BY
MUNEEB HASAN KHAN
GAMETOGENESIS
“Biological process by which
specialized, diploid cells undergo meiotic cell divisions to form mature, haploid gametes,
which are specialized generative
cells.”
·
Human gametes arise in embryonic life from Progenitor Germ Cells (PGCs) that: Form in epiblast in 2nd week.
Ø Migrate through primitive streak and into endoderm of umbilical
vesicle during gastrulation.
Ø Migrate to gonadal regions starting from 4th and arriving by end of 5th
week.
Ø Increase in number by mitotic
division
Ø Remain dormant during Infancy
Ø Undergo gametogenesis and cytodifferentiation to form gametes at puberty.
SPERMATOGENESIS:
·
Male gamete formation is a continuous process that begins at puberty and continues throughout life.
·
One cycle completes in 74 days and approximately 300 million sperms
are produced daily.
·
In seminiferous tubules, PGCs in germinal epithelium give rise to spermatogonia that are dormant in fetal life and infancy.
By
puberty, 3 types are seen:
1)
Type
A, Dark – reserve cells that produce a clone
of pale Type A cells.
2)
Type
A, Pale – produce type B cells as well as
increasing their own number. 3) Type B –divide mitotically into daughter cells.
- These daughter cells enlarge to form diploid primary spermatocytes, largest cells in the region – which enter
a prolonged
prophase (22 days)
- Then they rapidly undergo 1st
meiotic division to form 2 haploid
secondary spermatocytes.
- These undergo 2nd meiotic
division to form 4, nonmotile
haploid
spermatids.
- Until this stage, all progeny
of single type A cell clone connected by cytoplasmic bridges, due to incomplete cytokinesis.
- Spermatids differentiate into 4 sperms by spermiogenesis, involving:
Ø Acrosome formation from Golgi apparatus
Ø Condensation of nucleus
Ø Shedding of most of cytoplasm as residual bodies, which are phagocytosed by Sertoli cells. Flagellum/Tail formation from centrioles.
·
Mature Spermatozoa are haploid, motile cells with 22 autosomes and either X or Y sex
chromosome. They have 3 parts:
1) Head – contains nucleus and acrosome (cap-like, saccular organelle that covers anterior 2/3rd of head & contains
enzymes that help in penetration of ovum) 2) Neck – junction point of head and tail.
3) Tail – confers mobility and assists in transport & penetration. Has 3 segments:
a. Middle piece (contains mitochondria in a sheath for energy supply). b. Principle
piece
c. End piece
Supporting cells & Hormonal Control: Include
·
Leydig
cells –produce testosterone in response to LH from pituitary gland.
·
Sertoli
cells – line the seminiferous tubules.
Ø Bind testosterone to promote spermatogenesis.
Ø Bind follicle-stimulating
hormone to stimulate testicular fluid
production.
Ø Support, protect, nourish, and
assist in release of sperms.
OOGENESIS:
PRENATAL DEVELOPMENT:
·
PGCs in gonadal region differentiate into oogonia, that proliferate mitotically – reaching peak number of `7 million
at about 5th fetal month.
·
About 2 million of these enlarge and form primary oocytes before, which are:
o Arranged near surface of ovary
o Surrounded by a layer of squamous
cells i.e. primordial
follicle (derived from ovarian surface
epithelium and connective tissue)
o Acquire zona
pellucida (glycoproteinaceous layer secreted
by both oocyte and follicle) o Begin first mitotic
division that is arrested in diplotene stage
of prophase I until adolescence due to production
of oocyte
maturation inhibitor by follicular cells.
o Cannot perform mitosis (hence do not proliferate after birth)
·
Remaining 5 million oogonia degenerate
by atresia and are neither present at nor
formed after birth.
POSTNATAL MATURATION:
·
Majority of primary oocytes regress during infancy and only 40,00
remain by adolescence.
·
About 400 of these undergo further maturation & ovulation
usually at rate of once per
ovarian cycle.
·
A pool of 15-20 growing follicles is established and maintained in
ovary; usually 1 matures while the rest die by atresia, forming scar tissue i.e. corpus
atreticum.
·
Following events occur in maturing follicle:
1.
Primary oocyte completes 1st meiotic division in
response to an LH surge near ovulation to form 2 haploid cells:
a)
Secondary
oocyte – receives most of the cytoplasm
b)
1st
Polar Body – a small cell destined for
degeneration.
2.
Secondary oocyte undergoes second
meiotic division that proceeds upto metaphase, at which point ovulation occurs. 2 things can happen to it:
a)
If unfertilized, it degenerates and menstrual
phase occurs.
b)
If fertilized, meiosis completes and results in formation of mature
oocyte and 2nd
polar body.
3.
Both polar bodies are extruded into perivitelline space.
4.
Primordial follicle matures into Graafian
follicle, with its cells becoming first
cuboidal then columnar, & formation of granulosa, fluid-filled antrum and external theca
folliculi.
Supporting Cells & Hormonal Control:
Hypothalamus forms gonadotrophin-releasing
hormone at puberty that passes to anterior pituitary and causes it to release 2 hormones that regulate the ovarian
cycle:
1)
Follicle-stimulating
hormone:
i.
Stimulates growth of ovarian follicles
ii.
Promotes estrogen production by follicular cells and interstitial glands of ovary.
2)
Luteinizing hormone:
i.
Triggers ovulation by an upsurge in its levels
ii.
Inhibits FSH secretion to prevent anymore follicles from growing
iii. Stimulates progesterone secretion from corpus luteum.
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