Yamashita Toshihide, Tohyama Masaya
Department of Anatomy and Neuroscience, Graduate School of Medicine, Osaka University, 2-2 Yamadaoka, Suita, Osaka 565-0871, Japan.
Nat Neurosci. 2003 May;6(5):461-7. doi: 10.1038/nn1045.
The neurotrophin receptor p75(NTR) is involved in the regulation of axonal elongation by neurotrophins as well as several myelin components, including Nogo, myelin-associated glycoprotein (MAG) and myelin oligodendrocyte glycoprotein (OMgp). Neurotrophins stimulate neurite outgrowth by inhibiting Rho activity, whereas myelin-derived proteins activate RhoA and thereby inhibit growth. Here we show that direct interaction of the Rho GDP dissociation inhibitor (Rho-GDI) with p75(NTR) initiates the activation of RhoA, and this interaction between p75(NTR) and Rho-GDI is strengthened by MAG or Nogo. We also found that p75(NTR) facilitates the release of prenylated RhoA from Rho-GDI. The peptide ligand that is associated with the fifth alpha helix of p75(NTR) inhibits the interaction between Rho-GDI and p75(NTR), thus silencing the action mediated by p75(NTR). This peptide has potential as a therapeutic agent against the inhibitory cues that block regeneration in the central nervous system.
神经营养因子受体p75(NTR)参与神经营养因子以及包括Nogo、髓鞘相关糖蛋白(MAG)和髓鞘少突胶质细胞糖蛋白(OMgp)在内的几种髓鞘成分对轴突伸长的调节。神经营养因子通过抑制Rho活性来刺激神经突生长,而髓鞘衍生蛋白则激活RhoA,从而抑制生长。在此我们表明,Rho GDP解离抑制剂(Rho-GDI)与p75(NTR)的直接相互作用引发RhoA的激活,并且p75(NTR)与Rho-GDI之间的这种相互作用会因MAG或Nogo而增强。我们还发现p75(NTR)促进了法尼基化RhoA从Rho-GDI的释放。与p75(NTR)的第五个α螺旋相关的肽配体抑制Rho-GDI与p75(NTR)之间的相互作用,从而使p75(NTR)介导的作用沉默。这种肽具有作为治疗剂对抗中枢神经系统中阻碍再生的抑制性信号的潜力。