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Research for functional molecule involved in mechanical stress^induced increase in CaィイD12+ィエD1 from basement membrane

Research for functional molecule involved in mechanical stress^induced increase in CaィイD12+ィエD1 from basement membrane
机械应力^诱导基底膜CaiD12+D1增加的功能分子研究
批准号:
10672054
负责人:
OHATA Hisayuki
金额:
$1.47万
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:
1998
资助国家:
日本
项目状态:
已结题
起止时间:
1998 至 1999

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项目成果

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相关文献

中文摘要
翻译
We demonstrated that intracellular Ca i D12+i D 1 concentration([Ca I D 12+I D 1]I D 2 i I D 2)was increased in a restricted region with a diameter of less than a fewµm in lens epithelial cells loaded with fluo-4 when the cells were stimulated mechanically in the presence of lysophosphatidic acid(LPA),an intercellular phospholipid messenger.The Ca I D12+I D 1 response was inhibited by lowering extracelluar Ca I D 12+I D 1 concentration,but not by thapsigargin,suggesting that the Ca I D 12+I D 1 response is a Ca I D 12+I D 1 influx event.The Ca I D 12+I D 1 increase reached to the peak level in the starting region within 100 ms and concentrically diffused in a restricted region.We named the Ca I D 12+I D 1 influx“Ca I D 12+I D 1 spots”.In order to clarify the spatiotemporal characteristics of Ca I D 12+I D 1 spots,we visualized Ca I D 12+I D 1 spot phenomenon using a high-speed three-dimensional confocal system with a piezoelectric driven objective,which permits simultaneous imaging of focal and apical plan…More es of lens epithelial cells at each 37.6 ms interval.Ca I D12+I D 1 spots in the apical plane was more clearly visualized than that in the focal plane,suggesting that Ca I D 12+I D 1 spots reflect Ca I D 12+I D 1 influx on the apical membrane.From these results,we propose a hypothesis that Ca I D12+I D 1 spots is an elementary Ca I D 12+I D 1 influx event underlying localized cellular responses to mechanical stress.Furthermore,the involvement of Rho-mediated signal transduction and integrin signaling in Ca I D 12+I D 1 spots were investigated.Pretreatment of Clostridium botulinum exoenzyme C3 transferase,an inhibitor of Rho protein,or cytochalasin D,which depolymerizes the actin cytoskeleton,blocked formation of stress fibers,but not affect the Ca I D12+ii D1 spots。Additionally,genistein,an inhibitor of tyrosine kinase including pp 125 I D 1 FAK文件D1,did not inhibit the Ca I D 12+文件D 1 spots。On the other hand,GRGDSP,an inhibitor of integirn,partially inhibited the Ca I D12+I D 1 spots。These results suggest that LPA enhances the mechanical stress-induced Ca ei D12+ii D1 spots by modulating recognizing site of integirn to RGD sequence,but not by formation of actin stress fibers.Less:Less
英文摘要
We demonstrated that intracellular CaィイD12+ィエD1 concentration ([CaィイD12+ィエD1]ィイD2iィエD2) was increased in a restricted region with a diameter of less than a few μm in lens epithelial cells loaded with fluo-4 when the cells were stimulated mechanically in the presence of lysophosphatidic acid (LPA), an intercellular phospholipid messenger. The CaィイD12+ィエD1 response was inhibited by lowering extracelluar CaィイD12+ィエD1 concentration, but not by thapsigargin, suggesting that the CaィイD12+ィエD1 response is a CaィイD12+ィエD1 influx event. The CaィイD12+ィエD1 increase reached to the peak level in the starting region within 100 ms and concentrically diffused in a restricted region. We named the CaィイD12+ィエD1 influx "CaィイD12+ィエD1 spots". In order to clarify the spatiotemporal characteristics of CaィイD12+ィエD1 spots, we visualized CaィイD12+ィエD1 spot phenomenon using a high-speed three-dimensional confocal system with a piezoelectric driven objective, which permits simultaneous imaging of focal and apical plan … More es of lens epithelial cells at each 37.6 ms interval. CaィイD12+ィエD1 spots in the apical plane was more clearly visualized than that in the focal plane, suggesting that CaィイD12+ィエD1 spots reflect CaィイD12+ィエD1 influx on the apical membrane. From these results, we propose a hypothesis that CaィイD12+ィエD1 spots is an elementary CaィイD12+ィエD1 influx event underlying localized cellular responses to mechanical stress. Furthermore, the involvement of Rho-mediated signal transduction and integrin signaling in CaィイD12+ィエD1 spots were investigated. Pretreatment of Clostridium botulinum exoenzyme C3 transferase, an inhibitor of Rho protein, or cytochalasin D, which depolymerizes the actin cytoskeleton, blocked formation of stress fibers, but not affect the CaィイD12+ィエD1 spots. Additionally, genistein, an inhibitor of tyrosine kinase including pp125ィイD1FAKィエD1, did not inhibit the CaィイD12+ィエD1 spots. On the other hand, GRGDSP, an inhibitor of integirn, partially inhibited the CaィイD12+ィエD1 spots. These results suggest that LPA enhances the mechanical stress-induced CaィイD12+ィエD1 spots by modulating recognizing site of integirn to RGD sequence, but not by formation of actin stress fibers. Less
期刊论文(17)
专著(0)
科研奖励(0)
会议论文
Ohata,Hisayuki: "Confocal imaging analysis of intracellular ions in mixed cellular systems or in situ using two types of confocal microscopic systems" Methods in Enzymology,. 307(in press). (1999)
Ohata,Hisayuki:“使用两种类型的共焦显微系统对混合细胞系统或原位细胞内离子进行共焦成像分析”酶学方法,。
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Ohata, Hisayuki: "Confocal imaging analysis of intracellular ions in mixed cellular systems or in situ using two types of confocal microscopic systems"Methods in Enzymology. 307. 425-441 (1999)
Ohata,Hisayuki:“使用两种类型的共焦显微系统对混合细胞系统或原位细胞内离子进行共焦成像分析”酶学方法。
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16
    Shear stress-dependent vasospasm induced by lysophosphatidic acid
    • 批准号:
      21590240
    • 项目类别:
      Grant-in-Aid for Scientific Research (C)
    • 资助金额:
      $3.0万
    • 财政年份:
      2009
    • 负责人:
      OHATA Hisayuki
    • 依托单位:
    Effect of lysophosphatidic acid in fluid flow-response in vascular endothelial cells
    • 批准号:
      16590206
    • 项目类别:
      Grant-in-Aid for Scientific Research (C)
    • 资助金额:
      $2.24万
    • 财政年份:
      2004
    • 负责人:
      OHATA Hisayuki
    • 依托单位:
    Role of lysophosphatidic acid in fluid flow-response in vascular endothelial cells
    • 批准号:
      13672400
    • 项目类别:
      Grant-in-Aid for Scientific Research (C)
    • 资助金额:
      $1.92万
    • 财政年份:
      2001
    • 负责人:
      OHATA Hisayuki
    • 依托单位:
    海外基金