再髓鞘化
少突胶质细胞
神经科学
趋化因子受体
多发性硬化
CXCR4型
髓鞘
中枢神经系统
生物
趋化因子
趋化因子受体
受体
细胞生物学
免疫学
炎症
遗传学
作者
Tianci Chu,Lisa B. E. Shields,Yiping Zhang,Shiqing Feng,Christopher B. Shields,Jun Cai
标识
DOI:10.1177/1073858416685690
摘要
The chemokine CXCL12 plays a vital role in regulating the development of the central nervous system (CNS) by binding to its receptors CXCR4 and CXCR7. Recent studies reported that the CXCL12/CXCR4/CXCR7 axis regulates both embryonic and adult oligodendrocyte precursor cells (OPCs) in their proliferation, migration, and differentiation. The changes in the expression and distribution of CXCL12 and its receptors are tightly associated with the pathological process of demyelination in multiple sclerosis (MS), suggesting that modulating the CXCL12/CXCR4/CXCR7 axis may benefit myelin repair by enhancing OPC recruitment and differentiation. This review aims to integrate the current findings of the CXCL12/CXCR4/CXCR7 signaling pathway in the CNS and to highlight its role in oligodendrocyte development and demyelinating diseases. Furthermore, this review provides potential therapeutic strategies for myelin repair by analyzing the relevance between the pathological changes and the regulatory roles of CXCL12/CXCR4/CXCR7 during MS.
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