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平面细胞极性(PCP)蛋白通过在睾丸中的细胞骨架组织支持精子发生。

Planar cell polarity (PCP) proteins support spermatogenesis through cytoskeletal organization in the testis.

机构信息

The Second Affiliated Hospital and Yuying Children's Hospital, Wenzhou Medical University, Wenzhou, Zhejiang 325027, China; Institute of Reproductive Medicine, Nantong University School of Medicine, Nantong, Jiangsu 226001, China.

Institute of Reproductive Medicine, Nantong University School of Medicine, Nantong, Jiangsu 226001, China.

出版信息

Semin Cell Dev Biol. 2022 Jan;121:99-113. doi: 10.1016/j.semcdb.2021.04.008. Epub 2021 May 29.

Abstract

Few reports are found in the literature regarding the role of planar cell polarity (PCP) in supporting spermatogenesis in the testis. Yet morphological studies reported decades earlier have illustrated the directional alignment of polarized developing spermatids, most notably step 17-19 spermatids in stage V-early VIII tubules in the testis, across the plane of the epithelium in seminiferous tubules of adult rats. Such morphological features have unequivocally demonstrated the presence of PCP in developing spermatids, analogous to the PCP noted in hair cells of the cochlea in mammals. Emerging evidence in recent years has shown that Sertoli and germ cells express numerous PCP proteins, mostly notably, the core PCP proteins, PCP effectors and PCP signaling proteins. In this review, we discuss recent findings in the field regarding the two core PCP protein complexes, namely the Van Gogh-like 2 (Vangl2)/Prickle (Pk) complex and the Frizzled (Fzd)/Dishevelled (Dvl) complex. These findings have illustrated that these PCP proteins exert their regulatory role to support spermatogenesis through changes in the organization of actin and microtubule (MT) cytoskeletons in Sertoli cells. For instance, these PCP proteins confer PCP to developing spermatids. As such, developing haploid spermatids can be aligned and orderly packed within the limited space of the seminiferous tubules in the testes for the production of sperm via spermatogenesis. Thus, each adult male in the mouse, rat or human can produce an upward of 30, 50 or 300 million spermatozoa on a daily basis, respectively, throughout the adulthood. We also highlight critical areas of research that deserve attention in future studies. We also provide a hypothetical model by which PCP proteins support spermatogenesis based on recent studies in the testis. It is conceivable that the hypothetical model shown here will be updated as more data become available in future years, but this information can serve as the framework by investigators to unravel the role of PCP in spermatogenesis.

摘要

关于平面细胞极性(PCP)在支持睾丸生精作用的研究在文献中鲜有报道。然而,几十年前的形态学研究已经表明,极化的精原细胞具有定向排列,尤其是在睾丸生精小管的 V 期-早期 VIII 期小管中,第 17-19 步精原细胞在生精上皮的平面上排列。这些形态学特征明确证明了 PCP 存在于发育中的精原细胞中,类似于哺乳动物耳蜗毛细胞中的 PCP。近年来的新证据表明,支持细胞和生殖细胞表达许多 PCP 蛋白,其中最重要的是核心 PCP 蛋白、PCP 效应蛋白和 PCP 信号蛋白。在这篇综述中,我们讨论了近年来该领域关于两个核心 PCP 蛋白复合物的最新发现,即梵高样 2(Vangl2)/刺猬(Pk)复合物和卷曲(Fzd)/离散(Dvl)复合物。这些发现表明,这些 PCP 蛋白通过改变支持细胞中肌动蛋白和微管(MT)细胞骨架的组织来发挥其调节生精作用。例如,这些 PCP 蛋白赋予发育中的精原细胞 PCP。因此,发育中的单倍体精原细胞可以在睾丸生精小管的有限空间内排列有序,并整齐排列,以便通过生精作用产生精子。因此,在成年期,每只雄性小鼠、大鼠或人类每天分别可以产生多达 3 亿、5 亿或 30 亿个精子。我们还强调了未来研究中值得关注的关键研究领域。我们还根据睾丸中的最近研究提供了一个 PCP 蛋白支持生精作用的假设模型。可以想象,随着未来几年更多数据的出现,这里显示的假设模型将得到更新,但这些信息可以作为研究人员解开 PCP 在生精作用中的作用的框架。

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