Literature DB >> 20400506

Calnexin deficiency leads to dysmyelination.

Allison Kraus1, 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.

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Year:  2010        PMID: 20400506      PMCID: PMC2881815          DOI: 10.1074/jbc.M110.107201

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  30 in total

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