CAS Key Laboratory of Receptor Research, the National Center for Drug Screening, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, China.
School of Pharmacy, University of Chinese Academy of Sciences, Beijing, China.
Glia. 2022 Oct;70(10):1992-2008. doi: 10.1002/glia.24233. Epub 2022 Jun 27.
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.
髓鞘由中枢神经系统(CNS)中的少突胶质细胞(OLs)和外周的施万细胞形成,在支持神经元功能方面起着关键作用。OLs 由少突胶质前体细胞(OPCs)分化而来,对于发育过程中的髓鞘形成和 CNS 脱髓鞘疾病中的髓鞘修复很重要。了解髓鞘发育和髓鞘损伤后再髓鞘化的机制具有重要的临床意义。在这里,我们发现孤儿 G 蛋白偶联受体 GPR149 在 OPCs 中丰富,负调节 OPC 向 OL 的分化、髓鞘形成以及再髓鞘化。GPR149 的表达在 OPCs 分化为 OLs 期间下调。GPR149 缺失不影响 OPCs 的数量,但促进 OPC 向 OL 的分化,导致髓鞘更早发育。在铜诱导的脱髓鞘模型中,GPR149 缺失显著增强了髓鞘再生。进一步的研究表明,GPR149 可能通过 MAPK/ERK 通路调节 OL 分化和髓鞘形成。我们的研究表明,删除或阻断 GPR149 可能是促进脱髓鞘疾病中髓鞘修复的一种有趣方法。