Modulation of calcium signalling by mitochondria |
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Authors: | Ciara Walsh |
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Affiliation: | Department of Physiology, School of Biomedical Sciences, The University of Liverpool, Crown Street, Liverpool L69 3BX, UK |
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Abstract: | In this review we will attempt to summarise the complex and sometimes contradictory effects that mitochondria have on different forms of calcium signalling. Mitochondria can influence Ca2+ signalling indirectly by changing the concentration of ATP, NAD(P)H, pyruvate and reactive oxygen species — which in turn modulate components of the Ca2+ signalling machinery i.e. buffering, release from internal stores, influx from the extracellular solution, uptake into cellular organelles and extrusion by plasma membrane Ca2+ pumps. Mitochondria can directly influence the calcium concentration in the cytosol of the cell by importing Ca2+ via the mitochondrial Ca2+ uniporter or transporting Ca2+ from the interior of the organelle into the cytosol by means of Na+/Ca2+ or H+/Ca2+ exchangers. Considerable progress in understanding the relationship between Ca2+ signalling cascades and mitochondrial physiology has been accumulated over the last few years due to the development of more advanced optical techniques and electrophysiological approaches. |
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Keywords: | [Ca2+], calcium concentration ER, endoplasmic reticulum SR, sarcoplasmic reticulum [Ca2+]c, cytosolic Ca2+ concentration [Ca2+]m, mitochondrial Ca2+ concentration [Ca2+]er, Ca2+ concentration in endoplasmic reticulum IP3R, IP3 receptor RyR, ryanodine receptor, ROS, reactive oxygen species SOCE, store-operated Ca2+ entry ICRAC, calcium release-activated calcium current ACh, acetylcholine PMCA, plasma membrane Ca2+ ATPase SERCA, sarcoplasmic/endoplasmic reticulum Ca2+ ATPase Olig, Oligomycin IA, Iodoacetate Tg, thapsigargin STIM1, stromal interacting molecule one |
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