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Reciprocal influence of connexins and apical junction proteins on their expressions and functions
Authors:Mickaë  l Derangeon,Nicolas Bourmeyster,Jean-Claude Hervé  
Affiliation:a Institut de Physiologie et Biologie Cellulaires, Université de Poitiers, CNRS 6187; 40 avenue du recteur Pineau, Poitiers, F-86022, France
b Dominick P. Purpura Department of Neuroscience, Albert Einstein College of Medicine, Bronx, New York, USA
Abstract:Membranes of adjacent cells form intercellular junctional complexes to mechanically anchor neighbour cells (anchoring junctions), to seal the paracellular space and to prevent diffusion of integral proteins within the plasma membrane (tight junctions) and to allow cell-to-cell diffusion of small ions and molecules (gap junctions). These different types of specialised plasma membrane microdomains, sharing common adaptor molecules, particularly zonula occludens proteins, frequently present intermingled relationships where the different proteins co-assemble into macromolecular complexes and their expressions are co-ordinately regulated. Proteins forming gap junction channels (connexins, particularly) and proteins fulfilling cell attachment or forming tight junction strands mutually influence expression and functions of one another.
Keywords:42GPA9, Sertoli cell line   Caco-2, human colonic adenocarcinoma cells   Calu-3, human airway epithelial cell line   CHST8 cells, immortalized mouse hepatocytes   COS7, monkey African green kidney cells   HEK293 cells, human embryonic kidney 293 cells   MDCK, epithelial Madin-Darby canine kidney cells   Neuro2A, mouse neuroblastoma cells   NIH 3T3, mouse fibroblasts   NRK, rat kidney cells   PC-12, a neuron-like cell line originally cloned from rat phaeochromocytoma cells   ROS 17/2.8, osteosarcoma cell line
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