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血睾屏障与支持细胞功能:来自SCCx43KO小鼠的启示

Blood-testis barrier and Sertoli cell function: lessons from SCCx43KO mice.

作者信息

Gerber Jonathan, Heinrich Julia, Brehm Ralph

机构信息

Institute of AnatomyUniversity of Veterinary Medicine Hannover, Foundation, Bischofsholer Damm 15, 30173 Hannover, Germany.

Institute of AnatomyUniversity of Veterinary Medicine Hannover, Foundation, Bischofsholer Damm 15, 30173 Hannover, Germany

出版信息

Reproduction. 2016 Feb;151(2):R15-27. doi: 10.1530/REP-15-0366. Epub 2015 Nov 10.

Abstract

The gap junction protein connexin43 (CX43) plays a vital role in mammalian spermatogenesis by allowing for direct cytoplasmic communication between neighbouring testicular cells. In addition, different publications suggest that CX43 in Sertoli cells (SC) might be important for blood-testis barrier (BTB) formation and BTB homeostasis. Thus, through the use of the Cre-LoxP recombination system, a transgenic mouse line was developed in which only SC are deficient of the gap junction protein, alpha 1 (Gja1) gene. Gja1 codes for the protein CX43. This transgenic mouse line has been commonly defined as the SC specific CX43 knockout (SCCx43KO) mouse line. Within the seminiferous tubule, SC aid in spermatogenesis by nurturing germ cells and help them to proliferate and mature. Owing to the absence of CX43 within the SC, homozygous KO mice are infertile, have reduced testis size, and mainly exhibit spermatogenesis arrest at the level of spermatogonia, seminiferous tubules containing only SC (SC-only syndrome) and intratubular SC-clusters. Although the SC specific KO of CX43 does not seem to have an adverse effect on BTB integrity, CX43 influences BTB composition as the expression pattern of different BTB proteins (like OCCLUDIN, β-CATENIN, N-CADHERIN, and CLAUDIN11) is altered in mutant males. The supposed roles of CX43 in dynamic BTB regulation, BTB assembly and/or disassembly and its possible interaction with other junctional proteins composing this unique barrier are discussed. Data collectively indicate that CX43 might represent an important regulator of dynamic BTB formation, composition and function.

摘要

缝隙连接蛋白连接蛋白43(CX43)通过允许相邻睾丸细胞之间直接进行细胞质通讯,在哺乳动物精子发生过程中发挥着至关重要的作用。此外,不同的研究表明,支持细胞(SC)中的CX43可能对血睾屏障(BTB)的形成和BTB的稳态很重要。因此,通过使用Cre-LoxP重组系统,开发了一种转基因小鼠品系,其中只有支持细胞缺乏缝隙连接蛋白α1(Gja1)基因。Gja1编码CX43蛋白。这种转基因小鼠品系通常被定义为支持细胞特异性CX43敲除(SCCx43KO)小鼠品系。在生精小管内,支持细胞通过滋养生殖细胞来协助精子发生,并帮助它们增殖和成熟。由于支持细胞中缺乏CX43,纯合敲除小鼠不育,睾丸体积减小,主要表现为精子发生在精原细胞水平停滞,生精小管中仅含有支持细胞(仅支持细胞综合征)和管内支持细胞簇。尽管支持细胞特异性敲除CX43似乎对BTB的完整性没有不利影响,但CX43会影响BTB的组成,因为在突变雄性小鼠中,不同BTB蛋白(如闭合蛋白、β-连环蛋白、N-钙黏蛋白和Claudin11)的表达模式发生了改变。本文讨论了CX43在动态BTB调节、BTB组装和/或拆卸中的假定作用,以及它与构成这一独特屏障的其他连接蛋白可能的相互作用。总体数据表明,CX43可能是动态BTB形成、组成和功能的重要调节因子。

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