| Project/Area Number |
09680763
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Neurochemistry/Neuropharmacology
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| Research Institution | Osaka University |
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Principal Investigator |
NIINOBE Michio Osaka University, Insciture for Protein Research, Associate Professor, 蛋白質研究所, 助教授 (80135748)
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| Co-Investigator(Kenkyū-buntansha) |
ARUGA Jun The Institute of Physical and Chemical Rescarch, Researcher, ライフサイエンス筑波研究センター, 研究員 (10232076)
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| Project Period (FY) |
1997 – 1998
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| Project Status |
Completed (Fiscal Year 1998)
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| Budget Amount *help |
¥2,900,000 (Direct Cost: ¥2,900,000)
Fiscal Year 1998: ¥1,200,000 (Direct Cost: ¥1,200,000)
Fiscal Year 1997: ¥1,700,000 (Direct Cost: ¥1,700,000)
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| Keywords | synaptotagmin / synaptic vesicle / exocytosis / endocytosis / inositol polyphosphate / clathrin assembly protein / Alzheimeis disease / amyloid precursor protein / シナプス連絡 / ラット交感神経節細胞 / イノシトール6リン酸 |
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| Research Abstract |
C2A and C2B domains of synaptotagmin are functional domains which are involved in exo- and endocytosis of synaptic vesicles, and we have shown that exocytosis is suppressed with the binding of inositol polyphosphates (IP) to C2B domain.In this studies, we investigated about the details of function of both domains using mammalian cells, such as rat supeior cervical ganglion (SCG) neurons or bovine adrenal chromaffin cells, and also investigated about the binding protein to C2B domain.As an another approach, we investigated about the binding protein to the intracellular domain of amyloid precursor protein (APP), because neurotransmission was suppressed by injection of C-terminal peptide of APP into rat SCG neurons.
The results revealed that (1) IP inhibited Ca^<2+> -dependent fusion and spontaneous release, but the inhibition disappeared by the treatment with anti-C2B antibody, (2) C2A domain was involved in fusion step of synaptic vesicles as a Ca^<2+> sensor, while C2B domain was involved in both steps of exo- and endocytosis of synaptic vesicles, (3) clathrin assembly protein which is involved in endocytosis bound to C2B domain with high affinity, and this binding was inhibited by IP, (4) novel protein with a molecular mass of 115kDa which binds to the intracellular domain of APP was found in synaptosomes.
These results clearly demonstrated that synaptotagmin was a central key molecule which regulates the functions of synaptic vesicles via C2A and C2B domains.Further, it is possible that discover of the novel protein which binds to the intracellular domain of APP contributes to biochemical elucidation for Alzheimer's desease.The studies are now in progress about identification of the binding protein.
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