Comparison of cell type specific coupling between [Ca²⁺]_cyto and [Ca²⁺]_mito.

<p>(<b><i>A–E</i></b>) Fura-2/AM loaded cells expression 4mtD1GO-Cam were used to simultaneously record [Ca²⁺]_cyto (green traces) and [Ca²⁺]_mito (orange traces) in response to cell stimulation with IP₃-generating agonists. Respective zooms into the rising events are presented on right panels. (<b><i>A</i></b>) Representative traces of cytosolic and mitochondrial Ca²⁺ signals in Ea.hy926 in response to 100 µM histamine in the presence of 2 mM Ca²⁺. (<b><i>B</i></b>) Temporal correlation between [Ca²⁺]_cyto and [Ca²⁺]_mito in HeLa cells in response to 100 µM histamine in the presence of 2 mM Ca²⁺. (<b><i>C</i></b>) INS-1 cells were treated with a mixture of 100 µM CCh and 100 µM ATP in the absence of Ca²⁺. (<b><i>D</i></b>) [Ca²⁺]_cyto and [Ca²⁺]_mito in percentage of the respective maximal increases in response to the treatments shown in panels <i>A-C</i> are plotted against each other. Curves are representative for at least 4 independent experiments. (<b><i>E</i></b>) [Ca²⁺]_cyto and [Ca²⁺]_mito are plotted against each other for the Ca²⁺ extrusion phases during and after the removal of the IP₃-generating agonists as indicated in panels <i>A-C</i>. (<b><i>F</i></b>) Representative time course of changes of [Ca²⁺]_cyto in EA.hy926 cells in response to 100 µM histamine in the presence of 2 mM Ca²⁺ simultaneously measured with fura-2 and D1GO-Cam. The right panel shows the zoom into the rising event upon cell treatment with histamine.