Yamauchi Junji, Chan Jonah R, Shooter Eric M
Department of Neurobiology, Stanford University School of Medicine, Stanford, CA 94305-5125, USA.
Proc Natl Acad Sci U S A. 2003 Nov 25;100(24):14421-6. doi: 10.1073/pnas.2336152100. Epub 2003 Nov 12.
During development and nerve injury, complex interactions between glial cells and neurons are essential for establishing proper nerve function. Neurotrophins play multiple roles in the developing nervous system, including cell survival, growth, and differentiation. Here we show that migration of Schwann cells, isolated from sciatic nerves, is significantly enhanced by neurotrophin 3, but not by nerve growth factor or brain-derived neurotrophic factor. The neurotrophin-3-induced cell migration was also observed in Schwann cells isolated from sciatic nerves of p75NTR-/- mice, indicating that neurotrophin 3 enhances cell migration through TrkC. This effect was blocked by K252a, an inhibitor of the Trk receptor family. Additionally, the neurotrophin-3-induced cell migration depended on Rho GTPases (Rac1 and Cdc42) and c-Jun N-terminal kinase. We obtained the same results with Cos-7 cells expressing TrkC. Taken together, these results suggest that neurotrophin 3 activation of TrkC induces Schwann cell migration through the c-Jun N-terminal kinase signaling pathway.
在发育过程和神经损伤期间,神经胶质细胞与神经元之间的复杂相互作用对于建立正常的神经功能至关重要。神经营养因子在发育中的神经系统中发挥多种作用,包括细胞存活、生长和分化。在此我们表明,从坐骨神经分离出的雪旺细胞的迁移,被神经营养因子3显著增强,但未被神经生长因子或脑源性神经营养因子增强。在从p75NTR-/-小鼠坐骨神经分离出的雪旺细胞中也观察到了神经营养因子3诱导的细胞迁移,这表明神经营养因子3通过TrkC增强细胞迁移。这种效应被Trk受体家族的抑制剂K252a阻断。此外,神经营养因子3诱导的细胞迁移依赖于Rho GTP酶(Rac1和Cdc42)和c-Jun氨基末端激酶。我们用表达TrkC的Cos-7细胞获得了相同的结果。综上所述,这些结果表明神经营养因子3对TrkC的激活通过c-Jun氨基末端激酶信号通路诱导雪旺细胞迁移。