Role of Rab3 GDP/GTP exchange protein in synaptic vesicle trafficking at the mouse neuromuscular junction

被引:58
作者
Tanaka, M
Miyoshi, J
Ishizaki, H
Togawa, A
Ohnishi, K
Endo, K
Matsubara, K
Mizoguchi, A
Nagano, T
Sato, M
Sasaki, T
Takai, Y
机构
[1] Osaka Univ, Fac Med, Grad Sch Med, Dept Mol Biol & Biochem, Suita, Osaka 5650871, Japan
[2] JCR Pharmaceut Co Ltd, Japan Sci & Technol Corp, ERATO, Takai Biotimer Project, Kobe, Hyogo 6512241, Japan
[3] Kyoto Univ, Fac Med, Grad Sch Med, Dept Physiol, Kyoto 6068501, Japan
[4] Kyoto Univ, Fac Med, Grad Sch Med, Dept Anat & Neurobiol, Kyoto 6068501, Japan
[5] Fukui Med Univ, Fac Med, Dept Anat 2, Fukui 9101193, Japan
关键词
D O I
10.1091/mbc.12.5.1421
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The Rab3 small G protein family consists of four members, Rab3A, -3B, -3C, and -3D. Of these members, Rab3A regulates Ca2(+)-dependent neurotransmitter release. These small G proteins axe activated by Rab3 GDP/GTP exchange protein (Rab3 GEP). To determine the function of Rab3 GEP during neurotransmitter release, we have knocked out Rab3 GEP in mice. Rab3 GEP -/- mice developed normally but died immediately after birth. Embryos at E18.5 showed no evoked action potentials of the diaphragm and gastrocnemius muscles in response to electrical stimulation of the phrenic and sciatic nerves, respectively. In contrast, axonal conduction of the spinal cord and the phrenic nerve was not impaired. Total numbers of synaptic vesicles, especially those docked at the presynaptic plasma membrane, were reduced at the neuromuscular junction similar to 10-fold compared with controls, whereas postsynaptic structures and functions appeared normal. Thus, Rab3 GEP is essential for neurotransmitter release and probably for formation and trafficking of the synaptic vesicles.
引用
收藏
页码:1421 / 1430
页数:10
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