首页> 外文会议>American Society of Mechanical Engineers(ASME) Heat Transfer/Fluids Engineering Summer Conference 2004(HT/FED 2004) vol.4; 20040711-15; Charlotte,NC(US) >CORRELATION OF HSP70 EXPRESSION AND CELL VIABILITY FOLLOWING THERMAL STIMULATION OF AORTIC ENDOTHELIAL CELLS
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CORRELATION OF HSP70 EXPRESSION AND CELL VIABILITY FOLLOWING THERMAL STIMULATION OF AORTIC ENDOTHELIAL CELLS

机译:热刺激主动脉内皮细胞后HSP70表达与细胞活力的相关性

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The goal of this study was to determine the kinetics of HSP70 expression and variations in cell viability resulting from thermal preconditioning of the heart. Experiments were conducted to determine combinations of elevated temperatures and brief heating durations that could produce enhanced HSP70 levels while maintaining high cell viability. Bovine aortic endothelial cells were heated with a water bath at temperatures ranging from 44-50℃ and periods of 1-30 min consistent with anticipated protocols for cardiac preconditioning prior to surgery. Western blot and cell adhesion analysis in culture following heating were employed to determine HSP70 level and cell viability respectively. The results demonstrate that HSP70 expression and cell viability are not maximized simultaneously. To ensure cell viability greater than 90% required a heating protocol for which HSP70 expression was less than its maximum level. HSP70 expression increments from 2.3 to 3.6 times the value of the control can be achieved for thermal stimulation protocols varying from T = 46℃ for 10 min to T = 50℃ for 1 min while maintaining a cell viability of 90% or greater. An Arrhenius injury model was fit to the cell damage data yielding values for scaling and activation energy terms of A= 1.4x10~(66) s~(-1) and E_a = 4.1 x 10~5 J/mole.
机译:这项研究的目的是确定HSP70表达的动力学和心脏热预处理导致的细胞活力变化。进行实验以确定高温和短暂加热持续时间的组合,这些组合可以产生增强的HSP70水平,同时保持较高的细胞活力。牛主动脉内皮细胞用水浴加热,温度范围为44-50℃,时间为1-30分钟,这与手术前进行心脏预处理的预期方案一致。加热后在培养物中进行蛋白质印迹和细胞粘附分析,分别测定HSP70水平和细胞活力。结果表明,HSP70表达和细胞活力不能同时最大化。为确保细胞活力大于90%,需要使用加热规程,其HSP70表达低于其最大水平。对于热刺激方案,HSP70的表达从对照值的2.3倍增加到3.6倍,从T = 46℃持续10分钟到T = 50℃持续1分钟,同时保持细胞活力90%或更高。将Arrhenius损伤模型拟合到细胞损伤数据,得出标度和活化能项A = 1.4x10〜(66)s〜(-1)和E_a = 4.1 x 10〜5 J / mol的值。

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