Relationship between the development of the nerve cell and the expression of the neurotransmitter transporter
Relationship between the development of the nerve cell and the expression of the neurotransmitter transporter
批准号:
07680815
负责人:
KADOTA Tomoko
金额:
$1.6万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (C)
财政年份:
1995
资助国家:
日本
项目状态:
已结题
起止时间:
1995 至 1997
中文摘要
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英文摘要
In the present study we have produced monoclonal antibodies (MAbs) against oligopeptides of a dopamine transporter (DAT) protein. Using the antipeptide antibody, we have examined the expression of DAT in the neuron, especially the changes in subcellular localization of DAT during development. In this study we used PC12 cells, which are a clonal line of rat pheochromecytoma cells that secrete dopamine, epinephrine and acetylcholine and develop as neuron-like cells after treatment with nerve growth factor (NGF).An attempt to produce antipeptide antibodies against the oligopeptides specific in amino acid sequence to a rat dopamine transporter was made with an in vitro immunization method. Two monoclonal antibodies, Mabs H-1a and H-1b, were produced. Western blot analysis confirmed that the above antibodies recognized a -85,000 Da protein in a synaptosomal fraction prepared from the rat striatum but none in the fraction from the cerebellum. The specificity of the antibody to DAT was also c … More onfirmed by an antibody absorption test using two kinds of synthetic oligopeptides, one of which is specific only to DAT.These results have confirmed the specificity of the present antibody to DAT.The expression and subcellular localization of DAT were immunohistochemically examined with Mabs H-1a and H-1b in PC12 cells treated with NGF.The antibody labeled the surface of PC12 cells in control. When the cells were treated with NGF,the expression of DAT was significantly emphasized first in the cytoplasm and then on the surface of growth cones from the beginning of neurite outgrowth. The activity of DAT in the PC12 cells was pharmacologically confirmed by the uptake of [^3H] -dopamine and blockade by uptake inhibitors. The NGF treatment doubled the dopamine uptake activity. GBR12909, a specific inhibitor of DAT,blocked the [^3H] -dopamine at a concentration of 10^<-7> M.The expression of DAT and norepinephrine transporter (NET) mRNA in the PC12 cells was examined by reverse transcriptase-polmerase chain reaction (RT-PCR). DAT mRNA significantly increased in the NGF-treated cells after 7 days of incubation, whereas NET mRNA markedly decreased. Less
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Tomoko Kadota: "Synaptic spinules attendent on post-tetanic potentiation in cat sympathetic ganglion." Proceedings of Japan Academy. 72,SerB. 48-51 (1996)
Tomoko Kadota:“突触小刺参与猫交感神经节的强直后增强。”
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Tomoko Kadota: "Expression of dopamine transporter at the tips of growing neurites of PC12 cells." Journal of Histochemistry and Cytochemistry. 44. 989-996 (1996)
Tomoko Kadota:“多巴胺转运蛋白在 PC12 细胞生长的神经突尖端的表达。”
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門田朋子: "Na^+依存性伝達物質トランスポーター" 細胞. 27. 349-352 (1995)
Tomoko Kadota:“Na^+ 依赖性递质转运蛋白”细胞。27. 349-352 (1995)
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Mitsukai Fujita: "Developmental profiles of synaptophysin in granule cells of rat cerebellum: an immunohistocytochemical study." Journal of Electron Microscopy. 45. 185-194 (1996)
Mitsukai Fujita:“大鼠小脑颗粒细胞中突触素的发育概况:一项免疫组织细胞化学研究。”
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Tomoko Kadota: "Antipeptide antibody of dopamine transporter and its expression in the PC12h cells." Acta Anatomica Nipponica. 70. 248-251 (1995)
Tomoko Kadota:“多巴胺转运蛋白的抗肽抗体及其在 PC12h 细胞中的表达。”
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共 11 条
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:
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:
Expression and localization of the synapse specific proteins in central nervous system of the postnatal rat.
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批准号:01570026
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项目类别:Grant-in-Aid for General Scientific Research (C)
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资助金额:$1.15万
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财政年份:1989
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负责人:KADOTA Tomoko
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依托单位:
海外基金