FIRST YEAR EMBRYOLOGY: GAMETOGENESIS


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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