Using dual excitation and fixed emission fluorescence microscopy, we were able to measure changes in cytoplasmic free Ca2+ concentration ([Ca2+]i) and mitochondrial membrane potential simultaneously in the pancreatic β-cell. The β-cells were exposed to a combination of the Ca2+ indicator fura-2/AM and the indicator of mitochondrial membrane potential, rhodamine 123 (Rh123). Using simultaneous measurements of mitochondrial membrane potential and [Ca2+] i during glucose stimulation, it was possible to measure the time lag between the onset of mitochondrial hyperpolarization and changes in [Ca 2+]i. Glucose-induced oscillations in [Ca 2+]i were followed by transient depolarizations of mitochondrial membrane potential. These results are compatible with a model in which nadirs in [Ca2+]i oscillations are generated by a transient, Ca2+-induced inhibition of mitochondrial metabolism resulting in a temporary fall in the cytoplasmic ATP/ADP ratio, opening of plasma membrane KATP channels, repolarization of the plasma membrane, and thus transient closure of voltage-gated L-type Ca2+ channels.
CITATION STYLE
Kindmark, H., Köhler, M., Brown, G., Bränström, R., Larsson, O., & Berggren, P. O. (2001). Glucose-induced Oscillations in Cytoplasmic Free Ca2+ Concentration Precede Oscillations in Mitochondrial Membrane Potential in the Pancreatic β-Cell. Journal of Biological Chemistry, 276(37), 34530–34536. https://doi.org/10.1074/jbc.M102492200
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