首页> 美国卫生研究院文献>The Journal of Physiology >Analysis of cardiac mitochondrial Na+–Ca2+ exchanger kinetics with a biophysical model of mitochondrial Ca2+ handing suggests a 3: 1 stoichiometry
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Analysis of cardiac mitochondrial Na+–Ca2+ exchanger kinetics with a biophysical model of mitochondrial Ca2+ handing suggests a 3: 1 stoichiometry

机译:使用线粒体Ca2 +处理的生物物理模型分析心脏线粒体Na + -Ca2 +交换子动力学表明化学计量比为3:1

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摘要

Calcium is a key ion and is known to mediate signalling pathways between cytosol and mitochondria and modulate mitochondrial energy metabolism. To gain a quantitative, biophysical understanding of mitochondrial Ca2+ regulation, we developed a thermodynamically balanced model of mitochondrial Ca2+ handling and bioenergetics by integrating kinetic models of mitochondrial Ca2+ uniporter (CU), Na+–Ca2+ exchanger (NCE), and Na+–H+ exchanger (NHE) into an existing computational model of mitochondrial oxidative phosphorylation. Kinetic flux expressions for the CU, NCE and NHE were developed and individually parameterized based on independent data sets on flux rates measured in purified mitochondria. While available data support a wide range of possible values for the overall activity of the CU in cardiac and liver mitochondria, even at the highest estimated values, the Ca2+ current through the CU does not have a significant effect on mitochondrial membrane potential. This integrated model was then used to analyse additional data on the dynamics and steady-states of mitochondrial Ca2+ governed by mitochondrial CU and NCE. Our analysis of the data on the time course of matrix free [Ca2+] in respiring mitochondria purified from rabbit heart with addition of different levels of Na+ to the external buffer medium (with the CU blocked) with two separate models – one with a 2: 1 stoichiometry and the other with a 3: 1 stoichiometry for the NCE – supports the hypothesis that the NCE is electrogenic with a stoichiometry of 3: 1. This hypothesis was further tested by simulating an additional independent data set on the steady-state variations of matrix free [Ca2+] with respect to the variations in external free [Ca2+] in purified respiring mitochondria from rat heart to show that only the 3: 1 stoichiometry model predictions are consistent with the data. Based on these analyses, it is concluded that the mitochondrial NCE is electrogenic with a stoichiometry of 3: 1.
机译:钙是关键离子,并且已知其介导细胞质和线粒体之间的信号传导途径并调节线粒体能量代谢。为了对线粒体Ca 2 + 调控进行定量的生物物理理解,我们通过整合线粒体Ca 2的动力学模型建立了线粒体Ca 2 + 处理和生物能学的热力学平衡模型。 sup> 2 + 单端口(CU),Na + –Ca 2 + 交换子(NCE)和Na + –H + 交换器(NHE)转换为现有的线粒体氧化磷酸化计算模型。 CU,NCE和NHE的动力学通量表达式已开发出来,并基于在纯化的线粒体中测得的通量速率的独立数据集分别进行了参数化。尽管可用数据支持CU在心脏和肝脏线粒体中总体活动的可能范围很广,但即使在最高估计值下,通过CU的Ca 2 + 电流也没有显着影响对线粒体膜电位的影响然后使用该集成模型来分析线粒体CU和NCE控制的线粒体Ca 2 + 的动力学和稳态的其他数据。我们分析了在体外缓冲液中添加不同水平的Na + 的兔心脏呼吸线粒体中游离基质[Ca 2 + ]随时间变化的数据介质(具有封闭的CU)具有两个独立的模型-一个对NCE的化学计量比为2:1,另一个对化学计量比为3:1-支持以下假设:NCE是电动的,化学计量比为3:1。通过模拟关于矩阵自由[Ca 2 + ]相对于外部自由[Ca 2 + 的稳态变化的附加独立数据集,进一步测试了在大鼠心脏的纯化呼吸线粒体中的电泳,以表明只有3:1化学计量模型的预测与数据一致。根据这些分析,可以得出结论,线粒体NCE是电动的,化学计量比为3:1。

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