A p75NTR and Nogo receptor complex mediates repulsive signaling by myelin-associated glycoprotein

被引:371
作者
Wong, ST
Henley, JR
Kanning, KC
Huang, KH
Bothwell, M
Poo, M [1 ]
机构
[1] Univ Calif Berkeley, Dept Mol & Cell Biol, Div Neurobiol, Berkeley, CA 94720 USA
[2] Univ Washington, Dept Physiol & Biophys, Seattle, WA 98195 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1038/nn975
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Myelin-associated glycoprotein (MAG), an inhibitor of axon regeneration, binds with high affinity to the Nogo-66 receptor (NgR). Here we report that the p75 neurotrophin receptor (p75(NTR)) is a co-receptor of NgR for MAG signaling. In cultured human embryonic kidney (HEK) cells expressing NgR, p75(NTR) was required for MAG-induced intracellular Ca2+ elevation. Co-immunoprecipitation showed an association of NgR with p75NTR that can be disrupted by an antibody against p75(NTR) (NGFR5), and extensive coexpression was observed in the developing rat nervous system. Furthermore, NGFR5 abolished MAG-induced repulsive turning of Xenopus axonal growth cones and Ca2+ elevation, both in neurons and in NgR/p75(NTR)-expressing HEK cells. Thus we conclude that p75(NTR) is a co-receptor of NgR for MAG signaling and a potential therapeutic target for promoting nerve regeneration.
引用
收藏
页码:1302 / 1308
页数:7
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