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Mechanism of Presynaptic Function as Studied Using Giant Synaptosomes

Mechanism of Presynaptic Function as Studied Using Giant Synaptosomes
使用巨突触体研究突触前功能的机制
批准号:
62480418
负责人:
KIRINO Yutaka
金额:
$4.42万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for General Scientific Research (B)
财政年份:
1987
资助国家:
日本
项目状态:
已结题
起止时间:
1987 至 1988

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中文摘要
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英文摘要
1. This study has two main objectives. One is the detection and characterization of ion channels of synaptosomal membranes and synaptic vesicle membranes. For this purpose, we adopted reconstitution of biomembranes into planar lipid bilayer or into giant proteoliposomes. The second objective is the development of a new experimental system, which allow us to apply various techniques not applicable, so far, to the reconstitution system. For this purpose, we attempted to prepare giant biomembrane vesicles, by fusion of biomembrane vesicles without use of exo-genous phospholipids.2. We developed a simple method to obtain preparations of synaptosomes and synaptic vesicles from rat brain, which are minimal of contamina-tions by other membrane fractions.3. A rapid and simple method to prepare giant proteoliposomes without use of detergent has been established. This technique has some advantages over conventional methods involving the solubilization/dialysis procedure. Using this newly develop … More ed technique as well as the planar membrane technique, we have detected several kinds of cation and anion channels. Synaptosomal membrane contains voltage-independent potassium channels, which may contribute to the determination of resting potential. A calcium-dependent potassium channel was also observed. Two kinds of mono-valent cation channels and an anion channel were found to occur in the membrane of synaptic vesicles. These channels may play an important role in the exocytosis of neurotransmitters from presynaptic terminals.4. Using the treatment with a fusogenic compound such as polyethyleneglycol, electrofusion, partial digestion with proteases and/or freez-ing-thawing technique, we were able to prepare giant synaptosomes, 10-20 micrometers in diameter, without addition of exogenous lipid. Attempts to apply various procedures of electrophysiology and cell manipulation to these giant synaptosomes were made. Some of them had been so far impossible with reconstitute proteoliposomes. Insertion of a microelectrode and injection were carried out successfully. These results suggest that giant synaptosome should be a very useful system for the study of presynaptic functions and their mechanisms. Less
期刊论文(51)
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会议论文
Kazunori,Anzai: "Rapid Determination of Internal Volume of Membrane Vesicles with Stopped Flow-ESR Technique" Biochimica et Biophysica Acta. 937. 73-80 (1988)
Kazunori,Anzai:“用停流 ESR 技术快速测定膜囊泡的内部体积”生物化学和生物物理学学报。
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Kazunori,Anzai: Biochimica et Biopysica Acta. 937. 73-80 (1988)
安西一典:《生物化学与生物物理学学报》。
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通讯作者:
Higashi,Ken-ichiro: J.Biochem.101. 433-440 (1987)
东健一郎:J.Biochem.101。
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24
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