Citrullination of central nervous system proteins during the development of experimental autoimmune encephalomyelitis

被引:39
作者
Raijmakers, R
Vogelzangs, J
Croxford, JL
Wesseling, P
Van Venrooij, WJ
Pruijn, GJM
机构
[1] Nijmegen Ctr Mol Life Sci, Dept Biochem, NL-6500 HB Nijmegen, Netherlands
[2] Natl Ctr Neurol & Psychiat, Natl Inst Neurosci, Dept Immunol, Tokyo, Japan
[3] Northwestern Univ, Sch Med, Dept Microbiol & Immunol, Chicago, IL 60611 USA
[4] Radboud Univ, Nijmegen Med Ctr, Dept Pathol, NL-6500 HB Nijmegen, Netherlands
关键词
citrulline; experimental autoimmune encephalomyelitis; glial fibrillary acidic protein; multiple sclerosis; myelin basic protein; peptidyl arginine deiminase;
D O I
10.1002/cne.20529
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Immunization of mammals with central nervous system (CNS)-derived proteins or peptides induces experimental autoimmune encephalomyelitis (EAE), a disease resembling the human autoimmune disease multiple sclerosis (MS). Both diseases are accompanied by destruction of a part of the of the myelin sheaths, which surround neurites in the CNS. Previous studies in MS have described alterations in the citrullination of myelin basic protein, one of the main protein constituents of the myelin sheath. Here, we show that, also during the development of EAE in mice, hypercitrullination occurs in the areas of the spinal cord that show the highest degree of inflammation and that myelin basic protein and glial fibrillary acidic protein are among the hypercitrullinated proteins. We conclude that hypercitrullination of myelin proteins in the CNS is a common phenomenon in demyelinating disease. Hypercitrullination may cause conformational changes in proteins, so the affected proteins may be involved in the pathogenesis of CNS autoimmune disease by acting as autoreactive T-cell epitopes. This is the first report in which hypercitrullination of CNS proteins in EAE is described and in which proteins other than myelin basic protein are reported to be citrullinated during autoimmune-mediated CNS inflammation. (c) 2005 Wiley-Liss, Inc.
引用
收藏
页码:243 / 253
页数:11
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