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Role of pancreatitis-associated protein 1 on oxidative stress-induced cell death of pancreatic acinar cells

DC Field Value Language
dc.contributor.author김경환-
dc.contributor.author송지연-
dc.date.accessioned2015-04-24T16:52:33Z-
dc.date.available2015-04-24T16:52:33Z-
dc.date.issued2009-
dc.identifier.issn0077-8923-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/104339-
dc.description.abstractPreviously we showed that oxidative stress induces apoptosis of pancreatic acinar cells with nuclear loss of DNA repair proteins. Oxidative stress has an important role in the pathogenesis of pancreatitis. Pancreatitis-associated protein 1 (PAP-1) is a protein secreted upon induction of acute pancreatitis. In this study, we investigated the role of PAP-1 on oxidative stress-induced cell death of pancreatic acinar AR42J cells. AR42J cells were transfected with or without full-length sense cDNA of PAP-1 (PAP-1 S cDNA) or antisense cDNA of PAP-1 (PAP-1 AS cDNA) and received oxidative stress caused by glucose oxidase acting on beta-D-glucose, glucose/glucose oxidase. PAP-1 mRNA expression and cell viability were determined. As a result, oxidative stress induced PAP-1 mRNA expression in AR42J cells in a time-dependent manner. Cell viability decreased with the concentration of glucose oxides delivered to the cells that had received glucose. Oxidative stress-induced PAP-1 expression was augmented in the cells transfected with PAP-1 S cDNA compared with wild-type cells or cells transfected with control vector pcDNA. PAP-1 induction by oxidative stress decreased in the cells transfected with PAP-1 AS cDNA. Cell death caused by oxidative stress was inhibited in the cells transfected with PAP-1 S cDNA, but it increased in the cells transfected with PAP-1 AS cDNA. These results indicate that PAP-1 may be a defensive gene for oxidative stress-induced cell death of pancreatic acinar cells-
dc.description.statementOfResponsibilityopen-
dc.format.extent545~548-
dc.relation.isPartOfANNALS OF THE NEW YORK ACADEMY OF SCIENCES-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHAnimals-
dc.subject.MESHAntigens, Neoplasm/genetics-
dc.subject.MESHAntigens, Neoplasm/physiology*-
dc.subject.MESHApoptosis/physiology*-
dc.subject.MESHBiomarkers, Tumor/genetics-
dc.subject.MESHBiomarkers, Tumor/physiology*-
dc.subject.MESHCell Line, Tumor-
dc.subject.MESHCell Survival/physiology-
dc.subject.MESHDNA, Antisense/genetics-
dc.subject.MESHDNA, Complementary/genetics-
dc.subject.MESHGene Expression Regulation, Neoplastic-
dc.subject.MESHLectins, C-Type/genetics-
dc.subject.MESHLectins, C-Type/physiology*-
dc.subject.MESHOxidative Stress/physiology*-
dc.subject.MESHPancreatic Neoplasms/genetics-
dc.subject.MESHPancreatic Neoplasms/pathology-
dc.subject.MESHPancreatitis-Associated Proteins-
dc.subject.MESHRNA, Messenger/genetics-
dc.subject.MESHRNA, Messenger/metabolism-
dc.subject.MESHRats-
dc.subject.MESHReverse Transcriptase Polymerase Chain Reaction-
dc.subject.MESHTransfection-
dc.titleRole of pancreatitis-associated protein 1 on oxidative stress-induced cell death of pancreatic acinar cells-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Pharmacology (약리학)-
dc.contributor.googleauthorJoo Weon Lim-
dc.contributor.googleauthorJi Yeon Song-
dc.contributor.googleauthorJeong Yeon Seo-
dc.contributor.googleauthorHyeyoung Kim-
dc.contributor.googleauthorKyung Hwan Kim-
dc.identifier.doi10.1111/j.1749-6632.2009.04702.x-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA00311-
dc.contributor.localIdA02064-
dc.relation.journalcodeJ00181-
dc.identifier.eissn1749-6632-
dc.identifier.pmid19723102-
dc.identifier.urlhttp://onlinelibrary.wiley.com/doi/10.1111/j.1749-6632.2009.04702.x/abstract-
dc.subject.keywordpancreatitis-associated protein 1-
dc.subject.keywordcell death-
dc.subject.keywordpancreatic acinar cells-
dc.contributor.alternativeNameKim, Kyung Hwan-
dc.contributor.alternativeNameSong, Ji Yeon-
dc.contributor.affiliatedAuthorKim, Kyung Hwan-
dc.contributor.affiliatedAuthorSong, Ji Yeon-
dc.citation.volume1171-
dc.citation.startPage545-
dc.citation.endPage548-
dc.identifier.bibliographicCitationANNALS OF THE NEW YORK ACADEMY OF SCIENCES, Vol.1171 : 545-548, 2009-
dc.identifier.rimsid52605-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Pharmacology (약리학교실) > 1. Journal Papers

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