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Mitochondria adjust Ca signaling regime to a pattern of stimulation in salivary acinar cells
Authors:Olga Kopach  Ilya Kruglikov  Tatyana Pivneva  Nana Voitenko  Alexei Verkhratsky  Nataliya Fedirko
Affiliation:
  • a Department of General Physiology of Nervous System, Bogomoletz Institute of Physiology, Kiev 01024, Ukraine
  • b Department of Physiology and Neuroscience, New York University School of Medicine, NY 10016, USA
  • c Faculty of Life Sciences, The University of Manchester, United Kingdom
  • 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.
    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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