The document summarizes the female reproductive system, specifically the ovaries and oogenesis (egg formation). It describes the histology and structure of the ovaries, including the germinal epithelium, tunica albuginea, cortex, medulla, and ovarian follicles. It then explains the process of oogenesis, from primordial germ cells to primary oocytes surrounded by granulosa cells in primordial follicles. Upon stimulation by hormones, follicles develop through primary, secondary, and tertiary stages, with the release of a secondary oocyte at ovulation.
In testis, the immature male germ cell (spermatogonia ) produce sperms by spermatogenesis
The spermatogonia ( sing. Spermatogonium ) present on the inside of seminiferous tubules multiply by mitotic division and increase in numbers
Each spermatogonium is diploid and contains 46 chromosomes
Some of the spermatogonia called primary spermatocytes periodically undergo meiosis.A primary spermatocyte completes the first meiotic division (reduction division) leading to formation of two equal, haploid cells called secondary spermatocyte, which have only 23 chromosomes
The secondary spermatocyte undergo the second meiotic division to produce four equal, haploid spermatids
A brief account of different parts of sperm and its constitutions and,ovum parts and different envelops.all things are explained by a simple attractive diagram.
In testis, the immature male germ cell (spermatogonia ) produce sperms by spermatogenesis
The spermatogonia ( sing. Spermatogonium ) present on the inside of seminiferous tubules multiply by mitotic division and increase in numbers
Each spermatogonium is diploid and contains 46 chromosomes
Some of the spermatogonia called primary spermatocytes periodically undergo meiosis.A primary spermatocyte completes the first meiotic division (reduction division) leading to formation of two equal, haploid cells called secondary spermatocyte, which have only 23 chromosomes
The secondary spermatocyte undergo the second meiotic division to produce four equal, haploid spermatids
A brief account of different parts of sperm and its constitutions and,ovum parts and different envelops.all things are explained by a simple attractive diagram.
The physiological processes that regulate parturition and the onset of labor continue to be defined. It is clear, however, that labor onset represents the culmination of a series of biochemical changes in the uterus and cervix. These result from endocrine and paracrine signals emanating from both mother and fetus.
Anatomy of male and female reproductive system, Functions of male and female
reproductive system, sex hormones, physiology of menstruation, fertilization,
spermatogenesis, oogenesis, pregnancy and parturition
Giving overview of human embryonic development including spermatogenesis, oogenesis, fertilization, gastrulation, cleavage, extraembryonic layers and pregnancy
The topic discussed here is the Process of fertilization, different stages of fertilization, Implantation, Gastrulation, Formation of foetal membranes, Development of Embryo, Labor & Parturition
Oogenesis and follicular development Part 1 I Endocrine Physiology IHM Learnings
Oogenesis and follicular development Part 1 I Endocrine Physiology I
The slides will talk about
1. Introduction
2. Stages of follicular development
3. Primordial follicle
4. Preantral follicle (primary and secondary follicle)
5. Antral follicle
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This presentation explores a brief idea about the structural and functional attributes of nucleotides, the structure and function of genetic materials along with the impact of UV rays and pH upon them.
Professional air quality monitoring systems provide immediate, on-site data for analysis, compliance, and decision-making.
Monitor common gases, weather parameters, particulates.
Richard's aventures in two entangled wonderlandsRichard Gill
Since the loophole-free Bell experiments of 2020 and the Nobel prizes in physics of 2022, critics of Bell's work have retreated to the fortress of super-determinism. Now, super-determinism is a derogatory word - it just means "determinism". Palmer, Hance and Hossenfelder argue that quantum mechanics and determinism are not incompatible, using a sophisticated mathematical construction based on a subtle thinning of allowed states and measurements in quantum mechanics, such that what is left appears to make Bell's argument fail, without altering the empirical predictions of quantum mechanics. I think however that it is a smoke screen, and the slogan "lost in math" comes to my mind. I will discuss some other recent disproofs of Bell's theorem using the language of causality based on causal graphs. Causal thinking is also central to law and justice. I will mention surprising connections to my work on serial killer nurse cases, in particular the Dutch case of Lucia de Berk and the current UK case of Lucy Letby.
THE IMPORTANCE OF MARTIAN ATMOSPHERE SAMPLE RETURN.Sérgio Sacani
The return of a sample of near-surface atmosphere from Mars would facilitate answers to several first-order science questions surrounding the formation and evolution of the planet. One of the important aspects of terrestrial planet formation in general is the role that primary atmospheres played in influencing the chemistry and structure of the planets and their antecedents. Studies of the martian atmosphere can be used to investigate the role of a primary atmosphere in its history. Atmosphere samples would also inform our understanding of the near-surface chemistry of the planet, and ultimately the prospects for life. High-precision isotopic analyses of constituent gases are needed to address these questions, requiring that the analyses are made on returned samples rather than in situ.
(May 29th, 2024) Advancements in Intravital Microscopy- Insights for Preclini...Scintica Instrumentation
Intravital microscopy (IVM) is a powerful tool utilized to study cellular behavior over time and space in vivo. Much of our understanding of cell biology has been accomplished using various in vitro and ex vivo methods; however, these studies do not necessarily reflect the natural dynamics of biological processes. Unlike traditional cell culture or fixed tissue imaging, IVM allows for the ultra-fast high-resolution imaging of cellular processes over time and space and were studied in its natural environment. Real-time visualization of biological processes in the context of an intact organism helps maintain physiological relevance and provide insights into the progression of disease, response to treatments or developmental processes.
In this webinar we give an overview of advanced applications of the IVM system in preclinical research. IVIM technology is a provider of all-in-one intravital microscopy systems and solutions optimized for in vivo imaging of live animal models at sub-micron resolution. The system’s unique features and user-friendly software enables researchers to probe fast dynamic biological processes such as immune cell tracking, cell-cell interaction as well as vascularization and tumor metastasis with exceptional detail. This webinar will also give an overview of IVM being utilized in drug development, offering a view into the intricate interaction between drugs/nanoparticles and tissues in vivo and allows for the evaluation of therapeutic intervention in a variety of tissues and organs. This interdisciplinary collaboration continues to drive the advancements of novel therapeutic strategies.
Introduction:
RNA interference (RNAi) or Post-Transcriptional Gene Silencing (PTGS) is an important biological process for modulating eukaryotic gene expression.
It is highly conserved process of posttranscriptional gene silencing by which double stranded RNA (dsRNA) causes sequence-specific degradation of mRNA sequences.
dsRNA-induced gene silencing (RNAi) is reported in a wide range of eukaryotes ranging from worms, insects, mammals and plants.
This process mediates resistance to both endogenous parasitic and exogenous pathogenic nucleic acids, and regulates the expression of protein-coding genes.
What are small ncRNAs?
micro RNA (miRNA)
short interfering RNA (siRNA)
Properties of small non-coding RNA:
Involved in silencing mRNA transcripts.
Called “small” because they are usually only about 21-24 nucleotides long.
Synthesized by first cutting up longer precursor sequences (like the 61nt one that Lee discovered).
Silence an mRNA by base pairing with some sequence on the mRNA.
Discovery of siRNA?
The first small RNA:
In 1993 Rosalind Lee (Victor Ambros lab) was studying a non- coding gene in C. elegans, lin-4, that was involved in silencing of another gene, lin-14, at the appropriate time in the
development of the worm C. elegans.
Two small transcripts of lin-4 (22nt and 61nt) were found to be complementary to a sequence in the 3' UTR of lin-14.
Because lin-4 encoded no protein, she deduced that it must be these transcripts that are causing the silencing by RNA-RNA interactions.
Types of RNAi ( non coding RNA)
MiRNA
Length (23-25 nt)
Trans acting
Binds with target MRNA in mismatch
Translation inhibition
Si RNA
Length 21 nt.
Cis acting
Bind with target Mrna in perfect complementary sequence
Piwi-RNA
Length ; 25 to 36 nt.
Expressed in Germ Cells
Regulates trnasposomes activity
MECHANISM OF RNAI:
First the double-stranded RNA teams up with a protein complex named Dicer, which cuts the long RNA into short pieces.
Then another protein complex called RISC (RNA-induced silencing complex) discards one of the two RNA strands.
The RISC-docked, single-stranded RNA then pairs with the homologous mRNA and destroys it.
THE RISC COMPLEX:
RISC is large(>500kD) RNA multi- protein Binding complex which triggers MRNA degradation in response to MRNA
Unwinding of double stranded Si RNA by ATP independent Helicase
Active component of RISC is Ago proteins( ENDONUCLEASE) which cleave target MRNA.
DICER: endonuclease (RNase Family III)
Argonaute: Central Component of the RNA-Induced Silencing Complex (RISC)
One strand of the dsRNA produced by Dicer is retained in the RISC complex in association with Argonaute
ARGONAUTE PROTEIN :
1.PAZ(PIWI/Argonaute/ Zwille)- Recognition of target MRNA
2.PIWI (p-element induced wimpy Testis)- breaks Phosphodiester bond of mRNA.)RNAse H activity.
MiRNA:
The Double-stranded RNAs are naturally produced in eukaryotic cells during development, and they have a key role in regulating gene expression .
insect taxonomy importance systematics and classification
Female reproductive system 2 (Histology of Ovary, Oogenesis & Follicular Development)
1. FEMALE REPRODUCTIVE SYSTEM 2
1. HISTOLOGY OF OVARY
2.OOGENESIS AND FOLLICULAR
DEVELOPMENT
Mrs. Sarita Sharma
Assistant Professor
Department Of Pharmacology
Mumbai
2. OVARY
• FEMALE GONADS
They are paired glands THAT resmeble unshelled almonds in size and shape
Located one on either sides of uterus.
They are homologus to testes( same embryonic origin)
• OVARIES PRODUCE
1. Gametes, secondary oocytes that develope into mature ova(eggs) after
fertilization.
2. Hormones, including PROGESTRONE & ESTROGEN (FEMALE SEX HORMONES),
INHIBIN & RELAXIN
3. OVARIES (CONTI.)
A series of ligaments holds them in
position
• 1.Broad ligament of uterus, a fold
of parietal peritonium, attaches to
ovaries by double layered fold of
peritonium called mesovarium.
• 2. Ovarian ligament-ovary to
uterus
• 3. Suspensory ligament-ovary to
pelvic wall
• Each ovary contains a
hilum(hilus), a point of entrance &
4. HISTOLOGY OF OVARY
1: Germinal epithelium-layer of simple epithelium- covers surface of ovary
2: Tunica albuginea-whitish capsule of dense irregular connective tissue
located immediate after GE.
3: Ovarian cortex- deep to tunica albuginea. Consits of ovarian follicles,
surrounded by dense irregular connective tissues that contains collagen
fibers & fibroblast called stromal cells.
4: Ovarian medulla- deep to ovarian cortex. Consits of more loosely
arranged connective tissue & contains blood vessels, lymphatic vessels&
5. 5: ovarian Follicles- Present In Cortex & Consits Of Oocytes In Various
Development Stages+ cells Surrounding Them.
Surrounding Cells-forming A Single Layer-follicular Cells- Later In Development Forms
Several Layers-granulosa Cells. Surrounding Cells Nourish Developing Oocyte &
Begin To Secrete Estrogens As Follicle Grows Larger.
6: Mature (Graafian) Follicle- Large Fluid Filled Follicle I.E. Ready To Rupture &
Expel Its Secondary Oocyte, A Process Known As Ovulation.
7: Corpus Luteum- Yellow Body-remaining Part After Ovulation. Produce
Progestrone, Estrogen, Relaxin & Inhibin. Until It Degenarate Into Fibrous Scar Tissue
Called Corpus Albicans (white Body)
6.
7. OOGENESISAND FOLLICULAR DEVELOPMENT
• Formation of gametes in ovary is called as oogenesis.
• Oogenesis begins before females are born
• Essentially same steps of meiosis as spermatogenesis
• During early fetal development, primordial (primitive) germ cells migrate
from yolk sac to ovaries
• Germ cells then differentiate into oogonia – diploid (2n) stem cells
• Before birth, most germ cells degenerate – atresia
• A few develop into primary oocytes that enter meiosis I during fetal
development
• Each covered by single layer of flat follicular cells – primordial follicle
• About 200,000 to 2,000,000 at birth, 40,00 remain at puberty, and around 400
8. FOLLICULAR DEVELOPMENT
• Each month from puberty to menopause, FSH and LH stimulate the development of
several primordial follicles
• Usually, only one reaches ovulation
• Primordial follicles develop into primary follicles
• Primary oocyte surrounded by granulosa cells
• Forms zona pellucida between granulosa cells and primary oocyte
• Stromal cells begin to form theca folliculi
• Primary follicles develop into secondary follicles
• Theca differentiates into theca interna secreting estrogens and theca externa
• Granulosa cells secrete follicular fluid in antrum
• Innermost layer of granulosa cells attaches to zona pellucida forming corona
radiata
10. FOLLICULAR DEVELOPMENT
• Secondary follicle becomes mature (graffian) follicle
• Just before ovulation, diploid primary oocyte completes meiosis I (46
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• Produces 2 unequal sized haploid (n) cells – first polar body is discarded
and secondary oocyte
• At ovulation, secondary oocyte expelled with first polar body and corona radiata
• If fertilization does not occur, cells degenerate
• If a sperm penetrates secondary oocyte, meiosis II resumes
• Secondary oocyte splits into 2 cells of unequal size – second polar body (also
discarded) and ovum or mature egg
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