Mechanisms of transmission and plastcity at mammalian central synapses.
| Project/Area Number |
18H02530
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| Research Category |
Grant-in-Aid for Scientific Research (B)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Review Section |
Basic Section 46010:Neuroscience-general-related
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| Research Institution | Doshisha University |
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Principal Investigator |
Sakaba Takeshi 同志社大学, 脳科学研究科, 教授 (80609511)
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| Project Period (FY) |
2018-04-01 – 2021-03-31
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| Project Status |
Completed (Fiscal Year 2020)
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| Budget Amount *help |
¥17,680,000 (Direct Cost: ¥13,600,000、Indirect Cost: ¥4,080,000)
Fiscal Year 2020: ¥3,250,000 (Direct Cost: ¥2,500,000、Indirect Cost: ¥750,000)
Fiscal Year 2019: ¥4,940,000 (Direct Cost: ¥3,800,000、Indirect Cost: ¥1,140,000)
Fiscal Year 2018: ¥9,490,000 (Direct Cost: ¥7,300,000、Indirect Cost: ¥2,190,000)
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| Keywords | シナプス / 神経 / 可塑性 |
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| Outline of Final Research Achievements |
In order to understand the cellular mechanisms of transmission and plasticity at mammalian central synapses, we have applied simultaneous pre- and postsynaptic patch clamp to hippocampal mossy fiber synapses. We found that the intra-cellular Ca sensitivity for transmitter release was similar to the one at other synapse types, but the local Ca concentration at the transmitter release site was much lower, explaining low release probability of release at mossy fiber synapses. In addition, we found that cAMP-induced potentiation of transmitter release, important for short- and long-term plasticity, was mediated by accumulation of Ca channels near release sites, thereby increasing the local Ca concentration at the release site.
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| Academic Significance and Societal Importance of the Research Achievements |
本研究は、哺乳類中枢シナプスのシナプス前後部記録によって、厳密に伝達特性を測定し、それによって、伝達、可塑性の分子細胞メカニズムを明らかにした。海馬苔状線維シナプスではCa-伝達物質放出連関が特殊であり、それが伝達効率の低さの主要因となっていること、また可塑性因子であるcAMPによってCaチャネルクラスターが拡大し、それによって伝達物質放出量増大によってシナプス増強などの可塑性がおこることが明らかになった。
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Report
(4 results)
Research Products
(16 results)
