神经炎症
多发性硬化
实验性自身免疫性脑脊髓炎
小胶质细胞
发病机制
机制(生物学)
中枢神经系统
医学
脑脊髓炎
炎症
生物
疾病
神经科学
免疫学
病理
哲学
认识论
作者
Xizhong Jing,Yongjie Yao,Danning Wu,Hao Hong,Xu Feng,Na Xu,Yingfang Liu,Huanhuan Liang
标识
DOI:10.1073/pnas.2102642118
摘要
Significance Multiple sclerosis (MS) is a complex neuroinflammatory disorder that constitutes the major cause of nontraumatic disability in young adults. However, the underlying mechanism of this disease remains obscure. Here, we identified NMI and IFP35 as factors critical in the progress of MS and experimental autoimmune encephalomyelitis, as their dysregulation activates both microglia in the central nervous system and T cells in the periphery. This study expands our understanding of the pathogenesis of MS and aims to provide potential diagnostic and therapeutic targets.
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