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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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Prophase I Arrest of Mouse Oocytes Mediated by Natriuretic Peptide Precursor C Requires GJA1 (connexin-43) and GJA4 (connexin-37) Gap Junctions in the Antral Follicle and Cumulus-Oocyte Complex

TL;DR: Connexin mimetic peptides (CMPs) that specifically disrupt gap junction isoforms within cumulus-oocyte complexes (COCs) and isolated antral follicles in culture overcame NPPC-mediated meiotic arrest in both isolated COCs and antrals follicles.
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Granulosa cells regulate oocyte intracellular pH against acidosis in preantral follicles by multiple mechanisms.

TL;DR: These experiments identify the NHE isoforms involved in regulating oocytes pHi, indicate that gap junctions allow granulosa cells to exogenously regulate oocyte pHi against acidosis until the oocyte has acquired endogenous pHi regulation, and reveal that granul Rosa cells possess multiple mechanisms for carrying out this function.
Journal ArticleDOI

Dephosphorylation of juxtamembrane serines and threonines of the NPR2 guanylyl cyclase is required for rapid resumption of oocyte meiosis in response to luteinizing hormone.

TL;DR: The findings indicate that NPR2 dephosphorylation in the mural granulosa cells is essential for the normal progression of meiosis in response to LH and EGF receptor activation, and provide the first demonstration that a change in phosphorylation of a transmembrane guanylyl cyclase regulates a physiological process.
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