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视黄酸(RA)信号通路如何调节精子发生?

How does retinoic acid (RA) signaling pathway regulate spermatogenesis?

作者信息

Zhang Hua-Zhe, Hao Shuang-Li, Yang Wan-Xi

机构信息

The Sperm Laboratory, College of Life Sciences, Zhejiang University, Hangzhou, Zhejiang, China.

出版信息

Histol Histopathol. 2022 Nov;37(11):1053-1064. doi: 10.14670/HH-18-478. Epub 2022 Jun 6.

Abstract

Male sterility is a worldwide health problem which has troubled many unfortunate families and attracted widespread attention in the field of reproduction. Retinoic acid (RA) is a metabolite of vitamin A. Previous studies have shown that insufficient intake of vitamin A can lead to male infertility. Similarly, RA-deficiency can lead to abnormal spermatogenesis in men. RA signaling is inseparable from hormone stimulation, such as FSH, testosterone and others. It can regulate spermatogenesis as well, including the proliferation and differentiation of spermatogonia, meiosis, spermiogenesis and spermiation. To promote or inhibit spermatogenesis, RA regulates Stra8, Kit, GDNF, BMP4 and other factors in various pathways. At the self-renewal stage, RA inhibits spermatogonia renewal by directly or indirectly inhibiting DMRT, GDNF and Cyclin. At the stage of differentiation and meiosis, RA controls SSC differentiation through Kit induction and Nanos2 inhibition, and controls spermatogonia meiotic entry through up- regulation of Stra8. At the stage of spermiogenesis, RARα945;, as a key regulator, regulates spermatogenesis by up regulating Stra8 while binding with RA. Although RA plays an important role in all stages of spermatogenesis, RA signaling is more important in the early stage of spermatogonia (spg) differentiation and spermatocyte(spc) meiosis. According to the principle of RA signaling that regulates spermatogenesis, we also speculate on the future clinical application of RA, such as potential induction of SSC in vitro, contraception and restoring spermatogenesis. This paper reviews the regulatory pathways of RA, and prospects the clinical applications of RA signaling in the future.

摘要

男性不育是一个全球性的健康问题,困扰着许多不幸的家庭,并在生殖领域引起了广泛关注。视黄酸(RA)是维生素A的一种代谢产物。先前的研究表明,维生素A摄入不足会导致男性不育。同样,RA缺乏也会导致男性精子发生异常。RA信号传导与激素刺激密不可分,如促卵泡生成素(FSH)、睾酮等。它也能调节精子发生,包括精原细胞的增殖和分化、减数分裂、精子形成和精子释放。为了促进或抑制精子发生,RA在各种途径中调节Stra8、Kit、胶质细胞源性神经营养因子(GDNF)、骨形态发生蛋白4(BMP4)等因子。在自我更新阶段,RA通过直接或间接抑制双性缺失转录因子(DMRT)、GDNF和细胞周期蛋白来抑制精原细胞更新。在分化和减数分裂阶段,RA通过诱导Kit和抑制Nanos2来控制精原干细胞(SSC)分化,并通过上调Stra8来控制精原细胞减数分裂的进入。在精子形成阶段,RARα作为关键调节因子,在与RA结合的同时通过上调Stra8来调节精子发生。尽管RA在精子发生的所有阶段都起着重要作用,但RA信号传导在精原细胞(spg)分化和精母细胞(spc)减数分裂的早期更为重要。根据RA信号传导调节精子发生的原理,我们还推测了RA未来的临床应用,如体外潜在诱导SSC、避孕和恢复精子发生。本文综述了RA的调节途径,并展望了RA信号传导在未来的临床应用。

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