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Calnexin Deficiency Leads to Dysmyelination
Authors:Allison Kraus  Jody Groenendyk  Karen Bedard  Troy A. Baldwin  Karl-Heinz Krause  Michel Dubois-Dauphin  Jason Dyck  Erica E. Rosenbaum  Lawrence Korngut  Nansi J. Colley  Simon Gosgnach  Douglas Zochodne  Kathryn Todd  Luis B. Agellon  Marek Michalak
Abstract:Calnexin is a molecular chaperone and a component of the quality control of the secretory pathway. We have generated calnexin gene-deficient mice (cnx−/−) and showed that calnexin deficiency leads to myelinopathy. Calnexin-deficient mice were viable with no discernible effects on other systems, including immune function, and instead they demonstrated dysmyelination as documented by reduced conductive velocity of nerve fibers and electron microscopy analysis of sciatic nerve and spinal cord. Myelin of the peripheral and central nervous systems of cnx−/− mice was disorganized and decompacted. There were no abnormalities in neuronal growth, no loss of neuronal fibers, and no change in fictive locomotor pattern in the absence of calnexin. This work reveals a previously unrecognized and important function of calnexin in myelination and provides new insights into the mechanisms responsible for myelin diseases.
Keywords:Endoplasmic Reticulum (ER)   Membrane Proteins   Mouse   Neuroscience   Protein Folding   Calnexin   Myelin   Neuropathy
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