{ "labelLang" : "hun", "responseDate" : "2024-03-28 14:20", "content" : { "otype" : "JournalArticle", "mtid" : 3012680, "status" : "VALIDATED", "published" : true, "comment" : "Department of Pharmacology and Pharmacotherapy, Semmelweis University, Nagyvárad tér 4, Budapest, 1089, Hungary \n Department of Otorhinolaryngology, Head and Neck Surgery, Bajcsy-Zsilinszky Hospital, Budapest, Hungary \n Department of Otorhinolaryngology, Head and Neck Surgery, Semmelweis University, Budapest, Hungary \n Program in Neurosciences and Mental Health, The Hospital for Sick Children, Toronto, ON, Canada \n Department of Otolaryngology, Head and Neck Surgery, University Medical Center Groningen, University of Groningen, Groningen, Netherlands \n Pharmacological and Drug Safety Research, Gedeon Richter Plc, Budapest, Hungary \n Institute of Experimental Medicine, Hungarian Academy of Sciences, Budapest, Hungary \n Computational Cognitive Neuroimaging Laboratory, Computational Neuroscience and Cognitive Robotics Centre, University of Birmingham, Birmingham, United Kingdom \n Cited By :11 \n Export Date: 9 November 2022 \n CODEN: NERED \n Correspondence Address: Zelles, T.; Department of Pharmacology and Pharmacotherapy, Nagyvárad tér 4, Hungary; email: zelles.tibor@med.semmelweis-univ.hu \n Chemicals/CAS: adenosine triphosphate, 15237-44-2, 56-65-5, 987-65-5; calcium, 7440-70-2, 14092-94-5; cyclopiazonic acid, 18172-33-3, 83136-88-3; fura 2 acetoxymethyl ester, 105344-37-4, 108964-32-5; pyridoxal phosphate 6 azophenyl 2',4' disulfonic acid, 149017-66-3; Adenosine Triphosphate; Receptors, Purinergic P2X; Receptors, Purinergic P2Y; RNA, Messenger \n Funding details: K116654, NN107234 \n Funding details: TÉT_10-1-2011-0421 \n Funding text 1: This work was supported by the Hungarian-French Collaborative R&I Programme on Biotechnologies (TÉT_10-1-2011-0421) and the Hungarian Research and Development Fund (NN107234 and K116654). 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For the first time, we have performed functional ratiometric Ca2+ imaging (fura-2) in three different supporting cell types in the hemicochlea preparation of hearing mice to measure purinergic receptor-mediated Ca2+ signaling in pillar, Deiters' and Hensen's cells. Their resting [Ca2+]i was determined and compared in the same type of preparation. ATP evoked reversible, repeatable and dose-dependent Ca2+ transients in all three cell types, showing desensitization. Inhibiting the Ca2+ signaling of the ionotropic P2X (omission of extracellular Ca2+) and metabotropic P2Y purinergic receptors (depletion of intracellular Ca2+ stores) revealed the involvement of both receptor types. Detection of P2X2,3,4,6,7 and P2Y1,2,6,12,14 receptor mRNAs by RT-PCR supported this finding and antagonism by PPADS suggested different functional purinergic receptor population in pillar versus Deiters' and Hensen's cells. The sum of the extra- and intracellular Ca2+-dependent components of the response was about equal with the control ATP response (linear additivity) in pillar cells, and showed supralinearity in Deiters' and Hensen's cells. Calcium-induced calcium release might explain this synergistic interaction. The more pronounced Ca2+ leak from the endoplasmic reticulum in Deiters' and Hensen's cells, unmasked by cyclopiazonic acid, may also suggests the higher activity of the internal stores in Ca2+ signaling in these cells. 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