Zhou Xiu-Ping, Wu Kong-Yan, Liang Bin, Fu Xiu-Qing, Luo Zhen-Ge
Institute of Neuroscience, State Key Laboratory of Neuroscience, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai 200031, China.
Proc Natl Acad Sci U S A. 2008 Nov 4;105(44):17181-6. doi: 10.1073/pnas.0800846105. Epub 2008 Oct 28.
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.
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。