Tight junctions and the molecular basis for regulation of paracellular permeability

作者：James Melvin Anderson, Christina M. Van Itallie · 发表于：American Journal of Physiology-Gastrointestinal and Liver Physiology · 年份：1995 · DOI：10.1152/ajpgi.1995.269.4.g467 · 被引用次数：847 · 研究领域：Barrier Structure and Function Studies、S100 Proteins and Annexins、Cell Adhesion Molecules Research

Tight junctions create a regulated paracellular barrier to the movement of water, solutes, and immune cells between both epithelial and endothelial cells. Recent progress has been made in identifying the proteins that create this barrier. The transmembrane protein occludin is an excellent candidate for the sealing protein and is bound on the cytoplasmic membrane surface to the proteins ZO-1 and ZO-2. Functions for ZO-1 and ZO-2 are suggested by their invertebrate homologues, one of which is a tumor suppressor and another is required in epidermal growth factor receptor signaling. Multiple cellular signaling pathways affect assembly and sealing of junctions. Dynamic regulation of perijunctional actin has emerged as a unifying hypothesis for controlling paracellular permeability. Understanding and manipulating permeability will require a more detailed molecular characterization of tight junction proteins and in particular a characterization of how cell signaling regulates their attachment to the perijunctional cytoskeleton.