Calnexin Deficiency Leads to Dysmyelination

被引:58
作者
Kraus, Allison [1 ]
Groenendyk, Jody [1 ]
Bedard, Karen [1 ]
Baldwin, Troy A. [3 ]
Krause, Karl-Heinz [5 ,6 ,7 ]
Dubois-Dauphin, Michel [5 ,6 ,7 ]
Dyck, Jason [2 ]
Rosenbaum, Erica E. [8 ,9 ]
Korngut, Lawrence [10 ]
Colley, Nansi J. [8 ,9 ]
Gosgnach, Simon [2 ]
Zochodne, Douglas [10 ]
Todd, Kathryn [4 ]
Agellon, Luis B. [11 ]
Michalak, Marek [1 ]
机构
[1] Univ Alberta, Dept Biochem, Edmonton, AB T6G 2H7, Canada
[2] Univ Alberta, Dept Physiol, Sch Mol & Syst Med, Edmonton, AB T6G 2H7, Canada
[3] Univ Alberta, Dept Med Microbiol & Immunol, Sch Clin & Lab Sci, Edmonton, AB T6G 2H7, Canada
[4] Univ Alberta, Dept Psychiat, Ctr Neurosci, Edmonton, AB T6G 2H7, Canada
[5] Univ Geneva, Dept Pathol, CH-1211 Geneva 4, Switzerland
[6] Univ Geneva, Dept Immunol, CH-1211 Geneva 4, Switzerland
[7] Univ Geneva, Dept Clin Pathol, CH-1211 Geneva 4, Switzerland
[8] Univ Wisconsin, Dept Ophthalmol & Visual Sci, Dept Genet & Neurosci, Madison, WI 53792 USA
[9] Univ Wisconsin, Neurosci Training Program, Madison, WI 53792 USA
[10] Univ Calgary, Dept Clin Neurosci, Calgary, AB T2N 4N1, Canada
[11] McGill Univ, Sch Dietet & Human Nutr, Ste Anne De Bellevue, PQ H9X 3V9, Canada
基金
美国国家卫生研究院; 加拿大健康研究院; 瑞士国家科学基金会;
关键词
ENDOPLASMIC-RETICULUM; QUALITY-CONTROL; CALRETICULIN; CHAPERONE; ASSOCIATION; BINDING; OPSIN; DEATH; MICE; ER;
D O I
10.1074/jbc.M110.107201
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:18928 / 18938
页数:11
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