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dc.contributor.authorAgarwal, Shiuli
dc.contributor.authorVierbuchen, Tim
dc.contributor.authorGhosh, Sreya
dc.contributor.authorChan, Jennie
dc.contributor.authorJiang, Zhaozhao
dc.contributor.authorKandasamy, Richard Kumaran
dc.contributor.authorRicci, Emiliano
dc.contributor.authorFitzgerald, Katherine A.
dc.date.accessioned2023-01-09T09:12:57Z
dc.date.available2023-01-09T09:12:57Z
dc.date.created2021-02-11T14:32:24Z
dc.date.issued2020
dc.identifier.citationNature Communications. 2020, 11 6348-?.en_US
dc.identifier.issn2041-1723
dc.identifier.urihttps://hdl.handle.net/11250/3041806
dc.description.abstractLong non-coding RNAs are important regulators of biological processes including immune responses. The immunoregulatory functions of lncRNAs have been revealed primarily in murine models with limited understanding of lncRNAs in human immune responses. Here, we identify lncRNA LUCAT1 which is upregulated in human myeloid cells stimulated with lipopolysaccharide and other innate immune stimuli. Targeted deletion of LUCAT1 in myeloid cells increases expression of type I interferon stimulated genes in response to LPS. By contrast, increased LUCAT1 expression results in a reduction of the inducible ISG response. In activated cells, LUCAT1 is enriched in the nucleus where it associates with chromatin. Further, LUCAT1 limits transcription of interferon stimulated genes by interacting with STAT1 in the nucleus. Together, our study highlights the role of the lncRNA LUCAT1 as a post-induction feedback regulator which functions to restrain the immune response in human cells.en_US
dc.language.isoengen_US
dc.publisherNature Researchen_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titleThe long non-coding RNA LUCAT1 is a negative feedback regulator of interferon responses in humansen_US
dc.title.alternativeThe long non-coding RNA LUCAT1 is a negative feedback regulator of interferon responses in humansen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.source.pagenumber6348-?en_US
dc.source.volume11en_US
dc.source.journalNature Communicationsen_US
dc.identifier.doi10.1038/s41467-020-20165-5
dc.identifier.cristin1888901
dc.relation.projectNorges forskningsråd: 223255en_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode2


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