Mitochondrial Ca2+ concentrations in live cells: quantification methods and discrepancies

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Abstract

Intracellular Ca2+ signaling controls numerous cellular functions. Mitochondria respond to cytosolic Ca2+ changes by adapting mitochondrial functions and, in some cell types, shaping the spatiotemporal properties of the cytosolic Ca2+ signal. Numerous methods have been developed to specifically and quantitatively measure the mitochondrial-free Ca2+ concentrations ([Ca2+]m), but there are still significant discrepancies in the calculated absolute values of [Ca2+]m in stimulated live cells. These discrepancies may be due to the distinct properties of the methods used to measure [Ca2+]m, the calcium-free/bound ratio, and the cell-type and stimulus-dependent Ca2+ dynamics. Critical processes happening in the mitochondria, such as ATP generation, ROS homeostasis, and mitochondrial permeability transition opening, depend directly on the [Ca2+]m values. Thus, precise determination of absolute [Ca2+]m values is imperative for understanding Ca2+ signaling. This review summarizes the reported calibrated [Ca2+]m values in many cell types and discusses the discrepancies among these values. Areas for future research are also proposed.

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Fernandez-Sanz, C., De la Fuente, S., & Sheu, S. S. (2019, July 1). Mitochondrial Ca2+ concentrations in live cells: quantification methods and discrepancies. FEBS Letters. Wiley Blackwell. https://doi.org/10.1002/1873-3468.13427

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