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Tight junctions and the molecular basis for regulation of paracellular permeability

James M. AndersonChristina M. Van Itallie

Abstract

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.

Barrier Structure and Function StudiesS100 Proteins and AnnexinsCell Adhesion Molecules ResearchParacellular transportOccludinTight junctionCell biologyClaudinTransmembrane proteinActin cytoskeletonCytoplasmCell junctionBiology

MeSH terms

ActinsAnimalsEpithelial CellsEpitheliumHumansMembrane ProteinsPermeabilityPhosphoproteinsTight JunctionsOccludinZonula Occludens-1 ProteinZonula Occludens-2 Protein
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References
Barrier function of epithelia
American Journal of Physiology-Gastrointestinal and Liver Physiology · 1981 · 618 citations
Occludin: a novel integral membrane protein localizing at tight junctions.
The Journal of Cell Biology · 1993 · 2,521 citations
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