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C型利钠肽调节成年大鼠睾丸中的血睾屏障动态。

C-type natriuretic peptide regulates blood-testis barrier dynamics in adult rat testes.

作者信息

Xia Weiliang, Mruk Dolores D, Cheng C Yan

机构信息

Center for Biomedical Research, Population Council, 1230 York Avenue, New York, NY 10021.

出版信息

Proc Natl Acad Sci U S A. 2007 Mar 6;104(10):3841-6. doi: 10.1073/pnas.0610100104. Epub 2007 Feb 27.

Abstract

In adult rat testes, the blood-testis barrier (BTB) in the seminiferous epithelium must "open" (or "disassemble") to accommodate the migration of preleptotene spermatocytes from the basal to the adluminal compartment that occurs at stage VIII of the epithelial cycle. However, the molecule(s) and/or mechanism(s) that regulate this event are unknown. In this report, C-type natriuretic peptide (CNP) was shown to be a regulator of BTB dynamics. Although Sertoli and germ cells contributed to the pool of CNP in the seminiferous epithelium, its receptor, natriuretic peptide receptor B, resided almost exclusively in Sertoli cells. CNP also expressed stage-specifically and localized predominantly at the BTB in the seminiferous epithelium at stage VIII of the epithelial cycle. A synthetic CNP-22 peptide, when added to Sertoli cell cultures, was shown to perturb Sertoli cell tight junction in vitro, causing disappearance of BTB-associated proteins (JAM-A, occludin, N-cadherin, and beta-catenin) from the cell-cell interface. This inhibitory effect of CNP on the tight junction was confirmed by transient overexpression of CNP in these cells, which was mediated, at least in part, by accelerating the internalization of BTB integral membrane proteins. To validate these in vitro findings, CNP-22 was administered to testes at a dose of 0.35 or 3.5 mug per testis, which was shown to perturb the BTB integrity In vivo when the barrier function was assessed by monitoring the diffusion of a small molecular probe across the BTB. In summary, CNP secreted by Sertoli and germ cells into the BTB microenvironment regulates BTB dynamics during spermatogenesis.

摘要

在成年大鼠睾丸中,生精上皮中的血睾屏障(BTB)必须“打开”(或“解体”),以适应前细线期精母细胞从基底室迁移至管腔室,这一过程发生在上皮周期的第VIII阶段。然而,调节这一过程的分子和/或机制尚不清楚。在本报告中,C型利钠肽(CNP)被证明是BTB动态变化的调节因子。虽然支持细胞和生殖细胞都为生精上皮中的CNP库做出了贡献,但其受体利钠肽受体B几乎只存在于支持细胞中。CNP在上皮周期第VIII阶段的生精上皮中也呈现阶段特异性表达,且主要定位于BTB处。当将合成的CNP-22肽添加到支持细胞培养物中时,它在体外会扰乱支持细胞紧密连接,导致BTB相关蛋白(JAM-A、闭合蛋白、N-钙黏蛋白和β-连环蛋白)从细胞-细胞界面消失。CNP对紧密连接的这种抑制作用通过在这些细胞中瞬时过表达CNP得到证实,这至少部分是通过加速BTB整合膜蛋白的内化介导的。为了验证这些体外研究结果,将CNP-22以每个睾丸0.35或3.5微克的剂量注射到睾丸中,当通过监测小分子探针跨BTB的扩散来评估屏障功能时,结果显示它在体内会扰乱BTB的完整性。总之,支持细胞和生殖细胞分泌到BTB微环境中的CNP在精子发生过程中调节BTB的动态变化。

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