Mitochondrial regulation of cytosolic Ca2+ signals in smooth muscle
McCarron, John and Olson, Marnie and Chalmers, Susan (2012) Mitochondrial regulation of cytosolic Ca2+ signals in smooth muscle. Pflügers Archiv European Journal of Physiology, 464 (specia). pp. 51-62. (https://doi.org/10.1007/s00424-012-1108-9)
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The cytosolic Ca2+ concentration ([Ca2+]c) controls virtually every activity of smooth muscle, including contraction, migration, transcription, division and apoptosis. These processes may be activated by large (>10 μM) amplitude [Ca2+]c increases, which occur in small restricted regions of the cell or by smaller (<1 μM) amplitude changes throughout the bulk cytoplasm. Mitochondria contribute to the regulation of these signals by taking up Ca2+. However, mitochondria’s reported low affinity for Ca2+ is thought to require the organelle to be positioned close to ion channels and within a microdomain of high [Ca2+]. In cultured smooth muscle, mitochondria are highly dynamic structures but in native smooth muscle mitochondria are immobile, apparently strategically positioned organelles that regulate the upstroke and amplitude of IP3-evoked Ca2+ signals and IP3 receptor (IP3R) cluster activity. These observations suggest mitochondria are positioned within the high [Ca2+] microdomain arising from an IP3R cluster to exert significant local control of channel activity. On the other hand, neither the upstroke nor amplitude of voltage-dependent Ca2+ entry is modulated by mitochondria; rather, it is the declining phase of the transient that is regulated by the organelle. Control of the declining phase of the transient requires a high mitochondrial affinity for Ca2+ to enable uptake to occur over the normal physiological Ca2+ range (<1 μM). Thus, in smooth muscle, mitochondria regulate Ca2+ signals exerting effects over a large range of [Ca2+] (∼200 nM to at least tens of micromolar) to provide a wide dynamic range in the control of Ca2+ signals.
ORCID iDs
McCarron, John ORCID: https://orcid.org/0000-0002-3302-3984, Olson, Marnie and Chalmers, Susan ORCID: https://orcid.org/0000-0002-8073-7576;-
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Item type: Article ID code: 40056 Dates: DateEvent2012PublishedSubjects: Medicine > Therapeutics. Pharmacology Department: Faculty of Science > Strathclyde Institute of Pharmacy and Biomedical Sciences Depositing user: Pure Administrator Date deposited: 14 Jun 2012 14:10 Last modified: 11 Nov 2024 10:09 Related URLs: URI: https://strathprints.strath.ac.uk/id/eprint/40056