Reciprocal influence of connexins and apical junction proteins on their expressions and functions |
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Authors: | Mickaë l Derangeon,Nicolas Bourmeyster,Jean-Claude Hervé |
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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 |
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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. |
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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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