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DETERMINATION OF HYPERTHERMIC CELL KILLING MECHANISMS

DETERMINATION OF HYPERTHERMIC CELL KILLING MECHANISMS
高温杀死细胞机制的测定
批准号:
3459419
负责人:
Michael Jude Borrelli
金额:
$7.7万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
1988
资助国家:
美国
项目状态:
已结题
起止时间:
1988-07-15 至 1993-06-30

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英文摘要
Preliminary data suggests that hyperthermia-induced increases in intracellular free calcium concentrations ((Ca+2)i) are cytotoxic and contribute to the resultant cell killing. Hyperthermia induced changes in (Ca+2)i and total intracellular calcium will be measured, respectively, with the fluorescent calcium dye indo 1 and atomic absorption. Calcium cytotoxicity will be induced into nonheated cells using the calcium ionophore ionomycin, such that the cell killing level is similar to that observed following hyperthermia. If changes in intracellular calcium are similar in the heated and nonheated cells at isosurvival, altered intracellular calcium will be implicated as the, or one of the, cellular responses to hyperthermia that renders cells reproductively nonviable. A disparity in survival levels will indicate to what degree (if any) calcium cytotoxicity contributes to hyperthermic killing. Agonists and antagonists of calcium and calcium-regulated functions will be used to further establish the role of calcium in hyperthermic cell death and elucidate how calcium mediates its cytotoxic effects. Whole and permeabilized heated cells will be used to determine if (Ca+2)i increases because of a calcium influx from the extracellular medium or a release from intracellular stores. The same system will be used to determine how treated cells attempt to re-regulate calcium to homeostatic levels. (Ca+2)i will be measured in individual cell that will also be scored for the ability to form a colony in order to establish the threshold increase in (Ca+2)i required to kill a cell. Changes in the morphology and cytoplasmic distribution of the endoplasmic reticulum, mitochondria, and cytoskeleton will be monitored and quantified in these same cells to establish which aspects of the cell are damaged by altered (Ca+2)i and represent lethal lesion sites. Answers to the questions posed by this study will help determine how hyperthermia interacts with cells. This in turn will lead to a more educated application of this modality in the clinic.
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The Seventh Nanotechnology for Health Care Conference
  • 批准号:
    9805451
  • 项目类别:
  • 资助金额:
    $0.5万
  • 财政年份:
    2018
  • 负责人:
    Michael Jude Borrelli
  • 依托单位:
The Fifth Nanotechnology for Health Care Conference
  • 批准号:
    9094250
  • 项目类别:
  • 资助金额:
    $0.75万
  • 财政年份:
    2014
  • 负责人:
    Michael Jude Borrelli
  • 依托单位:
The Fifth Nanotechnology for Health Care Conference
  • 批准号:
    8849339
  • 项目类别:
  • 资助金额:
    $0.75万
  • 财政年份:
    2014
  • 负责人:
    Michael Jude Borrelli
  • 依托单位:
The Fifth Nanotechnology for Health Care Conference
  • 批准号:
    8792651
  • 项目类别:
  • 资助金额:
    $0.5万
  • 财政年份:
    2014
  • 负责人:
    Michael Jude Borrelli
  • 依托单位:
国内基金
海外基金
炎性反应中巨噬细胞激活诱导死亡(activation-induced cell death,AICD)的机理研究
  • 批准号:
    30330260
  • 项目类别:
    重点项目
  • 资助金额:
    105.0万元
  • 批准年份:
    2003
  • 负责人:
    顾军
  • 依托单位: