Proteomic analysis of pancreas derived from adult cloned pig

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dc.contributor.authorJung Il Chae-
dc.contributor.authorYoung Keun Cho-
dc.contributor.authorS K Cho-
dc.contributor.authorJ H Kim-
dc.contributor.authorY M Han-
dc.contributor.authorDeog Bon Koo-
dc.contributor.authorKyung Kwang Lee-
dc.date.accessioned2017-04-19T09:08:47Z-
dc.date.available2017-04-19T09:08:47Z-
dc.date.issued2008-
dc.identifier.issn0006-291X-
dc.identifier.uri10.1016/j.bbrc.2007.11.114ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/8233-
dc.description.abstractThe potential medical applications of animal cloning include xenotransplantation, but the complex molecular cascades that control porcine organ development are not fully understood. Still, it has become apparent that organs derived from cloned pigs may be suitable for transplantation into humans. In this study, we examined the pancreas of an adult cloned pig developed through somatic cell nuclear transfer (SCNT) using two-dimensional electrophoresis (2-DE) and Western blotting. Proteomic analysis revealed 69 differentially regulated proteins, including such apoptosis-related species as annexins, lamins, and heat shock proteins, which were unanimously upregulated in the SCNT sample. Among the downregulated proteins in SCNT pancreas were peroxiredoxins and catalase. Western blot results indicate that several antioxidant enzymes and the anti-apoptotic protein were downregulated in SCNT pancreas, whereas several caspases were upregulated. Together, these data suggest that the accumulation of reactive oxygen species (ROS) in the pancreas of an adult cloned pig leads to apoptosis.-
dc.publisherElsevier-
dc.titleProteomic analysis of pancreas derived from adult cloned pig-
dc.title.alternativeProteomic analysis of pancreas derived from adult cloned pig-
dc.typeArticle-
dc.citation.titleBiochemical and Biophysical Research Communications-
dc.citation.number2-
dc.citation.endPage387-
dc.citation.startPage379-
dc.citation.volume366-
dc.contributor.affiliatedAuthorJung Il Chae-
dc.contributor.affiliatedAuthorYoung Keun Cho-
dc.contributor.affiliatedAuthorDeog Bon Koo-
dc.contributor.affiliatedAuthorKyung Kwang Lee-
dc.contributor.alternativeName채정일-
dc.contributor.alternativeName조영근-
dc.contributor.alternativeName조성근-
dc.contributor.alternativeName김진회-
dc.contributor.alternativeName한용만-
dc.contributor.alternativeName구덕본-
dc.contributor.alternativeName이경광-
dc.identifier.bibliographicCitationBiochemical and Biophysical Research Communications, vol. 366, no. 2, pp. 379-387-
dc.identifier.doi10.1016/j.bbrc.2007.11.114-
dc.subject.keywordapoptosis-
dc.subject.keywordpancreas-
dc.subject.keywordpig-
dc.subject.keywordproteomic analysis-
dc.subject.keywordROS-
dc.subject.keywordsomatic cell cloning-
dc.subject.localapoptosis-
dc.subject.localApoptosis-
dc.subject.localpancreas-
dc.subject.localPancreas-
dc.subject.localPigs-
dc.subject.localpigs-
dc.subject.localPig-
dc.subject.localpig-
dc.subject.localProteomic analyses-
dc.subject.localProteomic analysis-
dc.subject.localproteomic analysis-
dc.subject.localReactive oxidative species-
dc.subject.localReactive oxygen species(ROS)-
dc.subject.localReactive oxygen species-
dc.subject.localReactive Oxygen Species (ROS)-
dc.subject.localReactive Oxygen Species-
dc.subject.localROS-
dc.subject.localReactive oxygen species (ROS)-
dc.subject.localreactive oxygen species-
dc.subject.localreactive oxygen species (ROS)-
dc.subject.localsomatic cell cloning-
dc.description.journalClassY-
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