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Role of tumor necrosis factor-α, interferon-γ and Fas-ligand on in vitro nitric oxide activity in the corpus luteum

dc.contributor.authorGalvão, A.M.
dc.contributor.authorSzóstek, Anna Z.
dc.contributor.authorSkarzynski, Dariusz J.
dc.contributor.authorFerreira-Dias, Graça M.
dc.date.accessioned2014-09-22T11:48:13Z
dc.date.available2014-09-22T11:48:13Z
dc.date.issued2013-10
dc.descriptionArticles in International Journalspor
dc.description.abstractNormal reproductive function involves the expression of inflammatory mediators. Regarding the corpus luteum (CL), cytokines promote the cross-talk between immune, vascular and steroidogenic cells, among others. Moreover, TNF, IFNG and FASL were shown to regulate equine CL establishment and regression. We hypothesized that cytokines action on equine CL may be mediated by nitric oxide (NO), through the regulation of endothelial NO synthase (eNOS) expression. TNF increased eNOS mRNA level and NO metabolite (nitrite) production during CL growth. Cytokines combined action (TNF + IFNG + FASL) promoted eNOS protein upregulation in mid-CL and nitrite production in mid and late-CL. However, in late-CL, TNF alone decreased nitrite secretion. These results indicate that in equine CL, cytokines TNF, IFNG and FASL regulate NO activity, via eNOS expression modulation.por
dc.identifier.citationGalvão, A.M., Szóstek, A.Z., Skarzynski, D.J., & Ferreira-Dias, G.M. (2013). Role of tumor necrosis factor-x, interferon-y and Fas-ligand on in vitro nitric oxide activity in the corpus luteum. Cytokine, 64(1), 18–21. doi: 10.1016/j.cyto.2013.07.015por
dc.identifier.doi10.1016/j.cyto.2013.07.015
dc.identifier.issn1043-4666
dc.identifier.urihttp://hdl.handle.net/10400.5/7196
dc.language.isoengpor
dc.publisherElsevier Ltd.por
dc.subjectTNF-αpor
dc.subjectIFN-γpor
dc.subjectFas-ligandpor
dc.subjectNitric oxidepor
dc.subjectCorpus luteumpor
dc.titleRole of tumor necrosis factor-α, interferon-γ and Fas-ligand on in vitro nitric oxide activity in the corpus luteumpor
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage21por
oaire.citation.startPage18por
oaire.citation.titleCytokinepor
oaire.citation.volume64(1)por
rcaap.rightsrestrictedAccesspor
rcaap.typearticlepor

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