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G protein-coupled receptor 37 is a negative regulator of oligodendrocyte differentiation and myelination

机译:G蛋白偶联受体37是少突胶质细胞分化和髓鞘形成的负调节剂

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摘要

While the formation of myelin by oligodendrocytes is critical for the function of the central nervous system, the molecular mechanism controlling oligodendrocyte differentiation remains largely unknown. Here we identify G protein-coupled receptor 37 (GPR37) as an inhibitor of late-stage oligodendrocyte differentiation and myelination. GPR37 is enriched in oligodendrocytes and its expression increases during their differentiation into myelin forming cells. Genetic deletion of Gpr37 does not affect the number of oligodendrocyte precursor cells, but results in precocious oligodendrocyte differentiation and hypermyelination. The inhibition of oligodendrocyte differentiation by GPR37 is mediated by suppression of an exchange protein activated by cAMP (EPAC)-dependent activation of Raf-MAPK-ERK1/2 module and nuclear translocation of ERK1/2. Our data suggest that GPR37 regulates central nervous system myelination by controlling the transition from early-differentiated to mature oligodendrocytes.
机译:尽管少突胶质细胞形成髓鞘对于中枢神经系统的功能至关重要,但控制少突胶质细胞分化的分子机制仍是未知之数。在这里,我们确定G蛋白偶联受体37(GPR37)为晚期少突胶质细胞分化和髓鞘形成的抑制剂。 GPR37富含少突胶质细胞,在分化为髓鞘形成细胞的过程中其表达增加。 Gpr37的遗传删除不影响少突胶质前体细胞的数量,但会导致早熟的少突胶质细胞分化和髓鞘过多。 GPR37对少突胶质细胞分化的抑制作用是通过抑制由cAMP(EPAC)依赖性的Raf-MAPK-ERK1 / 2模块激活和ERK1 / 2核易位激活的交换蛋白介导的。我们的数据表明,GPR37通过控制从早期分化的少突胶质细胞向成熟的少突胶质细胞的转变来调节中枢神经系统的髓鞘形成。

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