Perspectives on tight junction research

克洛丹 紧密连接 封堵器 并行传输 势垒函数 细胞结 细胞生物学 化学 生物 磁导率 遗传学 细胞
作者
Jörg–Dieter Schulzke,Dorothee Günzel,Lena John,Michael Fromm
出处
期刊:Annals of the New York Academy of Sciences [Wiley]
卷期号:1257 (1): 1-19 被引量:53
标识
DOI:10.1111/j.1749-6632.2012.06485.x
摘要

The tight junction connects neighboring epithelial or endothelial cells. As a general function, it seals the paracellular pathway and thus prevents back-leakage of just transported solutes and water. However, not all tight junctions are merely tight: some tight junction proteins build their own transport pathways by forming channels selective for small cations, anions, or water. Two families of tight junction proteins have been identified, claudins (27 members in mammals) and tight junction-associated MARVEL proteins ((TAMPs) occludin, tricellulin, and MarvelD3); an additional, structurally different, junction protein is junction adhesion molecule (JAM). Besides classification by genetic or molecular kinship, classification of tight junction proteins has been suggested according to permeability attributes. Recent studies describe specific cis and trans interactions and manifold physiologic regulations of claudins and TAMPs. In many inflammatory and infectious diseases they are found to be altered, for example, causing adversely increased permeability. Currently, attempts are being made to alter the paracellular barrier for therapeutic interventions or for transiently facilitating drug uptake. This overview concludes with a list of open questions and future topics in tight junction research.
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