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转化生长因子β3通过p38丝裂原活化蛋白激酶途径调节支持细胞紧密连接的动态变化。

Transforming growth factor beta3 regulates the dynamics of Sertoli cell tight junctions via the p38 mitogen-activated protein kinase pathway.

作者信息

Lui Wing-yee, Lee Will M, Cheng C Yan

机构信息

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

出版信息

Biol Reprod. 2003 May;68(5):1597-612. doi: 10.1095/biolreprod.102.011387. Epub 2002 Nov 27.

Abstract

Earlier studies have implicated the significance of transforming growth factor-beta3 (TGFbeta3) in the regulation of Sertoli cell tight junction (TJ) dynamics, possibly via its inhibitory effects on the expression of occludin, claudin-11, and zonula occludens-1 (ZO-1). Yet the mechanism by which TGFbeta3 regulates the Sertoli cell TJ-permeability barrier is not known. Using techniques of semiquantitative reverse transcription-PCR (RT-PCR), immunoblotting, immunohistochemistry, and inhibitors against different kinases coupled with physiological techniques to assess the Sertoli cell TJ barrier function, it was shown that this TGFbeta3-induced effect on Sertoli cell TJ dynamics is mediated via the p38 mitogen-activated protein (MAP) kinase pathway. First, the assembly of the Sertoli cell-TJ barrier was shown to be associated with a transient but significant decline in both the TGFbeta3 production and expression by Sertoli cells. Furthermore, addition of TGFbeta3 to Sertoli cell cultures during TJ assembly indeed perturbed the TJ barrier with an IC50 at approximately 9 pM. Second, the TGFbeta3-induced disruption of the TJ barrier was associated with a transient induction in MEKK2 but not the other upstream signaling molecules that mediate TGFbeta3 action, such as Smad2, Cdc42, Rac2, and N-Ras, suggesting this effect might be mediated via the p38 MAP kinase pathway. This postulate was confirmed by the observation that TGFbeta3 also induced the protein level of the activated and phosphorylated form of p38 MAP kinase at the time the TJ barrier was perturbed. Third, and perhaps the most important of all, this TGFbeta3-mediated inhibitory effect on the TJ barrier and the TGFbeta3-induced p-p38 MAP kinase production could be blocked by SB202190, a specific p38 MAP kinase inhibitor, but not U0126, a specific MEK1/2 kinase inhibitor. These results thus unequivocally demonstrate that TGFbeta3 utilizes the p38 MAP kinase pathway to regulate Sertoli cell TJ dynamics.

摘要

早期研究表明,转化生长因子-β3(TGFβ3)在调节支持细胞紧密连接(TJ)动态中具有重要意义,可能是通过其对闭合蛋白、紧密连接蛋白-11和闭锁小带蛋白-1(ZO-1)表达的抑制作用。然而,TGFβ3调节支持细胞TJ通透性屏障的机制尚不清楚。运用半定量逆转录聚合酶链反应(RT-PCR)、免疫印迹、免疫组织化学技术,以及针对不同激酶的抑制剂,并结合生理学技术来评估支持细胞TJ屏障功能,结果表明,TGFβ3对支持细胞TJ动态的这种诱导作用是通过p38丝裂原活化蛋白(MAP)激酶途径介导的。首先,支持细胞-TJ屏障的组装与支持细胞TGFβ3产生和表达的短暂但显著下降有关。此外,在TJ组装过程中向支持细胞培养物中添加TGFβ3确实会扰乱TJ屏障,其半数抑制浓度(IC50)约为9皮摩尔。其次,TGFβ3诱导的TJ屏障破坏与MEKK2的短暂诱导有关,但与介导TGFβ3作用的其他上游信号分子无关,如Smad2、Cdc42、Rac2和N-Ras,这表明这种作用可能是通过p38 MAP激酶途径介导的。这一假设通过以下观察得到证实:在TJ屏障受到扰乱时,TGFβ3还诱导了p38 MAP激酶的活化和磷酸化形式的蛋白水平升高。第三,也许最重要的是,这种TGFβ3介导的对TJ屏障的抑制作用以及TGFβ3诱导的p-p38 MAP激酶产生可以被特异性p38 MAP激酶抑制剂SB202190阻断,但不能被特异性MEK1/2激酶抑制剂U0126阻断。因此,这些结果明确表明,TGFβ3利用p38 MAP激酶途径来调节支持细胞TJ动态。

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