Antral And Tertiary Follicle Formation Flashcards

1
Q

The continued development of the oocyte to a mature state capable of being fertilized is

A

dependent upon the hormones of the menstrual cycle.

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2
Q

FSH stimulates a further increase in

A

GC numbers and is responsible for the formation of a fluid filled space within the growing follicle.

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3
Q

Fluid accumulation between cells commences when the follicle diameter reaches about

A

200-300 uM and these fluid-filled cavities coalesce to form a single cavity leading to a dramatic increase in follicular size.

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4
Q

6th week of fetal development: primordial germ cells (oogonia) migrate to

A

the ovarian cortex and multiply by mitosis.

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5
Q

Follicle assembly:

A

some oogonia are encapsulated by follicular cells → primordial folicle.

First stage of meiotic division arested > primary oocyte.

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6
Q

Then there is birth:

A

No further development until sexual maturity.

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7
Q

Upon sexual maturity:

A

Secretion of pituitary gonadotropins FSH and LH.

Primordial follicle activation: selected cohorts recruited to develop.

Follicular growth: increase in granulosa and cell number.

Steroidogenesis: increasing secretion of estrogen progressively inhibits the release of FSH and promotes LH release.

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8
Q

Upon ovulation, Corpus luteum formation:

A

progesterone secretion by corpus luteum maintained by low levels of LH.

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9
Q

Progesterone inhibits the expression of high levels of

A

LH secretion.

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10
Q

Following fertilization and implantation, Corpus luteum of pregnancy maintained by

A

HCG secreted by the developing conceptus.

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11
Q

Primordial follicle:

A

single layer of flattened granulosa cells.

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12
Q

Primary follicle:

A

single layer of cuboidal granulosa cells.

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13
Q

Secondary follicle:

A

two layers of granulosa and thecal cell differentiation.

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14
Q

Antral follicle:

A

fluid-filled antrum develops.

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15
Q

Graafian follicle:

A

mature follicle with distinct granulosa cells populations; mural and coronal.

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16
Q

The antrum grows by accumulating fluid derived from blood flowing through the thecal capillaries and secretion products from

A

follicular cells some of which (e.g. hyaluron and proteoglycans) create an osmotic gradient that participates in antrum growth.

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17
Q

Follicular fluid is thus a product of

A

transudation of plasma and secretions from the GC.

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18
Q

Cytokines are small- to medium-size proteins/glycoproteins that act

A

as intercellular mediators and growth factors.

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19
Q

Intrafollicular cytokines that regulate angiogenesis, steroidogenesis, oocyte maturation, leucocyte infiltration and follicle rupture/remodeling during ovulation are

A

readily detectable in follicular fluid

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20
Q

As the follicle size increases, the thecal layer

A

differentiates into the theca interna and theca externa.

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21
Q

The GC and theca become highly active steroidogenic cells. Under the influence of FSH and LH the

A

GCs continue to divide and more fluid fills the antrum.

22
Q

The theca interna becomes increasingly

A

vascularized as follicle development ensues while the GC layer remains avascular.

23
Q

As the volume of the antrum increases

A

the GCs become pressed against the wall of the follicle and are termed mural GCs.

24
Q

The oocyte is also eccentric and is attached to the mural GC by a stalk of

A

avascular GCs, the cumulus oophorus, and originate from a common progenitor in pre-antral follicles.

25
Antrum formation brings about physical
separation and differentiation of the two cell compartments.
26
The cumulus oocyte complex (COC) is comprised of three to four layers of cumulus cells (approximately 2000 cells) that
envelope the oocyte in tightly packed concentric layers.
27
Removal of the cumulus cells, even in the very final hours of maturation, oocytes will
severely compromise the ooyctes competence to fertilize.
28
Oocyte paracrine signaling to cumulus cells is
essential for cumulus expansion.
29
Two oocyte secreted morphogens, GDF9 and bone morphogenic protein 15 (BMP15) regulate
cumulus gene expression.
30
The GC immediately surrounding the oocyte, the corona radiata, are intimate connected to the oocyte via
specialized gap junctions that allow for nutrient exchange and transport of signaling molecules that regulate oocyte activity between the oocyte and GC.
31
The follicle is now called the tertiary Graafian or preovulatory follicle:
the follicle has increased from less than 0.1 mm as a newly recruited primary follicle to a 12-19 mm preovulatory follicle
32
Since the follicles are physically located within the ovarian cortexthis dramatic increase in the size ultimately leads to
one of the surfaces of the follicle coming in contact with the tunica albuginea.
33
The oocyte volume increases during follicle development but its genetic maturation
remains unchanged as a primary oocyte.
34
Recent evidence has demonstrated a functional role for the estradiol:
estrogen receptor system in follicular GC maintaining oocyte meiotic arest by regulating the expression of natriuretic peptide C (NPPC) and natriuretic peptide receptor 2 (NPR2).
35
Cyclic GMP diffuses into the oocyte via the large
network of gap junctions and inhibits phophodiesterase 3A (PDE3A) suppressing the hydrolysis of cyclic AMP.
36
High levels of cAMP in the oocyte suppress the activation of
MPF via the action of cAMP-dependent protein kinase A (PKA).
37
The maturing follicle begins to bulge on the ovarian surface forming a thinned area that looks like a blister (the stigma) from which the
oocyte will leave the ovary following rupture of the follicle at ovulation.
38
The anterior pituitary releases a surge of LH around Day 14 of a 28-day menstrual cycle. However, cumulus cells express few, if any, receptors for LH and hence the mechanism by which LH induced
cumulus cell expansion and oocyte maturation remain elusive.
39
This surge of LH is responsible for
the resumption of meiosis I and the ovulatory process.
40
After ovulation, the mature oocyte arrested in metaphase of meiosis II is picked-up by
the fimbria of the oviduct and transported to the distal 1/3 of oviduct (ampula).
41
Candidate regulatory factors include EGF-ike growth factors (such as amphiregulin, epiregulin and betacelulin) that have been shown to play critical roles in
mediating the actions of LH in pre-ovulatory follicles.
42
Amphiregulin is the dominant EGF-like molecule in humans and its presence in the follicle is stimulated
by the LH surge.
43
Amphiregulin activates EGF receptors within the follicle that trigger oocyte nuclear maturation, likely by autocrine and paracrine mechanisms, to propagate the LH signal to
granulosa and cumulus cells stimulating cumulus expansion, oocyte maturation and ovulation.
44
RAS and MAPK also appear to have important signaling roles in
ovarian follicles at the time of ovulation.
45
Reinitiation and completion of the second meiotic division is triggered by
fertilization and completes the process of oogenesis.
46
However, this final stage of oogenesis is short-lived. The 23 maternal chromosomes will join the 23 paternal chromosomes of the sperm within 18 hours by the process of
syngamy to form the diploid embryo.
47
In most menstrual cycles, only one follicle will continue to develop to the fully mature graafian stage (dominant follicle selection). The majority of growing follicles will undergo
atresia at some point during development involving degradation of all cell types in the follicle that appears to commence with different cell populations depending on the stage of follicle development at the time of atresia.
48
The oocyte is the first component to die in pre-antral bovine follicles whereas
the granulosa cells die first in later stage follicles.
49
Thecal cells appear to be more susceptible to cell death during
earlier stages of follicle development.
50
Death of follicular cells reportedly occurs by
programmed cell death (apoptosis)) as well as autophagy, necrosis and cornification.