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Sphingosine and FTY720 modulate pacemaking activity in interstitial cells of Cajal from mouse small intestine

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dc.contributor.authorNam, Joo Hyun-
dc.contributor.authorKim, Woo Kyung-
dc.contributor.authorKim, Byung Joo-
dc.date.accessioned2024-08-08T05:01:23Z-
dc.date.available2024-08-08T05:01:23Z-
dc.date.issued2013-09-
dc.identifier.issn1016-8478-
dc.identifier.issn0219-1032-
dc.identifier.urihttps://scholarworks.dongguk.edu/handle/sw.dongguk/18393-
dc.description.abstractInterstitial cells of Cajal (ICCs) are the pacemakers of the gastrointestinal tract, and transient receptor potential melastatin type 7 (TRPM7) and Ca2+ activated Cl- channels (ANO1) are candidate the generators of pacemaker potentials in ICCs. The effects of D-erythro-sphingosine (SPH) and structural analogues of SPH, that is, N,N-dimethyl-Derythro-sphingosine (N,N-DMS), FTY720, and FTY720-P on the pacemaking activities of ICCs were examined using the whole cell patch clamp technique. SPH, N,N-DMS, and FTY720 decreased the amplitudes of pacemaker potentials in ICC clusters, but resting membrane potentials displayed little change. Also, perfusing SPH, N,N-DMS, or FTY720 in the bath reduced both inward and outward TRPM7-like currents in single ICCs, and inhibited ANO1 currents. The another structural analogue of SPH, FTY720-P was ineffective at the pacemaker potentials in ICC clusters and the TRPM7-like currents in single ICCs. Furthermore, FTY720-P had no effect on ANO1. These results suggest that SPH, N,N-DMS, and FTY720 modulate the pacemaker activities of ICCs, and that TRPM7 and ANO1 channels affect intestinal motility.-
dc.format.extent10-
dc.language영어-
dc.language.isoENG-
dc.publisherKOREAN SOC MOLECULAR & CELLULAR BIOLOGY-
dc.titleSphingosine and FTY720 modulate pacemaking activity in interstitial cells of Cajal from mouse small intestine-
dc.typeArticle-
dc.publisher.location대한민국-
dc.identifier.doi10.1007/s10059-013-0091-0-
dc.identifier.scopusid2-s2.0-84898352222-
dc.identifier.wosid000324643100007-
dc.identifier.bibliographicCitationMOLECULES AND CELLS, v.36, no.3, pp 235 - 244-
dc.citation.titleMOLECULES AND CELLS-
dc.citation.volume36-
dc.citation.number3-
dc.citation.startPage235-
dc.citation.endPage244-
dc.type.docTypeArticle-
dc.identifier.kciidART001804111-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaCell Biology-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryCell Biology-
dc.subject.keywordPlusCHLORIDE CHANNELS-
dc.subject.keywordPlusTRPM7 CHANNEL-
dc.subject.keywordPlusRECEPTOR-
dc.subject.keywordPlusCURRENTS-
dc.subject.keywordPlusCONDUCTANCE-
dc.subject.keywordPlusACTIVATION-
dc.subject.keywordPlusMECHANISM-
dc.subject.keywordPlusBLOCKERS-
dc.subject.keywordPlusENTRY-
dc.subject.keywordAuthorANO1-
dc.subject.keywordAuthorinterstitial cells of Cajal-
dc.subject.keywordAuthorpacemaker potentials-
dc.subject.keywordAuthorSphingosine-
dc.subject.keywordAuthorTRPM7-
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