Biotechnology and Bioengineering Center and Department of Physiology, Medical College of Wisconsin, Milwaukee, Wisconsin.
PLoS One. 2010 Oct 8;5(10):e13278. doi: 10.1371/journal.pone.0013278.
Mitochondrial Ca(2+) uniporter is the primary influx pathway for Ca(2+) into respiring mitochondria, and hence plays a key role in mitochondrial Ca(2+) homeostasis. Though the mechanism of extra-matrix Ca(2+) dependency of mitochondrial Ca(2+) uptake has been well characterized both experimentally and mathematically, the mechanism of membrane potential (ΔΨ) dependency of mitochondrial Ca(2+) uptake has not been completely characterized. In this paper, we perform a quantitative reevaluation of a previous biophysical model of mitochondrial Ca(2+) uniporter that characterized the possible mechanism of ΔΨ dependency of mitochondrial Ca(2+) uptake. Based on a model simulation analysis, we show that model predictions with a variant assumption (Case 2: external and internal Ca(2+) binding constants for the uniporter are distinct), that provides the best possible description of the ΔΨ dependency, are highly sensitive to variation in matrix [Ca(2+)], indicating limitations in the variant assumption (Case 2) in providing physiologically plausible description of the observed ΔΨ dependency. This sensitivity is attributed to negative estimate of a biophysical parameter that characterizes binding of internal Ca(2+) to the uniporter. Reparameterization of the model with additional nonnengativity constraints on the biophysical parameters showed that the two variant assumptions (Case 1 and Case 2) are indistinguishable, indicating that the external and internal Ca(2+) binding constants for the uniporter may be equal (Case 1). The model predictions in this case are insensitive to variation in matrix [Ca(2+)] but do not match the ΔΨ dependent data in the domain ΔΨ≤120 mV. To effectively characterize this ΔΨ dependency, we reformulate the ΔΨ dependencies of the rate constants of Ca(2+) translocation via the uniporter by exclusively redefining the biophysical parameters associated with the free-energy barrier of Ca(2+) translocation based on a generalized, non-linear Goldman-Hodgkin-Katz formulation. This alternate uniporter model has all the characteristics of the previous uniporter model and is also able to characterize the possible mechanisms of both the extra-matrix Ca(2+) and ΔΨ dependencies of mitochondrial Ca(2+) uptake. In addition, the model is insensitive to variation in matrix [Ca(2+)], predicting relatively stable physiological operation. The model is critical in developing mechanistic, integrated models of mitochondrial bioenergetics and Ca(2+) handling.
线粒体钙单向转运体是 Ca2+进入呼吸线粒体的主要内流途径,因此在维持线粒体 Ca2+稳态中起着关键作用。尽管已经从实验和数学上很好地描述了细胞外基质 Ca2+对线粒体 Ca2+摄取的依赖性的机制,但膜电位(ΔΨ)对线粒体 Ca2+摄取的依赖性的机制尚未完全阐明。在本文中,我们对先前的线粒体钙单向转运体的生物物理模型进行了定量重新评估,该模型描述了线粒体 Ca2+摄取的 ΔΨ依赖性的可能机制。基于模型模拟分析,我们表明,提供对 ΔΨ依赖性的最佳描述的模型预测(假设 1:单向转运体的外部和内部 Ca2+结合常数是相同的)对基质 [Ca2+]的变化非常敏感,这表明假设 1(变体情况 2:单向转运体的外部和内部 Ca2+结合常数是不同的)在提供对观察到的 ΔΨ依赖性的生理上合理的描述方面存在局限性。这种敏感性归因于描述内部 Ca2+与单向转运体结合的生物物理参数的负估计。使用生物物理参数的附加非负约束对模型进行重新参数化表明,两种变体假设(假设 1 和假设 2)是不可区分的,这表明单向转运体的外部和内部 Ca2+结合常数可能相等(假设 1)。在这种情况下,模型预测对基质 [Ca2+]的变化不敏感,但与 ΔΨ≤120 mV 范围内的 ΔΨ 依赖性数据不匹配。为了有效地描述这种 ΔΨ 依赖性,我们通过专门根据广义的非线性 Goldman-Hodgkin-Katz 公式重新定义与 Ca2+转运的自由能势垒相关的生物物理参数,重新制定了通过单向转运体的 Ca2+转运的速率常数的 ΔΨ 依赖性。这个替代的单向转运体模型具有以前的单向转运体模型的所有特征,并且还能够描述细胞外基质 Ca2+和 ΔΨ 对线粒体 Ca2+摄取的依赖性的可能机制。此外,该模型对基质 [Ca2+]的变化不敏感,预测相对稳定的生理功能。该模型对于开发线粒体生物能量学和 Ca2+处理的机制性、综合模型至关重要。