Small GTPase Rab17 Regulates Dendritic Morphogenesis and Postsynaptic Development of Hippocampal Neurons

被引:35
|
作者
Mori, Yasunori [1 ]
Matsui, Takahide [1 ]
Furutani, Yutaka [2 ]
Yoshihara, Yoshihiro [2 ]
Fukuda, Mitsunori [1 ]
机构
[1] Tohoku Univ, Grad Sch Life Sci, Dept Dev Biol & Neurosci, Lab Membrane Trafficking Mech,Aoba Ku, Sendai, Miyagi 9808578, Japan
[2] RIKEN Brain Sci Inst, Lab Neurobiol Synapse, Wako, Saitama 3510198, Japan
关键词
SYNAPTIC VESICLE PROTEIN; LONG-TERM POTENTIATION; RECYCLING ENDOSOMES; AMPA RECEPTORS; FILOPODIA FORMATION; EPITHELIAL-CELLS; NMDA RECEPTOR; PC12; CELLS; TRAFFICKING; BINDING;
D O I
10.1074/jbc.M111.314385
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Neurons are compartmentalized into two morphologically, molecularly, and functionally distinct domains: axons and dendrites, and precise targeting and localization of proteins within these domains are critical for proper neuronal functions. It has been reported that several members of the Rab family small GTPases that are key mediators of membrane trafficking, regulate axon-specific trafficking events, but little has been elucidated regarding the molecular mechanisms that underlie dendrite-specific membrane trafficking. Here we show that Rab17 regulates dendritic morphogenesis and postsynaptic development in mouse hippocampal neurons. Rab17 is localized at dendritic growth cones, shafts, filopodia, and mature spines, but it is mostly absent in axons. We also found that Rab17 mediates dendrite growth and branching and that it does not regulate axon growth or branching. Moreover, shRNA-mediated knockdown of Rab17 expression resulted in a dramatically reduced number of dendritic spines, probably because of impaired filopodia formation. These findings have revealed the first molecular link between membrane trafficking and dendritogenesis.
引用
收藏
页码:8963 / 8973
页数:11
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