TY - JOUR
T1 - Calnexin deficiency leads to dysmyelination
AU - Kraus, Allison
AU - Groenendyk, Jody
AU - Bedard, Karen
AU - Baldwin, Troy A.
AU - Krause, Karl Heinz
AU - Dubois-Dauphin, Michel
AU - Dyck, Jason
AU - Rosenbaum, Erica E.
AU - Korngut, Lawrence
AU - Colley, Nansi J.
AU - Gosgnach, Simon
AU - Zochodne, Douglas
AU - Todd, Kathryn
AU - Agellon, Luis B.
AU - Michalak, Marek
PY - 2010/6/11
Y1 - 2010/6/11
N2 - 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.
AB - 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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U2 - 10.1074/jbc.M110.107201
DO - 10.1074/jbc.M110.107201
M3 - Article
C2 - 20400506
AN - SCOPUS:77953296950
SN - 0021-9258
VL - 285
SP - 18928
EP - 18938
JO - Journal of Biological Chemistry
JF - Journal of Biological Chemistry
IS - 24
ER -