髓鞘少突胶质细胞糖蛋白
多发性硬化
实验性自身免疫性脑脊髓炎
髓鞘
脑脊髓炎
医学
免疫学
中枢神经系统
脱髓鞘病
少突胶质细胞
发病机制
内科学
作者
S. Miyamura,Nagisa Matsuo,Kazuki Nagayasu,Hisashi Shirakawa,Shuji Kaneko
出处
期刊:Bio-protocol
[Bio-Protocol]
日期:2019-01-01
卷期号:9 (24)
被引量:12
标识
DOI:10.21769/bioprotoc.3453
摘要
Multiple sclerosis (MS) is the common demyelinating disease of human central nervous system. Among mouse models available to study MS, including the cuprizone application and lysolecithin-injection models, experimental autoimmune encephalomyelitis (EAE) model is widely used so that chronic EAE model of C57BL/6J can reflect the autoimmune pathogenesis of MS well. Here we introduce the EAE model based on C57BL/6J mice, which is generated by injection of myelin oligodendrocyte glycoprotein 35-55 (MOG 35-55) as an antigen. After immunization with complete Freund's adjuvant, clinical signs and changes in body weight are observed one or two weeks later. The EAE model will continue to be useful for development of therapeutics for MS.
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