Division of Newborn Medicine, Department of Medicine, Children's Hospital and Harvard Medical School, Boston, United States.
Department of Neurology, F. M. Kirby Neurobiology Center, Children's Hospital and Harvard Medical School, Boston, United States.
Elife. 2018 May 29;7:e33385. doi: 10.7554/eLife.33385.
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.
在中枢神经系统(CNS)中,少突胶质细胞(OL)谱系细胞调节髓鞘的形成和修复,它们感知并整合来自环境的信号,包括来自其他神经胶质细胞和细胞外基质(ECM)的信号。然而,协调这种复杂通讯的信号通路仍知之甚少。黏附 G 蛋白偶联受体 ADGRG1(也称为 GPR56)是人类、小鼠和斑马鱼 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,我们报告说,在细胞外基质蛋白层粘连蛋白存在的情况下,小胶质细胞衍生的转谷氨酰胺酶 2(TG2)向 OL 前体细胞(OPC)上的 ADGRG1 发出信号,并且 TG2/层粘连蛋白依赖性的 ADGRG1 激活促进 OPC 增殖。TG2/层粘连蛋白对 OPC 上的 ADGRG1 的信号传导另外改善了两种脱髓鞘小鼠模型中的髓鞘再生。这些发现确定了一种新的神经胶质细胞间信号通路,可促进髓鞘形成和修复,并提出了增强髓鞘再生的新策略。