Mizuno Tatsunori, Yamashita Toshihide, Tohyama Masaya
Department of Anatomy and Neuroscience, Graduate School of Medicine, Osaka University, Osaka, Japan.
J Neurochem. 2004 Oct;91(2):395-403. doi: 10.1111/j.1471-4159.2004.02717.x.
Several myelin-derived proteins are inhibitory cues that contribute to the lack of regeneration of the CNS and inhibit neurite outgrowth from some neurons in vitro. This inhibition is blocked if neurons are exposed to neurotrophins before encountering the inhibitors. Here, we demonstrate that chimaerin, one of the Rho GTPase activating proteins, is transcriptionally up-regulated after exposure to neurotrophins in post-natal cerebellar neurons. The expression of alpha chimaerin in the cerebellum is developmentally correlated with the abolishment of the inhibitory effect of myelin-associated glycoprotein (MAG). Ectopic expression of alpha chimaerin in cerebellar neurons results in resistance to MAG in regard to neurite outgrowth. These results suggest that up-regulated expression of chimaerin counteracts the activation of RhoA, which is a key molecule in transducing inhibitory signals in neurons.
几种髓磷脂衍生蛋白是抑制性信号,它们导致中枢神经系统缺乏再生,并在体外抑制某些神经元的神经突生长。如果神经元在遇到抑制剂之前暴露于神经营养因子,这种抑制作用就会被阻断。在此,我们证明,Rho GTPase激活蛋白之一的嵌合蛋白在出生后小脑神经元暴露于神经营养因子后转录上调。小脑α-嵌合蛋白的表达在发育上与髓鞘相关糖蛋白(MAG)抑制作用的消除相关。小脑神经元中α-嵌合蛋白的异位表达导致神经突生长对MAG产生抗性。这些结果表明,嵌合蛋白表达上调可抵消RhoA的激活,而RhoA是在神经元中传导抑制信号的关键分子。