The orphan G protein-coupled receptor GPR149 is a negative regulator of myelination and remyelination

被引:8
|
作者
Suo, Na [1 ]
He, Bingqing [1 ,2 ,3 ]
Cui, Shihao [1 ,2 ]
Yang, Ying [1 ,2 ,3 ]
Wang, Min [1 ]
Yuan, Qianting [1 ]
Xie, Xin [1 ,2 ,3 ,4 ,5 ]
机构
[1] Chinese Acad Sci, Natl Ctr Drug Screening, Shanghai Inst Mat Med, CAS Key Lab Receptor Res, Shanghai 201203, Peoples R China
[2] Univ Chinese Acad Sci, Sch Pharm, Beijing, Peoples R China
[3] ShanghaiTech Univ, Sch Life Sci & Technol, Shanghai, Peoples R China
[4] Chinese Acad Sci, Shanghai Inst Mat Med, State Key Lab Drug Res, Shanghai, Peoples R China
[5] Univ Chinese Acad Sci, Sch Pharmaceut Sci & Technol, Hangzhou Inst Adv Study, Hangzhou, Peoples R China
基金
中国国家自然科学基金;
关键词
GPR149; MAPK; ERK pathway; myelination; oligodendrocyte; oligodendrocyte progenitor cell; remyelination; OLIGODENDROCYTE PROGENITOR CELLS; GROWTH-FACTOR; SCHWANN-CELLS; MATURE OLIGODENDROCYTES; THERAPEUTIC TARGET; ERK ACTIVATION; BASIC-PROTEIN; DIFFERENTIATION; BRAIN; MECHANISMS;
D O I
10.1002/glia.24233
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Myelin sheath, formed by oligodendrocytes (OLs) in the central nervous system (CNS) and Schwann cells in periphery, plays a critical role in supporting neuronal functions. OLs, differentiated from oligodendrocyte precursor cells (OPCs), are important for myelination during development and myelin repair in CNS demyelinating disease. To identify mechanisms of myelin development and remyelination after myelin damage is of great clinical interest. Here we show that the orphan G protein-coupled receptor GPR149, enriched in OPCs, negatively regulate OPC to OL differentiation, myelination, as well as remyelination. The expression of GPR149 is downregulated during OPCs differentiation into OLs. GPR149 deficiency does not affect the number of OPCs, but promotes OPC to OL differentiation which results in earlier development of myelin. In cuprizone-induced demyelination model, GPR149 deficiency significantly enhances myelin regeneration. Further study indicates that GPR149 may regulate OL differentiation and myelin formation via MAPK/ERK pathway. Our study suggests that deleting or blocking GPR149 might be an intriguing way to promote myelin repair in demyelinating diseases.
引用
收藏
页码:1992 / 2008
页数:17
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