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Ion channel coupling and membrane plasticity in nucleus and mitochondria

Ion channel coupling and membrane plasticity in nucleus and mitochondria
细胞核和线粒体中的离子通道耦合和膜可塑性
批准号:
23590254
负责人:
MARUYAMA Yoshio
金额:
$3.41万
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:
2011
资助国家:
日本
项目状态:
已结题
起止时间:
2011 至 2013

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中文摘要
翻译
将腔内Ca2+浓度固定在超过10微摩尔浓度的核/内质网制剂(核膜:NE)中,并将其置于膜片钳记录技术的全NE配置中,我观察到膜电容的增加,即膜面积的测量。在原位膜片钳条件下记录的膜电容在显微镜下波动。结果表明,NE膜系统表现出反映时间膜囊泡和塌陷的特征性波动,这一过程受腔内Ca2+浓度控制。NE膜具有丰富的离子通道和水通道。这些活性膜可能有助于维持NE的组装、管腔和核膜的结构。此外,我用激光共聚焦显微镜观察到,在NE制备过程中,有一层厚膜堆积,在一个小点上堆叠成层,假设与核孔对应。
英文摘要
Fixing the lumen Ca2+-concentration at over 10 micro molar concentration in a nuclear/endoplasmic reticulum preparation (nuclear envelope: NE), which is subjected into whole-NE configuration of the patch-clamp recording techniques, I observed increases of membrane electrical capacitance, the measure of the membrane area. The membrane capacitance, recorded under in situ patch-clamp condition, fluctuated microscopically. The result suggests that the NE membrane system shows a characteristic undulation reflecting temporal membrane vesiculation and collapse, and the process is under control of the lumen Ca2+ concentration. The NE membrane is rich in ion- and water- channels. Those active membrane may component contribute to maintain NE assembly, the structure of the lumen and the nuclear membranes. Further, I observed with laser confocal microscopy in the NE preparation, a thick membrane accumulation, stacking into layers at a small spot, assumingly corresponding to the nucleic pore.
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会议论文
Decreased Expression of a Novel Prostaglandin Transporter, OAT-PG, Facilitates Renocortical PGE(2) Accumulation during Rat Pregnancy
新型前列腺素转运蛋白 OAT-PG 表达下降促进大鼠妊娠期间肾皮质 PGE(2) 积累
DOI: 10.1159/000353977
发表时间: 2013
期刊: Gynecol Obstet Invest
影响因子: --
作者: [Kazama I, Matsubara M, Kanai Y, Hatano R, Asano S, Endo Y, Toyama H, Ejima Y, Kurosawa S, Maruyama Y]
通讯作者: Maruyama Y
Amphipaths differentially modulate membrane surface deformation in rat peritoneal mast cells during exocytosis
双亲细胞在胞吐作用过程中差异调节大鼠腹膜肥大细胞的膜表面变形
DOI: 10.1159/000350079
发表时间: 2013
期刊: Cell Physiol Biochem
影响因子: --
作者: [Kazama I, Maruyama Y, Takahashi S, Kokumai T]
通讯作者: Kokumai T
Inner mitochondrial maxi-K⁺channels in neonatal renal tubular cells : novel therapeutic targets to control apoptosis
新生儿肾小管细胞内线粒体 maxi-K⁺ 通道:控制细胞凋亡的新治疗靶点
DOI: 10.1016/j.mehy.2012.03.013
发表时间: 2012
期刊: Med Hypotheses
影响因子: 4.7
作者: [Kazama I, Maruyama Y]
通讯作者: Maruyama Y
DOI: 10.3109/08923973.2012.666249
发表时间: 2012-10-01
期刊: IMMUNOPHARMACOLOGY AND IMMUNOTOXICOLOGY
影响因子: 3.3
作者: [Kazama, Itsuro, Maruyama, Yoshio, Murata, Yoshimichi]
通讯作者: Murata, Yoshimichi
共 8 条
    Dynamics of vesicle formation controlled by cellular messenger signaling
    • 批准号:
      09470006
    • 项目类别:
      Grant-in-Aid for Scientific Research (B)
    • 资助金额:
      $8.26万
    • 财政年份:
      1997
    • 负责人:
      MARUYAMA Yoshio
    • 依托单位:
    Features of granule motion and of vesicular fusion by local cell signaling
    • 批准号:
      06454148
    • 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
    • 依托单位:
    Dynamics of vesicular tronsformation in maclear complex.
    • 批准号:
      06557004
    • 项目类别:
      Grant-in-Aid for Developmental Scientific Research (B)
    • 资助金额:
      $7.62万
    • 财政年份:
      1994
    • 负责人:
      MARUYAMA Yoshio
    • 依托单位:
    Control of granular fusion by small molecular GTP-binding protein
    • 批准号:
      04670052
    • 项目类别:
      Grant-in-Aid for General Scientific Research (C)
    • 资助金额:
      $1.34万
    • 财政年份:
      1992
    • 负责人:
      MARUYAMA Yoshio
    • 依托单位:
    海外基金