Angelow Susanne, Yu Alan S L
Division of Nephrology, Department of Medicine, University of Southern California Keck School of Medicine, Los Angeles, California 90033, USA.
Curr Opin Nephrol Hypertens. 2007 Sep;16(5):459-64. doi: 10.1097/MNH.0b013e32820ac97d.
Claudins are tight junction proteins that form paracellular barriers and pores. The purpose of this timely review is to provide an update on the exciting new advances in our understanding of claudin biology and their relevance to renal physiology and pathophysiology.
Accumulating evidence from numerous studies indicates that the primary role of claudins is to determine the permeability and charge selectivity of the paracellular pathway to small ions. Studies in which claudins are overexpressed in cell lines have potential limitations and need to be interpreted cautiously. Ribonucleic acid interference is a novel approach to functional characterization. Claudins are believed to assemble into multimers by homophilic and heterophilic side-by-side and head-to-head interaction; however, there is still limited evidence for this. The roles of a few claudins in the renal tubule, including claudins 2, 8, 10, 16 and 19, have now been elucidated.
These findings reveal tantalizing clues to claudin biology and function. Much remains unknown, however, and these findings will hopefully encourage further research in this important area.
紧密连接蛋白是形成细胞旁屏障和孔道的紧密连接蛋白。本次及时综述的目的是就我们对紧密连接蛋白生物学的理解及其与肾脏生理学和病理生理学的相关性方面令人兴奋的新进展提供最新信息。
众多研究积累的证据表明,紧密连接蛋白的主要作用是决定细胞旁途径对小离子的通透性和电荷选择性。在细胞系中过表达紧密连接蛋白的研究存在潜在局限性,需要谨慎解读。核糖核酸干扰是一种功能表征的新方法。紧密连接蛋白被认为通过同型和异型的并排及头对头相互作用组装成多聚体;然而,对此仍证据有限。现在已经阐明了一些紧密连接蛋白在肾小管中的作用,包括紧密连接蛋白2、8、10、16和19。
这些发现揭示了紧密连接蛋白生物学和功能的诱人线索。然而,仍有许多未知之处,希望这些发现能鼓励在这一重要领域进行进一步研究。