SlideShare a Scribd company logo
1 of 36
APOPTOSIS
Dr. JILSHA
OBJECTIVES
• Introduction
• History of apoptosis
• Difference between apoptosis and necrosis
• Functional significance
• Reasons for apoptosis
• Mechanism and regulation of apoptosis
• Changes in apoptosis
• Examples of apoptosis
• Detection and recent advances
• Applied physiology
INTRODUCTION
• Apoptosis is defined as the natural or programmed cell death that occurs
under genetic control.
• When cells are no longer needed or become a threat to the organism, they
undergo PCD or apoptosis.
• Apoptosis is a Greek word meaning “falling off”.
• Since the cell’s own genes play an active role in its demise, apoptosis can also
be called as cell suicide.
.
HISTORY
• German scientist Carl Vogt put forth the principle of apoptosis in
1842.
• Walther Flemming, an anatomist described the process of
programmed cell death. in 1885.
• John Kerr in 1965, while studying tissues using electron microscopy,
was able to distinguish apoptosis from traumatic cell death.
• In a signal article published in 1972, John F. Kerr, Andrew H. Wyllie
and A. R. Curie coined the term “apoptosis”.
• Kerr received the Paul Ehrlich and Ludwig Darmstaedter prize on
March 14, 2000 for his description of apoptosis.
• The 2002 Nobel prize in Medicine was awarded to Sydney Brenner, H.
Robert Hovitz and John Sulston for their work in identifying genes
that control apoptosis.
APOPTOSIS vs NECROSIS
• Cell death occurs in two ways : necrosis and apoptosis.
• Apoptosis should be distinguished from necrosis in which the healthy
cells are destroyed by some injury inflicted on the cells.
• Since necrosis is caused by some external process, it can also be
called as cell murder.
FACT
About 10 million cells are
produced every day in human
body by mitosis. An equal
number of cells die by
apoptosis. Thus maintaining
homeostasis.
FUNCTIONAL SIGNIFICANCE
• The purpose of apoptosis is to remove unwanted cells without
causing any stress or damage to the neighboring cells.
• It plays a role in cellular homeostasis.
• Useful in removal of cell that is damaged beyond repair by toxins or
viruses.
• It is an essential event during developmental stages and in adults.
Therefore, decreased apoptosis has been implicated in the
genesis of malignancy and autoimmune diseases.
REASONS FOR APOPTOSIS
• Withdrawal of positive signals
• Growth factors for neurons
• IL – 2
• Receipt of negative signals
• Increased levels of oxidants within the cell
• Damage to DNA by oxidants
• Death activators
• TNF α
• TNF β
• Fas ligand
MECHANISM
• Apoptosis is initiated by two stimuli:
• Extrinsic pathway
• Intrinsic pathway
• In extrinsic pathway, the stimulus is received from outside of the cell and in
intrinsic pathway, the stimulus arises from within the cell.
• Both the pathways lead to activation of cysteine proteases in the cell called
caspases which triggers apoptosis.
• Caspases are synthesized in the cell as precursors named procaspase.
FACT
There are 12
confirmed caspases
in humans and
10 in mice, carrying
out a variety of
cellular functions.
CASPASES
stands for
cysteine-aspartic
proteases
• There are three types of caspases
• Inflammatory caspases : Caspases 1,4 and 5.
• Initiator caspases : Caspases 2, 8, 9, 10.
• Effector caspases : Caspases 3, 6 and 7.
• In the case of apoptosis, the process starts with activation of
caspase 8 or 9 which inturn activates caspase 3 & 7 which then
activate other caspases resulting in a cascade.
REGULATION OF APOPTSIS
• Certain intracellular proteins provide signal for the final programmed cell death.
• Pro-apoptotic proteins : BAX and BAC
• Anti-apoptotic proteins: BCL-2, BCL-X, MCL-1
• Apoptosis depends upon the balance between the pro and anti apoptotic proteins. In
a healthy cell, anti-apoptotic proteins binds with pro-apoptotic proteins thereby
blocking their action.
• If a cell is damaged or it stops receiving survival signals, Bcl – 2 and Bcl –x are
blocked in turn. Bax and Bac are then free to punch a series of channels in the
mitochondria.
INTRINSIC PATHWAY
• Also known as mitochondrial pathway.
• Internal stimuli may be due to cellular stress, viral infections, increase
in the concentration of intracellular oxidants, heat, radiation, nutrient
deprivation, hypoxia, increased intracellular calcium concentration,
damage to the DNA etc.,
INTRINSIC PATHWAY
INTERNAL STIMULI
Damage to
mitochondrial
membrane increasing
permeability
Entry of
Cytochrome C into
the cytoplasm
Cytochrome binds to
Apaf – 1 forming
apoptosome
Apoptosome
activates procaspase
9 to caspase 9
• Mitochondrial proteins called SMACs (Second Mitochondria derived
Activator of Caspases) are also released into the cell’s cytosol
following increased mitochondrial permeability.
• SMAC binds to anti – apoptotic proteins thereby deactivating them
and therefore allowing apoptosis to proceed.
EXTRINSIC PATHWAY
• The extrinsic pathway of apoptosis begins outside a cell, when conditions in the
extracellular environment determine that a cell must die.
• External stimuli are various ligands that bind with cell surface to activate apoptosis.
• TNF and Fas Ligands are some examples of ligands that activates Caspase 8.
• These ligands are called death ligands and they bind with Death receptors like
TNFR1.
• Ligand binding causes the receptors to cluster and ultimately form a Death
Inducing Signalling Complex (DISC).
• Upon DISC formation caspase cascade activation takes place.
• Activation of Caspases results in:
• Shrinkage of cell
• DNA fragmentation
• Chromatin condensation(pyknosis)
CHANGES IN APOPTOSIS
PATHOPHYSIOLOGICAL
• Apoptotic cells become round or oval and reduce in size.
• Cytoplasm becomes intensely eosinophilic.
• Though cytoplasm is reduced, organelles remain almost normal.
• Chromatic condensation occurs.
• Nuclear fragmentation occurs.
• Apoptotic bodies contain compacted organelles.
• Phagocytosis of apoptotic bodies occur by macrophages. The phagocytic cells
secrete cytokines like IL-10 and TGF-β which inhibit inflammation of neighbouring
tissues.
BIOCHEMICAL CHANGES
• Proteolysis of cytoskeletal proteins.
• Cross – linking of protein molecules.
• Fragmentation of nuclear chromatin by activation of nuclease.
• A glycoprotein – thrombospondin and a phosphoprotein –
phosphatidylserine appear on the outer surface of apoptotic bodies for
recognition by macrophages.
PHYSIOLOGICAL PROCESSES
• The separation of fingers and toes in a developing human embryo occurs because
cells between the digits undergo apoptosis.
• Endometrial shedding in menstrual cycles.
• Regression of lactating breast after cessation of breastfeeding.
• Normal shedding of intestinal epithelium.
• Involution of thymus after childhood.
• Degeneration and regeneration of neurons within the CNS and formation of
synapse.
• Regression of duct system during sex differentiation in the foetus.
PATHOLOGICAL PROCESSES
• Tumor cell death on exposure to chemotherapeutic agents.
• Transplant cell death by cytotoxic T cells that cause transplant
rejection.
• Cell death induced by viral infections.
• Cell death induced by radiation, hypoxia.
• Degenerative diseases like Alzheimer’s disease, Parkinson’s disease
etc.,
DETECTION OF APOPTOSIS
• DNA fragmentation assay by electrophoresis.
• TUNEL (terminal deoxynucleotidyl transferase dUTP nick end
labeling) staining.
• Demonstration of chromatic condensation by H & E staining.
• Estimation of cytosolic cytochrome – C, activated caspase and
annexin – V.
APPLIED PHYSIOLOGY
• Understanding the concept of apoptosis has promising role in future regenerative medicine.
• Disorders with reduced apoptosis:
• Cancer
• Autoimmune diseases – SLE, Myasthenia gravis
• Inflammatory diseases – BA, IBD
• Viral infections – Herpes, pox, adenovirus
• Disorders with increased apoptosis :
• Alzheimer’s disease, Parkinson’s disease
• Myocardial infarction, stroke.
• AIDS
RECENT ADVANCES
• Caspase inhibitors such as N – benzyloxycarbonyl – Val – Ala – Asp
fluoromethyl – ketone (Z – VAD) were being investigated for the treatment
of neurodegenerative disorders like :
• Alzheimer’s disease
• ALS
• Huntington’s disease
• Parkinson’s disease
• Another promising compound that is currently under evaluation is
Minocycline which is better than other caspase inhibitors with less side
effects.
SUMMARY
• Apoptosis is defined as the natural or programmed cell death.
• The purpose of apoptosis is to remove unwanted cells.
• May be physiological or pathological.
• There are two pathways – extrinsic and intrinsic pathway.
• It is regulated by pre and anti apoptotic proteins.
• Several changes occur in the apoptotic cells which is finally
phagocytosed by macrophages.
• Has a promising role in regenerative medicine.
Apoptosis

More Related Content

What's hot

What's hot (20)

Apoptosis
ApoptosisApoptosis
Apoptosis
 
Apoptosis
Apoptosis Apoptosis
Apoptosis
 
Apoptosis, program cell death
Apoptosis, program cell deathApoptosis, program cell death
Apoptosis, program cell death
 
Apoptosis
ApoptosisApoptosis
Apoptosis
 
Apoptosis
ApoptosisApoptosis
Apoptosis
 
Necrosis and apoptosis
Necrosis and apoptosisNecrosis and apoptosis
Necrosis and apoptosis
 
Apoptosis
ApoptosisApoptosis
Apoptosis
 
Apoptosis
ApoptosisApoptosis
Apoptosis
 
Necrosis and apoptosis
Necrosis and apoptosisNecrosis and apoptosis
Necrosis and apoptosis
 
Apoptosis
ApoptosisApoptosis
Apoptosis
 
Apoptosis
ApoptosisApoptosis
Apoptosis
 
Apoptosis
ApoptosisApoptosis
Apoptosis
 
Apoptosis
ApoptosisApoptosis
Apoptosis
 
Apoptosis (Programm of cell death)
Apoptosis (Programm of cell death)Apoptosis (Programm of cell death)
Apoptosis (Programm of cell death)
 
Apoptosis
ApoptosisApoptosis
Apoptosis
 
Apoptosis in health and diseases
Apoptosis in health and diseasesApoptosis in health and diseases
Apoptosis in health and diseases
 
Apoptosis.ppt
Apoptosis.pptApoptosis.ppt
Apoptosis.ppt
 
Apoptosis for first semester
Apoptosis   for first semesterApoptosis   for first semester
Apoptosis for first semester
 
Tumour supressor gene
Tumour supressor geneTumour supressor gene
Tumour supressor gene
 
Apoptosis
Apoptosis Apoptosis
Apoptosis
 

Similar to Apoptosis

apopwqgdcbhuredgbcfyhhvhcctosis (1).pptx
apopwqgdcbhuredgbcfyhhvhcctosis (1).pptxapopwqgdcbhuredgbcfyhhvhcctosis (1).pptx
apopwqgdcbhuredgbcfyhhvhcctosis (1).pptx
SarithaRani4
 
apoptosis lecture-powerpoint slides (1) (1).pdf
apoptosis lecture-powerpoint slides (1) (1).pdfapoptosis lecture-powerpoint slides (1) (1).pdf
apoptosis lecture-powerpoint slides (1) (1).pdf
SrimathideviJ
 
APOPTOSIS.pptx
APOPTOSIS.pptxAPOPTOSIS.pptx
APOPTOSIS.pptx
Gowthun
 

Similar to Apoptosis (20)

Apoptosis basics + microphotographs
Apoptosis basics + microphotographsApoptosis basics + microphotographs
Apoptosis basics + microphotographs
 
physiology of apoptosis first year mbbs medical.pdf
physiology of apoptosis first year mbbs medical.pdfphysiology of apoptosis first year mbbs medical.pdf
physiology of apoptosis first year mbbs medical.pdf
 
apopwqgdcbhuredgbcfyhhvhcctosis (1).pptx
apopwqgdcbhuredgbcfyhhvhcctosis (1).pptxapopwqgdcbhuredgbcfyhhvhcctosis (1).pptx
apopwqgdcbhuredgbcfyhhvhcctosis (1).pptx
 
Apoptosis - programmed cell death that occurs in multicellular organisms
Apoptosis - programmed cell death that occurs in multicellular organismsApoptosis - programmed cell death that occurs in multicellular organisms
Apoptosis - programmed cell death that occurs in multicellular organisms
 
Apoptosis
ApoptosisApoptosis
Apoptosis
 
apoptosis lecture-powerpoint slides (1) (1).pdf
apoptosis lecture-powerpoint slides (1) (1).pdfapoptosis lecture-powerpoint slides (1) (1).pdf
apoptosis lecture-powerpoint slides (1) (1).pdf
 
APOPTOSIS
APOPTOSISAPOPTOSIS
APOPTOSIS
 
Apoptosis.pptx
Apoptosis.pptxApoptosis.pptx
Apoptosis.pptx
 
Cell injury apoptosis lect 08jan 2020
Cell injury apoptosis lect 08jan 2020Cell injury apoptosis lect 08jan 2020
Cell injury apoptosis lect 08jan 2020
 
Apoptosis
ApoptosisApoptosis
Apoptosis
 
Apoptosis / dental crown & bridge courses
Apoptosis / dental crown & bridge coursesApoptosis / dental crown & bridge courses
Apoptosis / dental crown & bridge courses
 
Apoptosis
ApoptosisApoptosis
Apoptosis
 
APOPTOSIS.pptx
APOPTOSIS.pptxAPOPTOSIS.pptx
APOPTOSIS.pptx
 
Apoptosis
ApoptosisApoptosis
Apoptosis
 
Apoptosis
ApoptosisApoptosis
Apoptosis
 
Apoptosis
Apoptosis Apoptosis
Apoptosis
 
Apoptosis definition, mechanism , Apoptosis vs necrosis, Assays of apoptosis,...
Apoptosis definition, mechanism , Apoptosis vs necrosis, Assays of apoptosis,...Apoptosis definition, mechanism , Apoptosis vs necrosis, Assays of apoptosis,...
Apoptosis definition, mechanism , Apoptosis vs necrosis, Assays of apoptosis,...
 
Intrinsic and Extrinsic Pathway of Apoptosis
Intrinsic and Extrinsic  Pathway of ApoptosisIntrinsic and Extrinsic  Pathway of Apoptosis
Intrinsic and Extrinsic Pathway of Apoptosis
 
DPT - Cell injury and Cell death
DPT - Cell injury and Cell deathDPT - Cell injury and Cell death
DPT - Cell injury and Cell death
 
Role of apoptosis in physiology and diseases i
Role of apoptosis in physiology and diseases iRole of apoptosis in physiology and diseases i
Role of apoptosis in physiology and diseases i
 

More from Jilsha Cecil (8)

Intercellular junctions
Intercellular junctionsIntercellular junctions
Intercellular junctions
 
Lymphatic system and lymph
Lymphatic system and lymphLymphatic system and lymph
Lymphatic system and lymph
 
Erythropoiesis
ErythropoiesisErythropoiesis
Erythropoiesis
 
Leukopoiesis
LeukopoiesisLeukopoiesis
Leukopoiesis
 
Blood indices
Blood indicesBlood indices
Blood indices
 
White blood cells - morphology, functions and variations
White blood cells - morphology, functions and variationsWhite blood cells - morphology, functions and variations
White blood cells - morphology, functions and variations
 
Transport across cell membrane
Transport across cell membraneTransport across cell membrane
Transport across cell membrane
 
Cell membrane
Cell membraneCell membrane
Cell membrane
 

Recently uploaded

Pests of cotton_Borer_Pests_Binomics_Dr.UPR.pdf
Pests of cotton_Borer_Pests_Binomics_Dr.UPR.pdfPests of cotton_Borer_Pests_Binomics_Dr.UPR.pdf
Pests of cotton_Borer_Pests_Binomics_Dr.UPR.pdf
PirithiRaju
 
Biogenic Sulfur Gases as Biosignatures on Temperate Sub-Neptune Waterworlds
Biogenic Sulfur Gases as Biosignatures on Temperate Sub-Neptune WaterworldsBiogenic Sulfur Gases as Biosignatures on Temperate Sub-Neptune Waterworlds
Biogenic Sulfur Gases as Biosignatures on Temperate Sub-Neptune Waterworlds
Sérgio Sacani
 
Asymmetry in the atmosphere of the ultra-hot Jupiter WASP-76 b
Asymmetry in the atmosphere of the ultra-hot Jupiter WASP-76 bAsymmetry in the atmosphere of the ultra-hot Jupiter WASP-76 b
Asymmetry in the atmosphere of the ultra-hot Jupiter WASP-76 b
Sérgio Sacani
 
Pests of cotton_Sucking_Pests_Dr.UPR.pdf
Pests of cotton_Sucking_Pests_Dr.UPR.pdfPests of cotton_Sucking_Pests_Dr.UPR.pdf
Pests of cotton_Sucking_Pests_Dr.UPR.pdf
PirithiRaju
 

Recently uploaded (20)

Human & Veterinary Respiratory Physilogy_DR.E.Muralinath_Associate Professor....
Human & Veterinary Respiratory Physilogy_DR.E.Muralinath_Associate Professor....Human & Veterinary Respiratory Physilogy_DR.E.Muralinath_Associate Professor....
Human & Veterinary Respiratory Physilogy_DR.E.Muralinath_Associate Professor....
 
Justdial Call Girls In Indirapuram, Ghaziabad, 8800357707 Escorts Service
Justdial Call Girls In Indirapuram, Ghaziabad, 8800357707 Escorts ServiceJustdial Call Girls In Indirapuram, Ghaziabad, 8800357707 Escorts Service
Justdial Call Girls In Indirapuram, Ghaziabad, 8800357707 Escorts Service
 
Molecular markers- RFLP, RAPD, AFLP, SNP etc.
Molecular markers- RFLP, RAPD, AFLP, SNP etc.Molecular markers- RFLP, RAPD, AFLP, SNP etc.
Molecular markers- RFLP, RAPD, AFLP, SNP etc.
 
Pests of cotton_Borer_Pests_Binomics_Dr.UPR.pdf
Pests of cotton_Borer_Pests_Binomics_Dr.UPR.pdfPests of cotton_Borer_Pests_Binomics_Dr.UPR.pdf
Pests of cotton_Borer_Pests_Binomics_Dr.UPR.pdf
 
Biogenic Sulfur Gases as Biosignatures on Temperate Sub-Neptune Waterworlds
Biogenic Sulfur Gases as Biosignatures on Temperate Sub-Neptune WaterworldsBiogenic Sulfur Gases as Biosignatures on Temperate Sub-Neptune Waterworlds
Biogenic Sulfur Gases as Biosignatures on Temperate Sub-Neptune Waterworlds
 
Locating and isolating a gene, FISH, GISH, Chromosome walking and jumping, te...
Locating and isolating a gene, FISH, GISH, Chromosome walking and jumping, te...Locating and isolating a gene, FISH, GISH, Chromosome walking and jumping, te...
Locating and isolating a gene, FISH, GISH, Chromosome walking and jumping, te...
 
❤Jammu Kashmir Call Girls 8617697112 Personal Whatsapp Number 💦✅.
❤Jammu Kashmir Call Girls 8617697112 Personal Whatsapp Number 💦✅.❤Jammu Kashmir Call Girls 8617697112 Personal Whatsapp Number 💦✅.
❤Jammu Kashmir Call Girls 8617697112 Personal Whatsapp Number 💦✅.
 
Asymmetry in the atmosphere of the ultra-hot Jupiter WASP-76 b
Asymmetry in the atmosphere of the ultra-hot Jupiter WASP-76 bAsymmetry in the atmosphere of the ultra-hot Jupiter WASP-76 b
Asymmetry in the atmosphere of the ultra-hot Jupiter WASP-76 b
 
Thyroid Physiology_Dr.E. Muralinath_ Associate Professor
Thyroid Physiology_Dr.E. Muralinath_ Associate ProfessorThyroid Physiology_Dr.E. Muralinath_ Associate Professor
Thyroid Physiology_Dr.E. Muralinath_ Associate Professor
 
9999266834 Call Girls In Noida Sector 22 (Delhi) Call Girl Service
9999266834 Call Girls In Noida Sector 22 (Delhi) Call Girl Service9999266834 Call Girls In Noida Sector 22 (Delhi) Call Girl Service
9999266834 Call Girls In Noida Sector 22 (Delhi) Call Girl Service
 
Site Acceptance Test .
Site Acceptance Test                    .Site Acceptance Test                    .
Site Acceptance Test .
 
GBSN - Microbiology (Unit 1)
GBSN - Microbiology (Unit 1)GBSN - Microbiology (Unit 1)
GBSN - Microbiology (Unit 1)
 
Zoology 5th semester notes( Sumit_yadav).pdf
Zoology 5th semester notes( Sumit_yadav).pdfZoology 5th semester notes( Sumit_yadav).pdf
Zoology 5th semester notes( Sumit_yadav).pdf
 
GBSN - Microbiology (Unit 2)
GBSN - Microbiology (Unit 2)GBSN - Microbiology (Unit 2)
GBSN - Microbiology (Unit 2)
 
Pests of cotton_Sucking_Pests_Dr.UPR.pdf
Pests of cotton_Sucking_Pests_Dr.UPR.pdfPests of cotton_Sucking_Pests_Dr.UPR.pdf
Pests of cotton_Sucking_Pests_Dr.UPR.pdf
 
High Class Escorts in Hyderabad ₹7.5k Pick Up & Drop With Cash Payment 969456...
High Class Escorts in Hyderabad ₹7.5k Pick Up & Drop With Cash Payment 969456...High Class Escorts in Hyderabad ₹7.5k Pick Up & Drop With Cash Payment 969456...
High Class Escorts in Hyderabad ₹7.5k Pick Up & Drop With Cash Payment 969456...
 
Forensic Biology & Its biological significance.pdf
Forensic Biology & Its biological significance.pdfForensic Biology & Its biological significance.pdf
Forensic Biology & Its biological significance.pdf
 
module for grade 9 for distance learning
module for grade 9 for distance learningmodule for grade 9 for distance learning
module for grade 9 for distance learning
 
Proteomics: types, protein profiling steps etc.
Proteomics: types, protein profiling steps etc.Proteomics: types, protein profiling steps etc.
Proteomics: types, protein profiling steps etc.
 
9654467111 Call Girls In Raj Nagar Delhi Short 1500 Night 6000
9654467111 Call Girls In Raj Nagar Delhi Short 1500 Night 60009654467111 Call Girls In Raj Nagar Delhi Short 1500 Night 6000
9654467111 Call Girls In Raj Nagar Delhi Short 1500 Night 6000
 

Apoptosis

  • 2. OBJECTIVES • Introduction • History of apoptosis • Difference between apoptosis and necrosis • Functional significance • Reasons for apoptosis • Mechanism and regulation of apoptosis • Changes in apoptosis • Examples of apoptosis • Detection and recent advances • Applied physiology
  • 3. INTRODUCTION • Apoptosis is defined as the natural or programmed cell death that occurs under genetic control. • When cells are no longer needed or become a threat to the organism, they undergo PCD or apoptosis. • Apoptosis is a Greek word meaning “falling off”. • Since the cell’s own genes play an active role in its demise, apoptosis can also be called as cell suicide. .
  • 4. HISTORY • German scientist Carl Vogt put forth the principle of apoptosis in 1842.
  • 5. • Walther Flemming, an anatomist described the process of programmed cell death. in 1885.
  • 6. • John Kerr in 1965, while studying tissues using electron microscopy, was able to distinguish apoptosis from traumatic cell death. • In a signal article published in 1972, John F. Kerr, Andrew H. Wyllie and A. R. Curie coined the term “apoptosis”. • Kerr received the Paul Ehrlich and Ludwig Darmstaedter prize on March 14, 2000 for his description of apoptosis.
  • 7. • The 2002 Nobel prize in Medicine was awarded to Sydney Brenner, H. Robert Hovitz and John Sulston for their work in identifying genes that control apoptosis.
  • 8. APOPTOSIS vs NECROSIS • Cell death occurs in two ways : necrosis and apoptosis. • Apoptosis should be distinguished from necrosis in which the healthy cells are destroyed by some injury inflicted on the cells. • Since necrosis is caused by some external process, it can also be called as cell murder.
  • 9.
  • 10.
  • 11. FACT About 10 million cells are produced every day in human body by mitosis. An equal number of cells die by apoptosis. Thus maintaining homeostasis.
  • 12. FUNCTIONAL SIGNIFICANCE • The purpose of apoptosis is to remove unwanted cells without causing any stress or damage to the neighboring cells. • It plays a role in cellular homeostasis. • Useful in removal of cell that is damaged beyond repair by toxins or viruses. • It is an essential event during developmental stages and in adults. Therefore, decreased apoptosis has been implicated in the genesis of malignancy and autoimmune diseases.
  • 13. REASONS FOR APOPTOSIS • Withdrawal of positive signals • Growth factors for neurons • IL – 2 • Receipt of negative signals • Increased levels of oxidants within the cell • Damage to DNA by oxidants • Death activators • TNF α • TNF β • Fas ligand
  • 14. MECHANISM • Apoptosis is initiated by two stimuli: • Extrinsic pathway • Intrinsic pathway • In extrinsic pathway, the stimulus is received from outside of the cell and in intrinsic pathway, the stimulus arises from within the cell. • Both the pathways lead to activation of cysteine proteases in the cell called caspases which triggers apoptosis. • Caspases are synthesized in the cell as precursors named procaspase.
  • 15. FACT There are 12 confirmed caspases in humans and 10 in mice, carrying out a variety of cellular functions. CASPASES stands for cysteine-aspartic proteases
  • 16. • There are three types of caspases • Inflammatory caspases : Caspases 1,4 and 5. • Initiator caspases : Caspases 2, 8, 9, 10. • Effector caspases : Caspases 3, 6 and 7. • In the case of apoptosis, the process starts with activation of caspase 8 or 9 which inturn activates caspase 3 & 7 which then activate other caspases resulting in a cascade.
  • 17. REGULATION OF APOPTSIS • Certain intracellular proteins provide signal for the final programmed cell death. • Pro-apoptotic proteins : BAX and BAC • Anti-apoptotic proteins: BCL-2, BCL-X, MCL-1 • Apoptosis depends upon the balance between the pro and anti apoptotic proteins. In a healthy cell, anti-apoptotic proteins binds with pro-apoptotic proteins thereby blocking their action. • If a cell is damaged or it stops receiving survival signals, Bcl – 2 and Bcl –x are blocked in turn. Bax and Bac are then free to punch a series of channels in the mitochondria.
  • 18. INTRINSIC PATHWAY • Also known as mitochondrial pathway. • Internal stimuli may be due to cellular stress, viral infections, increase in the concentration of intracellular oxidants, heat, radiation, nutrient deprivation, hypoxia, increased intracellular calcium concentration, damage to the DNA etc.,
  • 19. INTRINSIC PATHWAY INTERNAL STIMULI Damage to mitochondrial membrane increasing permeability Entry of Cytochrome C into the cytoplasm Cytochrome binds to Apaf – 1 forming apoptosome Apoptosome activates procaspase 9 to caspase 9
  • 20. • Mitochondrial proteins called SMACs (Second Mitochondria derived Activator of Caspases) are also released into the cell’s cytosol following increased mitochondrial permeability. • SMAC binds to anti – apoptotic proteins thereby deactivating them and therefore allowing apoptosis to proceed.
  • 21.
  • 22. EXTRINSIC PATHWAY • The extrinsic pathway of apoptosis begins outside a cell, when conditions in the extracellular environment determine that a cell must die. • External stimuli are various ligands that bind with cell surface to activate apoptosis. • TNF and Fas Ligands are some examples of ligands that activates Caspase 8. • These ligands are called death ligands and they bind with Death receptors like TNFR1. • Ligand binding causes the receptors to cluster and ultimately form a Death Inducing Signalling Complex (DISC). • Upon DISC formation caspase cascade activation takes place.
  • 23.
  • 24.
  • 25. • Activation of Caspases results in: • Shrinkage of cell • DNA fragmentation • Chromatin condensation(pyknosis)
  • 26. CHANGES IN APOPTOSIS PATHOPHYSIOLOGICAL • Apoptotic cells become round or oval and reduce in size. • Cytoplasm becomes intensely eosinophilic. • Though cytoplasm is reduced, organelles remain almost normal. • Chromatic condensation occurs. • Nuclear fragmentation occurs. • Apoptotic bodies contain compacted organelles. • Phagocytosis of apoptotic bodies occur by macrophages. The phagocytic cells secrete cytokines like IL-10 and TGF-β which inhibit inflammation of neighbouring tissues.
  • 27. BIOCHEMICAL CHANGES • Proteolysis of cytoskeletal proteins. • Cross – linking of protein molecules. • Fragmentation of nuclear chromatin by activation of nuclease. • A glycoprotein – thrombospondin and a phosphoprotein – phosphatidylserine appear on the outer surface of apoptotic bodies for recognition by macrophages.
  • 28.
  • 29. PHYSIOLOGICAL PROCESSES • The separation of fingers and toes in a developing human embryo occurs because cells between the digits undergo apoptosis. • Endometrial shedding in menstrual cycles. • Regression of lactating breast after cessation of breastfeeding. • Normal shedding of intestinal epithelium. • Involution of thymus after childhood. • Degeneration and regeneration of neurons within the CNS and formation of synapse. • Regression of duct system during sex differentiation in the foetus.
  • 30.
  • 31. PATHOLOGICAL PROCESSES • Tumor cell death on exposure to chemotherapeutic agents. • Transplant cell death by cytotoxic T cells that cause transplant rejection. • Cell death induced by viral infections. • Cell death induced by radiation, hypoxia. • Degenerative diseases like Alzheimer’s disease, Parkinson’s disease etc.,
  • 32. DETECTION OF APOPTOSIS • DNA fragmentation assay by electrophoresis. • TUNEL (terminal deoxynucleotidyl transferase dUTP nick end labeling) staining. • Demonstration of chromatic condensation by H & E staining. • Estimation of cytosolic cytochrome – C, activated caspase and annexin – V.
  • 33. APPLIED PHYSIOLOGY • Understanding the concept of apoptosis has promising role in future regenerative medicine. • Disorders with reduced apoptosis: • Cancer • Autoimmune diseases – SLE, Myasthenia gravis • Inflammatory diseases – BA, IBD • Viral infections – Herpes, pox, adenovirus • Disorders with increased apoptosis : • Alzheimer’s disease, Parkinson’s disease • Myocardial infarction, stroke. • AIDS
  • 34. RECENT ADVANCES • Caspase inhibitors such as N – benzyloxycarbonyl – Val – Ala – Asp fluoromethyl – ketone (Z – VAD) were being investigated for the treatment of neurodegenerative disorders like : • Alzheimer’s disease • ALS • Huntington’s disease • Parkinson’s disease • Another promising compound that is currently under evaluation is Minocycline which is better than other caspase inhibitors with less side effects.
  • 35. SUMMARY • Apoptosis is defined as the natural or programmed cell death. • The purpose of apoptosis is to remove unwanted cells. • May be physiological or pathological. • There are two pathways – extrinsic and intrinsic pathway. • It is regulated by pre and anti apoptotic proteins. • Several changes occur in the apoptotic cells which is finally phagocytosed by macrophages. • Has a promising role in regenerative medicine.