The adhesion GPCR Gpr56 regulates oligodendrocyte development via interactions with Gα12/13 and RhoA

被引:116
作者
Ackerman, Sarah D. [1 ]
Garcia, Cynthia [2 ]
Piao, Xianhua [3 ,4 ]
Gutmann, David H. [2 ]
Monk, Kelly R. [1 ,5 ]
机构
[1] Washington Univ, Sch Med, Dept Dev Biol, St Louis, MO 63110 USA
[2] Washington Univ, Sch Med, Dept Neurol, St Louis, MO 63110 USA
[3] Boston Childrens Hosp, Dept Med, Div Newborn Med, Boston, MA 02115 USA
[4] Harvard Univ, Sch Med, Boston, MA 02115 USA
[5] Washington Univ, Sch Med, Hope Ctr Neurol Disorders, St Louis, MO 63110 USA
关键词
PROTEIN-COUPLED-RECEPTOR; IN-VIVO; EXTRACELLULAR-MATRIX; ZEBRAFISH EMBRYOS; SONIC HEDGEHOG; CELL MIGRATION; SCHWANN-CELLS; MYELINATION; DIFFERENTIATION; GPR126;
D O I
10.1038/ncomms7122
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
In the vertebrate central nervous system, myelinating oligodendrocytes are postmitotic and derive from proliferative oligodendrocyte precursor cells (OPCs). The molecular mechanisms that govern oligodendrocyte development are incompletely understood, but recent studies implicate the adhesion class of G protein-coupled receptors (aGPCRs) as important regulators of myelination. Here, we use zebrafish and mouse models to dissect the function of the aGPCR Gpr56 in oligodendrocyte development. We show that gpr56 is expressed during early stages of oligodendrocyte development. In addition, we observe a significant reduction of mature oligodendrocyte number and myelinated axons in gpr56 zebrafish mutants. This reduction results from decreased OPC proliferation, rather than increased cell death or altered neural precursor differentiation potential. Finally, we show that these functions are mediated by G alpha(12/13) proteins and Rho activation. Together, our data establish Gpr56 as a regulator of oligodendrocyte development.
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页数:14
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