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dc.contributor.authorKästle, Matthias
dc.contributor.authorMerten, Camilla
dc.contributor.authorHartig, Roland
dc.contributor.authorKaehne, Thilo
dc.contributor.authorLiaunardy-Jopeace, Ardiyanto
dc.contributor.authorWoessner, Nadine M.
dc.contributor.authorSchamel, Wolfgang W.
dc.contributor.authorJames, John
dc.contributor.authorMinguet, Susana
dc.contributor.authorSimeoni, Luca
dc.contributor.authorSchraven, Burkhart
dc.date.accessioned2020-12-22T19:00:41Z
dc.date.available2020-12-22T19:00:41Z
dc.date.issued2020-11-23
dc.date.submitted2020-05-15
dc.identifier.others12964-020-00673-z
dc.identifier.other673
dc.identifier.urihttps://www.repository.cam.ac.uk/handle/1810/315469
dc.descriptionFunder: DFG
dc.descriptionFunder: Projekt DEAL
dc.description.abstractAbstract: Background: Upon engagement of the T-cell receptor (TCR), the Src-family protein tyrosine kinase p56Lck phosphorylates components of the TCR (e.g. the TCRζ chains), thereby initiating T-cell activation. The enzymatic activity of Lck is primarily regulated via reversible and dynamic phosphorylation of two tyrosine residues, Y394 and Y505. Lck possesses an additional highly conserved tyrosine Y192, located within the SH2 domain, whose role in T-cell activation is not fully understood. Methods: Knock-in mice expressing a phospho-mimetic (Y192E) form of Lck were generated. Cellular and biochemical characterization was performed to elucidate the function of Y192 in primary T cells. HEK 293T and Jurkat T cells were used for in vitro studies. Results: Co-immunoprecipitation studies and biochemical analyses using T cells from LckY192E knock-in mice revealed a diminished binding of LckY192E to CD45 and a concomitant hyperphosphorylation of Y505, thus corroborating previous data obtained in Jurkat T cells. Surprisingly however, in vitro kinase assays showed that LckY192E possesses a normal enzymatic activity in human and murine T cells. FLIM/FRET measurements employing an LckY192E biosensor further indicated that the steady state conformation of the LckY192E mutant is similar to Lckwt. These data suggest that Y192 might regulate Lck functions also independently from the Lck/CD45-association. Indeed, when LckY192E was expressed in CD45−/−/Csk−/− non-T cells (HEK 293T cells), phosphorylation of Y505 was similar to Lckwt, but LckY192E still failed to optimally phosphorylate and activate the Lck downstream substrate ZAP70. Furthermore, LckY19E was recruited less to CD3 after TCR stimulation. Conclusions: Taken together, phosphorylation of Y192 regulates Lck functions in T cells at least twofold, by preventing Lck association to CD45 and by modulating ligand-induced recruitment of Lck to the TCR. Major findings: Our data change the current view on the function of Y192 and suggest that Y192 also regulates Lck activity in a manner independent of Y505 phosphorylation. FN7ZF7ULbDVsMsT6Sckwh1Video Abstract
dc.languageen
dc.publisherBioMed Central
dc.rightsAttribution 4.0 International (CC BY 4.0)en
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en
dc.subjectResearch
dc.subjectLck
dc.subjectT-cell activation
dc.subjectTCR signaling
dc.subjectZap70
dc.subjectKnock-in mice
dc.subjectY192
dc.subjectSignal transduction
dc.subjectPLA
dc.titleTyrosine 192 within the SH2 domain of the Src-protein tyrosine kinase p56 Lck regulates T-cell activation independently of Lck/CD45 interactions
dc.typeArticle
dc.date.updated2020-12-22T19:00:39Z
prism.issueIdentifier1
prism.publicationNameCell Communication and Signaling
prism.volume18
dc.identifier.doi10.17863/CAM.62576
dcterms.dateAccepted2020-10-13
rioxxterms.versionofrecord10.1186/s12964-020-00673-z
rioxxterms.versionVoR
rioxxterms.licenseref.urihttp://creativecommons.org/licenses/by/4.0/
dc.contributor.orcidSchraven, Burkhart [0000-0003-4321-7405]
dc.identifier.eissn1478-811X


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Attribution 4.0 International (CC BY 4.0)
Except where otherwise noted, this item's licence is described as Attribution 4.0 International (CC BY 4.0)