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dc.contributor.authorTakiguchi, Naomien
dc.contributor.authorTakahashi, Yukien
dc.contributor.authorNishikawa, Makiyaen
dc.contributor.authorMatsui, Yurikoen
dc.contributor.authorFukuhara, Yasushien
dc.contributor.authorOushiki, Daihien
dc.contributor.authorKiyose, Kazukien
dc.contributor.authorHanaoka, Kenjiroen
dc.contributor.authorNagano, Tetsuoen
dc.contributor.authorTakakura, Yoshinobuen
dc.contributor.alternative高橋, 有己ja
dc.contributor.alternative高倉, 喜信ja
dc.date.accessioned2012-10-02T05:08:55Z-
dc.date.available2012-10-02T05:08:55Z-
dc.date.issued2011-04-
dc.identifier.issn0724-8741-
dc.identifier.urihttp://hdl.handle.net/2433/159458-
dc.description.abstractPurpose : Hydrodynamic injection has been shown to reactivate silenced transgene expression in mouse liver. In this study, the roles of inflammatory cytokines and reactive oxygen species (ROS) in the reactivation were examined. Methods : Production of inflammatory cytokines and ROS by hydrodynamic injection of saline was examined in mice that had received a hydrodynamic injection of a plasmid expressing Gaussia luciferase. The level of reporter gene expression was used as an indicator of the reactivation. The involvement of cytokines and ROS was examined by depleting Kupffer cells or by pre-administration of antioxidants, respectively. Results : A hydrodynamic injection of saline induced a significant production of interleukin (IL)-6. Depleting Kupffer cells using clodronate liposomes markedly reduced the IL-6 production but had no significant effect on the transgene expression. On the other hand, an injection of catalase or N-acetylcysteine significantly inhibited the hydrodynamic injection-induced reactivation of silenced transgene expression. The silenced expression was also reactivated by carbon tetrachloride, an inducer of oxidative stress in the liver, in a dose-dependent manner, and this reactivation was significantly inhibited by catalase. Conclusions : These findings show a positive correlation between the generation of ROS and the reactivation of silenced transgene expression after hydrodynamic injections.en
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherSpringeren
dc.rightsThe final publication is available at www.springerlink.comen
dc.rightsこの論文は出版社版でありません。引用の際には出版社版をご確認ご利用ください。ja
dc.rightsThis is not the published version. Please cite only the published version.en
dc.subjecthydrodynamic injectionen
dc.subjectinflammationen
dc.subjectliveren
dc.subjectplasmid DNAen
dc.subjectreactive oxygen speciesen
dc.subject.meshAnimalsen
dc.subject.meshCarbon Tetrachloride/pharmacologyen
dc.subject.meshClodronic Acid/pharmacologyen
dc.subject.meshDNA/administration & dosageen
dc.subject.meshDNA/geneticsen
dc.subject.meshEnzyme-Linked Immunosorbent Assayen
dc.subject.meshGene Expression/drug effectsen
dc.subject.meshGene Silencing/drug effectsen
dc.subject.meshGene Transfer Techniquesen
dc.subject.meshHydrodynamicsen
dc.subject.meshInjections, Intravenousen
dc.subject.meshInterleukin-6/blooden
dc.subject.meshInterleukin-6/immunologyen
dc.subject.meshIsotonic Solutions/administration & dosageen
dc.subject.meshIsotonic Solutions/pharmacologyen
dc.subject.meshKupffer Cells/drug effectsen
dc.subject.meshKupffer Cells/pathologyen
dc.subject.meshLiposomesen
dc.subject.meshLiver/immunologyen
dc.subject.meshLiver/metabolismen
dc.subject.meshLiver/pathologyen
dc.subject.meshLuciferases/geneticsen
dc.subject.meshMaleen
dc.subject.meshMiceen
dc.subject.meshMice, Inbred ICRen
dc.subject.meshMicroscopy, Fluorescenceen
dc.subject.meshPlasmids/administration & dosageen
dc.subject.meshPlasmids/geneticsen
dc.subject.meshReactive Oxygen Species/metabolismen
dc.subject.meshTransgenesen
dc.subject.meshTumor Necrosis Factor-alpha/blooden
dc.subject.meshTumor Necrosis Factor-alpha/immunologyen
dc.titlePositive correlation between the generation of reactive oxygen species and activation/reactivation of transgene expression after hydrodynamic injections into mice.en
dc.typejournal article-
dc.type.niitypeJournal Article-
dc.identifier.ncidAA10632083-
dc.identifier.jtitlePharmaceutical researchen
dc.identifier.volume28-
dc.identifier.issue4-
dc.identifier.spage702-
dc.identifier.epage711-
dc.relation.doi10.1007/s11095-010-0331-3-
dc.textversionauthor-
dc.identifier.pmid21116691-
dcterms.accessRightsopen access-
dc.identifier.pissn0724-8741-
dc.identifier.eissn1573-904X-
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