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首页> 外文期刊>American Journal of Physiology >Modeling the effect of stretch and plasma membrane tension on Na+-K+-ATPase activity in alveolar epithelial cells.
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Modeling the effect of stretch and plasma membrane tension on Na+-K+-ATPase activity in alveolar epithelial cells.

机译:模拟拉伸和质膜张力对肺泡上皮细胞中Na + -K + -ATPase活性的影响。

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While a number of whole cell mechanical models have been proposed, few, if any, have focused on the relationship among plasma membrane tension, plasma membrane unfolding, and plasma membrane expansion and relaxation via lipid insertion. The goal of this communication is to develop such a model to better understand how plasma membrane tension, which we propose stimulates Na(+)-K(+)-ATPase activity but possibly also causes cell injury, may be generated in alveolar epithelial cells during mechanical ventilation. Assuming basic relationships between plasma membrane unfolding and tension and lipid insertion as the result of tension, we have captured plasma membrane mechanical responses observed in alveolar epithelial cells: fast deformation during fast cyclic stretch, slower, time-dependent deformation via lipid insertion during tonic stretch, and cell recovery after release from stretch. The model estimates plasma membrane tension and predicts Na(+)-K(+)-ATPase activation for a specified cell deformation time course. Model parameters were fit to plasma membrane tension, whole cell capacitance, and plasma membrane area data collected from the literature for osmotically swollen and shrunken cells. Predictions of membrane tension and stretch-stimulated Na(+)-K(+)-ATPase activity were validated with measurements from previous studies. As a proof of concept, we demonstrate experimentally that tonic stretch and consequent plasma membrane recruitment can be exploited to condition cells against subsequent cyclic stretch and hence mitigate stretch-induced responses, including stretch-induced cell death and stretch-induced modulation of Na(+)-K(+)-ATPase activity. Finally, the model was exercised to evaluate plasma membrane tension and potential Na(+)-K(+)-ATPase stimulation for an assortment of traditional and novel ventilation techniques.
机译:虽然已经提出了许多全细胞力学模型,但很少有(如果有的话)集中在质膜张力,质膜展开和质膜通过脂质插入而扩张和松弛之间的关系。这种交流的目的是开发这样一种模型,以更好地了解我们提出的质膜张力如何刺激肺泡上皮细胞在刺激过程中产生Na(+)-K(+)-ATPase活性,但也可能引起细胞损伤。机械通风。假设由于张力的结果,质膜展开与张力和脂质插入之间存在基本关系,我们已经捕获到了在肺泡上皮细胞中观察到的质膜机械反应:快速循环拉伸过程中快速变形,补品拉伸过程中通过脂质插入而产生了较慢的时间依赖性变形,以及从舒展状态释放后的细胞恢复。该模型估计质膜张力,并预测Na(+)-K(+)-ATPase在特定细胞变形时间过程中的活化。模型参数适合质膜张力,全细胞电容以及从文献中收集的有关渗透性肿胀和收缩细胞的质膜面积数据。膜张力和拉伸刺激的Na(+)-K(+)-ATPase活性的预测已从以前的研究中得到验证。作为概念的证明,我们通过实验证明了滋补拉伸和随后的质膜募集可以被利用来调节细胞对抗后续的循环拉伸,从而减轻拉伸诱导的反应,包括拉伸诱导的细胞死亡和拉伸诱导的Na(+)调节)-K(+)-ATPase活性。最后,对模型进行了评估,以评估各种传统和新型通风技术的质膜张力和潜在的Na(+)-K(+)-ATPase刺激。

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