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MicroRNA-146a controls IFN-g production and functional plasticity of murine gd T cells by targeting Nod1

dc.contributor.authorSchmolka, Nina
dc.contributor.authorPapotto, Pedro H.
dc.contributor.authorRomero, Paula Vargas
dc.contributor.authorAmado, Tiago
dc.contributor.authorEnguita, Francisco J.
dc.contributor.authorAmorim, Ana
dc.contributor.authorGordon, Katrina E.
dc.contributor.authorBoldin, Mark
dc.contributor.authorSerre, Karine
dc.contributor.authorBuck, Amy H.
dc.contributor.authorGomes, Anita Quintal
dc.contributor.authorSilva-Santos, Bruno
dc.date.accessioned2019-05-16T15:58:27Z
dc.date.available2019-05-16T15:58:27Z
dc.date.issued2018-03
dc.description.abstractγδ T cells have emerged as key providers of the proinflammatory cytokines interleukin 17 (IL-17) and interferon-γ (IFN-γ) in various models of infection, inflammation, and autoimmunity. Our previous epigenetic and transcriptional analyses have shown that whereas CD27+ γδ T cells are committed to IFN-γ expression, the IL-17 producing CD27- subset has limited plasticity to co-express both cytokines under inflammatory conditions (Schmolka et al. Nat Immunol 2013). To further understand the molecular control of this plasticity we now investigated the potential role of microRNA (miRNA)-mediated post-transcriptional regulation.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationSchmolka N, Papotto, PH, Paula VP, Amado T, Gomes AQ, Silva-Santos B, et al. MicroRNA-146a controls IFN-g production and functional plasticity of murine gd T cells by targeting Nod1. In: 12th World Immune Regulation Meeting, Bern (Switzerland), March 14-17, 2018.pt_PT
dc.identifier.urihttp://hdl.handle.net/10400.21/10032
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/pt_PT
dc.subjectImmunologypt_PT
dc.subjectInflammatory cytokinespt_PT
dc.subjectAutoimmunitypt_PT
dc.subjectFunctional plasticitypt_PT
dc.titleMicroRNA-146a controls IFN-g production and functional plasticity of murine gd T cells by targeting Nod1pt_PT
dc.typeconference object
dspace.entity.typePublication
oaire.citation.conferencePlaceBernapt_PT
rcaap.rightsopenAccesspt_PT
rcaap.typeconferenceObjectpt_PT

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