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TASK-2 Expression Levels are Increased in Mouse Cryopreserved Ovaries

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dc.contributor.author강다원-
dc.contributor.authorChang Yong Choe-
dc.contributor.authorChang-Woon Kim-
dc.contributor.authorAe Jin Goo-
dc.contributor.author한재희-
dc.date.accessioned2022-12-26T21:51:15Z-
dc.date.available2022-12-26T21:51:15Z-
dc.date.issued2015-
dc.identifier.issn2671-4639-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/17518-
dc.description.abstractCryopreservation affects osmotic tolerance and intracellular ion concentration through changes in expression levels of water and ion channels. Control of these changes is important for cell survival after cryopreservation. Relatively little is known about changes in K+ channel expression compared to water channel expression. This study was performed to investigate changes in TASK-2 channel (KCNK5: potassium channel, subfamily K, member 5), a member of two-pore domain K+ channel family, in cryopreserved mouse ovaries. Cryopreservation increased TASK-2 mRNA expression in mouse ovaries. In addition, TASK-2 protein expression was upregulated in vitrified and slowly frozen ovaries. TASK-2 protein was expressed in all area of granulosa cells that surround the oocyte within the follicle, except nucleus. Viability of cells overexpressed with TASK-2 was higher than that of vector-transfected cells. Our results found that TASK-2 expression was increased by cryopreservation and overexpression of TASK-2 decreased cryopreservation-induced cell death. These results suggest that TASK-2 upregulation might reduce cryodamage.-
dc.format.extent6-
dc.language영어-
dc.language.isoENG-
dc.publisher사단법인 한국동물생명공학회-
dc.titleTASK-2 Expression Levels are Increased in Mouse Cryopreserved Ovaries-
dc.title.alternativeTASK-2 Expression Levels are Increased in Mouse Cryopreserved Ovaries-
dc.typeArticle-
dc.publisher.location대한민국-
dc.identifier.bibliographicCitation한국동물생명공학회지, v.30, no.4, pp 277 - 282-
dc.citation.title한국동물생명공학회지-
dc.citation.volume30-
dc.citation.number4-
dc.citation.startPage277-
dc.citation.endPage282-
dc.identifier.kciidART002070386-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClasskci-
dc.subject.keywordAuthorcryopreservation-
dc.subject.keywordAuthorovary-
dc.subject.keywordAuthorTASK-2 channel-
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