Mitochondria adjust Ca signaling regime to a pattern of stimulation in salivary acinar cells |
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Authors: | Olga Kopach Ilya Kruglikov Tatyana Pivneva Nana Voitenko Alexei Verkhratsky Nataliya Fedirko |
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Affiliation: | a Department of General Physiology of Nervous System, Bogomoletz Institute of Physiology, Kiev 01024, Ukraineb Department of Physiology and Neuroscience, New York University School of Medicine, NY 10016, USAc Faculty of Life Sciences, The University of Manchester, United Kingdom |
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Abstract: | The salivary acinar cells have unique Ca2+ signaling machinery that ensures an extensive secretion. The agonist-induced secretion is governed by Ca2+ signals originated from the endoplasmic reticulum (ER) followed by a store-operated Ca2+ entry (SOCE). During tasting and chewing food a frequency of parasympathetic stimulation increases up to ten fold, entailing cells to adapt its Ca2+ machinery to promote ER refilling and ensure sustained SOCE by yet unknown mechanism. By employing a combination of fluorescent Ca2+ imaging in the cytoplasm and inside cellular organelles (ER and mitochondria) we described the role of mitochondria in adjustment of Ca2+ signaling regime and ER refilling according to a pattern of agonist stimulation. Under the sustained stimulation, SOCE is increased proportionally to the degree of ER depletion. Cell adapts its Ca2+ handling system directing more Ca2+ into mitochondria via microdomains of high [Ca2+] providing positive feedback on SOCE while intra-mitochondrial tunneling provides adequate ER refilling. In the absence of an agonist, the bulk of ER refilling occurs through Ca2+-ATPase-mediated Ca2+ uptake within subplasmalemmal space. In conclusion, mitochondria play a key role in the maintenance of sustained SOCE and adequate ER refilling by regulating Ca2+ fluxes within the cell that may represent an intrinsic adaptation mechanism to ensure a long-lasting secretion. |
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Keywords: | ACh, acetylcholine [Ca2+]cyt, cytosolic Ca2+ concentration ER, endoplasmic reticulum PM, plasma membrane InsP3, inositol 1,4,5-trisphosphate [Ca2+]ER, ER Ca2+ concentration [Ca2+]mit, mitochondrial Ca2+ concentration SOC, store-operated channel SOCE, store-operated Ca2+ entry PMCA, Ca2+ ATPase of PM SERCA, Ca2+ ATPase of the ER NCX, mitochondrial Na+/Ca2+ exchanger TRPC1, transient receptor potential channel 1 TG, thapsigargin EM, electron microscopy FCCP, p-trifluoromethoxy carbonyl cyanide phenyl hydrazone CGP37157, 7-Chloro-5-(2-chlorophenyl)-1,5-dihydro-4,1-benzothiaze pin-2(3H)-one |
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