Project/Area Number |
61480116
|
Research Category |
Grant-in-Aid for General Scientific Research (B)
|
Allocation Type | Single-year Grants |
Research Field |
General pharmacology
|
Research Institution | Okazaki National Research Institutes, National Institute for Physiological Sciences (1988) Gunma University (1986-1987) |
Principal Investigator |
OBATA Kunihiko Okazaki National Research Insitiutes, Professor, 生理学研究所, 教授 (60013976)
|
Co-Investigator(Kenkyū-buntansha) |
INOUE Hiroshi Gunma University School of Medicine, Assistant Professor, 医学部, 助手 (30125827)
|
Project Period (FY) |
1986 – 1988
|
Project Status |
Completed (Fiscal Year 1988)
|
Budget Amount *help |
¥7,000,000 (Direct Cost: ¥7,000,000)
Fiscal Year 1988: ¥500,000 (Direct Cost: ¥500,000)
Fiscal Year 1987: ¥1,000,000 (Direct Cost: ¥1,000,000)
Fiscal Year 1986: ¥5,500,000 (Direct Cost: ¥5,500,000)
|
Keywords | Synaptic vesicle / Brain-specific proteins / Monoclonal antibodies / Immuno histochemistry / Immunoelectron microscopy / Western blot / 小脳 / シナプス小胞 / 免疫電子顕微鏡 / ウェスタンブロット / 蛋白質 / イムノブロット(ウェスタンブロット) / 海馬 |
Research Abstract |
Synaptic vesicles are clustered within the presynaptic nerve terminals and contain neurotransmitter substances which are released via exocytosis during the synaptic transmission. Chemical architecture of the synaptic vesicles remains almost unknown except for synapsin I which is associated and dissociated with the vesicle membrane and thus controls fusion of the vesicles with the presynaptic cell memmbrane. In order to identify other vesicle-specific proteins, we produced a library of monoclonal antibodies against synaptic vesicle fraction purified from the guinea pig cerebral cortex. Four different groups of the antibodies identified four vesicle specific proteins of 30, 36, 3, and 65 kilodalons. We named them SVP (synaptic vesicle protein) 30, 36, 38 and 65. Unlike synapsin I, SVPs were integrated within the vesicle membrane. SVP 65 were phosphorylated in the presence of calcium. SVP 38 was considered to be identical with synaptophysin and p38 which were independently discovered in West germany and the United States. Immunohistochemistry of the mammalisn nervous tissue with anti-SVP antibodies has demonstrated several aspects in development and organization of the synapses in the central and peripheral nervous system. For exzmple, time course of development of various synapses was confirmed in the cerebellum. Physiological roles of the SVPs in the synaptic transmission remain to be elucidated in future.
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