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dc.contributor.authorSengiku, Atsushien
dc.contributor.authorUeda, Masakatsuen
dc.contributor.authorKono, Jinen
dc.contributor.authorSano, Takeshien
dc.contributor.authorNishikawa, Nobuyukien
dc.contributor.authorKunisue, Sumihiroen
dc.contributor.authorTsujihana, Kojiroen
dc.contributor.authorLiou, Louis S.en
dc.contributor.authorKanematsu, Akihiroen
dc.contributor.authorShimba, Shigekien
dc.contributor.authorDoi, Masaoen
dc.contributor.authorOkamura, Hitoshien
dc.contributor.authorOgawa, Osamuen
dc.contributor.authorNegoro, Hiromitsuen
dc.contributor.alternative上田, 政克ja
dc.contributor.alternative河野, 仁ja
dc.contributor.alternative國末, 純宏ja
dc.contributor.alternative土居, 雅夫ja
dc.contributor.alternative岡村, 均ja
dc.contributor.alternative小川, 修ja
dc.contributor.alternative根来, 宏光ja
dc.date.accessioned2018-09-03T06:30:26Z-
dc.date.available2018-09-03T06:30:26Z-
dc.date.issued2018-01-31-
dc.identifier.issn2045-2322-
dc.identifier.urihttp://hdl.handle.net/2433/234202-
dc.description.abstractDay-night changes in the storage capacity of the urinary bladder are indispensable for sound sleep. Connexin 43 (Cx43), a major gap junction protein, forms hemichannels as a pathway of ATP in other cell types, and the urinary bladder utilizes ATP as a mechanotransduction signals to modulate its capacity. Here, we demonstrate that the circadian clock of the urothelium regulates diurnal ATP release through Cx43 hemichannels. Cx43 was expressed in human and mouse urothelium, and clock genes oscillated in the mouse urothelium accompanied by daily cycles in the expression of Cx43 and extracellular ATP release into the bladder lumen. Equivalent chronological changes in Cx43 and ATP were observed in immortalized human urothelial cells, but these diurnal changes were lost in both arrhythmic Bmal1-knockout mice and in BMAL1-knockdown urothelial cells. ATP release was increased by Cx43 overexpression and was decreased in Cx43 knockdown or in the presence of a selective Cx43 hemichannel blocker, which indicated that Cx43 hemichannels are considered part of the components regulating ATP release in the urothelium. Thus, a functional circadian rhythm exists in the urothelium, and coordinates Cx43 expression and function as hemichannels that provide a direct pathway of ATP release for mechanotransduction and signalling in the urothelium.en
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherSpringer Natureen
dc.rights© The Author(s) 2018. This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.en
dc.titleCircadian coordination of ATP release in the urothelium via connexin43 hemichannelsen
dc.typejournal article-
dc.type.niitypeJournal Article-
dc.identifier.jtitleScientific reportsen
dc.identifier.volume8-
dc.relation.doi10.1038/s41598-018-20379-0-
dc.textversionpublisher-
dc.identifier.artnum1996-
dc.addressDepartment of Urology, Graduate School of Medicine, Kyoto Universityen
dc.addressDepartment of Urology, Graduate School of Medicine, Kyoto Universityen
dc.addressDepartment of Urology, Graduate School of Medicine, Kyoto Universityen
dc.addressDepartment of Urology, Graduate School of Medicine, Kyoto Universityen
dc.addressDepartment of Urology, Japanese Red Cross Otsu Hospitalen
dc.addressDepartment of Systems Biology, Graduate School of Pharmaceutical Sciences, Kyoto Universityen
dc.addressDepartment of Systems Biology, Graduate School of Pharmaceutical Sciences, Kyoto University・Department of Dermatology, Graduate School of Medicine, Kyoto Universityen
dc.addressDepartment of Urology, Cambridge Health Allianceen
dc.addressDepartment of Urology, Hyogo College of Medicineen
dc.addressDepartment of Health Science, School of Pharmacy, Nihon Universityen
dc.addressDepartment of Systems Biology, Graduate School of Pharmaceutical Sciences, Kyoto Universityen
dc.addressDepartment of Systems Biology, Graduate School of Pharmaceutical Sciences, Kyoto Universityen
dc.addressDepartment of Urology, Graduate School of Medicine, Kyoto Universityen
dc.addressDepartment of Urology, Graduate School of Medicine, Kyoto Universityen
dc.identifier.pmid29386573-
dcterms.accessRightsopen access-
datacite.awardNumber15H05682-
datacite.awardNumber25893100-
jpcoar.funderName日本学術振興会ja
jpcoar.funderName日本学術振興会ja
jpcoar.funderName.alternativeJapan Society for the Promotion of Science (JSPS)en
jpcoar.funderName.alternativeJapan Society for the Promotion of Science (JSPS)en
出現コレクション:学術雑誌掲載論文等

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