Wong Ching-Hang, Cheng C Yan
Population Council, 1230 York Avenue, New York, NY 10021, USA.
Dev Biol. 2005 Oct 1;286(1):1-15. doi: 10.1016/j.ydbio.2005.08.001.
Mitogen-activated protein kinases (MAPKs) are important regulators of many cellular processes. In mammalian testes, these kinases are involved in controlling cell division, differentiation, survival and death, and are therefore critical to spermatogenesis. Recent studies have also illustrated their involvement in junction restructuring in the seminiferous epithelium, especially at the ectoplasmic specialization (ES), a testis-specific adherens junction (AJ) type. ES contributes to the adhesion between Sertoli cells at the blood-testis barrier, as well as between Sertoli and developing spermatids (step 9 and beyond) at the adluminal compartment. MAPKs regulate AJ dynamics in the testis via their effects on the turnover of junction-associated protein complexes, the production of proteases and protease inhibitors, and the cytoskeleton structure. In this review, roles of the three major MAPK members, namely extracellular signal-regulated kinase (ERK), c-Jun N-terminal kinase (JNK), and p38 MAPK, in ES dynamics are critically discussed. An integrated model of how these three MAPKs regulate adhesion function in the seminiferous epithelium is also presented. This model will serve as the framework for future investigation in the field.
丝裂原活化蛋白激酶(MAPKs)是许多细胞过程的重要调节因子。在哺乳动物睾丸中,这些激酶参与控制细胞分裂、分化、存活和死亡,因此对精子发生至关重要。最近的研究还表明它们参与了生精上皮中的连接重组,特别是在睾丸特异性黏附连接(AJ)类型的外质特化(ES)处。ES有助于血睾屏障处支持细胞之间以及管腔隔室中支持细胞与发育中的精子细胞(第9阶段及以后)之间的黏附。MAPKs通过影响连接相关蛋白复合物的周转、蛋白酶和蛋白酶抑制剂的产生以及细胞骨架结构来调节睾丸中的AJ动态。在这篇综述中,将批判性地讨论细胞外信号调节激酶(ERK)、c-Jun氨基末端激酶(JNK)和p38 MAPK这三种主要MAPK成员在ES动态中的作用。还提出了这三种MAPKs如何调节生精上皮中黏附功能的综合模型。该模型将作为该领域未来研究的框架。