Expression and localization of the synapse specific proteins in central nervous system of the postnatal rat.
Expression and localization of the synapse specific proteins in central nervous system of the postnatal rat.
批准号:
01570026
负责人:
KADOTA Tomoko
金额:
$1.15万
依托单位国家:
日本
项目类别:
Grant-in-Aid for General Scientific Research (C)
财政年份:
1989
资助国家:
日本
项目状态:
已结题
起止时间:
1989 至 1990
中文摘要
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英文摘要
1. Postsynaptic density specific protein, 82K proteinA fraction of synaptic junctional complex (SJC) was prepared from rat brain synaptosomes and served as an antigen material to produce monoclonal antibodies for examining the component proteins of the SJC. An antibody, SJ-8, was obtained, which recognized a protein with a molecular weight of 82,000 dalton (82K protein) in the SJC preparation in immunoblotting analysis. The immunohistochemical localization of the 82K protein was studied with the rat cerebellum. The antibody SJ-8 labeled the peripheral area of the Purkinje and granule cells. Small punctate areas were also stained in the molecular layer with SJ-8. Intracellular localization of the protein was examined with the rat brain synaptosomes. Immunoelectron microscopy demonstrated that SJ-8 strongly labeled the postsynaptic density and also a fibrous network spreading out of it. However, the antibody did not label the pre- and postsynaptic membrane.2. Expression of synaptophysin … More in the rat cerebellumExpression and intracellular localization of synaptophysin was examined in cerebellar cortex of the perinatal rat. Rats, 1-7 days after birth, were fixed by perfusion via the heart with 4% paraformaldehyde. The cerebellar cortex was dissected out and cut into 40 mum thick slices with a vibratome. After blocking with 1% bovine serum albumin, the slices were incubated with the antibody against synaptophysin. Then, slices were reacted with FITC- conjugated anti-mouse IgG and examined with a light microscopy equipped with epifluorescence. Specimens from perinatal rats did not show any positive reactions. Several positive spots appeared around the Purkinje cells and granule cells three days after birth. Small punctates of reaction were also observed in the molecular layer. These positive reactions significantly increased 7 days after birth. The reaction pattern in the cerebellar cortex after 2 weeks was similar to that of adult rats. The development of positive reaction may involve the synaptogenesis in the cerebellar cortex. Synaptophysin might be transported from the perikaryon to the nerve ending via the axon before the synaptogenesis. The transporting system of the protein is immunocytochemically examined. Less
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Tomoko Kadota: "Localization of a 82 KDa protein in postsynaptic density." Neuroscience Research.
Tomoko Kadota:“突触后密度中 82 KDa 蛋白质的定位。”
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通讯作者:
門田 朋子: "シナプトファイシン" 生体の科学. 41. 349-350 (1990)
门田智子:“突触素”生物科学 41. 349-350 (1990)。
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門田 朋子: "神経伝達時におけるシナプス小胞の動態" 日本電子顕微鏡. 21. 103-113 (1990)
Tomoko Kadota:“神经传递过程中突触小泡的动力学”日本电子显微镜 21. 103-113 (1990)。
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Kadota, T., Fujita, M., Moroi, K., Hori, M. and Kadota, K.: "Localization of a 82 KDa protein in postsynaptic density." Neuroscience Research.
Kadota, T.、Fujita, M.、Moroi, K.、Hori, M. 和 Kadota, K.:“突触后密度中 82 KDa 蛋白质的定位”。
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Functional morphology on the synaptic plasticity : Rapid remodeling of the synapse during long-term potentiation.
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批准号:10680698
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$2.3万
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财政年份:1998
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负责人:KADOTA Tomoko
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依托单位:
Relationship between the development of the nerve cell and the expression of the neurotransmitter transporter
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批准号:07680815
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$1.6万
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财政年份:1995
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负责人:KADOTA Tomoko
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依托单位:
Regulated secretion and cytoskeleton in synapses.
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批准号:04670035
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项目类别:Grant-in-Aid for General Scientific Research (C)
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资助金额:$1.41万
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财政年份:1992
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负责人:KADOTA Tomoko
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依托单位:
国内基金
海外基金
星形胶质细胞通过Siah介导糖尿病海马神经元突触损伤的机制研究
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批准号:81171023
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项目类别:面上项目
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资助金额:55.0万元
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批准年份:2011
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负责人:赵延欣
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依托单位: