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在小鼠胚胎中构建卵巢器官发生的途径。

Building pathways for ovary organogenesis in the mouse embryo.

机构信息

Department of Veterinary Biosciences, University of Illinois at Urbana-Champaign, Illinois, USA.

出版信息

Curr Top Dev Biol. 2010;90:263-90. doi: 10.1016/S0070-2153(10)90007-0.

Abstract

Despite its significant role in oocyte generation and hormone production in adulthood, the ovary, with regard to its formation, has received little attention compared to its male counterpart, the testis. With the exception of germ cells, which undergo a female-specific pattern of meiosis, morphological changes in the fetal ovary are subtle. Over the past 40 years, a number of hypotheses have been proposed for the organogenesis of the mammalian ovary. It was not until the turn of the millennium, thanks to the advancement of genetic and genomic approaches, that pathways for ovary organogenesis that consist of positive and negative regulators have started to emerge. Through the action of secreted factors (R-spondin1, WNT4, and follistatin) and transcription regulators (beta-catenin and FOXL2), the developmental fate of the somatic cells is directed toward ovarian, while testicular components are suppressed. In this chapter, we review the history of studying ovary organogenesis in mammals and present the most recent discoveries using the mouse as the model organism.

摘要

尽管卵巢在卵子生成和成年期激素产生方面起着重要作用,但与睾丸相比,其形成过程却很少受到关注。除了经历女性特有的减数分裂的生殖细胞外,胎儿卵巢的形态变化很小。在过去的 40 年中,人们提出了许多关于哺乳动物卵巢发生的假说。直到千禧年之交,由于遗传和基因组方法的进步,包含正负调节剂的卵巢发生途径才开始显现。通过分泌因子(R-spondin1、WNT4 和 follistatin)和转录调节因子(β-连环蛋白和 FOXL2)的作用,体细胞的发育命运被导向卵巢,而睾丸成分则被抑制。在本章中,我们回顾了研究哺乳动物卵巢发生的历史,并介绍了使用小鼠作为模型生物的最新发现。

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