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dc.contributor.authorFinlay, Daviden
dc.contributor.authorGardiner, Clairen
dc.date.accessioned2020-10-22T13:00:14Z
dc.date.available2020-10-22T13:00:14Z
dc.date.issued2020en
dc.date.submitted2020en
dc.identifier.citationJessica F. Walls, Jeff J. Subleski, Erika M. Palmieri, Marieli Gonzalez Cotto, Clair M. Gardiner, Daniel W. McVicar, David K. Finlay, Metabolic but not transcriptional regulation by PKM2 is important for Natural Killer cell responses, eLIFE, 2020en
dc.identifier.otherYen
dc.descriptionPUBLISHEDen
dc.description.abstractNatural Killer (NK) cells have an important role in immune responses to viruses and tumours. Integrating changes in signal transduction pathways and cellular metabolism is essential for effective NK cells responses. The glycolytic enzyme Pyruvate Kinase Muscle 2 (PKM2) has described roles in regulating glycolytic flux and signal transduction, particularly gene transcription. While PKM2 expression is robustly induced in activated NK cells, mice lacking PKM2 in NK cells showed no defect in NK cell metabolism, transcription or antiviral responses to MCMV infection. NK cell metabolism was maintained due to compensatory PKM1 expression in PKM2-null NK cells. To further investigate the role of PKM2, we used TEPP-46, which increases PKM2 catalytic activity while inhibiting any PKM2 signalling functions. NK cells activated with TEPP-46 had reduced effect or function due to TEPP-46-induced increases in oxidative stress. Overall, PKM2-regulated glycolytic metabolism and redox status, not transcriptional control, facilitate optimal NK cells responses.en
dc.language.isoenen
dc.relation.ispartofserieseLIFEen
dc.rightsYen
dc.titleMetabolic but not transcriptional regulation by PKM2 is important for Natural Killer cell responsesen
dc.typeJournal Articleen
dc.type.supercollectionscholarly_publicationsen
dc.type.supercollectionrefereed_publicationsen
dc.identifier.peoplefinderurlhttp://people.tcd.ie/finlayden
dc.identifier.peoplefinderurlhttp://people.tcd.ie/gardinecen
dc.identifier.rssinternalid220925en
dc.identifier.doihttp://dx.doi.org/10.7554/eLife.59166en
dc.rights.ecaccessrightsopenAccess
dc.subject.TCDThemeImmunology, Inflammation & Infectionen
dc.subject.TCDTagGLUCOSE METABOLISMen
dc.subject.TCDTagImmunometabolismen
dc.subject.TCDTagNATURAL KILLER CELLSen
dc.subject.TCDTagPKM2en
dc.subject.TCDTagVIRAL-INFECTIONen
dc.identifier.orcid_id0000-0003-2716-6679en
dc.status.accessibleNen
dc.contributor.sponsorScience Foundation Ireland (SFI)en
dc.contributor.sponsorGrantNumber18/ERCS/6005en
dc.contributor.sponsorWellcome Trusten
dc.contributor.sponsorGrantNumber106811/Z/15/Zen
dc.identifier.urihttp://hdl.handle.net/2262/93884


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