Adhesion G-protein coupled receptors and extracellular matrix proteins: Roles in myelination and glial cell development

被引:29
|
作者
Mehta, Paulomi [1 ]
Piao, Xianhua [1 ]
机构
[1] Harvard Med Sch, Boston Childrens Hosp, Dept Med, Div Newborn Med, Boston, MA USA
基金
美国国家卫生研究院;
关键词
development; signaling; injury response; BILATERAL FRONTOPARIETAL POLYMICROGYRIA; OLIGODENDROCYTE PROGENITOR MATURATION; CHONDROITIN SULFATE PROTEOGLYCANS; ADOLESCENT IDIOPATHIC SCOLIOSIS; CONGENITAL MUSCULAR-DYSTROPHY; PERIPHERAL-NERVE MYELINATION; SCHWANN-CELLS; PRION PROTEIN; TISSUE TRANSGLUTAMINASE; DEMYELINATED LESIONS;
D O I
10.1002/dvdy.24473
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
Adhesion G protein-coupled receptors (aGPCRs) are a large family of transmembrane proteins that play important roles in many processes during development, primarily through cell-cell and cell-extracellular matrix (ECM) interactions. In the nervous system, they have been linked to the complex process of myelination, both in the central and peripheral nervous system. GPR126 is essential in Schwann cell-mediated myelination in the peripheral nervous system (PNS), while GPR56 is involved in oligodendrocyte development central nervous system (CNS) myelination. VLGR1 is another aGPCR that is associated with the expression of myelin-associated glycoprotein (MAG) which has inhibitory effects on the process of nerve repair. The ECM is composed of a vast array of structural proteins, three of which interact specifically with aGPCRs: collagen III/GPR56, collagen IV/GPR126, and laminin-211/GPR126. As druggable targets, aGPCRs are valuable in their ability to unlock treatment for a wide variety of currently debilitating myelin disorders. Developmental Dynamics 246:275-284, 2017. (c) 2016 Wiley Periodicals, Inc.
引用
收藏
页码:275 / 284
页数:10
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