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维持减数分裂阻滞以及诱导从小窦卵泡体外发育而来的小鼠卵母细胞-颗粒细胞复合体中的卵母细胞成熟。

Maintenance of meiotic arrest and the induction of oocyte maturation in mouse oocyte-granulosa cell complexes developed in vitro from preantral follicles.

作者信息

Eppig J J

机构信息

Jackson Laboratory, Bar Harbor, Maine 04609.

出版信息

Biol Reprod. 1991 Dec;45(6):824-30. doi: 10.1095/biolreprod45.6.824.

DOI:10.1095/biolreprod45.6.824
PMID:1666849
Abstract

During the development of oocyte-granulosa cell complexes from preantral follicles in vitro, oocytes grow and acquire competence to undergo germinal vesicle breakdown (GVB). In the culture system used here, GVB-competent oocytes were maintained in meiotic arrest solely by endogenous physiological mechanisms of the granulosa cells without supplementation with meiosis-arresting substances. Addition of mycophenolic acid, an inhibitor of inosine monophosphate (IMP) dehydrogenase, induced GVB in about 70% of the GVB-competent oocytes grown in vitro. The mechanism for meiotic arrest in this system is, therefore, similar to that for arrest in vivo insofar as it requires the participation of the IMP dehydrogenase pathway. Rp-cyclic adenosine monophosphothioate, a membrane-permeable antagonist to cAMP, induced GVB by about 30% of the competent oocytes. Cyclic AMP-dependent pathways, therefore, participate in the physiological mechanism by which mouse granulosa cells maintain meiotic arrest. Complexes were grown for 10 days in medium containing 0, 1, 5, or 10 ng/ml FSH, were stimulated with either 1 microgram/ml FSH or LH, and were assessed for GVB and cumulus expansion. GVB was stimulated by FSH whether or not the complexes were grown in medium containing FSH, but LH or hCG induced GVB only when the complexes were grown in medium containing FSH. Cumulus expansion occurred in response to either FSH or LH only when complexes were grown in medium containing FSH. FSH, therefore, promotes the differentiation of granulosa cells from preantral follicles in vitro so that LH can stimulate GVB and cumulus expansion.

摘要

在体外从窦前卵泡发育卵母细胞-颗粒细胞复合体的过程中,卵母细胞生长并获得进行生发泡破裂(GVB)的能力。在此处使用的培养系统中,具有GVB能力的卵母细胞仅通过颗粒细胞的内源性生理机制维持减数分裂阻滞,无需添加减数分裂阻滞物质。添加肌苷单磷酸(IMP)脱氢酶抑制剂霉酚酸可诱导约70%体外培养的具有GVB能力的卵母细胞发生GVB。因此,该系统中减数分裂阻滞的机制与体内阻滞机制相似,因为它需要IMP脱氢酶途径的参与。Rp-环磷酸腺苷硫代酸盐是一种可透过细胞膜的cAMP拮抗剂,可诱导约30%具有能力的卵母细胞发生GVB。因此,环磷酸腺苷依赖性途径参与了小鼠颗粒细胞维持减数分裂阻滞的生理机制。复合体在含有0、1、5或10 ng/ml促卵泡激素(FSH)的培养基中培养10天,用1微克/ml FSH或促黄体生成素(LH)刺激,并评估GVB和卵丘扩展情况。无论复合体是否在含有FSH的培养基中培养,FSH均可刺激GVB,但只有当复合体在含有FSH的培养基中培养时,LH或人绒毛膜促性腺激素(hCG)才会诱导GVB。只有当复合体在含有FSH的培养基中培养时,FSH或LH才会引起卵丘扩展。因此,FSH可促进体外窦前卵泡颗粒细胞的分化,从而使LH能够刺激GVB和卵丘扩展。

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