单位:[1]Childrens Hosp, Dept Med, Div Newborn Med, Boston, MA 02115 USA[2]Harvard Med Sch, Boston, MA 02115 USA[3]Childrens Hosp, Dept Neurol, FM Kirby Neurobiol Ctr, Boston, MA 02115 USA[4]Huazhong Univ Sci & Technol, Tongji Med Coll, Tongji Hosp, Wuhan, Hubei, Peoples R China华中科技大学同济医学院附属同济医院[5]Washington Univ, Sch Med, Dept Dev Biol, St Louis, MO USA[6]KBRI, Dept Neural Dev & Dis, Daegu, South Korea[7]Univ Michigan, Med Ctr, Dept Pharmacol, Ann Arbor, MI 48109 USA[8]Univ Oregon, Inst Neurosci, Eugene, OR 97403 USA[9]Korea Brain Res Inst, Convergence Brain Res Dept, Daegu, South Korea[10]Oregon Hlth & Sci Univ, Vollum Inst, L474, Portland, OR 97201 USA
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.
基金:
National Institute of Neurological Disorders and Stroke [NS085201, NS087801, NS079445]; National Multiple Sclerosis Society [FG 2063-A1/2, RG-1501-02577]; National Research Foundation of Korea [2015M3C7A1029037]; Ministry of Science, ICT and Future Planning [18-BR-02-02]; National Multiple Sclerosis Society; Ministry of Science & ICT (MSIT), Republic of Korea [18-BR-02] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS); National Research Foundation of Korea [2015M3C7A1029037] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
第一作者单位:[1]Childrens Hosp, Dept Med, Div Newborn Med, Boston, MA 02115 USA[2]Harvard Med Sch, Boston, MA 02115 USA[3]Childrens Hosp, Dept Neurol, FM Kirby Neurobiol Ctr, Boston, MA 02115 USA
通讯作者:
通讯机构:[1]Childrens Hosp, Dept Med, Div Newborn Med, Boston, MA 02115 USA[2]Harvard Med Sch, Boston, MA 02115 USA[3]Childrens Hosp, Dept Neurol, FM Kirby Neurobiol Ctr, Boston, MA 02115 USA[5]Washington Univ, Sch Med, Dept Dev Biol, St Louis, MO USA[10]Oregon Hlth & Sci Univ, Vollum Inst, L474, Portland, OR 97201 USA
推荐引用方式(GB/T 7714):
Giera Stefanie,Luo Rong,Ying Yanqin,et al.Microglial transglutaminase-2 drives myelination and myelin repair via GPR56/ADGRG1 in oligodendrocyte precursor cells[J].ELIFE.2018,7:doi:10.7554/eLife.33385.
APA:
Giera, Stefanie,Luo, Rong,Ying, Yanqin,Ackerman, Sarah D.,Jeong, Sung-Jin...&Piao, Xianhua.(2018).Microglial transglutaminase-2 drives myelination and myelin repair via GPR56/ADGRG1 in oligodendrocyte precursor cells.ELIFE,7,
MLA:
Giera, Stefanie,et al."Microglial transglutaminase-2 drives myelination and myelin repair via GPR56/ADGRG1 in oligodendrocyte precursor cells".ELIFE 7.(2018)