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Molecular mechanism of synaptic plasticity

Molecular mechanism of synaptic plasticity
突触可塑性的分子机制
批准号:
07278101
负责人:
SHIMIZU Takao
金额:
$72.9万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research on Priority Areas
财政年份:
1995
资助国家:
日本
项目状态:
已结题
起止时间:
1995 至 1998

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中文摘要
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英文摘要
Synaptic plasticity is considered to be a fundamental mechanism of memory and learning. In this project, more than 140 scientists with different disciplines have worked to elucidate the underlying molecular mechanisms of neuronal plasticity and its biological significance. Many important molecules (glutamate receptor channels, protein kinases, receptors for lipid mediators, small GTP binding proteins etc) were cloned by these members, and their genetically deficient mice were established. By backcrossing, most mice are now congenic for more strict analyses. Using these mice, we found that NMDA receptors and protein kinases C are important for synaptic plasticity as well as synaptic maturation. Lipid mediators (prostaglandin, leukotrienes, PAF), small G-proteins are also involved in plasticity and neuronal cell migration. Using subtraction technology and others, we found various LTP or LTD-induced genes, and ther functions are currently under investigations.
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Mori, M. et al.: "Predominant expression of platelet-activating factor receptor in the rat microglia"Journal of Neuroscience. 16. 3590-3600 (1996)
Mori, M. 等人:“大鼠小胶质细胞中血小板激活因子受体的主要表达”神经科学杂志。
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通讯作者:
Sakimura K. et al.: "Reduced hippocamal LTP and spatial learning in mice lacking NMDA receptor e1 subunit"Nature. 373. 151-155 (1995)
Sakimura K. 等人:“缺乏 NMDA 受体 e1 亚基的小鼠海马 LTP 和空间学习能力降低”Nature。
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Yokomizo, T. et al.: "A G-protein-coupled receptor for leukotniene B4 that mediates chemotaxis"Nature. 387. 620-624 (1997)
Yokomizo, T. 等人:“介导趋化性的白细胞介素 B4 的 G 蛋白偶联受体”。
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Kasai, H. et al.: "Multiple and diverse forms of regulated exocytosis revealed in wild tyno acid defective PC19 cells"Proc. Natl. Acad. Sai. U.S.A.. 96. 945-999 (1999)
Kasai, H. 等人:“在野生泰诺酸缺陷型 PC19 细胞中揭示了多种形式的受控胞吐作用”Proc.
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