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dc.creatorBaron, Rebecca M. 
dc.creatorKwon, Min?Young 
dc.creatorCastano, Ana P. 
dc.creatorGhanta, Sailaja 
dc.creatorRiascos?Bernal, Dario F. 
dc.creatorLópez Guzmán, Silvia 
dc.creatorMacias, Alvaro Andres 
dc.creatorIth, Bonna 
dc.creatorSchissel, Scott L. 
dc.creatorLederer, James A. 
dc.creatorReeves, Raymond 
dc.creatorYet, Shaw?Fang 
dc.creatorLayne, Matthew D. 
dc.creatorXiaoli, Liu 
dc.creatorPerrella, Mark A. 
dc.date.accessioned2020-08-06T16:21:19Z
dc.date.available2020-08-06T16:21:19Z
dc.date.created2018-07-05
dc.identifier.issnISSN: 0741-5400
dc.identifier.issnEISSN: 1938-3673
dc.identifier.urihttps://repository.urosario.edu.co/handle/10336/26325
dc.description.abstractHigh mobility group (HMG) proteins are a family of architectural transcription factors, with HMGA1 playing a role in the regulation of genes involved in promoting systemic inflammatory responses. We speculated that blocking HMGA1?mediated pathways might improve outcomes from sepsis. To investigate HMGA1 further, we developed genetically modified mice expressing a dominant negative (dn) form of HMGA1 targeted to the vasculature. In dnHMGA1 transgenic (Tg) mice, endogenous HMGA1 is present, but its function is decreased due to the mutant transgene. These mice allowed us to specifically study the importance of HMGA1 not only during a purely pro?inflammatory insult of endotoxemia, but also during microbial sepsis induced by implantation of a bacterial?laden fibrin clot into the peritoneum. We found that the dnHMGA1 transgene was only present in Tg and not wild?type (WT) littermate mice, and the mutant transgene was able to interact with transcription factors (such as NF??B), but was not able to bind DNA. Tg mice exhibited a blunted hypotensive response to endotoxemia, and less mortality in microbial sepsis. Moreover, Tg mice had a reduced inflammatory response during sepsis, with decreased macrophage and neutrophil infiltration into tissues, which was associated with reduced expression of monocyte chemotactic protein?1 and macrophage inflammatory protein?2. Collectively, these data suggest that targeted expression of a dnHMGA1 transgene is able to improve outcomes in models of endotoxin exposure and microbial sepsis, in part by modulating the immune response and suggest a novel modifiable pathway to target therapeutics in sepsis.
dc.format.mimetypeapplication/pdf
dc.language.isoeng
dc.relation.ispartofJournal of Leukocyte Biology, ISSN: 0741-5400; EISSN: 1938-3673, Vol.104, No.4 (October, 2018); pp.677-689
dc.relation.urihttps://jlb.onlinelibrary.wiley.com/doi/abs/10.1002/JLB.4HI0817-333RR
dc.sourceJournal of Leukocyte Biology
dc.titleFrontline Science: Targeted expression of a dominant-negative high mobility group A1 transgene improves outcome in sepsis
dc.typearticle
dc.publisherJohn Wiley and Sons
dc.subject.keywordArchitectural transcription factor
dc.subject.keywordChemokines
dc.subject.keywordImmune response
dc.subject.keywordTransgenic Mice
dc.rights.accesRightsinfo:eu-repo/semantics/restrictedAccess
dc.type.spaArtículo
dc.rights.accesoRestringido (Acceso a grupos específicos)
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersion
dc.identifier.doihttps://doi.org/10.1002/JLB.4HI0817-333RR
dc.title.TranslatedTitleCiencia de primera línea: la expresión dirigida de un transgén del grupo A1 de alta movilidad dominante-negativo mejora el resultado en la sepsis
dc.relation.citationEndPage689
dc.relation.citationIssueNo. 4
dc.relation.citationStartPage677
dc.relation.citationTitleJournal of Leukocyte Biology
dc.relation.citationVolumeVol. 104


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