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精子发生过程中微丝的动态变化和调控。

The dynamics and regulation of microfilament during spermatogenesis.

机构信息

The Sperm Laboratory, College of Life Sciences, Zhejiang University, Hangzhou 310058, China.

The Sperm Laboratory, College of Life Sciences, Zhejiang University, Hangzhou 310058, China.

出版信息

Gene. 2020 Jun 20;744:144635. doi: 10.1016/j.gene.2020.144635. Epub 2020 Mar 31.

Abstract

Spermatogenesis is a highly complex physiological process which contains spermatogonia proliferation, spermatocyte meiosis and spermatid morphogenesis. In the past decade, actin binding proteins and signaling pathways which are critical for regulating the actin cytoskeleton in testis had been found. In this review, we summarized 5 actin-binding proteins that have been proven to play important roles in the seminiferous epithelium. Lack of them perturbs spermatids polarity and the transport of spermatids. The loss of Arp2/3 complex, Formin1, Eps8, Palladin and Plastin3 cause sperm release failure suggesting their irreplaceable role in spermatogenesis. Actin regulation relies on multiple signal pathways. The PI3K/Akt signaling pathway positively regulate the mTOR pathway to promote actin reorganization in seminiferous epithelium. Conversely, TSC1/TSC2 complex, the upstream of mTOR, is activated by the LKB1/AMPK pathway to inhibit cell proliferation, differentiation and migration. The increasing researches focus on the function of actin binding proteins (ABPs), however, their collaborative regulation of actin patterns and potential regulatory signaling networks remains unclear. We reviewed ABPs that play important roles in mammalian spermatogenesis and signal pathways involved in the regulation of microfilaments. We suggest that more relevant studies should be performed in the future.

摘要

精子发生是一个高度复杂的生理过程,包含精原细胞增殖、精母细胞减数分裂和精子形成。在过去的十年中,已经发现了许多对调节睾丸中肌动蛋白细胞骨架至关重要的肌动蛋白结合蛋白和信号通路。在这篇综述中,我们总结了 5 种已被证明在生精上皮中发挥重要作用的肌动蛋白结合蛋白。这些蛋白的缺失会扰乱精子的极性和运动。Arp2/3 复合物、formin1、Eps8、palladin 和 Plastin3 的缺失会导致精子释放失败,表明它们在精子发生中不可替代的作用。肌动蛋白的调节依赖于多种信号通路。PI3K/Akt 信号通路正向调节 mTOR 通路,促进生精上皮中肌动蛋白的重组。相反,mTOR 的上游 TSC1/TSC2 复合物被 LKB1/AMPK 通路激活,抑制细胞增殖、分化和迁移。越来越多的研究集中在肌动蛋白结合蛋白(ABPs)的功能上,然而,它们对肌动蛋白模式的协同调节以及潜在的调节信号网络仍然不清楚。我们综述了在哺乳动物精子发生中起重要作用的 ABPs 以及参与微丝调节的信号通路。我们建议在未来进行更多相关的研究。

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