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TrkB介导的香叶基香叶基转移酶I激活促进树突形态发生。

TrkB-mediated activation of geranylgeranyltransferase I promotes dendritic morphogenesis.

作者信息

Zhou Xiu-Ping, Wu Kong-Yan, Liang Bin, Fu Xiu-Qing, Luo Zhen-Ge

机构信息

Institute of Neuroscience, State Key Laboratory of Neuroscience, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai 200031, China.

出版信息

Proc Natl Acad Sci U S A. 2008 Nov 4;105(44):17181-6. doi: 10.1073/pnas.0800846105. Epub 2008 Oct 28.

Abstract

Dendrite morphogenesis is regulated by neuronal activity or neurotrophins, which may function by activating intrinsic signaling proteins, including Rho family GTPases. Here we report that activity- and brain-derived neurotrophic factor (BDNF)-dependent dendritic morphogenesis requires activation of geranylgeranyltransferase I (GGT), a prenyltransferase that mediates lipid modification of Rho GTPases. Dendritic arborization in cultured hippocampal neurons was promoted by over-expression of GGT, and reduced by inhibition or down-regulation of GGT. Furthermore, GGT was activated by neuronal depolarization or BDNF, both of which promote dendritic arborization, in cultured hippocampal neurons. Moreover, exploration of a novel environment caused activation of GGT in the mice hippocampus, suggesting that neural activity activates GGT in vivo. Interestingly, GGT was physically associated with tropomyosin-related kinase B (TrkB), the receptor for BDNF, and this association was enhanced by depolarization. Disrupting the GGT-TrkB interaction or down-regulating GGT activity attenuated depolarization- or BDNF-induced dendrite development. Finally, the GGT effect on dendrite arborization was prevented by over-expressing Rac1 with the prenylation site deleted or mutated. Thus depolarization- or BDNF-dependent dendrite development may be mediated by GGT-induced prenylation of Rho GTPases.

摘要

树突形态发生受神经元活动或神经营养因子调控,它们可能通过激活包括Rho家族GTP酶在内的内在信号蛋白发挥作用。在此我们报告,依赖于活动和脑源性神经营养因子(BDNF)的树突形态发生需要香叶基香叶基转移酶I(GGT)的激活,GGT是一种介导Rho GTP酶脂质修饰的异戊二烯基转移酶。在培养的海马神经元中,GGT的过表达促进了树突分支,而GGT的抑制或下调则减少了树突分支。此外,在培养的海马神经元中,神经元去极化或BDNF均可激活GGT,二者均能促进树突分支。而且,探索新环境会导致小鼠海马体中GGT的激活,这表明神经活动在体内激活了GGT。有趣的是,GGT与BDNF的受体原肌球蛋白相关激酶B(TrkB)存在物理关联,而去极化可增强这种关联。破坏GGT-TrkB相互作用或下调GGT活性会减弱去极化或BDNF诱导的树突发育。最后,通过过表达缺失或突变异戊二烯化位点的Rac1可阻止GGT对树突分支的影响。因此,去极化或BDNF依赖的树突发育可能由GGT诱导的Rho GTP酶异戊二烯化介导。

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