Department of Molecular Neuroscience, Graduate School of Medicine, Osaka University, 2-2 Yamadaoka, Suita, Osaka 565-0871, Japan.
Cell Death Dis. 2011 Sep 1;2(9):e198. doi: 10.1038/cddis.2011.85.
The Nogo receptor and paired immunoglobulin-like receptor B (PIR-B) are receptors for three myelin-derived axon-growth inhibitors, including myelin-associated glycoprotein (MAG). In this study, we report that the p75 receptor is required for the signal transduction of PIR-B, which interacted with p75 upon ligand binding. In addition, p75 was required for activation of Src homology 2-containing protein tyrosine phosphatase (SHP), which is induced by MAG binding to PIR-B. Mice carrying a mutation in the p75 gene showed promotion of axonal regeneration after optic nerve injury. Thus, our results indicate that p75 has a critical role in axon growth inhibition in specific neuronal tracts.
神经生长抑制因子受体和配对免疫球蛋白样受体 B(PIR-B)是三种髓鞘源性轴突生长抑制剂的受体,包括髓鞘相关糖蛋白(MAG)。在这项研究中,我们报告说 p75 受体是 PIR-B 信号转导所必需的,p75 受体在配体结合时与 PIR-B 相互作用。此外,p75 还需要激活 Src 同源性 2 结构域蛋白酪氨酸磷酸酶(SHP),该酶由 MAG 与 PIR-B 结合诱导。携带 p75 基因突变的小鼠在视神经损伤后表现出轴突再生的促进作用。因此,我们的结果表明 p75 在特定神经元束的轴突生长抑制中起关键作用。