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dc.contributor.authorTangerås, Line Haugstad
dc.contributor.authorSilva, Gabriela
dc.contributor.authorStødle, Guro
dc.contributor.authorGierman, Lobke
dc.contributor.authorSkei, Bente
dc.contributor.authorCollett, Karin
dc.contributor.authorBeversmark, Anne Lise
dc.contributor.authorSkråstad, Ragnhild Bergene
dc.contributor.authorThomsen, Liv Cecilie Vestrheim
dc.contributor.authorBjørge, Line
dc.contributor.authorIversen, Ann-Charlotte
dc.date.accessioned2020-05-04T08:29:01Z
dc.date.available2020-05-04T08:29:01Z
dc.date.created2018-12-13T17:27:06Z
dc.date.issued2018
dc.identifier.citationPlacenta. 2018, 72-73 53-61.en_US
dc.identifier.issn0143-4004
dc.identifier.urihttps://hdl.handle.net/11250/2653143
dc.description.abstractNormal pregnancy is characterized by an elevated inflammatory state involving the placenta. The placental inflammation is further increased in preeclampsia, resulting in release of harmful danger signals to the maternal circulation. Activation of toll-like receptors (TLR)2 and TLR4 by endogenous danger signals plays a role in inflammatory diseases. Placental TLR2 and TLR4 expression has been reported, and high mobility group box 1 (HMGB1) is a likely endogenous activator of these receptors. We aimed to examine HMGB1 activation of TLR2 and TLR4 as mechanisms of placental inflammation in normal and preeclamptic pregnancies, by combined analysis of expression and function of the ligand HMGB1, the receptors TLR2 and TLR4, and the cytokine responder interleukin (IL)-8.en_US
dc.language.isoengen_US
dc.publisherElsevieren_US
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/deed.no*
dc.titlePlacental inflammation by HMGB1 activation of TLR4 at the syncytiumen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionacceptedVersionen_US
dc.source.pagenumber53-61en_US
dc.source.volume72-73en_US
dc.source.journalPlacentaen_US
dc.identifier.doi10.1016/j.placenta.2018.10.011
dc.identifier.cristin1642997
dc.relation.projectNorges forskningsråd: 223255en_US
dc.description.localcode© 2018. This is the authors’ accepted and refereed manuscript to the article. This manuscript version is made available under the CC-BY-NC-ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/en_US
cristin.ispublishedtrue
cristin.fulltextpostprint
cristin.qualitycode1


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Attribution-NonCommercial-NoDerivatives 4.0 Internasjonal
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