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dc.creatorStojanović, Ivana D.
dc.creatorSaksida, Tamara
dc.creatorStošić-Grujičić, Stanislava
dc.date.accessioned2015-08-28T10:26:51Z
dc.date.available2015-08-28T10:26:51Z
dc.date.issued2013
dc.date.issued2013sr
dc.identifier.issn0354-4664sr
dc.identifier.otherRad_konverzija_381sr
dc.identifier.urihttps://radar.ibiss.bg.ac.rs/handle/123456789/324
dc.description.abstractIn diabetes, pancreatic islets are subjected to high levels of inflammatory mediators that can lead to beta cell destruction. We recently showed that pancreatic islet cells derived from MIF-deficient (MIF-KO) mice are resistant to apoptosis induction by the cytotoxic stimuli of cytokines. Here we show that MIF-KO islets under cytokine (IFN-γ+TNF- α+IL-1β) stimulation express and secrete significantly lower amounts of IL-1β, while the expression of caspase-1 mRNA is not influenced by MIF deficiency. These data suggest that MIF-KO islets possess an innate defect in the process of IL-1 β synthesis and secretion.en
dc.description.sponsorshipnullsr
dc.language.isoengsr
dc.rightsopenAccesssr
dc.sourceArchives of Biological Sciencessr
dc.subjectPancreatic isletsENG
dc.subjectMacrophage Migration Inhibitory Factor (MIF)ENG
dc.subjectIL-1βENG
dc.subjectcaspase-1ENG
dc.titleDeficiency of macrophage migration inhibitory factor (MIF) inhibits cytokine-induced IL-1β generation in murine pancreatic islet cellsen
dc.typearticlesr
dc.rights.licenseARR
dcterms.abstractСтошић-Грујичић, Станислава Д.; Саксида, Тамара; Стојановић, Ивана;
dc.citation.issue1sr
dc.citation.volume65sr
dc.citation.spage9sr
dc.citation.epage15sr
dc.type.versionpublishedVersionsr
dc.identifier.fulltexthttps://radar.ibiss.bg.ac.rs//bitstream/id/2434/Rad_konverzija_381.pdf
dc.citation.rankM23
dc.identifier.rcubhttps://hdl.handle.net/21.15107/rcub_ibiss_324


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Приказ основних података о документу