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支持细胞-支持细胞和支持细胞-生殖细胞相互作用及其在精子发生过程中曲细精管上皮生殖细胞移动中的意义。

Sertoli-Sertoli and Sertoli-germ cell interactions and their significance in germ cell movement in the seminiferous epithelium during spermatogenesis.

作者信息

Mruk Dolores D, Cheng C Yan

机构信息

Population Council, Center for Biomedical Research, New York, New York 10021, USA.

出版信息

Endocr Rev. 2004 Oct;25(5):747-806. doi: 10.1210/er.2003-0022.

DOI:10.1210/er.2003-0022
PMID:15466940
Abstract

Spermatogenesis is the process by which a single spermatogonium develops into 256 spermatozoa, one of which will fertilize the ovum. Since the 1950s when the stages of the epithelial cycle were first described, reproductive biologists have been in pursuit of one question: How can a spermatogonium traverse the epithelium, while at the same time differentiating into elongate spermatids that remain attached to the Sertoli cell throughout their development? Although it was generally agreed upon that junction restructuring was involved, at that time the types of junctions present in the testis were not even discerned. Today, it is known that tight, anchoring, and gap junctions are found in the testis. The testis also has two unique anchoring junction types, the ectoplasmic specialization and tubulobulbar complex. However, attention has recently shifted on identifying the regulatory molecules that "open" and "close" junctions, because this information will be useful in elucidating the mechanism of germ cell movement. For instance, cytokines have been shown to induce Sertoli cell tight junction disassembly by shutting down the production of tight junction proteins. Other factors such as proteases, protease inhibitors, GTPases, kinases, and phosphatases also come into play. In this review, we focus on this cellular phenomenon, recapping recent developments in the field.

摘要

精子发生是一个单倍体精原细胞发育成256个精子的过程,其中一个精子将使卵子受精。自20世纪50年代首次描述上皮周期的阶段以来,生殖生物学家一直在追寻一个问题:精原细胞如何穿过上皮组织,同时分化成长形精子细胞,而精子细胞在整个发育过程中始终附着于支持细胞?尽管人们普遍认为这涉及连接结构的重组,但当时甚至还未识别出睾丸中存在的连接类型。如今,已知睾丸中存在紧密连接、锚定连接和缝隙连接。睾丸还有两种独特的锚定连接类型,即外质特化和球管复合体。然而,最近的注意力已转向识别“打开”和“关闭”连接的调节分子,因为这些信息将有助于阐明生殖细胞移动的机制。例如,细胞因子已被证明可通过停止紧密连接蛋白的产生来诱导支持细胞紧密连接的解体。蛋白酶、蛋白酶抑制剂、GTP酶、激酶和磷酸酶等其他因素也发挥作用。在本综述中,我们聚焦于这一细胞现象,概述该领域的最新进展。

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