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Microglial transglutaminase-2 drives myelination and myelin repair via GPR56/ADGRG1 in oligodendrocyte precursor cells

机译:小胶质转谷氨酰胺酶2通过少突胶质前体细胞中的GPR56 / ADGRG1驱动髓鞘形成和髓鞘修复

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摘要

In the central nervous system (CNS), myelin formation and repair are regulated by oligodendrocyte (OL) lineage cells, which sense and integrate signals from their environment, including from other glial cells and the extracellular matrix (ECM). The signaling pathways that coordinate this complex communication, however, remain poorly understood. The adhesion G protein-coupled receptor ADGRG1 (also known as GPR56) is an evolutionarily conserved regulator of OL development in humans, mice, and zebrafish, although its activating ligand for OL lineage cells is unknown. Here, we report that microglia-derived transglutaminase-2 (TG2) signals to ADGRG1 on OL precursor cells (OPCs) in the presence of the ECM protein laminin and that TG2/laminin-dependent activation of ADGRG1 promotes OPC proliferation. Signaling by TG2/laminin to ADGRG1 on OPCs additionally improves remyelination in two murine models of demyelination. These findings identify a novel glia-to-glia signaling pathway that promotes myelin formation and repair, and suggest new strategies to enhance remyelination.
机译:在中枢神经系统(CNS)中,髓鞘的形成和修复受少突胶质细胞(OL)谱系细胞的调节,这些谱系细胞感知并整合来自其环境的信号,包括来自其他神经胶质细胞和细胞外基质(ECM)的信号。然而,协调这种复杂通信的信号通路仍然知之甚少。粘附G蛋白偶联受体ADGRG1(也称为GPR56)是人,小鼠和斑马鱼中OL发育的进化保守调节剂,尽管其OL谱系细胞的激活配体尚不清楚。在这里,我们报告小胶质细胞源转谷氨酰胺酶2(TG2)信号在存在ECM蛋白层粘连蛋白的情况下在OL前体细胞(OPC)上向ADGRG1传递信号,并且依赖于TG2 / laminin的ADGRG1活化促进了OPC增殖。 TG2 / laminin在OPC上向ADGRG1发出的信号还改善了两种脱髓鞘小鼠模型中的髓鞘再生。这些发现确定了促进髓磷脂形成和修复的新的神经胶质间信号通路,并提出了增强髓鞘再生的新策略。

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