prevent abnormalities to lipoprotein patterns or quantitative changes to protein bands caused by irradiation. Overall, the results suggest salicin has radioprotective abilities against gamma irradiation effects on various electrophoretic patterns in brain tissue.
This document summarizes a study that evaluated the potential of an adeno-associated virus (AAV) vector delivering a peptide derived from the Nrf2 protein to target the Nrf2 signaling pathway in the retina. The Nrf2 peptide was fused to a cell-penetrating peptide sequence (Tat-peptide) and expressed from an AAV vector. In vitro, the TatNrf2mer peptide induced antioxidant gene expression, blocked IL-1β secretion, and protected cells from oxidative injury. In mouse models, TatNrf2mer expression partially protected photoreceptor function and decreased inflammatory cytokines and cells in models of retinal oxidative injury and uveitis. The results suggest this AAV-delivered TatNrf
The antimicrobial mechanism of ECA water against pseudomonas aeruginosa and ...Trevor William Sievert
This study investigated the antimicrobial mechanism of electrochemically activated water (anolyte) against Pseudomonas aeruginosa and Escherichia coli using SDS-PAGE protein analysis. Bacteria were treated with different concentrations of anolyte and their protein profiles analyzed via SDS-PAGE. Undiluted and 10-1 diluted anolyte were most effective, causing fewer and fainter protein bands compared to untreated bacteria, indicating protein destruction. Dilute anolyte caused extra protein bands, suggesting oxidative stress and protein fragmentation. The results provide insight into anolyte's antimicrobial action by affecting bacterial proteins.
Evaluation of salicin isolated from salix subserrata as a radioprotectorRam Sahu
1) The study investigated the radioprotective effects of salicin, a compound found in willow trees, against gamma radiation damage in rat spleen tissue.
2) Irradiation significantly increased lipid peroxidation in spleen tissue but salicin treatment reduced this effect.
3) Ultrastructural examination found no abnormalities in control or salicin groups but irradiation caused lesions and cell loss, which salicin provided some protection against.
4) Changes to protein and enzyme patterns from irradiation were detected electrophoretically and salicin treatment prevented some of these qualitative effects.
This document summarizes research on a class of compounds called thiazolides and their potential as antiviral agents, specifically against hepatitis B virus (HBV). Key points:
1. Thiazolides show promise as novel antiviral agents that could help treat HBV infections by acting through a non-resistance inducing mechanism. Nitazoxanide is a broad-spectrum thiazolide currently used as an antiparasitic drug.
2. The study synthesized and tested a wide range of thiazolide analogs for anti-HBV activity. Compound 3 showed potent and selective inhibition of HBV replication with low toxicity.
3. Structure-activity relationship analysis found good correlation
The document discusses research into identifying potential ganglioside-binding proteins in Borrelia burgdorferi that causes Lyme disease. Bioinformatics analysis identified VlsE1 as a top hit that is known to be involved in late-stage Lyme disease. VlsE1 was cloned and expressed, and expression studies showed that 0.1 mM IPTG produced the best yield of soluble VlsE1. While some VlsE1 remained insoluble, work is ongoing to optimize expression and purification conditions to study the potential function of VlsE1 in binding gangliosides.
This study investigated the allergenic properties of recombinant pro- and mature forms of the major house dust mite allergens Der p 1 and Der f 1. The recombinant mature forms exhibited similar structure and allergenicity as the natural allergens. However, the recombinant proforms had different structures than the mature forms and showed reduced allergenicity in IgE binding and histamine release assays using patient sera. Molecular modeling suggested the prodomains block major IgE epitopes on the mature allergen surfaces. This indicates the prodomains reduce allergenicity by masking key epitopes.
This summary provides the key information from the document in 3 sentences:
The study investigated the allergenicity of recombinant proforms and mature forms of the house dust mite allergens Der p 1 and Der f 1. It found that the prodomains of Der p 1 and Der f 1, which are cysteine proteases, reduced allergenicity compared to the mature forms. Molecular modeling revealed that the prosegments are anchored at regions on the mature portion that contain major conformational IgE epitopes commonly recognized in patients.
Ameliorative effect of salicin against gamma irradiation inducedRam Sahu
This document summarizes a study that investigated the radioprotective effects of salicin against gamma irradiation-induced changes in the brain tissue of male rats. The study found that salicin administration reduced lipid peroxidation and minimized changes to protein patterns caused by irradiation. Specifically, salicin showed the highest protective effect against irradiation in rats that received salicin treatment after irradiation. However, salicin was not able to fully prevent abnormalities to lipoprotein patterns or quantitative changes to protein bands caused by irradiation. Overall, the results suggest salicin has radioprotective abilities against gamma irradiation effects on various electrophoretic patterns in brain tissue.
This document summarizes a study that evaluated the potential of an adeno-associated virus (AAV) vector delivering a peptide derived from the Nrf2 protein to target the Nrf2 signaling pathway in the retina. The Nrf2 peptide was fused to a cell-penetrating peptide sequence (Tat-peptide) and expressed from an AAV vector. In vitro, the TatNrf2mer peptide induced antioxidant gene expression, blocked IL-1β secretion, and protected cells from oxidative injury. In mouse models, TatNrf2mer expression partially protected photoreceptor function and decreased inflammatory cytokines and cells in models of retinal oxidative injury and uveitis. The results suggest this AAV-delivered TatNrf
The antimicrobial mechanism of ECA water against pseudomonas aeruginosa and ...Trevor William Sievert
This study investigated the antimicrobial mechanism of electrochemically activated water (anolyte) against Pseudomonas aeruginosa and Escherichia coli using SDS-PAGE protein analysis. Bacteria were treated with different concentrations of anolyte and their protein profiles analyzed via SDS-PAGE. Undiluted and 10-1 diluted anolyte were most effective, causing fewer and fainter protein bands compared to untreated bacteria, indicating protein destruction. Dilute anolyte caused extra protein bands, suggesting oxidative stress and protein fragmentation. The results provide insight into anolyte's antimicrobial action by affecting bacterial proteins.
Evaluation of salicin isolated from salix subserrata as a radioprotectorRam Sahu
1) The study investigated the radioprotective effects of salicin, a compound found in willow trees, against gamma radiation damage in rat spleen tissue.
2) Irradiation significantly increased lipid peroxidation in spleen tissue but salicin treatment reduced this effect.
3) Ultrastructural examination found no abnormalities in control or salicin groups but irradiation caused lesions and cell loss, which salicin provided some protection against.
4) Changes to protein and enzyme patterns from irradiation were detected electrophoretically and salicin treatment prevented some of these qualitative effects.
This document summarizes research on a class of compounds called thiazolides and their potential as antiviral agents, specifically against hepatitis B virus (HBV). Key points:
1. Thiazolides show promise as novel antiviral agents that could help treat HBV infections by acting through a non-resistance inducing mechanism. Nitazoxanide is a broad-spectrum thiazolide currently used as an antiparasitic drug.
2. The study synthesized and tested a wide range of thiazolide analogs for anti-HBV activity. Compound 3 showed potent and selective inhibition of HBV replication with low toxicity.
3. Structure-activity relationship analysis found good correlation
The document discusses research into identifying potential ganglioside-binding proteins in Borrelia burgdorferi that causes Lyme disease. Bioinformatics analysis identified VlsE1 as a top hit that is known to be involved in late-stage Lyme disease. VlsE1 was cloned and expressed, and expression studies showed that 0.1 mM IPTG produced the best yield of soluble VlsE1. While some VlsE1 remained insoluble, work is ongoing to optimize expression and purification conditions to study the potential function of VlsE1 in binding gangliosides.
This study investigated the allergenic properties of recombinant pro- and mature forms of the major house dust mite allergens Der p 1 and Der f 1. The recombinant mature forms exhibited similar structure and allergenicity as the natural allergens. However, the recombinant proforms had different structures than the mature forms and showed reduced allergenicity in IgE binding and histamine release assays using patient sera. Molecular modeling suggested the prodomains block major IgE epitopes on the mature allergen surfaces. This indicates the prodomains reduce allergenicity by masking key epitopes.
This summary provides the key information from the document in 3 sentences:
The study investigated the allergenicity of recombinant proforms and mature forms of the house dust mite allergens Der p 1 and Der f 1. It found that the prodomains of Der p 1 and Der f 1, which are cysteine proteases, reduced allergenicity compared to the mature forms. Molecular modeling revealed that the prosegments are anchored at regions on the mature portion that contain major conformational IgE epitopes commonly recognized in patients.
This document discusses a study investigating the potential mutagenic effects of the synthetic food dye tartrazine (E102) using the plant Allium cepa. The results showed that tartrazine caused reductions in mitotic index, increases in mitotic abnormalities, and decreases in DNA and RNA content in A. cepa roots in a concentration- and time-dependent manner. Tartrazine also induced changes to the protein banding pattern in A. cepa seeds. However, administering the antioxidant vitamin C was found to minimize the toxic effects caused by tartrazine. The study demonstrates the genotoxic effects of tartrazine and the protective action of vitamin C against this DNA damage.
Developing DNA topoisomerases as targets for antibacterial chemotherapywarwick_amr
Dr. Sara Henderson
Collaborators:
Dr. Steve Hearnshaw (JIC)
Dr. Ben Bax (GSK)
Dr. Thomas Germe (GSK)
Dr. Sean Ekins (Collaborative Drug Discovery)
Dr. Shantanu Karkare (JNCASR)
Dr. Fred Collin (GSK)
Dr. Natassja Bush (JIC)
Dr. Jenny Pritchard (GSK)
Dr. Clara Franch (GSK)
Funding:
BBSRC, MRC, EU (mm4tb, ENABLE)
Thank you!
42
The document summarizes a study that used an integrated molecular approach to examine the response of the Pacific oyster, Crassostrea gigas, to multiple stressors. The study exposed oysters to copper, a common pollutant, and Vibrio tubiashii, a bacterial pathogen. It measured the expression of genes involved in stress response, including heat shock protein 70 (Hsp70), metallothionein IV, and copper oxidase, at the mRNA and protein levels. The results showed that V. tubiashii inhibited the expression of metallothionein IV and copper oxidase, leaving the oysters more vulnerable to copper toxicity. The study demonstrated how one stressor can compromise an
This document discusses Staphylococcus aureus and antibiotic resistance. It analyzed 34 isolated S. aureus samples from a hospital in China. Antibiotic susceptibility testing found high resistance to erythromycin (95.2%) but no mutations conferring resistance to fusidic acid or mupirocin. Multilocus sequence typing of resistance genes identified mutations in genes related to macrolide and mupirocin resistance in 23 of 28 samples. The overuse of antibiotics is increasing resistance, demonstrating the need for prudent antibiotic use and resistance monitoring to preserve treatment options.
in silico validation of efficacy of phytochemicals from Passiflora edulis sim...Sneya Fernandes
This document summarizes an in silico study validating phytochemicals from Passiflora edulis Sims against SARS-CoV-2. 130 phytochemicals were screened against the SARS-CoV-2 main protease protein using molecular docking. Prulaurasin showed the strongest binding and hydrogen bonding. It and 4 other compounds were analyzed further. Prulaurasin demonstrated the best drug-likeness properties including solubility, pharmacokinetics, and no violations of Lipinski's rules. The study concludes Prulaurasin is the best lead compound and recommends further in vitro and in vivo testing to validate its anti-SARS-CoV-2 activity suggested by in silico screening.
Gabriela Mattos received a BSc in Biochemistry and Molecular Biology from Dalhousie University in 2016, where she conducted honors thesis research on the regulatory role of deubiquitinating enzymes in apolipoprotein B-100 synthesis and degradation under the supervision of Dr. Roger McLeod. She has skills in laboratory techniques and software programs, and is fluent in English, Portuguese, and French. She has experience as a research assistant and has presented her research at conferences. Currently, she works as a banquet server and is seeking opportunities in research.
The document summarizes a study that found two fungi isolated from a Brazilian mangrove forest were able to extracellularly synthesize spherical silver nanoparticles (Ag NP) that were 35±10 nm in size. The Ag NP were characterized through various techniques and showed pronounced antimicrobial activity against pathogenic fungi and bacteria. In particular, Ag NP produced by Aspergillus tubingensis were highly effective at inhibiting Pseudomonas aeruginosa growth. This is the first report of extracellular Ag NP synthesis and antimicrobial properties of Ag NP produced by fungi isolated from a Brazilian mangrove, opening possibilities for obtaining biogenic Ag NP with positive surface potential and new applications.
Evaluation of the coexpressed gene network of dreb2 aAlexander Decker
This document analyzes the coexpressed gene network of DREB2A in Arabidopsis thaliana. DREB2A is involved in responses to drought and salt stress. The network was analyzed using the ATTED-II database. Several genes were found to be closely coexpressed with DREB2A, including heat shock protein 70B (Hsp70b) and a heat stress transcription factor. These interacting genes play important roles in protecting plants from pathogen attack and helping proteins maintain proper folding under heat and salt stress. The expression patterns of DREB2A and four directly connected genes in the network vary across developmental stages and stress conditions, indicating their involvement in maintaining equilibrium under different environmental perturbations.
11.evaluation of the coexpressed gene network of dreb0002www.iiste.org call f...Alexander Decker
This document analyzes the co-expressed gene network of DREB2A in Arabidopsis thaliana. DREB2A is a transcription factor involved in responses to drought and salt stress. The study uses the ATTED-II database to identify genes that are co-expressed with DREB2A. Several of the top co-expressed genes play roles in stress response pathways, such as heat shock proteins Hsp70b and heat stress transcription factors. The co-expressed network reveals that DREB2A interacts with proteins important for protecting plants from pathogens and stress-induced protein denaturation. Analysis of the co-expressed genes' expression patterns under different conditions provides insight into how their coordinated expression helps maintain homeostasis in response to
J. Antimicrob. Chemother.-2014-Aldape-jac-dku325Dustin Heeney
Tigecycline suppresses toxin production and sporulation in Clostridium difficile strains. At subinhibitory concentrations, tigecycline stimulated increased toxin gene expression in both historical and hypervirulent C. difficile strains, but only increased toxin protein production in the historical strain. Tigecycline dramatically suppressed toxin production in the hypervirulent strain. Tigecycline also dose-dependently reduced spore production in both strains. These findings suggest that tigecycline treatment could control C. difficile disease progression and limit its spread by disrupting sporulation and toxin production.
This study screened selected bioflavonoids from medicinal plants as potential inhibitors of the main protease (Mpro) of COVID-19 using molecular docking. Rutin showed the highest binding affinity to Mpro, while resveratol showed the lowest. Nelfinavir and lopinavir, used as standards, also showed strong binding. Apigenin, luteolin, and naringin exhibited good inhibition potential. Further research is needed to validate these bioflavonoids as COVID-19 treatments and investigate their effects on other viral targets.
This study examines the antimicrobial and antibiofilm activity of a 5-kDa peptide fraction isolated from the coelomocytes (immune cells) of the sea urchin Paracentrotus lividus. The peptide fraction, called 5-CC, showed inhibitory activity against both Gram-positive and Gram-negative bacteria, as well as fungi, with minimum inhibitory concentrations ranging from 253.7 to 15.8 mg ml-1. 5-CC also inhibited the formation of Staphylococcus aureus and Staphylococcus epidermidis biofilms. At sub-MIC concentrations, 5-CC inhibited the formation of young (6-hour) and mature (24-hour) biofilms of
Synthesis, Anti-HIV activity and Cytotoxicity of N-Substituted Phthalimide de...pharmaindexing
A series of novel N-substituted phthalimide derivatives were synthesized by reacting phthalic anhydride with primary aromatic amines. The chemical structures of the synthesized compounds were characterized using spectral analysis. The compounds were screened for antiviral activity against HIV-1 and HIV-2 in MT-4 cells and were found to exhibit cytotoxicity with CC50 values ranging from 84-125 μg/ml. None of the compounds showed significant anti-HIV activity.
Antibiotic Susceptibility Pattern of Pyogenic Bacterial Isolates in Sputum.IOSR Journals
Drugs Have Been Used For The Treatment Of Infectious Diseases Since 17th Century , However
Chemotherapy As A Science Has Began With Paul Ehrlich In The First Decade Of 20th Century . Paul Ehrlich
(1854-1915) Was One Of The Earliest Pioneers In The Field Of Antimicrobial Chemotherapy .1Ehrlich
Formulated The Principles Of “Selective Toxicity” ,I.E; Selective Inhibition Of The Growth Of Microorganisms
Without Damage To The Host.2 Resistance Has Been Documented Not Only Against Antibiotics Of
Natural And Semi- Synthetic Origin , But Also Against Purely Synthetic Compounds (Flouroquinolone) Or
Those Which Do Not Even Enter The Cells (Vancomycin) .3 However , The Euphoria Over The Potential
Conquest Of Infectious Diseases Was Short-Lived .Almost As Soon As Antibacterial Drugs Were Deployed ,
Bacteria Responded By Manifesting Various Forms Of Resistance.4 Considered As “Wonder Drugs”
Antibiotics Are Often Prescribed Inappropriately And Inadequately And Have Thus Became One Of The
Highly Abused Agents.5
In vitro experiments of prokaryotic and eukaryotic antimicrobial peptide cyto...AI Publications
These proteinaceous molecules, called antimicrobial peptides (AMPs), are a varied collection of antimicrobial peptides. The ability of AMPs to combat gut infections necessitates further study of the AMP-GI tract interaction. These peptides need to be tested in vitro for cytotoxicity before they may be considered for use in clinical infections. Using the MTT conversion assay, neutral red dye absorption assay, and a comparison to vancomycin, researchers examined the cytotoxicity of gallidermin, nisin A, natural magainin peptides, and melittin in two gastrointestinal cell types (HT29 and Caco-2). Sheep erythrocyte hemolytic activity was also studied, and the influence of AMPs on paracellular permeability was assessed using transepithelial resistance (TEER) and TEM. Gallidermin, nisin A, magainin I, magainin II, and melittin were the least cytotoxic AMPs. To our knowledge, only Melittin and NIS caused considerable hemolysis. There are two distinct ways that melittin and nisin differ in their ability to kill bacteria. It was the only AMP that had an effect on the permeability of the paracellular space. Intestinal tight junctions and cell–cell adhesion were destroyed by long-term melittin therapy, as were microvilli, cell debris, and cell–cell adhesion. Antimicrobial activity and low cytotoxicity make Gallidermin a promising therapeutic drug. The antibacterial properties of Melittin are limited, but its ability to transport poorly bioavailable medicines may be useful.
The study analyzed 100 multidrug-resistant Acinetobacter baumannii isolates from intensive care unit patients in Tehran, Iran between 2006 and 2011 to evaluate changes in genotypic diversity and antimicrobial susceptibility patterns. Resistance to antimicrobials tested increased between 0-30% within 5 years. By 2011, 6-100% of isolates were resistant to each agent tested. Genotypic changes among isolates were also drastic, with novel international clone variants comprising 36% of isolates in 2011. Resistance is growing for last-resort antimicrobials such as colistin and tigecycline.
This document describes research on cloning and expressing the domain III region of the dengue virus envelope protein (DENV EDIII) from serotypes 3 and 4. Key findings include:
1) DENV EDIII from serotypes 3 and 4 were successfully cloned and expressed in E. coli, and the recombinant proteins were purified using nickel affinity and size exclusion chromatography.
2) The purified recombinant EDIII proteins were able to fold correctly and form stable monomers, as shown through analytical methods like SDS-PAGE and gel filtration chromatography.
3) In mouse studies, immunization with the recombinant EDIII proteins, especially when combined with adjuvants, induced strong humoral and cellular immune responses as measured by
This document describes the design, synthesis, and evaluation of novel antimicrobial dipeptidomimetic compounds. A library of linear and branched dipeptidomimetics was created by modifying spermine with tryptophan residues at different positions and with different N-terminal tags. Eight compounds showed good antibacterial activity against methicillin-resistant Staphylococcus aureus (MRSA) and methicillin-resistant Staphylococcus epidermidis. Two lead compounds were nonhemolytic, rapidly bactericidal against MRSA, and did not induce resistance after multiple passages. These compounds were also effective against MRSA biofilms by inhibiting formation and reducing viability of mature biofilms. The membrane interactions and lower
1) O documento descreve um jacaré, que vive na água, é verde e carnívoro, comendo peixes e tendo presas grandes.
2) Ele também tem muitos dentes, pés e a pele pode ser usada para fazer objetos, embora humanos o temam.
3) O jacaré não gosta de humanos.
Carbonaceous fullerene containing mineral shungite andAlexander Decker
This document discusses a mathematical model of the interaction between two natural minerals, shungite and zeolite, with water. Shungite is a carbon-containing mineral found in Russia, while zeolite is an aluminosilicate mineral found in Bulgaria. The minerals were treated with water and their energy spectra were analyzed using non-equilibrium and differential-equilibrium methods. Both shungite and zeolite were found to restructure the hydrogen bond energy between water molecules, increasing local maxima in the differential non-equilibrium spectra. The document proposes uses for these minerals in water treatment and purification due to their adsorption, catalytic, and bactericidal properties.
This document discusses a study investigating the potential mutagenic effects of the synthetic food dye tartrazine (E102) using the plant Allium cepa. The results showed that tartrazine caused reductions in mitotic index, increases in mitotic abnormalities, and decreases in DNA and RNA content in A. cepa roots in a concentration- and time-dependent manner. Tartrazine also induced changes to the protein banding pattern in A. cepa seeds. However, administering the antioxidant vitamin C was found to minimize the toxic effects caused by tartrazine. The study demonstrates the genotoxic effects of tartrazine and the protective action of vitamin C against this DNA damage.
Developing DNA topoisomerases as targets for antibacterial chemotherapywarwick_amr
Dr. Sara Henderson
Collaborators:
Dr. Steve Hearnshaw (JIC)
Dr. Ben Bax (GSK)
Dr. Thomas Germe (GSK)
Dr. Sean Ekins (Collaborative Drug Discovery)
Dr. Shantanu Karkare (JNCASR)
Dr. Fred Collin (GSK)
Dr. Natassja Bush (JIC)
Dr. Jenny Pritchard (GSK)
Dr. Clara Franch (GSK)
Funding:
BBSRC, MRC, EU (mm4tb, ENABLE)
Thank you!
42
The document summarizes a study that used an integrated molecular approach to examine the response of the Pacific oyster, Crassostrea gigas, to multiple stressors. The study exposed oysters to copper, a common pollutant, and Vibrio tubiashii, a bacterial pathogen. It measured the expression of genes involved in stress response, including heat shock protein 70 (Hsp70), metallothionein IV, and copper oxidase, at the mRNA and protein levels. The results showed that V. tubiashii inhibited the expression of metallothionein IV and copper oxidase, leaving the oysters more vulnerable to copper toxicity. The study demonstrated how one stressor can compromise an
This document discusses Staphylococcus aureus and antibiotic resistance. It analyzed 34 isolated S. aureus samples from a hospital in China. Antibiotic susceptibility testing found high resistance to erythromycin (95.2%) but no mutations conferring resistance to fusidic acid or mupirocin. Multilocus sequence typing of resistance genes identified mutations in genes related to macrolide and mupirocin resistance in 23 of 28 samples. The overuse of antibiotics is increasing resistance, demonstrating the need for prudent antibiotic use and resistance monitoring to preserve treatment options.
in silico validation of efficacy of phytochemicals from Passiflora edulis sim...Sneya Fernandes
This document summarizes an in silico study validating phytochemicals from Passiflora edulis Sims against SARS-CoV-2. 130 phytochemicals were screened against the SARS-CoV-2 main protease protein using molecular docking. Prulaurasin showed the strongest binding and hydrogen bonding. It and 4 other compounds were analyzed further. Prulaurasin demonstrated the best drug-likeness properties including solubility, pharmacokinetics, and no violations of Lipinski's rules. The study concludes Prulaurasin is the best lead compound and recommends further in vitro and in vivo testing to validate its anti-SARS-CoV-2 activity suggested by in silico screening.
Gabriela Mattos received a BSc in Biochemistry and Molecular Biology from Dalhousie University in 2016, where she conducted honors thesis research on the regulatory role of deubiquitinating enzymes in apolipoprotein B-100 synthesis and degradation under the supervision of Dr. Roger McLeod. She has skills in laboratory techniques and software programs, and is fluent in English, Portuguese, and French. She has experience as a research assistant and has presented her research at conferences. Currently, she works as a banquet server and is seeking opportunities in research.
The document summarizes a study that found two fungi isolated from a Brazilian mangrove forest were able to extracellularly synthesize spherical silver nanoparticles (Ag NP) that were 35±10 nm in size. The Ag NP were characterized through various techniques and showed pronounced antimicrobial activity against pathogenic fungi and bacteria. In particular, Ag NP produced by Aspergillus tubingensis were highly effective at inhibiting Pseudomonas aeruginosa growth. This is the first report of extracellular Ag NP synthesis and antimicrobial properties of Ag NP produced by fungi isolated from a Brazilian mangrove, opening possibilities for obtaining biogenic Ag NP with positive surface potential and new applications.
Evaluation of the coexpressed gene network of dreb2 aAlexander Decker
This document analyzes the coexpressed gene network of DREB2A in Arabidopsis thaliana. DREB2A is involved in responses to drought and salt stress. The network was analyzed using the ATTED-II database. Several genes were found to be closely coexpressed with DREB2A, including heat shock protein 70B (Hsp70b) and a heat stress transcription factor. These interacting genes play important roles in protecting plants from pathogen attack and helping proteins maintain proper folding under heat and salt stress. The expression patterns of DREB2A and four directly connected genes in the network vary across developmental stages and stress conditions, indicating their involvement in maintaining equilibrium under different environmental perturbations.
11.evaluation of the coexpressed gene network of dreb0002www.iiste.org call f...Alexander Decker
This document analyzes the co-expressed gene network of DREB2A in Arabidopsis thaliana. DREB2A is a transcription factor involved in responses to drought and salt stress. The study uses the ATTED-II database to identify genes that are co-expressed with DREB2A. Several of the top co-expressed genes play roles in stress response pathways, such as heat shock proteins Hsp70b and heat stress transcription factors. The co-expressed network reveals that DREB2A interacts with proteins important for protecting plants from pathogens and stress-induced protein denaturation. Analysis of the co-expressed genes' expression patterns under different conditions provides insight into how their coordinated expression helps maintain homeostasis in response to
J. Antimicrob. Chemother.-2014-Aldape-jac-dku325Dustin Heeney
Tigecycline suppresses toxin production and sporulation in Clostridium difficile strains. At subinhibitory concentrations, tigecycline stimulated increased toxin gene expression in both historical and hypervirulent C. difficile strains, but only increased toxin protein production in the historical strain. Tigecycline dramatically suppressed toxin production in the hypervirulent strain. Tigecycline also dose-dependently reduced spore production in both strains. These findings suggest that tigecycline treatment could control C. difficile disease progression and limit its spread by disrupting sporulation and toxin production.
This study screened selected bioflavonoids from medicinal plants as potential inhibitors of the main protease (Mpro) of COVID-19 using molecular docking. Rutin showed the highest binding affinity to Mpro, while resveratol showed the lowest. Nelfinavir and lopinavir, used as standards, also showed strong binding. Apigenin, luteolin, and naringin exhibited good inhibition potential. Further research is needed to validate these bioflavonoids as COVID-19 treatments and investigate their effects on other viral targets.
This study examines the antimicrobial and antibiofilm activity of a 5-kDa peptide fraction isolated from the coelomocytes (immune cells) of the sea urchin Paracentrotus lividus. The peptide fraction, called 5-CC, showed inhibitory activity against both Gram-positive and Gram-negative bacteria, as well as fungi, with minimum inhibitory concentrations ranging from 253.7 to 15.8 mg ml-1. 5-CC also inhibited the formation of Staphylococcus aureus and Staphylococcus epidermidis biofilms. At sub-MIC concentrations, 5-CC inhibited the formation of young (6-hour) and mature (24-hour) biofilms of
Synthesis, Anti-HIV activity and Cytotoxicity of N-Substituted Phthalimide de...pharmaindexing
A series of novel N-substituted phthalimide derivatives were synthesized by reacting phthalic anhydride with primary aromatic amines. The chemical structures of the synthesized compounds were characterized using spectral analysis. The compounds were screened for antiviral activity against HIV-1 and HIV-2 in MT-4 cells and were found to exhibit cytotoxicity with CC50 values ranging from 84-125 μg/ml. None of the compounds showed significant anti-HIV activity.
Antibiotic Susceptibility Pattern of Pyogenic Bacterial Isolates in Sputum.IOSR Journals
Drugs Have Been Used For The Treatment Of Infectious Diseases Since 17th Century , However
Chemotherapy As A Science Has Began With Paul Ehrlich In The First Decade Of 20th Century . Paul Ehrlich
(1854-1915) Was One Of The Earliest Pioneers In The Field Of Antimicrobial Chemotherapy .1Ehrlich
Formulated The Principles Of “Selective Toxicity” ,I.E; Selective Inhibition Of The Growth Of Microorganisms
Without Damage To The Host.2 Resistance Has Been Documented Not Only Against Antibiotics Of
Natural And Semi- Synthetic Origin , But Also Against Purely Synthetic Compounds (Flouroquinolone) Or
Those Which Do Not Even Enter The Cells (Vancomycin) .3 However , The Euphoria Over The Potential
Conquest Of Infectious Diseases Was Short-Lived .Almost As Soon As Antibacterial Drugs Were Deployed ,
Bacteria Responded By Manifesting Various Forms Of Resistance.4 Considered As “Wonder Drugs”
Antibiotics Are Often Prescribed Inappropriately And Inadequately And Have Thus Became One Of The
Highly Abused Agents.5
In vitro experiments of prokaryotic and eukaryotic antimicrobial peptide cyto...AI Publications
These proteinaceous molecules, called antimicrobial peptides (AMPs), are a varied collection of antimicrobial peptides. The ability of AMPs to combat gut infections necessitates further study of the AMP-GI tract interaction. These peptides need to be tested in vitro for cytotoxicity before they may be considered for use in clinical infections. Using the MTT conversion assay, neutral red dye absorption assay, and a comparison to vancomycin, researchers examined the cytotoxicity of gallidermin, nisin A, natural magainin peptides, and melittin in two gastrointestinal cell types (HT29 and Caco-2). Sheep erythrocyte hemolytic activity was also studied, and the influence of AMPs on paracellular permeability was assessed using transepithelial resistance (TEER) and TEM. Gallidermin, nisin A, magainin I, magainin II, and melittin were the least cytotoxic AMPs. To our knowledge, only Melittin and NIS caused considerable hemolysis. There are two distinct ways that melittin and nisin differ in their ability to kill bacteria. It was the only AMP that had an effect on the permeability of the paracellular space. Intestinal tight junctions and cell–cell adhesion were destroyed by long-term melittin therapy, as were microvilli, cell debris, and cell–cell adhesion. Antimicrobial activity and low cytotoxicity make Gallidermin a promising therapeutic drug. The antibacterial properties of Melittin are limited, but its ability to transport poorly bioavailable medicines may be useful.
The study analyzed 100 multidrug-resistant Acinetobacter baumannii isolates from intensive care unit patients in Tehran, Iran between 2006 and 2011 to evaluate changes in genotypic diversity and antimicrobial susceptibility patterns. Resistance to antimicrobials tested increased between 0-30% within 5 years. By 2011, 6-100% of isolates were resistant to each agent tested. Genotypic changes among isolates were also drastic, with novel international clone variants comprising 36% of isolates in 2011. Resistance is growing for last-resort antimicrobials such as colistin and tigecycline.
This document describes research on cloning and expressing the domain III region of the dengue virus envelope protein (DENV EDIII) from serotypes 3 and 4. Key findings include:
1) DENV EDIII from serotypes 3 and 4 were successfully cloned and expressed in E. coli, and the recombinant proteins were purified using nickel affinity and size exclusion chromatography.
2) The purified recombinant EDIII proteins were able to fold correctly and form stable monomers, as shown through analytical methods like SDS-PAGE and gel filtration chromatography.
3) In mouse studies, immunization with the recombinant EDIII proteins, especially when combined with adjuvants, induced strong humoral and cellular immune responses as measured by
This document describes the design, synthesis, and evaluation of novel antimicrobial dipeptidomimetic compounds. A library of linear and branched dipeptidomimetics was created by modifying spermine with tryptophan residues at different positions and with different N-terminal tags. Eight compounds showed good antibacterial activity against methicillin-resistant Staphylococcus aureus (MRSA) and methicillin-resistant Staphylococcus epidermidis. Two lead compounds were nonhemolytic, rapidly bactericidal against MRSA, and did not induce resistance after multiple passages. These compounds were also effective against MRSA biofilms by inhibiting formation and reducing viability of mature biofilms. The membrane interactions and lower
1) O documento descreve um jacaré, que vive na água, é verde e carnívoro, comendo peixes e tendo presas grandes.
2) Ele também tem muitos dentes, pés e a pele pode ser usada para fazer objetos, embora humanos o temam.
3) O jacaré não gosta de humanos.
Carbonaceous fullerene containing mineral shungite andAlexander Decker
This document discusses a mathematical model of the interaction between two natural minerals, shungite and zeolite, with water. Shungite is a carbon-containing mineral found in Russia, while zeolite is an aluminosilicate mineral found in Bulgaria. The minerals were treated with water and their energy spectra were analyzed using non-equilibrium and differential-equilibrium methods. Both shungite and zeolite were found to restructure the hydrogen bond energy between water molecules, increasing local maxima in the differential non-equilibrium spectra. The document proposes uses for these minerals in water treatment and purification due to their adsorption, catalytic, and bactericidal properties.
This document reviews approaches for colon-specific drug delivery (CDDS). It compares earlier approaches like prodrugs, pH-dependent systems, and microbial-triggered systems, which had limitations, to newer approaches like pressure-controlled colonic delivery capsules, CODESTM, and osmotic controlled drug delivery (ORDS-CT) systems. These novel approaches are unique in achieving in vivo site specificity and feasibility of manufacturing. Factors that must be considered in colon targeted drug delivery system design include anatomy and physiology of the colon, pH levels in different colon regions, colonic microflora and enzymes, transit of materials through the colon, and drug absorption in the colon.
This document provides a summary of a short story called "Two Kinds" by Amy Tan. It is told through the perspective of Jing-Mei Woo, a young Chinese-American girl, and her mother Suyuan Woo. The summary focuses on their daily lives - Suyuan works long hours at a Chinese restaurant while trying to push Jing-Mei to succeed academically. Jing-Mei struggles to meet her mother's high expectations. Their neighbor, Mr. Chong, provides help and support to both Suyuan and Jing-Mei. The story explores their mother-daughter relationship and experiences navigating two cultures.
Jerry Brunetti is a cancer survivor who rejected chemotherapy in favor of improving his diet and immune system. He focused on detoxifying heavy metals from his body, consuming fermented and nutrient-dense foods like raw dairy, and boosting vitamins A and D which are important for cancer recovery. Jerry believes environmental toxins, viruses, and an immune system weakened by poor nutrition contributed to his cancer diagnosis. He advocates holistic farming practices that produce healthy, nutritious food to prevent disease.
This document provides details about Stop 1 of the field trip - the H-Area Seepage Basin Extraction, Treat and Re-Injection Project at the Savannah River Site. It describes how unlined seepage basins were previously used to dispose of wastewater from separations facilities until 1988. Groundwater monitoring showed contamination with tritium, nitrate, heavy metals and radionuclides. The project extracts contaminated groundwater from the area, treats it to remove contaminants, and then re-injects the treated water back into the aquifer. The goal is to reduce contaminant levels in the groundwater plume.
This document provides an introduction to pollution prevention and regulations for small quantity generators of hazardous waste. It encourages generators to implement pollution prevention techniques to reduce their generation of hazardous waste, noting the financial and liability benefits of doing so. The document outlines the federal and state regulatory requirements that apply to small quantity generators if they produce hazardous waste above certain thresholds. These include requirements for proper waste accumulation, storage, disposal, recordkeeping, and reporting.
Bio h2o2 International produces a hydrogen peroxide product called Bio h2o2 that is stabilized with an organic polyalcohol instead of toxic chemicals like benzene and silver. Standard hydrogen peroxide decomposes over time, reducing its effectiveness and potentially creating safety hazards, but Bio h2o2 is more stable. Unlike standard hydrogen peroxide, Bio h2o2 is non-toxic, biodegradable, and safe for use in applications like plant protection, livestock disease prevention, water treatment, and food decontamination.
This study evaluated the efficacy of Hydrated Sodium Calcium Aluminosilicate (HSCAS) and turmeric powder, individually and combined, to counteract the toxic effects of aflatoxin in broiler chickens. Five groups of 100 broiler chicks each were fed either an uncontaminated diet, an aflatoxin-contaminated diet, or an aflatoxin-contaminated diet supplemented with HSCAS, turmeric powder, or both. Treatment with HSCAS or turmeric powder alone improved performance and reduced organ damage compared to the untreated contaminated group. Both additives also improved immune response and biochemical parameters in contaminated birds. The study concludes that adding HSC
Raman study of the polarizing forces promoting catalysis in 4 chlorbenzoyl-co...John Clarkson
J. Clarkson, P.J. Touge, K.L. Taylor, D. Dunaway-Mariano & P.R. Carey, “Raman Study of the Polarizing Forces Promoting Catalysis in 4-Chlorbenzoyl-CoA Dehalogenase”, Biochemistry, 36, 10192-10199, 1997.
This document discusses computational modelling of the metalloenzyme cytochrome P450 TxtE to understand its mechanism for nitrating L-tryptophan. Quantum mechanical calculations were performed on ferric superoxide and nitric oxide, as well as L-tryptophan and nitrogen dioxide, to observe how nitration occurs. QM/MM calculations using ONIOM were also set up to model the active site of the full P450 TxtE enzyme. The results provide insight into whether neutral or positive nitrogen dioxide is involved in the nitration reaction catalyzed by this enzyme.
Possible Toxicity of Glyphosate and Links to AutismAfonte4
Glyphosate, the active ingredient in Roundup herbicide, inhibits the shikimate pathway in both plants and bacteria. This pathway is responsible for the production of aromatic amino acids like tryptophan and phenylalanine. When ingested, glyphosate can disrupt gut bacteria in humans by inhibiting this pathway. This can lead to decreased production of important neurotransmitters and signaling molecules as well as vitamin deficiencies. Imbalances in gut bacteria from glyphosate exposure cause similar gastrointestinal issues seen in autism. While not proven, it is possible that disrupting the shikimate pathway through increased glyphosate use could contribute to the symptoms of autism spectrum disorder by impacting amino acid production and microbiome
Proton pump inhibitors present and future a reviewGulzar Alam
This document provides an overview of proton pump inhibitors (PPIs), including a brief history of their development and their use in treating acid-related disorders. It discusses the physiology of acid secretion in the stomach and the discovery of the proton pump. It also summarizes several acid-related disorders like ulcers, GERD, and Zollinger-Ellison syndrome that are treated by inhibiting acid secretion. The document reviews the clinical significance and advantages of PPIs compared to previous drugs while also mentioning some limitations and efforts to develop new treatments.
This document provides an overview of chemistry concepts including:
- The SI system and units such as meters, kilograms, and moles.
- Properties of pure substances like physical properties that can be observed without changing composition versus chemical properties involving changes in composition.
- Stoichiometry principles where chemical equations represent mole ratios in chemical reactions and can be used to calculate amounts of reactants and products.
- Gas laws including Boyle's, Charles', and Gay-Lussac's laws describing the relationships between gas properties of pressure, volume, temperature and amount.
This study examined the residues of the pesticide endosulfan in the milk of goats following ingestion of endosulfan through their diet. 12 goats were divided into 3 groups - a control group and two treatment groups that received either 15 mg or 30 mg of endosulfan per goat, daily, for 25 days. Milk samples were collected and analyzed for endosulfan residues. Residues gradually increased during treatment and peaked on the last day, then declined after treatment ended. The half-life of decline was approximately 8.67-8.88 days. There were no significant effects on feed intake, milk yield, milk composition or blood parameters in the treated goats.
This document provides an overview of matter and its different states. It begins by defining matter as anything that has mass and occupies space. It then discusses the particulate nature of matter and describes the three common states of matter - solids, liquids, and gases. It explains the characteristic properties of each state, including how solids have a definite shape but liquids and gases do not. Temperature and pressure can cause changes between the different states. The document also introduces the concepts of elements, compounds, and mixtures as different ways of classifying matter based on its chemical composition.
Determination of temperature regions in thermal degradation of ligninMichal Jablonsky
In this paper, industrial lignins were characterized by elemental analysis (EA) and thermogravimetry (TG). The aim was to find the main intervals of lignin degradation and maximum rate of their degradation. The results obtained can be helpful in finding the applicability of the materials at their thermal decomposition. The differences between individual lignins have been confirmed by EA and TG.
This document provides an overview and analysis of Prakash Chand Baliwal's internship project at GAIL (India) Limited in Vijaipur, Madhya Pradesh. The project involved studying the propane refrigeration unit and analyzing naphtha losses at the loading gantry. Key points include:
- Baliwal successfully completed his internship from June 20th to July 21st, where he studied the LPG extraction process and operation of equipment at the Vijaipur gas processing plant.
- The project calculated the refrigeration capacity of the plant's evaporators and condensers, and analyzed the work done by compressors. It also studied naphtha leakage at the loading gantry
Structural Studies on Pyrene-Based Blue-Light Emitting Molecules and Ion-Sens...Thomas Warwick
The document discusses structural studies performed on six calixarenes and two pyrene-based blue light emitting molecules. Single crystal X-ray diffraction experiments were conducted to determine the absolute structures of the crystalline samples. The results include structures that appear optimized and poorly optimized for their intended purposes as ion sensors or light emitters, with discussion of reasons why and discovery of 2:1 host-guest binding behavior for a thiacalixarene.
RESEARCH BRAIN 07 Ameliorative Potential of Sitagliptin and/or Calcipotriol o...AHMED ASHOUR
Background: Alzheimer's disease (AD) is a progressive neuropsychiatric disorder that causes
dementia. It mostly affects people older than 65 years. The exact mechanisms of AD are not
fully understood but affection of apoptosis, oxidative stress and neuroinflammation may be
contributing factors. Aim: To evaluate the ability of sitagliptin and/or calcipotriol to attenuate
lipopolysaccharide (LPS)-induced AD in mice and to elucidate their possible mechanisms of
action. Methods: Sixty male Balb/c mice were divided into 6 equal groups: Control; LPS; LPS
+ carboxymethyl cellulose; LPS + Sitagliptin; LPS + Calcipotriol; and LPS + Sitagliptin +
Calcipotriol group. Behavioral tests, tissue catalase (CAT), superoxide dismutase (SOD) and
thiobarbituric acid derivatives (TBARS) were assessed. Also, tissue transforming growth factor
beta-1 (TGF-1), ec ac aa (TNF-) ad ee 6 (IL-6) were
determined. Parts of the hippocampus were subjected to histopathological,
immunohistochemical and electron microscopic examination. Results: Administration of
sitagliptin and/or calcipotriol prior to LPS injection induced significant increase in the
recognition index, tissue CAT and SOD associated with significant decrease in tissue TBARS,
TNF-, IL-6 and TGF-1 ad ca ee e aca,
immunohistochemical and electron microscopic picture compared to LPS group. These changes
were significant in sitagliptin/calcipotriol combination group compared to the use of each of
these drugs alone. Conclusion: Sitagliptin/calcipotriol combin
The document summarizes a study on the protein profiles of gamma ray irradiated blood stages of Plasmodium berghei, the malaria parasite, for developing a malaria vaccine candidate. Key findings include:
1) Protein profiles differed between infected and uninfected blood, indicating exported parasite proteins. Higher irradiation doses and dose rates resulted in more protein bands.
2) A dose of 150 Gy and dose rate of 380 Gy/hour altered protein profiles the most for vaccine development.
3) Protein profiles depended on parasite density in blood and differed between P. berghei and other rodent malaria species.
4) Profiles were unaffected by infection duration but depended on parasite composition in blood stages. Altered proteins could
Cloning and Expression of Outer Membrane Protein Omp38 Derived from Aeromonas hydrophila in Escherichia coli
http://dx.doi.org/10.21276/SSR-IIJLS.2019.5.3.8
Does allicin combined with vitamin B-complex have superior potentials than al...Prof. Hesham N. Mustafa
BACKGROUND:
The current article aims to explore the protective potentials of α-tocopherol alone and the combination of allicin and vitamin B-complex against lead-acetate neurotoxicity on the cerebellar cortex.
MATERIALS AND METHODS:
Forty rats were divided into four groups (n=10). Group 1 was the control group. Group 2 received 10 mg/kg body weight (BW) of lead acetate. Group 3 was exposed to 10 mg/kg BW of lead acetate plus a combination of allicin (100 mg/kg BW) and vit. B-complex (40 mg/kg BW). Group 4 was administered lead acetate (10 mg/kg BW) and α-tocopherol (100 mg/kg BW). The animals received treatment for sixty days by oral gavage. All the groups were studied ultrastructurally and immunohistochemically with glial fibrillary acidic protein (GFAP).
RESULTS:
The affected groups revealed shrunken and degenerated Purkinje cells with irregular nuclei. The cytoplasm comprised several lysosomes, unhealthy mitochondria, and dilated Golgi saccules. The myelinated nerve fibers demonstrated breaking of the myelin sheaths, apparent vacuoles, and broad axonal spaces. Immunohistochemically, there was a tremendous surge in GFAP-positive astrocytes in the lead acetate-treated group. These histological and ultrastructural variations were ameliorated by the administration of α-tocopherol and the combination of allicin and vit. B complex. Moreover, an apparent decrease in the number of GFAP-positive astrocytes was obvious in the protected groups.
CONCLUSIONS:
Although both α-tocopherol and the combination of allicin and vit. B-complex can be used as possible adjuvant therapies to ameliorate nervous system ailments attributable to lead acetate, α-tocopherol showed more protective potential.
KEYWORDS:
Allicin; Astrocytes; GFAP; Myelin Figure; Oligodendrocyte; Purkinje cells
This document describes research into using the recombinant dense granule antigen GRA7 from Toxoplasma gondii for serodiagnosis of toxoplasmosis. The GRA7 gene was amplified from T. gondii genomic DNA and inserted into an expression vector. The recombinant GRA7 protein was expressed in E. coli and purified. Western blot analysis showed human sera reacted with the 29 kDa rGRA7 antigen. ELISA tests using rGRA7 showed sensitivity of 96% for IgM detection and 89% for IgG detection, with specificity of 90% for both, demonstrating its potential usefulness for toxoplasmosis diagnosis.
1) Mice lacking the gene encoding miR-122a (Mir122a-/- mice) developed steatohepatitis, fibrosis, and hepatocellular carcinoma at a high frequency and in a sex-dependent manner similar to humans.
2) Mir122a-/- mice exhibited impaired lipid metabolism including reduced expression of the microsomal triglyceride transfer protein MTTP, contributing to steatosis.
3) Restoring MTTP or miR-122a expression in Mir122a-/- mice reduced disease manifestations by reversing steatosis, inflammation, and fibrosis and improving liver function.
This document discusses research on the effects of omalizumab (anti-IgE therapy) treatment in patients with severe persistent asthma over 4 years. It lists 15 publications by the author on outcomes related to omalizumab therapy, including effects on oxidative stress markers, cytokines, quality of life, and side effects. The author has studied how omalizumab impacts factors involved in coagulation, fibrinolysis, angiogenesis and inflammation.
IRF5 Promotes the Progression of Hepatocellular Carcinoma and is Regulated by...JohnJulie1
The IRF family of proteins involves in the tumor progression. However, but the functions of IRF5 in the tumorigenesis are largely unknown. Here, IRF5 was found to be up-regulated in hepatocellular carcinoma (HCC). Interfering with IRF5 inhibited the growth and tumorigenic ability of HCC cells.
IRF5 Promotes the Progression of Hepatocellular Carcinoma and is Regulated by...NainaAnon
1. The study found that IRF5 was upregulated in hepatocellular carcinoma (HCC) tissues compared to normal tissues based on mRNA and protein levels.
2. Overexpression of IRF5 promoted the growth and colony formation of HCC cells in vitro, while silencing IRF5 inhibited HCC cell growth and proliferation.
3. TRIM35 was found to interact with and promote the degradation of IRF5. TRIM35 expression was negatively correlated with IRF5 levels in HCC clinical samples.
IRF5 Promotes the Progression of Hepatocellular Carcinoma and is Regulated by...daranisaha
The IRF family of proteins involves in the tumor progression. However, but the functions of IRF5 in the tumorigenesis are largely unknown. Here, IRF5 was found to be up-regulated in hepatocellular carcinoma (HCC). Interfering with IRF5 inhibited the growth and tumorigenic ability of HCC cells. When studying the molecular mechanism, it was found that TRIM35 interacted with IRF5, promoting the ubiquitination and degradation of IRF5. In the clinical specimens of HCC, TRIM35 was negatively correlated with the expression of IRF5. These observations reveal the oncogenic function of IRF5 in the progression of HCC, suggesting that IRF5 is a promising target for the therapy of HCC.
IRF5 Promotes the Progression of Hepatocellular Carcinoma and is Regulated by...semualkaira
The IRF family of proteins involves in the tumor progression. However, but the functions of IRF5 in the tumorigenesis are largely unknown. Here, IRF5 was found to be up-regulated in hepatocellular carcinoma (HCC). Interfering with IRF5 inhibited the growth and tumorigenic ability of HCC cells. When studying the molecular mechanism, it was found that TRIM35 interacted with IRF5, promoting the ubiquitination and degradation of IRF5. In the clinical specimens of HCC, TRIM35 was negatively correlated with the expression of IRF5. These observations reveal the oncogenic function of IRF5 in the progression of HCC, suggesting that IRF5 is a promising target for the therapy of HCC.
IRF5 Promotes the Progression of Hepatocellular Carcinoma and is Regulated by...eshaasini
The IRF family of proteins involves in the tumor progression. However, but the functions of IRF5 in the tumorigenesis are largely unknown. Here, IRF5 was found to be up-regulated in hepatocellular carcinoma (HCC). Interfering with IRF5 inhibited the growth and tumorigenic ability of HCC cells. When studying the molecular mechanism, it was found that TRIM35 interacted with IRF5, promoting the ubiquitination and degradation of IRF5. In the clinical specimens of HCC, TRIM35 was negatively correlated with the expression of IRF5. These observations reveal the oncogenic function of IRF5 in the progression of HCC, suggesting that IRF5 is a promising target for the therapy of HCC.
IRF5 Promotes the Progression of Hepatocellular Carcinoma and is Regulated by...semualkaira
The IRF family of proteins involves in the tumor progression. However, but the functions of IRF5 in the tumorigenesis are largely unknown. Here, IRF5 was found to be up-regulated in hepatocellular carcinoma (HCC). Interfering with IRF5 inhibited the growth and tumorigenic ability of HCC cells. When studying the molecular mechanism, it was found that TRIM35 interacted with IRF5, promoting the ubiquitination and degradation of IRF5. In the clinical specimens of HCC, TRIM35 was negatively correlated with the expression of IRF5. These observations reveal the oncogenic function of IRF5 in the progression of HCC, suggesting that IRF5 is a promising target for the therapy of HCC.
IRF5 Promotes the Progression of Hepatocellular Carcinoma and is Regulated by...semualkaira
The IRF family of proteins involves in the tumor progression. However, but the functions of IRF5 in the tumorigenesis are largely unknown. Here, IRF5 was found to be up-regulated in hepatocellular carcinoma (HCC). Interfering with IRF5 inhibited the growth and tumorigenic ability of HCC cells. When studying the molecular mechanism, it was found that TRIM35 interacted with IRF5, promoting the ubiquitination and degradation of IRF5. In the clinical specimens of HCC, TRIM35 was negatively correlated with the expression of IRF5. These observations reveal the oncogenic function of IRF5 in the progression of HCC, suggesting that IRF5 is a promising target for the therapy of HCC.
The document describes a study that used functional genomics to discover the molecular basis of colistin resistance in Shewanella algae MARS 14. Researchers constructed a genomic expression library of S. algae MARS 14 in E. coli and screened it to select clones resistant to colistin. Sequencing of the resistant clones identified a unique gene, ethanolamine phosphotransferase (EptA), in all clones. EptA overexpression was found to confer colistin resistance by modifying LPS and increasing 27-fold in expression in S. algae MARS 14.
This study investigated the effects of antioxidant supplementation on lipid profiles and hematological parameters in malaria-induced albino rats. Rats were infected with malaria parasites and treated with anti-malarial drugs. They were divided into three groups: Group A received antioxidants (foods), Group B received nutraceuticals, and Group C served as the control. After 12 weeks, hematological parameters like PCV, WBC, RBC, and HGB significantly increased more in Groups A and B compared to Group C. Lipid levels like TG and LDL also significantly increased more in Groups A and B versus Group C. However, CHOL and HDL levels non-significantly decreased more in Groups A and B versus Group C.
IOSR Journal of Pharmacy and Biological Sciences(IOSR-JPBS) is an open access international journal that provides rapid publication (within a month) of articles in all areas of Pharmacy and Biological Science. The journal welcomes publications of high quality papers on theoretical developments and practical applications in Pharmacy and Biological Science. Original research papers, state-of-the-art reviews, and high quality technical notes are invited for publications.
Isolation, in vitro antidiabetic, antioxidant activity and molecular docking ...iosrjce
The document describes the isolation and characterization of two pentacyclic triterpenoids, friedelin and 3β-friedelinol, from the stem bark of Syzygium alternifolium. The compounds were tested for their antidiabetic and antioxidant activities. Friedelin and 3β-friedelinol showed significant inhibition of α-glucosidase and α-amylase enzymes, decreasing plasma glucose levels and demonstrating antidiabetic effects. They also exhibited antioxidant properties by scavenging free radicals in the DPPH inhibition assay. Molecular docking studies confirmed the binding of friedelin and 3β-friedelinol to α-glucosidase and
Antimicrobial Susceptibility Pattern, Biochemical Characteristics and Biotypi...albertdivis
The current study was attempted to investigate the effect of biofield treatment on Salmonella paratyphi A (S. paratyphi A) in terms of antimicrobial susceptibility assay, biochemical characteristics and biotyping.
This document summarizes a study that evaluated the use of a recombinant Toxoplasma gondii surface antigen 1 (SAG1) for the serodiagnosis of acute and chronic Toxoplasma infections in humans. The researchers cloned the SAG1 gene from T. gondii genomic DNA and expressed the recombinant protein in E. coli. They then used the recombinant SAG1 antigen in ELISA tests to detect IgM and IgG antibodies in human sera, comparing it to a commercial ELISA kit. The recombinant SAG1 ELISA showed 93% sensitivity and 95% specificity for IgG detection, and 87% sensitivity and 95% specificity for IgM detection, demonstrating its potential as a diagnostic tool for toxoplasmosis
2. protect against disease development [5e7]. ES-62 activity is
dependent on an unusual post-translational attachment of phos-
phorylcholine (PC) [reviewed in Ref. [8]] and indeed PC attached to
ovalbumin [6] or albumin [9] can mimic ES-62 in protecting against
CIA. As a consequence of this, we hypothesized that it could be
possible to synthesize novel small drug-like PC-based molecular
analogues (SMAs) that mimic ES-62 activity: indeed, recently we
produced a sulfone termed 11a that protects against CIA and ap-
pears to do so using the same mechanism of action as ES-62,
namely inhibiting TLR-mediated pro-inflammatory cytokine re-
sponses, by partially downregulating MyD88 expression [9]. Here,
we describe another novel sulfone, 12b, which also inhibits disease
development in mice sensitized and challenged with collagen, but
which contains additional previously unsuspected immunomodu-
latory properties. In particular, we have found 12b to modulate the
expression of a number of genes associated with the inflammatory
response, particularly those linked to IL-1b signalling, and which
appear to be counter-regulated by activation of the transcription
factor, NRF2 that plays a crucial cytoprotective role in the response
to oxidative stress [10]. SMA-12b may thus be prototypic of a novel
class of compounds of use in treating RA, in particular in those
patients resistant to TNF-targeting biologics [11].
2. Materials and methods
2.1. Animals
Jirds and mice were bred and/or maintained in the Biological
Services Units of the Universities of Glasgow and Strathclyde in
accordance with Home Office UK Licenses PPL60/3119, PPL60/3580,
PPL60/3791, PPL60/4300, PIL60/12183 and PIL60/12950 and the
permission of the Ethics Review Board of both Universities.
Collagen-induced arthritis (CIA) was induced in male DBA/1 mice
(8e10 weeks old; Harlan Olac; Bicester, UK) by intradermal im-
munization with bovine type II collagen (CII, MD Biosciences) in
complete Freund's adjuvant (FCA) and mice were treated with
purified endotoxin-free 12b (1 mg/dose) or PBS subcutaneously on
days À2, 0 and 21 and scored for development of arthritis as pre-
viously described [5e7]. In addition, the therapeutic effects of 12b
were tested where following the onset of arthritis (mean score
3.25 ± 0.55), mice were treated subcutaneously with PBS or 12b
(1 mg/dose) every 3 days (d0, d3 and d6). The Nrf2À/À
animals that
were created by Itoh et al. [12] and provided kindly by Ken Itoh and
Masayuki Yamamoto were backcrossed over six generations onto a
C57BL/6 background.
2.2. Chemical synthesis and preparation of SMAs
Endotoxin-free ES-62 and SMAs-11a, -12b and -19o (for struc-
tures see Supplemental Fig. 1) were prepared as described previ-
ously, with the SMAs to !95% purity as shown by HPLC and 1
H
NIMR [7,9,13]. The SMAs were reconstituted at 100 mg/ml in cell
culture-tested dimethyl sulfoxide (DMSO; SigmaeAldrich) and
then diluted in RPMI medium, or PBS when used in vivo, to 1 mg/ml
and stored in microcentrifuge tubes at À20 C. Compounds were
filter-sterilised using a Millex-GP (0.22 mm; Millipore) filter unit
prior to use in culture. All reagents and plasticware used were
sterile and pyrogen free.
2.3. Analysis of pathology and IL-1b expression in the joint
Decalcified joint tissue section (7 mm) preparation, Haematox-
ylin and Eosin (H E) and Trichrome staining and detection via
immunofluorescence were performed as previously described
[7,13]. The extent of synovitis, pannus formation, and destruction of
bone and cartilage was determined using a graded scale: grade 0,
no signs of inflammation; grade 1, mild inflammation with hyper-
plasia of the synovial lining and minor cartilage damage; grades 2
through 4, increasing degrees of inflammatory cell infiltrate and
destruction of bone and cartilage. To detect IL-1b expression, sec-
tions were incubated with sodium citrate buffer (10 mM Sodium
Citrate, 0.05% Tween 20, pH 6.0) for antigen retrieval and stained
with a rabbit anti-mouse IL-1b antibody (Abcam; rabbit IgG isotype
control) with DAPI as a counterstain, at 4 C for 12 h, followed by
detection using a biotinylated goat anti-rabbit IgG antibody and
streptavidineAlexa Fluor 647. Immunofluorescence images were
obtained using an LSM 510 META confocal laser coupled to an
Axiovert 200 microscope (Zeiss) and analysed by Zeiss LSM Image
Browser software.
2.4. Ex vivo analysis
Draining lymph node (DLN) cells (106
/ml) were
incubated ± 50 ng/ml PMA plus 500 ng/ml ionomycin for 1 h before
addition of 10 mg/ml Brefeldin A (SigmaeAldrich, UK) for a further
5 h at 37 C with 5% CO2. Live cells were discriminated by the LIVE/
DEAD fixable aqua dye (Invitrogen) and phenotypic markers were
labelled using anti-CD4-PerCP, anti-CD8-FITC or anti-gd-PE (Bio-
Legend) antibodies before the cells were fixed and permeabilised
using BioLegend protocols. Cells were then labelled using anti-
IFNg-Pacific Blue or anti-IL-17A-APC (BioLegend) antibodies for
30 min prior to flow cytometry and gated according to appropriate
isotype controls as described previously [7]. IL-12p40 and IL-17
levels in serum or DLN, bmM and peritoneal exudate cell (PEC)
supernatants were detected by ELISA using kits from BioLegend as
described previously [7] whilst levels of IL-1b were determined by
ELISA using kits from eBioscience according to the manufacturer's
recommendations.
2.5. In vitro analysis of bone marrow-derived macrophages (bmMs)
Macrophages were prepared from bone marrow progenitor cells
obtained from 6- to 8-wk-old male BALB/c mice and DBA/1 mice
with CIA or C57BL/6, MyD88 and NRF2 knockout mice. Bone
marrow progenitor cells were cultured for 7 days at 37/5% CO2 in
complete Dulbecco's modified Eagle's medium (DMEM; GIBCO)
supplemented with 20% L929 cell culture supernatant (contains
CSF-1), 10% heat-inactivated Fetal Calf Serum (HI FCS), 2 mM L-
glutamine (GIBCO), 50 U/ml penicillin (GIBCO) and 50 mg/ml
streptomycin (GIBCO) with fresh medium being added on day 4
[14]. The cells were analysed by flow cytometry, and were shown
routinely to be !99% positive for CD11b and F4/80 markers.
BmMs were cultured in RPMI medium (PAA Laboratories) sup-
plemented with 10% HI FCS, 2 mM L-glutamine, 50 U/ml penicillin
and 50 mg/ml streptomycin (complete RPMI) in triplicate (2 Â 105
cells/well) in 96-well plates and were rested overnight prior to
exposure to the indicated concentration of SMAs for 18 h. In some
experiments, bmMs were then stimulated with either Salmonella
minnesota lipopolysaccharide (100 or where indicated, 1000 ng/ml
LPS; Sigma), BLP (10 ng/ml Pam3CSK4; Axxora Ltd) or CpG
(0.01 mM; Source Bioscience Autogen) for 24 h and cell superna-
tants analysed for cytokine production by ELISA. ELISAs were per-
formed according to the manufacturer's instructions, using paired
antibodies from BD Bioscience Pharmingen for IL-12p40 and IL-6
and RD systems for IL-1b.
2.6. TransAm (NFkB p65)
BmMs were cultured in 6 well plates (4 Â 106
cells/well) in
complete RPMI medium. After 24 h, the medium was changed and
J. Rzepecka et al. / Journal of Autoimmunity 60 (2015) 59e7360
3. the cells were pretreated with or without SMAs (5 mg/ml) for 18 h
before being stimulated with 100 ng/ml LPS, 100 ng/ml BLP or 1 mM
CpG for 1 h. Treatment with the SMAs alone did not activate NFkB
p65 (results not shown). Activated NFkB p65 was measured in
nuclear fractions (isolated using a Nuclear Extraction Kit; Active-
Motif) by the ELISA-based TransAM kit (ActiveMotif) according to
the manufacturer's instructions.
2.7. Flow cytometric analysis of cell death
Cell death was determined by 7-Amino Actinomycin D (7-AAD;
BD Pharmingen) staining of bmMs after stimulation with com-
pounds 12b and 19o. bmMs (2 Â 105
/well) were pretreated with
SMAs (5 mg/ml) for 18 h prior to being stimulated with either
100 ng/ml S. minnesota LPS (Sigma), 100 ng/ml BLP (Pam3CSK4) or
0.01 mM CpG for 24 h. The ability of the compounds to spontane-
ously induce cell death was also tested. The cells were washed in
PBS containing 1% FCS, then subsequently incubated with 5 mL of 7-
AAD for 10 min on ice in the dark. Flow cytometry was conducted
using a FACS Canto immunocytometry system (Becton Dickinson
Pharmingen) and data were processed using FlowJo software (Tree
Star Inc., OR USA).
2.8. Laser scanning cytometry (LSC)
BmMs (104
/well) from mice with CIA treated with either PBS or
12b (1 mg/ml) were incubated for 18 h in Lab-Tek chamber slides
(Nunc) before being stimulated with LPS (100 ng/ml) for 15 min
then fixed with 4% formaldehyde for 15 min [15]. Samples were
quenched with 50 mM ammonium chloride (Fisher Scientific) for
10 min, washed, permeabilised with 0.1% Triton X-100 (Sigma) in
PBS for 20 min and then washed and incubated for 20 min with PBS
containing 1% BSA and 10% normal goat serum (Sigma). Cells were
then incubated with anti-phospho-p65 (pp65; Cell Signalling) or
the relevant isotype control rabbit IgG (Santa Cruz Biotech Inc) in
PBS containing 1% BSA and 10% normal goat serum overnight at
4 C. The cells were washed, and incubated with fluorescein-
conjugated anti-rabbit IgG (Vector Laboratories) at 10 mg/ml in 1%
BSA, 10% normal goat serum in PBS for 1 h in the dark. Cells were
washed and stained with DAPI (Invitrogen) as a counterstain. Cells
were washed again, and the slides mounted in Vectashield (Vector
Laboratories) for analysis by LSC. LSC data were analysed using
WinCyte software (CompuCyte). Using the relocation feature of the
LSC, areas with the average representative fluorescence were
relocated to and digital images of the stained cells were obtained
using a Hammamatsu camera and Openlab software (Improvision)
[15].
2.9. Cell lysates and Western blotting
BmMs (2 Â 106
cells/sample) were lysed by the addition of ice-
cold, modified RIPA buffer (50 mM Tris, pH 7.4, 150 mM sodium
chloride, 2% (v/v) NP-40, 0.25% (w/v) sodium deoxycholate, 1 mM
EGTA, 1x Halt protease and phosphatase inhibitors [Pierce]) and
solubilised on ice for 30 min. Protein (30 mg) samples were resolved
on the XCell SureLock Mini-Cell kit with NuPAGE Novex high-
performance pre-cast Bis-Tris gels and NuPAGE buffers and re-
agents (Invitrogen Life Technologies). Proteins were transferred to
nitrocellulose (Amersham) or PVDF (Millipore, Watford, UK) and
membranes were blocked by incubating for 1 h in 5% non-fat milk
in TBS/Tween (0.5 M NaCl and 20 mM Tris pH7.5 with 0.1% (v/v)
Tween-20) at RT. Membranes were incubated with primary anti-
body diluted in 5% BSA in TBS/Tween buffer overnight at 4 C,
washed with TBS/Tween and incubated with the appropriate
horseradish peroxidase (HRP)-conjugated secondary antibody in
5% non-fat milk in TBS/Tween for 1 h at RT. Membranes were then
washed with TBS/Tween and protein bands were visualised using
the ECL detection system. Quantification of the bands was per-
formed using ImageJ software (National Institute of Health, NIH).
2.10. Microarray
BmMs (2 Â 106
cells/well in 6-well plates) were incubated with
medium, 12b, 19o (both 5 mg/ml) or ES-62 (2 mg/ml) for 4 h. Cells
were harvested into RLT buffer and RNA prepared using the RNeasy
Mini kit (Qiagen) and residual DNA cleared with DNaseI (Invi-
trogen), according to the manufacturers' protocols. Checking of
RNA quality, cDNA preparation and microarray were performed at
the Glasgow Polyomics Facility at the University of Glasgow using
standard Affymetrix protocols. Triplicate biological replicates were
hybridised to Affymetrix Mouse Gene 1.0 ST arrays representing
over 28,000 genes. Bioinformatical data analysis was commis-
sioned in the Bioinformatic Services Miltenyi Biotec GmbH (Ber-
gisch-Gladbach, Germany). Briefly, raw microarray data were
preprocessed using GC-RMA method and corrected for batch effect.
The normalized log2 intensities values were centered to the median
of all samples for each transcript cluster ID, i.e. the median was
subtracted from each individual log2 expression value. Such ratio
data in log2 space were used to create heat maps in which red
shading indicates a stronger expression of the representative gene
in comparison to the median of the total sample, and green rep-
resents a relative downregulation, respectively. Next, the different
samples were compared to each other by a correlation analysis in
order to get an impression of inter-sample similarity or variability.
The obtained inter-experiment correlation coefficients based on
the normalized log2 intensities were generated for all samples and
displayed in clustered images. Positive correlation is indicated by
shades of yellow (higher correlation ¼ brighter color), while less
well correlated samples are indicated by shades of black. In order to
select differentially regulated transcripts between SMA-12b-
stimulated and unstimulated samples the following selection
criteria were applied: adjusted p value 0.1 (calculated by the
method of Benjamini and Hochberg) and at least 1.5-fold expres-
sion difference. All differentially expressed genes were analysed
through the use of IPA (Ingenuity®
Systems, www.ingenuity.com)
software to detect up-stream regulators (transcription factors, TF)
that may be responsible for the observed changes in the gene
expression using experimentally observed relationships between
TFs and genes. The IPA TF analytical tool determines a z-score that
establishes whether gene-expression changes for known targets of
each TF are consistent with what is reported as “activation” in the
literature (z 0, TF predicted as “activated”), or if the changes
reflect inhibition as described in the literature (z 0, TF predicted
as “inhibited”). Z-scores greater than 2 or -2 are considered sig-
nificant. Next, all of the significantly down-regulated TFs i.e. RelA,
NFkB1 and HMGB1 were displayed as a network to graphically
represent the molecular relationships between molecules. Mole-
cules are represented as nodes, and the biological relationship
between two nodes is represented as a line. All relationships are
supported by at least one reference from the literature, from a
textbook, or from canonical information stored in the Ingenuity
Knowledge Base. The intensity of the node color indicates the de-
gree of up- (red) or down- (green) regulation. Nodes are displayed
using various shapes that represent the functional class of the gene
product. For signalling pathways, an arrow pointing from node A to
node B indicates that A causes B to be activated (e.g. by binding,
phosphorylation, dephosphorylation, etc) and for ligands/receptors
pathways: an arrow pointing from a ligand to a receptor signifies
that the ligand binds the receptor and subsequently leads to acti-
vation of the receptor. This binding event does not necessarily
J. Rzepecka et al. / Journal of Autoimmunity 60 (2015) 59e73 61
4. directly activate the receptor; activation of the receptor could be
caused by events secondary to the ligand/receptor-binding event.
Solid lines indicate direct interactions whereas dotted lines, indi-
rect interactions.
2.11. qRT-PCR
Total RNA was extracted using an RNeasy plus kit (Qiagen) and
1 mg of RNA was used to synthesize cDNA (Applied Biosystems).
TaqMan®
RT-PCR was performed using the following TaqMan®
Gene
Expression Assays: IL-1b (Mm01336189_m1), chemokine receptor
5 (CCR5: Mm01216171_m1), chemokine receptor 2 (CCR2: Mm00
438270_m1), chemokine ligand 10 (CXCL10; Mm00445235_m1),
complement component 5a receptor 1 (C5AR1; Mm00500292_s1),
CD274 (PD-L1) (Mm00452054_m1), CD200 receptor 1 (CD200R1:
Mm02605260_s1), NLRP3 (Mm00840904_ml), NLRC4
(Mm01233149_ml), glutamate-cysteine ligase, modifier subunit
(GCLM; Mm00514996_ml), glutamate-cysteine ligase, catalytic
subunit (GCLC: Mm00802655_ml) and haem oxygenase 1 (HMOX1;
Mm00516005_ml), all from Applied Biosystems. Polymerase chain
reactions were performed in triplicate in a StepOne sequence de-
tector (Applied Biosystems). Data analysis was performed using the
Applied Biosystems sequence detection software and samples were
normalized to the reference reporter mouse glyceraldehyde 3-
phosphate dehydrogenase (GAPDH; Mm99999915_g1) endoge-
nous control.
2.12. Statistical analysis of data
Parametric data were analysed by the unpaired one-tailed Stu-
dent's t test or by 1-way ANOVA. Normalised data were analysed by
the KruskaleWallis test whilst the ManneWhitney test was used
for analysis of clinical CIA scores where *p 0.05, **p 0.01 and
***p 0.001.
3. Results
3.1. SMA-12b protects against CIA
We have recently provided proof of concept that screening of
PC-based compounds for their ability to suppress TLR2-, TLR4- and
TLR9-mediated production of Th1/Th17-promoting cytokines (IL-
12p40 and IL-6) by macrophages allows the selection of SMAs, such
as the sulfone 11a, that mimic the ability of ES-62 to protect against
CIA by suppressing pathogenic IFNg and IL-17 production [9].
Although another sulfone, 12b, could also significantly reduce IL-
12p40 secretion, it was not as effective with respect to IL-6 [9].
Nevertheless, it was found to be as effective as ES-62 [5e7,13] and
11a [9] in preventing the development of arthritis in the prophy-
lactic CIA mouse model, as indicated by reduction in each of
articular score (Fig. 1A), hind paw width (Fig. 1B) and disease
incidence (Fig. 1C; score !2). Furthermore, importantly as with ES-
62 [5] and SMA-11a (unpublished), when SMA-12b was adminis-
tered therapeutically after the onset of arthritis; it protected against
further disease development (Fig. 1D).
Consistent with the in vitro screening studies, whilst 12b- or
PBS-treated mice undergoing CIA in the prophylactic model did not
display altered numbers of leukocytes in the peritoneal exudate
(PEC; Fig. 1E) or frequencies of macrophages within this population
(Fig. 1F) when compared to healthy naïve mice, we observed
significantly elevated levels of IL-12p40 in the peritoneal fluid of
mice undergoing CIA that were reduced to the levels observed in
naïve mice by in vivo exposure to 12b (Fig. 1G). Similarly, the low
levels of IL-12p40 spontaneously secreted ex vivo by DLN cells were
reduced to levels comparable to those produced by naive cells, in
cultures derived from 12b-treated mice undergoing CIA (Fig. 1H).
However, unlike ES-62 and 11a, SMA-12b did not suppress the
number of total DLN cells or CD4þ
, CD8þ
and gd T cells (Fig. 1I and
results not shown). Moreover, although there was a trend towards
reduction in the number of IFNg-producing DLN cells, specifically
CD4þ
, CD8þ
and gd T cells following PMA/Ionomycin stimulation,
this did not reach statistical significance (Fig. 1J and results not
shown). Furthermore, 12b did not reduce the number of PMA/
ionomycin-stimulated DLN or CD4þ
or gd T cells that were
capable of producing IL-17 (Fig. 1K and results not shown) or lower
the serum levels of IL-17 in mice undergoing CIA (Fig. 1L). This lack
of modulation of IL-17/IFNg responses in vivo was rather surprising
as IL-12p40, as a component of both IL-12p70 and IL-23, is a ther-
apeutic target (ustekinumab) in inflammatory autoimmune dis-
eases [16,17] due to its ability to promote differentiation and/or
maintenance of Th1 and Th17 cells. Nevertheless, these studies
demonstrated that despite exhibiting some potential to suppress
the cytokine milieu associated with Th17/Th1-driven pathogenesis
in arthritis, both in vitro and in vivo, the protection afforded by 12b
did not appear to depend on suppressing the Th17/Th1 phenotype
associated with pathogenesis in CIA.
3.2. SMA-12b modulates inflammatory response gene expression in
bmMs
To investigate the mechanism(s) underlying the protection
against CIA afforded by SMA-12b, genome-wide microarray of
macrophages was undertaken. Bioinformatical analysis revealed
that whilst ES-62 and an SMA, 19o, that had been found not to
modulate TLR-driven proinflammatory cytokine production in the
in vitro screens [9], essentially did not alter the gene expression
profile, treatment of macrophages with 12b for 4 h resulted in 364
genes being up-regulated and 496 genes being down-regulated in
comparison to un-stimulated cells (a complete list of the affected
genes and associated information provided by Ingenuity Pathway
Analysis is shown in Supplementary Table 1). Indeed, tree structure
analysis of sample clusters according to their degree of similarity
shows that only 12b-stimulated cells clearly separated from the
three other experimental conditions (Fig. 2A), with the 30 most
down- and up-regulated genes shown (Fig. 2B). Furthermore, it was
noted that when examining all of the data, a number of genes of
possible relevance to RA were affected (Supplementary Table 2). For
example, several associated with pro-inflammatory cytokine re-
sponses (e.g., IL-1b) and cell migration and recruitment, particu-
larly of monocytes (e.g., NR4A1, CXCL10, CXCL3, CCR2, CX3CR1 and
TREM) were down regulated and many of these were members of
the top 30 downregulated genes. At the same time, some genes that
play an inhibitory role in inflammation e.g., CD200R1 and CD274
(PD-L1) and have recently been identified as therapeutic targets in
RA [18,19] were up-regulated. The data for a number of these key
genes have been validated by qRT-PCR (Fig. 2C).
3.3. SMA-12b inhibits the secretion of IL-1b
IL-1b was found to be the most downregulated gene in bmMs
exposed to SMA-12b (Supplementary Tables 1 and 2) and so we
next attempted to obtain evidence linking this effect of the SMA to
the release of IL-1b. First, we determined whether 12b inhibited
LPS-mediated secretion of IL-1b by bmMs and this was found to be
the case (Fig. 3A). We then investigated mice undergoing CIA and
found that DLN cells from SMA-12b-treated mice displayed
reduced ConA-stimulated IL-1b production relative to cells from
mice undergoing CIA treated with PBS or from naïve mice (Fig. 3B).
Finally, crucially it was found that staining of IL-1b production in
the joint reveals that this is greatly inhibited in mice that show
J. Rzepecka et al. / Journal of Autoimmunity 60 (2015) 59e7362
5. reduced disease development as a consequence of exposure to 12b
(Fig. 3CD).
3.4. SMA-12b is predicted to target transcription factors
To identify the transcription factors potentially responsible for
the observed SMA-12b-mediated changes in macrophage gene
expression, we used IPA for Transcription Factors (TFs). This soft-
ware predicted, based on prior knowledge of expected effects be-
tween transcriptional regulators and their known target genes, the
activation z-scores of 3 TFs - RelA (À2.996), NFkB1 (À2.223) and
HMGB1 (À2.168) to be significantly inhibited by SMA 12b and 6 TFs,
NFE2L2 (NRF2; 3.630), NKX2-3 (3.300), CBFB (2.630), TRIM24
(2.611), RXRA (2.213) and DACH1 (2.000) to be significantly acti-
vated. The TF with the lowest activation z-score and therefore the
most inhibited by 12b was RelA, the p65 signalling element of the
NFkB pathway. Consistent with this, we found that SMA-12b in-
hibits p65 NFkB activation in bmMs stimulated with each of TLR2
(BLP), TLR4 (LPS) and TLR9 (CpG) ligands in vitro (Fig. 4A). More-
over, exposure of mice undergoing CIA to 12b in vivo resulted in
bmMs with reduced capacity for phosphorylation and consequent
activation of p65 (pp65) in response to stimulation with LPS ex vivo
(Fig. 4B). RelA-regulated genes with changes in their mRNA levels
following exposure of cells to 12b that correlated with inhibition of
RelA are shown in Fig. 4C and include IL-1b, as reported earlier the
most repressed gene amongst all those tested in the microarray
Fig. 1. SMA-12b protects against CIA in an IL-17-independent manner. Development of CIA by (A) Mean Arthritis Score (PBS, n ¼ 15; 12b, n ¼ 13; data pooled from 2 independent
experiments) and (B) hind paw width (PBS, n ¼ 7; 12b, n ¼ 6; data from single experiment), where results are expressed as mean scores ± SEM for PBS or 12b-treatment groups of
collagen-exposed mice. Incidence (C), indicated by % of mice developing a severity score !2 is shown (PBS, n ¼ 15; 12b, n ¼ 13). (D) Following development of arthritis (d0), mice
were treated every 3 days with PBS or 12b (both n ¼ 6) and score for each mouse normalised to that at day 0. Peritoneal cavity cells were counted (E) (PBS, n ¼ 11; 12b, n ¼ 12; naive,
n ¼ 6) and frequency of F4/80þ
cells determined by FACS (F) (PBS, n ¼ 13; 12b; n ¼ 12, naive, n ¼ 5). Peritoneal fluid was concentrated and IL-12p40 measured by ELISA (G) (PBS,
n ¼ 14; 12b, n ¼ 10; naive, n ¼ 7). For E-G, each value represents data from individual mice with data pooled from two independent experiments. (H) IL-12p40 spontaneously
released by DLN cells from mice undergoing CIA and treated as indicated are shown where data are presented as the mean values of individual mice from one experiment (naïve,
n ¼ 3; PBS, n ¼ 7; 12b, n ¼ 6). (I) Total numbers of DLN cells of individual mice from the naïve (n ¼ 3), PBS-treated (n ¼ 14) and 12b-treated (n ¼ 13) groups are shown. (J) The
number of IFNg-expressing DLN cells and (K), IL-17-expressing DLN cells following stimulation with PMA/ionomycin from individual mice is shown (naïve, n ¼ 3; PBS, n ¼ 12; 12b,
n ¼ 12). (L) Serum IL-17 levels are plotted as mean values of triplicate IL-17 analyses from individual mice (PBS, n ¼ 14; 12b, n ¼ 13). *p 0.05; **p 0.01 and ***p 0.001.
J. Rzepecka et al. / Journal of Autoimmunity 60 (2015) 59e73 63
6. (Supplementary Table 1). As mentioned above, IPA also projected
inhibition of activity of another member of the NFkB family, namely
NFkB1 (Fig. 4C), the 105 kD protein that is processed to produce the
p50 TF and consistent with this, 12b down-regulated transcript
levels of a number of NFkB1-dependent genes (Fig. 4C). Many genes
whose expression was changed by SMA-12b and whose direction of
change supported inhibition of RelA were present in this group of
genes confirming that these two TFs act in concert to regulate gene
expression levels and are both 12b targets. Collectively, these data
suggest that 12b acts to suppress the hyperactive NF-kB (p65 and
p50) signalling that promotes recruitment of inflammatory cells
and generation of pro-inflammatory mediators such as IL-1b in RA
joints [20].
To address the mechanisms responsible for suppressing NF-kB
signalling, we turned to the TFs that were predicted by the IPA to be
activated by SMA-12b (Fig. 4D) and, on the basis of the changes in
the expression profile of their target genes, NFE2L2 (NRF2) was
ascribed the highest activation score. Interestingly, therefore, given
the convergence of hypoxia, reactive oxygen species (ROS) and the
inflammasome in promoting the inflammation and angiogenesis
that leads to joint damage in RA [21e25], a large group of genes,
involved in protection against oxidative stress and controlled by
this TF were up-regulated by SMA-12b (Supplementary Tables 1
and 2). For example, 12b drove increased expression of genes tak-
ing part in synthesis, regeneration and utilization of glutathione
such as GCLM, GCLC, SLC7A11, GSTA3 and GSR (Fig. 4D). In addition,
SMA-12b also increased mRNA levels of TXNRD1 and PRDX1, which
are engaged in thioredoxin production, regeneration and utiliza-
tion, as well as NQO1 and HMOX1 that play a role in quinone
detoxification and iron sequestration, respectively.
That NF-kB-associated TFs and NRF2 were inversely targeted
was particularly interesting as there is evidence in the literature
that these elements counter-regulate [26,27] and also that NRF2
protects against joint damage in the antibody-induced arthritis
(AIA) model of RA by limiting oxidative stress-induced cartilage
destruction [28]. By contrast, crosstalk between NF-kB and
Fig. 2. SMA-12b modulates gene expression in bmMs. (A) The tree structure indicates clusters of samples according to their degree of similarity. Positive correlation is indicated by
shades of yellow (higher correlation ¼ brighter colour), while less well correlated samples are indicated by shades of black. The colour bar on top of the tree indicates the treatment
group assignment: green, none; blue, 12b; red, 19o and yellow, ES-62, of samples from 3 independent experiments. (B) Excerpt of a clustered heat map (Euclidean distance,
complete linkage) showing 30 most down-regulated and 30 most up-regulated reporters in triplicate samples from 3 independent experiments (aec) of 12b-treated macrophages
compared to un-treated cells (medium). (C) Microarray data were validated for selected target genes by qRT-PCR where the levels of the gene of interest were normalized to the
level of GAPDH and expressed as a fold change for 12b (and 19o) with respect to the medium control. Data shown are means from three biological replicates.
J. Rzepecka et al. / Journal of Autoimmunity 60 (2015) 59e7364
7. Fig. 3. SMA-12b inhibits IL-1b production. (A) BmMs from BALB/c mice pre-treated with the indicated concentration (mg/ml) of 12b or medium alone were then stimulated with LPS
(1 mg/ml) and IL-1b release determined by ELISA. Data presented are the mean values ± SD for replicate cultures (medium, n ¼ 7; none, n ¼ 6; 12b(0.2), n ¼ 4; 12b(1), n ¼ 8 and
12b(5), n ¼ 8) from 3 individual mice (except for 12b(0.2) cultures where data were only obtained for 2 mice). (B) DLN cells from naive DBA/1 mice or DBA/1 mice undergoing CIA
treated with either PBS or 12b were stimulated with ConA (1 mg/ml) and levels of released IL-1b determined. Data shown are the mean values for individual mice (naive, n ¼ 3; PBS,
n ¼ 7; 12b, n ¼ 6). (C) Joint sections from individual mice representative of each treatment group were assessed for histopathology (10Â magnification; H E and Trichrome
staining; scale bars 100 mm, no zoom) and also IL-1b expression by immunofluorescence (magnification 20Â: scale bars 200 mm and scan zoom 0.7; 40Â: scale bars 100 mm and scan
zoom 0.7 for naive and 1.5 for PBS and 12b). Isotype controls were negative and the strong IL-1b staining in the naïve (40Â) image reflects high production of IL-1b (31kD) by
keratinocytes in the portion of skin in the section included as an additional control for validation of the antibody specificity. Parameters of histopathology were scored (D) with the
data presented as mean values from individual mice ± SEM (n ¼ 14 for PBS-; n ¼ 12 for 12b-treatment groups). *p 0.05; **p 0.01 and ***p 0.001.
8. Fig. 4. SMA-12b inhibits TLR-induced NFkB activation in macrophages. (A) BmMs were pre-incubated for 18 h with SMAs (5 mg/ml) and then stimulated with 100 ng/ml LPS, 10 ng/ml
BLP or 1 mM CpG for 1 h. “None” represents no SMA pre-treatment and “medium”, no PAMP treatment. p65 activation was measured by the TransAM assay and data presented are
mean values ± SEM from three independent experiments, *p 0.05; **p 0.01 (B) BmM from CIA mice treated with PBS or 12b were incubated with medium or LPS (100 ng/ml) and
assessed for expression of pp65 (green) against a DAPI (blue) nuclear counterstain. Histograms are presented showing gating of pp65þ
cells relative to the isotype control; the
increase in pp65 expression by LPS-treated cells relative to that in unstimulated bmMs and the levels of pp65 expression in LPS-stimulated bmMs derived from CIA mice exposed to
PBS or 12b (200 individual cells/group) were analysed. Data are then presented as the mean values ± SD, n ¼ 3, of the difference in mean fluorescence integral (DMFI) of LPS-
stimulated cells relative to their medium controls. IPA prediction of 12b-mediated down-regulation of RelA/NFkB1 (C) and up-regulation of NRF2 NFE2L2; (D) signalling based on
expression of their target genes by microarray analysis is shown. Genes down-regulated or up-regulated by 12b are shown in green and red, respectively.
9. Hypoxia-Inducible Factors (HIFs) has been shown to be arthrito-
genic [21]. It was therefore decided to further explore, including a
comparison with SMA-11a, whether SMA-12b inversely targeted
key NF-kB- (IL-1b, inflammasome genes) and NRF2- (HMOX1, GCLC
and GCLM) dependent genes that may play roles in counter-
regulating inflammation in RA.
3.5. SMA-12b modulates transcript levels of IL-1b/inflammasome
and NRF2-controlled genes
Inflammasomes are closely associated with IL-1b as they form
molecular platforms that drive the proteolytic cleavage by caspase-
1, which results in release of bioactive IL-1b. Indeed, ROS-
dependent NF-kB signalling via the NLRP3 inflammasome has
been implicated in IL-1b-mediated pathogenesis in RA [22,23]. It
was therefore interesting that in addition to IL-1b being the gene
most repressed by 12b, the SMA down-regulated, albeit not as
profoundly, levels of genes encoding several inflammasome mol-
ecules, including NLRP3 (À1.51 vs unstimulated) and NLRC4 (À1.69
vs unstimulated) (Supplementary Tables 1 and 2). We therefore
further explored the modulation of IL-1b and these inflammasome
genes in macrophages by SMA-12b and also, for comparison, the
effects of 11a (both at 5 mg/ml; Fig. 5AeC). This confirmed that 12b
downregulated steady-state expression of IL-1b and NLRC4 mRNA
within 4 h but this was not the case for 11a. Moreover, whilst both
SMAs downregulated NLRP3 expression within 4 h, significant
suppression of NLRP3 mRNA was observed at 2 h with 12b, but not
with 11a. We next investigated the effects of 11a and 12b on the
mRNA levels of IL-1b and the inflammasome genes after simulta-
neous exposure of the cells to a pro-inflammatory stimulus, in this
case, LPS (Fig. 5DeF). Under these pro-inflammatory conditions,
12b, but not 11a, also suppressed LPS-mediated upregulation of IL-
1b and NLRP3. Although, 12b did not significantly inhibit the
transient LPS-mediated upregulation of NLRC4, levels of this
inflammasome component were reduced below basal levels within
4 h under all LPS-stimulated conditions tested. These differential
effects may reflect that, for example, unlike NLRP3 that requires
additional pro-inflammatory signals including bacterial TLR ligands
Fig. 5. SMA-12b downregulates genes associated with production of bioactive IL-1b in bmMs. The effect of exposure of bmMs to SMAs-11a and -12b (both at 5 mg/ml) over 4 h on the
steady state- and LPS-induced mRNA levels of IL-1b (A D); NLRP3 (B E) and NLRC4 (C F) as assessed by qRT-PCR where the levels of the gene of interest were normalized to the
level of GAPDH and expressed as a fold change with respect to the medium control. Data are presented as the means ± SEM of the mean of replicate values pooled from 3 individual
experiments. *p 0.05; **p 0.01 and ***p 0.001. Black* represent significance between 12b (or 11a) and control whereas grey* represents significant differences between 12b-
and 11a-treated cells.
J. Rzepecka et al. / Journal of Autoimmunity 60 (2015) 59e73 67
10. for full induction, NLRC4 exhibits high levels of expression under
steady-state conditions, and hence exposure to LPS may induce
confounding effects in this case [24].
Likewise, as the IPA analysis revealed that SMA-12b increased
levels of many antioxidant genes controlled by the transcription
factor NRF2 (Fig. 6A), we assessed whether 12b and 11a (both at
5 mg/ml) differentially modulated the expression levels of HMOX1
(the most up-regulated gene from the antioxidant family) and two
genes, GCLC and GCLM that are crucially involved in biosynthesis of
glutathione, under steady-state and pro-inflammatory (LPS-TLR4
signalling) conditions. Consistent with the microarray data,12b, but
not 11a, was able to strongly upregulate expression of all 3 genes
between 2 and 4 h (Fig. 6BeD). By contrast, LPS acted to down-
regulate HMOX1, GCLC and GCLM expression: however, this was
prevented by 12b and indeed, even in the presence of LPS, this SMA,
but not 11a, was able to induce their expression (Fig. 6EeG).
3.6. SMA-12b suppresses IL-1b and inflammasome genes via NRF2
NRF2 and NF-kB have been reported to counter-regulate gene
induction and consistent with this, 12b downregulated NF-kB-
regulated IL-1b and inflammasome genes whilst up-regulating
expression of NRF2-controlled anti-oxidant genes (Figs. 5 and 6).
We therefore hypothesised that deficiency in NRF2 could inhibit
the ability of 12b to dampen-down genes classically known to
depend on NFkB e.g. IL-1b. As predicted, while 12b significantly
down-regulated the levels of IL-1b mRNA in a dose-dependent
manner in bmM from WT mice, this was not apparent in NRF2
KO macrophages (Fig. 7A). Similarly, the 12b-induced down-
regulation in the levels of NLRP3 and NLRC4 (Fig. 7B and C) was
shown to be NRF2-dependent, as there was no significant differ-
ences in the mRNA levels of these genes between control and 12b-
treated bmM from NRF2 KO mice, although it should be noted that
NRF2 deficiency itself appeared to impact on the steady-state levels
of NLRP3 and particularly, perhaps mimicking the effects of LPS,
NLRC4 expression. NRF2-deficiency was validated by the suppres-
sion of 12b-mediated induction of GCLC observed in WT bmM
(Fig. 7D). Of note, the counter-regulation of inflammasome and
anti-oxidant genes that we are witnessing appears to be associated
with SMA-12b protection against CIA as analysis showed increased
levels of mRNA for GCLC (129%) and HMOX (121%) yet reduced
levels of NLRP3 (74%) in splenocytes from 12b-treated relative to
PBS-treated mice with CIA.
We next investigated the ability of 12b to suppress LPS-
production of IL-1b in NRF2-deficient bmM and found it to be
lost (Fig. 8A). By contrast, 12b-mediated inhibition of LPS-
stimulated IL-12p40 or IL-6 production remained intact despite
NRF2 deficiency (Fig. 8A results not shown). This latter result
presumably reflects that 12b, similarly to the parent molecule ES-
62 and SMA-11a [9], downregulates steady-state levels of MyD88
Fig. 6. SMA-12b upregulates mRNA levels of anti-oxidant genes that are NRF2 targets. (A) IPA prediction of 12b-mediated activation of NRF2 cytoprotective/anti-oxidant pathways
based on 12b-modulation of expression of NRF2 target genes as assessed by microarray analysis. The effect of exposure of bmMs to SMAs-11a and -12b over 4 h (both at 5 mg/ml) on
the steady state- and LPS-induced mRNA levels of HMOX1 (B E); GCLC (C F) and GCLM (D G) as assessed by qRT-PCR where the levels of the gene of interest were normalized
to the level of GAPDH and expressed as a fold change with respect to the medium control. Data are presented as the means ± SEM of values pooled from 3 individual experiments.
*p 0.05; **p 0.01 and ***p 0.001. Black* represent significance between 12b (or 11a) and control whereas grey* represents significant differences between 12b- and 11a-treated
cells.
J. Rzepecka et al. / Journal of Autoimmunity 60 (2015) 59e7368
11. expression in bmM (Fig. 8B; for 12b, 67.68 ± 8.34% of medium
alone levels where n ¼ 3 and p 0.05). By contrast, we have
recently reported that LPS upregulates MyD88 expression in
bmMs [9], and in two further independent experiments we have
shown that pre-exposure to 12b also resulted in downregulation
of MyD88 expression in LPS-treated bmM (Fig. 8C and D). In
addition to being essential for TLR4-mediated IL-12p40 production
by bmMs [29], MyD88 is required for LPS-induction of IL-1b as
well as for the NF-kB-mediated induction of NLRP3 and IL-1b by
TLRs important in CIA/RA, such as TLR2 [30e32] and IL-1R [33,34]
that do not couple via the TRIF, MyD88-independent pathway
[35]: thus, we investigated whether 12b-mediated inhibition of IL-
1b production was also associated with downregulation of MyD88
signalling. This revealed that although steady-state levels of IL-1b
mRNA (Fig. 8E) are partially reduced by MyD88 deficiency, expo-
sure to 12b resulted in a further reduction in levels. Steady-state
levels of NLRP3, NLRC4, GCLC and HMOX1 expression and their
modulation by 12b were predominantly independent of MyD88
expression (Fig. 8E and results not shown). Thus with respect to
IL-1b, these data suggest that SMA 12b acts to inhibit pathogenic
production of this cytokine by a dual-pronged mechanism,
involving downregulation of MyD88 in addition to upregulation of
NRF2 activation and converging at the level of the inflammasome
(Fig. 8F).
4. Discussion
ES-62 is an immunomodulatory molecule secreted by the filarial
nematode, A. viteae that exerts anti-inflammatory effects on both
the innate and adaptive arms of the immune response to promote
parasite survival and, as a consequence, exhibits therapeutic po-
tential in a number of autoimmune and allergic inflammatory
disorders [36]. However, due to being a large and potentially
immunogenic protein, ES-62 is in reality not suitable for develop-
ment as a therapy. Nevertheless, its anti-inflammatory activity is
due to post-translational decoration with PC, allowing us to
recently construct a library of drug-like compounds based around
this active PC moiety as a potential starting point in the develop-
ment of novel anti-inflammatory drugs as therapies in autoimmune
inflammation.
The sulfone SMA-12b was selected for screening for anti-
inflammatory actions in the mouse CIA model on the basis that
its ability to inhibit PAMP-induced IL-12p40 and to a lesser degree
IL-6 production should dampen down subsequent Th1/Th17
polarisation [9], a phenotype associated with pathology in this
model [7,37]. This strategy has recently provided proof of concept
with respect to the protective actions of the related SMA, 11a [9].
Like ES-62 and 11a, SMA-12b was found to afford protection against
CIA in both prophylactic and therapeutic studies but detailed
analysis of the former revealed that even allowing for 12b's reduced
effectiveness at lowering IL-6 responses, such protection clearly did
not appear to reflect the significant suppression of Th1/Th17 re-
sponses that had been noted with 11a.
As an approach to understanding how SMA-12b might be pro-
tecting against CIA in the light of its limited effects on Th1/Th17
responses, we turned to microarray analysis employing bmMs. This
indicated that 12b was able to suppress IL-1b and associated
inflammasome gene expression and also production of IL-1b
Fig. 7. SMA-12b-mediated changes in gene expression are abrogated in NRF2-deficient bmMs. The effect of exposure (4 h) of bmMs from wild type and NRF2-deficient (NRF2 KO)
C57BL/6 mice to SMA-12b on the mRNA levels of IL-1b (A; n ¼ 5); NLRP3 (B; n ¼ 5); NLRC4 (C; n ¼ 6) and GCLC (D; n ¼ 6) as assessed by qRT-PCR. The levels of the gene of interest
were normalized to GAPDH and expressed as a fold change with respect to the relevant wild type medium control. Data are presented as the means ± SEM, where n represents
matched replicate cultures of individual wild type and KO mice. *p 0.05; **p 0.01 and ***p 0.001 where significance is for WT SMA treatments relative to the wild type “none”
condition as indicated by black* and grey* indicates significance between “none” WT and “none” KO samples.
J. Rzepecka et al. / Journal of Autoimmunity 60 (2015) 59e73 69
12. protein. Moreover, analysis of the joints of CIA mice successfully
treated with SMA-12b indicated a reduction in the level of IL-1b-
expressing cells in the synovium. This represents a key finding
given the importance of this cytokine in induction of pathology in
both CIA [38] and RA [39] as evidenced by the effectiveness of IL-1-
targeting biologics such as anakinra in suppressing the infiltration
of inflammatory cells and joint damage in RA patients [33]. Sub-
sequent IPA for Transcription factors (TF) helped provide an
explanation for the effect on IL-1b by revealing that NF-kB signal-
ling, which can promote both IL-1b production and effector re-
sponses and has been implicated in joint pathogenesis in CIA [20],
was likely to be inhibited by SMA-12b and this was confirmed by
functional analysis, both in vitro and ex vivo. At the same time, IPA
indicated activation of NRF2; a key component of the response to
oxidative stress [40,41]. This result was consistent with the obser-
vation that the two TFs are known to counter-regulate each other
[26,27,42] and indeed NRF2À/À
mice were subsequently employed
to show the importance of this TF to the inhibitory effects on pro-
duction of the NF-kB target, IL-1b.
A key question is how SMA-12b is able to promote NRF2 acti-
vation. Like 12b, SMA-11a can cause inhibition of NF-kB [9] but it
does not appear to activate NRF2 (Fig. 6). The major difference
between 11a and 12b is that the latter is a quaternary ammonium
salt as opposed to a tertiary amine, a structural difference that
would be expected to have a substantial influence both on binding
to receptors (through differences in hydrogen bonding ability and
steric bulk) and on access to cells and cellular compartments (12b is
permanently positively charged). The 4-substituent on the benzene
ring (bromo in 11a and methyl in 12b) is also significantly different,
particularly in terms of size, and might also influence receptor
binding. However the most plausible explanation for the difference
in effect on NRF2 is that 12b but not 11a is likely to be converted by
b-elimination within the cell to a vinyl sulfone [43], a structure
recently shown to cause activation of NRF2 [44]. The 12b-derived
vinyl sulfone, as an electrophile, could in theory interact with thiol-
groups on cysteine residues of the NRF2 repressor protein, Keap-1,
and based on recent ideas reported in the literature [45] this could
cause a conformational change that would allow release of NRF2,
and translocation to the nucleus to drive expression of target genes
such as HMOX1 which, like NRF2 itself [28], has been shown to be
protective against inflammatory arthritis. Indeed, like 12b, HMOX1
appears to achieve protection in the CIA model by reducing each of
NF-kB activation, production of IL-1b by synovial cells, and synovial
fibroblast hyperplasia (pannus formation) [46]. Further support for
12b mediating activation of NRF2 by interacting with Keap1 is
provided by the recent report of a crystal structure of the Btb
domain of Keap1 with a triterpenoid antagonist bound through a
sulfide link at residue C151 (Protein Data Bank 4cxt) [47]. Thus,
future work designed to fully optimize the structure of SMA-12b in
Fig. 8. SMA-12b-mediated suppression IL-1b is abrogated in NRF2 KO but not MyD88 KO
bmMs. (A) BmMs from wild type and NRF2-deficient (WT and NRF2 KO) C57BL/6 mice
were incubated with 12b (18 h) prior to exposure to medium (“None”) or LPS (100 ng/
ml) for a further 24 h and IL-b and IL-12p40 release measured by ELISA. Data presented
are the % responses (normalised to the wild type LPS response; 100%) and the
means ± SEM (of mean values of triplicate cultures) from matched individual wild type
and NRF2 KO mice (IL-1b: n ¼ 3 and IL-12p40; n ¼ 6). Western blot analysis of MyD88
expression in BALB/c bmMs (B) treated with ES-62 (2 mg/ml) or 12b (1 mg/ml) for 20 h.
bmMs pretreated with 12b (2 h) were then stimulated with LPS overnight and MyD88
expression assessed by western blotting (C) or flow cytometry (D; black ¼ LPS;
grey ¼ LPS þ SMA-12b). The effect of exposure (4 h) of bmMs from wild type and
MyD88-deficient (MyD88 KO) C57BL/6 mice to 12b (E) on the mRNA levels of IL-1b
(n ¼ 4); NLRP3 (n ¼ 3) and GCLC (n ¼ 6) as assessed by qRT-PCR. The levels of the
genes were normalized to GAPDH and expressed as a fold change with respect to the
relevant WT medium control. Data (A E) are presented as the means ± SEM, where n
represents matched cultures from individual wild type and KO mice. *p 0.05;
**p 0.01 and ***p 0.001 where for black *, significance is relative to the corre-
sponding wild type control and for grey**, significance is relative to the corresponding
KO control. (F) Model of SMA-12b action in CIA: 12b protection predominantly reflects
activation of NRF2 signalling to counteract MyD88-integrated inflammasome-
mediated IL-1b production whilst 11a preferentially targets MyD88-driven induction
of the IL-17 inflammatory axis.
J. Rzepecka et al. / Journal of Autoimmunity 60 (2015) 59e7370
13. the drive towards the clinic will have particular focus on the role of
vinyl sulfone conversion.
In addition to inducing NRF2-dependent inhibition of bioactive
IL-1b production, 12b (like ES-62 and 11a but not 19o [9]) down-
regulates MyD88 expression: as this key TLR/IL-1R signal trans-
ducer is also critical for IL-1R (and for DAMP/TLR) coupling to the
inflammasome [48], such downregulation amplifies suppression of
IL-1b and associated transduction of its pathogenic effector func-
tions (Fig. 8F). Moreover, by inducing TLR/IL-1R-
hyporesponsiveness, MyD88 downregulation not only also pro-
vides a molecular mechanism for the observed 12b-mediated
NRF2-independent inhibition of TLR-mediated IL-6 and IL-12 pro-
duction but potentially impacts on IL-1R/TLR driven-MyD88-
ARNO-Arf6 signalling that plays a key role in vascular leakage and
consequent induction of inflammatory arthritis and joint damage
[49e51].
Although 12b does not suppress IFNg responses in CIA to the
extent that they are inhibited by ES-62 and 11a, its ability to sup-
press expression of downstream effectors of IFNg signalling such as
IRFs (as evidenced by microarray analysis) may reflect MyD88
downregulation as this adaptor molecule appears to play a critical
role in transducing effector immune responses in IFNg-activated
macrophages [52]. Similarly, MyD88-signalling in Meningococcal
sepsis has been associated with high serum levels of C5a [53], a pro-
inflammatory mediator that enhances TLR4/MyD88-mediated IL-
17F production by macrophages [54] and is pathogenic in
arthritis [55e57] due to its promotion of proinflammatory cell
migration [58] and osteoclastogenesis, particularly in synergism
with IL-1b [59]. Moreover, as osteoclasts, the cells responsible for
bone resorption in chronically inflamed joints, can arise from the
same progenitors as macrophages, it is intriguing in the context of
RA that microarray analysis suggests that 12b can downregulate the
transcription factor NFAT-C1, which has been proposed to be a
master regulator of the osteoclast transcriptome [60] and can be
induced in a TLR2/MyD88-dependent manner [61]. Thus, given the
important role of spontaneous TLR2 signalling in synovial inflam-
mation in RA [30] and reports that whilst TLR4 can preferentially
couple to IL-6/IL-17 signalling, TLR2 signalling primarily results in
IL-1b production in mice exposed to Mycoplasma arthritidis
mitogen, a superantigen that induces inflammation resulting in
arthritis, skin necrosis and shock [62], our microarray findings that
TLR2, IL-1b and C5aR all appear to be targets of 12b in macrophages
may further explain the differential protective effects of 12b and
11a in CIA.
Finally, further analysis of the microarray data reveals that the
expression of a large number of genes apparently not related to
inflammation and immunity are also modulated by SMA-12b.
Amongst the 30 most down-regulated genes are: (i) Nr4al (NUR77;
7.75-fold decrease), a member of the steroid-thyroid hormone-
retinoid receptor superfamily that acts as a nuclear transcription
factor/orphan nuclear receptor and is currently being explored with
respect to roles in cancer [63] and insulin resistance leading to
type-2 diabetes [64]; (ii) Gpr65 (5.59-fold decrease), which acts as a
receptor for psychosine [65]; (iii) x99383 (4.34-fold decrease), an
RNA-specific editase of glutamate receptors [66]; (iv) Nuak1 (3.4-
fold decrease), a serine/threonine protein kinase involved in a
number of different biological processes relating to cell adhesion,
senescence and proliferation [67] and (v) Ccrn4l (3.17-fold
decrease), which intriguingly has a suggested role as a circadian
clock effector (Nocturnin) [68] that promotes obesity [68,69].
Amongst the 30 most-upregulated genes are: (i) Ednrb (14.37-fold
increase), the endothelin receptor type B [70]; (ii) Slc16a9 (12.9-
fold increase), solute carrier 16, member 9, a monocarboxylic acid
transporter [71]; (iii) RragD (6.42-fold increase), a Rag-like GTPase
[72]; (iv) Ppap2b (6.09-fold increase), a plasma membrane-located
phosphatidic acid phosphatase [73] and (v) Ext1 (5.94-fold in-
crease), an ER-located glycosyltransferase involved in heparin sul-
fate biosynthesis [74]. Clearly, genes covering a wide range of
functions (or possible functions) are being targeted and it is un-
certain whether changes in expression of any of these genes or
other non-immunity/inflammation genes affected by SMA-12b
contribute to its protective effects against CIA. However, given the
recent focus on how insulin resistance and consequent obesity
[75,76] and circadian rhythms [77] impact on autoimmune in-
flammatory diseases such as RA, and that NRF2-dependent path-
ways act to protect against the dysfunction of metabolic pathways
and biological clocks that exacerbates inflammatory diseases
[78e80], it would be of interest in the future to proceed to deter-
mine whether experimentally knocking out/down or increasing the
expression of such individual genes most affected by 12b offers any
protection against disease in mouse models of RA and other in-
flammatory disorders.
5. Conclusion
In spite of initial therapeutic success, IL-1-targeting biologics
were superseded by TNF-blockers in the treatment of RA, although
lately there has been a resurgence of interest in such reagents [33].
This reflects recent proposals that IL-1 and IL-6 rather than TNF
may be critical in the transition from acute to chronic disease [81]
and, perhaps consistent with this, that patients refractory to TNF
therapy respond better to IL-1-modulation rather than alternative
TNF treatments [11]. This raises the possibility of using SMAs, such
as 11a and 12b with complementary inflammatory targets in a
stratified/personalized manner, taking into account both the dif-
ferential kinetics of particular cytokines depending on the stage of
the disease and also their site of action (such as the joint). For
example, whilst IL-17 is secreted in high levels during the initiation
phase of arthritis, this production is much reduced at the chronic
stage [82]. Perhaps particularly pertinent to this suggestion, recent
data suggest that certain synovial phenotypes are associated with
responsiveness to biologic therapies: thus, good responses to anti-
TNFa correlated with an IL-1-associated myeloid synovial signature
whereas lymphoid synovial phenotypes, reflective of IL-17-driven
pathogenesis, were less responsive to TNF blocking [83]. At the
same time, targeting of C5a/C5aR [55e57] and TLR2 [32] has shown
promise in experimental models of arthritis and thus the increasing
evidence of crosstalk between complement, TLR and IL-1R signal-
ling in inflammatory pathologies such as RA, for example by pro-
moting cellular migration and osteoclastogenesis [59] makes SMAs
that potentially target all three convergent pathways an attractive
proposition for development of novel treatments for RA. Encour-
agingly, therefore, in consideration of the route to the clinic, our
early preliminary data suggest that ES-62 and 11a but not 12b can
inhibit LPS-stimulated IL-6 production from PBMC from RA patients
and also that (at least) ES-62 can similarly reduce IL-17 production.
Moreover, SMA-12b modulates expression of a number of genes in
human mast cells similarly to that witnessed with mouse macro-
phages (unpublished data). Furthermore, and in line with the
observed lack of toxicity of 11a and 12b in vitro, preliminary ADMET
data show no hERG liability or cytochrome p450 enzyme inhibition
associated with these compounds (Supplementary Fig. 1 and data
not shown). Finally, the recent dramatic success of IL-1-blocking
therapies in a wide range of autoinflammatory syndromes in-
dicates that there may be more widespread application of such
complementary drugs in a diverse range of these previously
intractable and debilitating conditions, as well as to more common
IL-1-mediated disorders such as post-infarction heart failure
[33,84,85].
J. Rzepecka et al. / Journal of Autoimmunity 60 (2015) 59e73 71
14. Funding
This work was funded by grants from the Wellcome Trust
(086852), the Bioscience and Biotechnology Research Council
(BBSRC: E013929), MRC (Confidence in Concept) and Arthritis
Research UK (18413). DTR and MC were awarded studentships
funded by the Wellcome Trust and FL by the BBSRC respectively.
Author contributions
WH, MMH, CJS and JR conceived the study. JR, MAP, LA, DTR, MC
and FL performed the experiments. JH and AK synthesised the ES-
62 small molecule analogues and LA and FL manufactured ES-62.
PJM and MLA prepared the NRF2À/À
mice. WH, MMH and JR
wrote the paper. WH, MMH, JR, LA, CJS and MAP evaluated and
interpretated the emerging data. All authors critiqued and proof
read the manuscript and approved the final version.
Non-author contributions
Padraic Fallon of Trinity College, Dublin and Susanne Hartmann
of Freie Universitat, Berlin, kindly provided tissues from MyD88À/À
mice.
Conflicts on interest
The authors have no conflicts of interest.
Appendix A. Supplementary data
Supplementary data related to this article can be found online at
http://dx.doi.org/10.1016/j.jaut.2015.04.005.
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