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TRPM7 Is Involved in Volume Regulation in Salivary Glands

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dc.contributor.authorKim, J. M.-
dc.contributor.authorChoi, S.-
dc.contributor.authorPark, K.-
dc.creator박경표-
dc.date.accessioned2019-04-24T08:31:02Z-
dc.date.available2020-04-05T08:31:02Z-
dc.date.created2018-08-30-
dc.date.issued2017-08-
dc.identifier.citationJournal of Dental Research, Vol.96 No.9, pp.1044-1050-
dc.identifier.issn0022-0345-
dc.identifier.urihttps://hdl.handle.net/10371/147978-
dc.description.abstractUnder hypotonic conditions, the regulatory volume decrease (RVD) is essential to maintain physiological homeostasis and functions in diverse biological systems. Intracellular Ca2+ has been reported as an important mediator of this response, but the underlying Ca2+ mechanism responsible for RVD is still controversial. Here we investigate the role of Ca2+ in the RVD response using live-cell imaging, microspectrofluorimetry, and a patch-clamp technique. A typical RVD was observed in submandibular gland acinar cells after swelling in a hypotonic solution, whereas intracellular Ca2+ chelation completely inhibited the RVD response. The incidence and magnitude of the Ca2+ transient were proportional to the degree of hypotonicity of the extracellular medium, and there was a close relationship between intracellular Ca2+ concentration and the volumetric changes of the cells. Notably, this response was mediated by Ca2+-induced Ca2+ release, which is triggered by Ca2+ influx via stretch-activated TRPM7 channels. Furthermore, we detected the generation of Cl- currents in the swelling acinar cells upon hypotonic stress, and the current profile matched that of the Ca2+-activated Cl- currents. A specific inhibitor of Cl- currents also inhibited the RVD response. In conclusion, an intracellular Ca2+ increase in response to osmotically induced cell swelling plays a critical role in RVD in salivary gland acinar cells.-
dc.language영어-
dc.language.isoenen
dc.publisherSAGE Publications-
dc.titleTRPM7 Is Involved in Volume Regulation in Salivary Glands-
dc.typeArticle-
dc.identifier.doi10.1177/0022034517708766-
dc.citation.journaltitleJournal of Dental Research-
dc.identifier.wosid000406054800011-
dc.identifier.scopusid2-s2.0-85025664695-
dc.description.srndOAIID:RECH_ACHV_DSTSH_NO:T201719757-
dc.description.srndRECH_ACHV_FG:RR00200001-
dc.description.srndADJUST_YN:-
dc.description.srndEMP_ID:A001677-
dc.description.srndCITE_RATE:5.38-
dc.description.srndDEPT_NM:치의과학과-
dc.description.srndEMAIL:kppark@snu.ac.kr-
dc.description.srndSCOPUS_YN:Y-
dc.citation.endpage1050-
dc.citation.number9-
dc.citation.startpage1044-
dc.citation.volume96-
dc.description.isOpenAccessN-
dc.contributor.affiliatedAuthorPark, K.-
dc.identifier.srndT201719757-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusPAROTID ACINAR-CELLS-
dc.subject.keywordPlusCORNEAL EPITHELIAL-CELLS-
dc.subject.keywordPlusACTIVATED CA2+ ENTRY-
dc.subject.keywordPlusCHLORIDE CHANNELS-
dc.subject.keywordPlusINTRACELLULAR CALCIUM-
dc.subject.keywordPlusLACRIMAL GLAND-
dc.subject.keywordPlusDECREASE RVD-
dc.subject.keywordPlusLINE SMG-C6-
dc.subject.keywordPlusRELEASE-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordAuthorcell biology-
dc.subject.keywordAuthorcell signaling-
dc.subject.keywordAuthormechanotransduction-
dc.subject.keywordAuthormolecular biology-
dc.subject.keywordAuthorphysiology-
dc.subject.keywordAuthorsignal transduction-
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