Peroxiredoxin I participates in the protection of reactive oxygen species-mediated cellular senescence = 세포 노화에서 활성산소에 의한 퍼록시레독신 I 역할

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dc.contributor.authorYoung-Ho Park-
dc.contributor.authorH S Kim-
dc.contributor.authorJong-Hee Lee-
dc.contributor.authorSeon A Choi-
dc.contributor.authorJ M Kim-
dc.contributor.authorG T Oh-
dc.contributor.authorS W Kang-
dc.contributor.authorSun-Uk Kim-
dc.contributor.authorDae Yeul Yu-
dc.date.accessioned2018-01-11T02:53:13Z-
dc.date.available2018-01-11T02:53:13Z-
dc.date.issued2017-
dc.identifier.issn1225-8687-
dc.identifier.uri10.5483/BMBRep.2017.50.10.121ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/17517-
dc.description.abstractPeroxiredoxin I (Prx I) plays an important role as a reactive oxygen species (ROS) scavenger in protecting and maintaining cellular homeostasis; however, the underlying mechanisms are not well understood. Here, we identified a critical role of Prx I in protecting cells against ROS-mediated cellular senescence by suppression of p16INK4a expression. Compared to wild-type mouse embryonic fibroblasts (WT-MEFs), Prx I-/- MEFs exhibited senescence-associated phenotypes. Moreover, the aged Prx I-/- mice showed an increased number of cells with senescence associated-β-galactosidase (SA-β-gal) activity in a variety of tissues. Increased ROS levels and SA-β-gal activity, and reduction of chemical antioxidant in Prx I-/- MEF further supported an essential role of Prx I peroxidase activity in cellular senescence that is mediated by oxidative stress. The up-regulation of p16INK4a expression in Prx I-/- and suppression by overexpression of Prx I indicate that Prx I possibly modulate cellular senescence through ROS/p16INK4a pathway-
dc.publisherKorea Soc-Assoc-Inst-
dc.titlePeroxiredoxin I participates in the protection of reactive oxygen species-mediated cellular senescence = 세포 노화에서 활성산소에 의한 퍼록시레독신 I 역할-
dc.title.alternativePeroxiredoxin I participates in the protection of reactive oxygen species-mediated cellular senescence-
dc.typeArticle-
dc.citation.titleBMB Reports-
dc.citation.number10-
dc.citation.endPage533-
dc.citation.startPage528-
dc.citation.volume50-
dc.contributor.affiliatedAuthorYoung-Ho Park-
dc.contributor.affiliatedAuthorJong-Hee Lee-
dc.contributor.affiliatedAuthorSeon A Choi-
dc.contributor.affiliatedAuthorSun-Uk Kim-
dc.contributor.affiliatedAuthorDae Yeul Yu-
dc.contributor.alternativeName박영호-
dc.contributor.alternativeName김현선-
dc.contributor.alternativeName이종희-
dc.contributor.alternativeName최선아-
dc.contributor.alternativeName김진만-
dc.contributor.alternativeName오구택-
dc.contributor.alternativeName강상원-
dc.contributor.alternativeName김선욱-
dc.contributor.alternativeName유대열-
dc.identifier.bibliographicCitationBMB Reports, vol. 50, no. 10, pp. 528-533-
dc.identifier.doi10.5483/BMBRep.2017.50.10.121-
dc.subject.keywordAntioxidant enzyme-
dc.subject.keywordCellular senescence-
dc.subject.keywordOxidative stress-
dc.subject.keywordp16INK4a-
dc.subject.keywordPeroxiredoxin-
dc.subject.localAnti-oxidant enzyme-
dc.subject.localAntioxidant Enzymes-
dc.subject.localAntioxidant enzyme-
dc.subject.localAntioxidant enzymes-
dc.subject.localantioxidant enzyme-
dc.subject.localantioxidant enzymes-
dc.subject.localCellular senescence-
dc.subject.localcellular senescence-
dc.subject.localCellular Senescence-
dc.subject.localOXIDATIVE STRESS-
dc.subject.localOxidative Stress-
dc.subject.localOxidative stre-
dc.subject.localOxidative stress-
dc.subject.localoxidative stress-
dc.subject.localP16INK4A-
dc.subject.localp16INK4a-
dc.subject.localPeroxiredoxin-
dc.subject.localPeroxiredoxins-
dc.subject.localperoxiredoxin-
dc.description.journalClassY-
Appears in Collections:
Ochang Branch Institute > Division of National Bio-Infrastructure > Futuristic Animal Resource & Research Center > 1. Journal Articles
Ochang Branch Institute > Division of National Bio-Infrastructure > National Primate Research Center > 1. Journal Articles
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