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Open AccessJournal ArticleDOI

Regulation of germ cell development by intercellular signaling in the mammalian ovarian follicle.

TLDR
Oocyte differentiation depends on continuous signaling interactions with the somatic cells of the follicle and may be regulated by extracellular vesicles newly identified in follicular fluid and at TZP tips, which could mediate intercellular transfer of macromolecules.
Abstract
Prior to ovulation, the mammalian oocyte undergoes a process of differentiation within the ovarian follicle that confers on it the ability to give rise to an embryo. Differentiation comprises two phases-growth, during which the oocyte increases more than 100-fold in volume as it accumulates macromolecules and organelles that will sustain early embryogenesis; and meiotic maturation, during which the oocyte executes the first meiotic division and prepares for the second division. Entry of an oocyte into the growth phase appears to be triggered when the adjacent granulosa cells produce specific growth factors. As the oocyte grows, it elaborates a thick extracellular coat termed the zona pellucida. Nonetheless, cytoplasmic extensions of the adjacent granulosa cells, termed transzonal projections (TZPs), enable them to maintain contact-dependent communication with the oocyte. Through gap junctions located where the TZP tips meet the oocyte membrane, they provide the oocyte with products that sustain its metabolic activity and signals that regulate its differentiation. Conversely, the oocyte secretes diffusible growth factors that regulate proliferation and differentiation of the granulosa cells. Gap junction-permeable products of the granulosa cells prevent precocious initiation of meiotic maturation, and the gap junctions also enable oocyte maturation to begin in response to hormonal signals received by the granulosa cells. Development of the oocyte or the somatic compartment may also be regulated by extracellular vesicles newly identified in follicular fluid and at TZP tips, which could mediate intercellular transfer of macromolecules. Oocyte differentiation thus depends on continuous signaling interactions with the somatic cells of the follicle. WIREs Dev Biol 2018, 7:e294. doi: 10.1002/wdev.294 This article is categorized under: Gene Expression and Transcriptional Hierarchies > Cellular Differentiation Signaling Pathways > Cell Fate Signaling Early Embryonic Development > Gametogenesis.

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Disruption of gap junctional communication within the ovarian follicle induces oocyte maturation

TL;DR: Because experimentally induced breakdown of communication within the ovarian follicle is associated with a drop in intraoocyte cAMP concentrations and results in resumption of meiosis, this could be the physiological mechanism employed by LH to stimulate oocyte maturation.
Journal ArticleDOI

Oocyte stage-specific effects of MTOR determine granulosa cell fate and oocyte quality in mice

TL;DR: It is shown that conditional knockout (cKO) of Mtor in either primordial or growing oocytes caused infertility but differentially affected oocyte quality, granulosa cell fate, and follicular development.
Journal Article

Effect of cell shape and packing density on granulosa cell proliferation and formation of multiple layers during early follicle development in the ovary

TL;DR: It is proposed that the basement membrane and/or theca cells that surround the follicle provide an important confinement for rapidly dividing columnar cells so that they attain maximum packing density, which restricts lateral mitosis and promotes inwardly oriented cell divisions and subsequent multilayering.
Journal ArticleDOI

Molecular regulation of follicle-stimulating hormone synthesis, secretion and action.

TL;DR: Several key players that regulate FSH synthesis, sorting, secretion and action in gonads and extragonadal tissues have been identified in a physiological setting and it is anticipated that several exciting new discoveries uncovering all aspects of FSH biology will soon be forthcoming.
Journal ArticleDOI

Mammalian Oocytes Locally Remodel Follicular Architecture to Provide the Foundation for Germline-Soma Communication

TL;DR: It is shown that TZP number and germline-soma communication are strikingly reduced in reproductively aged females, and an inability of somatic follicle cells to respond appropriately to oocyte-derived cues may contribute to human infertility.
References
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Journal ArticleDOI

Quantification of healthy follicles in the neonatal and adult mouse ovary: evidence for maintenance of primordial follicle supply

TL;DR: The hypothesis of postnatal follicle renewal in postnatal and adult ovaries of C57BL/6 mice is supported and no evidence for ovarian germline stem cells is found.
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Oocyte-granulosa cell interactions during mouse follicular development: regulation of kit ligand expression and its role in oocyte growth.

TL;DR: Elucidation of the molecular mechanisms that promote the development of healthy oocytes with good developmental competence has potential applications for improving fertility and for in vitro growth systems for oocytes from domestic animals and humans.
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Oocyte-somatic cell interactions in the human ovary-novel role of bone morphogenetic proteins and growth differentiation factors.

TL;DR: This review summarizes the current knowledge on the physiological role and molecular determinants of these ovarian regulatory factors within the human germline-somatic regulatory loop and indicates that GDF8 is an intra-ovarian factor that may play a novel role in regulating ovarian functions in the human ovary.
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Oocyte Regulation of Kit Ligand Expression in Mouse Ovarian Follicles

TL;DR: The hypothesis that oocytes regulate granulosa cell kit ligand mRNA levels in a way that is characteristic of the stage of growth and development of the oocyte is supported and the results suggest that oocyte play a major role in promoting dynamic changes in gene expression by granuloso cells appropriate to the stageof follicular development.
Journal ArticleDOI

Experimental evidence showing that no mitotically active female germline progenitors exist in postnatal mouse ovaries

TL;DR: The results provide evidence that supports the traditional view that no postnatal follicular renewal occurs in mammals, and no mitotically active Ddx4-expressing female germline progenitors exist in postnatal mouse ovaries.
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