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Dynamics of vesicular tronsformation in maclear complex.

Dynamics of vesicular tronsformation in maclear complex.
麦克莱尔复合物中囊泡变形的动力学。
批准号:
06557004
负责人:
MARUYAMA Yoshio
金额:
$7.62万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Developmental Scientific Research (B)
财政年份:
1994
资助国家:
日本
项目状态:
已结题
起止时间:
1994 至 1995

项目摘要

项目成果

MARUYAMA Yoshio的其他基金

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相关文献

中文摘要
翻译
胰腺腺泡细胞的外核膜是粗糙的内质网(ER)膜。采用去核法收集核膜,采用标准膜片钳技术对这些制剂的外膜进行膜片钳处理。在单通道和全电流水平上,发现1)电压和Ca^<2+>激活的大k通道电流,2)一种向外的整流k通道电流,3)一种向内的整流cl通道电流。这些通道可能通过调节ip_3和/或环adp核糖依赖的Ca^<2+>-从内质网释放,促进细胞Ca^<2+>-信号转导。采用相敏电容测量方法,对膜电容变化的时间过程进行了监测。在局部斑块-膜水平上,这些变化是随机发生的,可以解释为可逆的囊泡形成(膜转化)。步骤的大小分布采用负指数曲线拟合,表明膜转化能量似乎只有一个能量峰。在全内质网水平上增加腔内Ca^<2+>-浓度,膜电容增加。这表明囊泡可逆地转化为帽状,囊泡内部与内质网腔之间有连接。结果提示内质网腔Ca^<2+>参与了囊泡运输。
英文摘要
The outer nuclear membrane of pancreatic acinar cells serves as a rough endoplasmic reticulum (ER) membrane. Collecting nuclear envelopes by enucleation, the standard patch-clamp techniques were applied to the outer membrane of these preparation. At the single channel and whole-current level, 1) voltage and Ca^<2+>-activated large K-channel current, 2) a type of outward-going rectifier K-channel current, 3) a type of inward-going rectifier Cl-channel current, were found. These channels may contribute to cellular Ca^<2+>-signaling through regulating IP_3-and/or cyclic ADP-ribose-dependent Ca^<2+>-release from the ER.Applying a phase-sensitive capacitance measurement to the ER preparation, the time course of the changes in membrane capacitance were monitored. At the local patch-membrane level, the changes occurred at random as discrete on-and off-steps, which can be interpreted as reversible vesicle formation (membrane transformation). The size distribution of the steps were fitted by a negative exponential curve, suggesting the membrane transformation energy seems to have a single energy peak. Increasing the lumenal Ca^<2+>-concentration at the whole-ER level, a rise in the membrane capacitance was found. This indicates that the vesicles are reversibly transformed to caps with a connection between the vesicle interior and the ER lumen. The result suggests the involvement of the ER lumenal Ca^<2+> in the vesicular transport.
期刊论文(18)
专著(0)
科研奖励(0)
会议论文
Maruyama, Y.: "Delay in granular fusion evoked by repetitive cytosolic Ca^<2+> spikes in mouse pancreatic acinar cells" Cell Calcium. 16. 419-430 (1994)
Maruyama, Y.:“小鼠胰腺腺泡细胞中重复的胞质 Ca^2 尖峰引起的颗粒融合延迟”细胞钙。
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通讯作者:
丸山芳夫: "膜容量測定法" 日本生理学雑誌. 56. 363-368 (1994)
Yoshio Maruyama:“膜电容测量方法”日本生理学杂志 56. 363-368 (1994)。
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Maruyama, Y.: "Ca^<2+>-activated K^+-channels in the nuclear envelope isolated from single pancreatic acinar cells." Pflugers Archiv. 430. 148-150 (1995)
Maruyama,Y.:“从单个胰腺腺泡细胞中分离出核膜中的 Ca ^ 2 -激活的 K ^ -通道。”
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Shimade,H.: "A sodium coupled neutral aminoacid cotransporter inhibited by the volatile anaesthtic halothane in megakaryocytes." Jap.J.Physiology. 45. 165-176 (1995)
Shimade,H.:“巨核细胞中被挥发性麻醉剂氟烷抑制的钠偶联中性氨基酸协同转运蛋白。”
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共 17 条
    Ion channel coupling and membrane plasticity in nucleus and mitochondria
    • 批准号:
      23590254
    • 项目类别:
      Grant-in-Aid for Scientific Research (C)
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    • 财政年份:
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    Features of granule motion and of vesicular fusion by local cell signaling
    • 批准号:
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    • 项目类别:
      Grant-in-Aid for General Scientific Research (B)
    • 资助金额:
      $4.22万
    • 财政年份:
      1994
    • 负责人:
      MARUYAMA Yoshio
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    • 批准号:
      04670052
    • 项目类别:
      Grant-in-Aid for General Scientific Research (C)
    • 资助金额:
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