Cell-type dependent effects of mCa2+ uptake on cytosolic Ca2+ signals. Stimulation of secretory cells elicits cytosolic Ca2+ transients that are rapidly transmitted to the mitochondria, resulting in large mCa2+ transients. Modulation of net mCa2+ uptake affects the magnitude of both the cytosolic Ca2+ transient and the mitochondrial Ca2+ transient, and impacts physiologically relevant cellular functions. For example, increased net mCa2+ uptake in adrenal chromaffin cells can limit the magnitude of the cytosolic Ca2+ transient and thereby limit the amount of cytosolic Ca2+ available to stimulate secretion of catecholamines such as norepinephrine (NE). In other cell types, however, mitochondrial Ca2+ signals are not coupled as directly to each cytosolic Ca2+ transient. For example, cardiomyocytes do not generally appear to have beat-to-beat oscillations in mCa2+ content that mirror cytosolic Ca2+ transients. Rather, alterations in the amplitude and/or frequency of cytosolic Ca2+ transients drive integrated changes in mCa2+ concentration. For instance, sympathetic stimulation of cardiomyocytes increases the amplitude and frequency of cytosolic Ca2+ transients, causing a progressive increase in mCa2+ concentration over time. [Ca2+], Ca2+ concentration; [cytoCa2+], cytosolic [Ca2+]; [mitoCa2+], mitochondrial [Ca2+]; see glossary for other abbreviations.