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dc.contributor.authorLILJEROOS Marien_GB
dc.contributor.authorVUOLTEENAHO Reettaen_GB
dc.contributor.authorMORATH SIEGFRIEDen_GB
dc.contributor.authorHARTUNG THOMASen_GB
dc.contributor.authorHALLMAN Mikkoen_GB
dc.contributor.authorOJANIEMI Marjaen_GB
dc.date.accessioned2010-02-25T14:43:43Z-
dc.date.available2007-03-28en_GB
dc.date.available2010-02-25T14:43:43Z-
dc.date.issued2007en_GB
dc.date.submitted2007-01-15en_GB
dc.identifier.citationCELLULAR SIGNALLING vol. 19 p. 625-633en_GB
dc.identifier.urihttp://publications.jrc.ec.europa.eu/repository/handle/JRC35940-
dc.description.abstractLipoteichoic acid (LTA) of Gram-positive bacteria initiates innate immune responses via Toll-like receptor-2 (TLR2), resulting in the activation of intracellular signaling and production of inflammatory cytokines in macrophages. Although Bruton's tyrosine kinase (Btk) is biologically important molecule implicated in immune regulation and recently in TLR signaling its importance for LTA-TLR2 mediated responses has not been evaluated. In this study, we detected Btk in the LTA signaling complex with TLR2 and PI 3-kinase (PI3K). The constitutive interaction of these proteins was mediated via PI3K Src homology (SH3) -domain. Both Btk and PI3K were activated by LTA stimulation and the LTA induced cytokine expression was differentially modulated by these kinases. LTA induced the activation of nuclear factor kappaB (NFkappaB), however, only Btk inhibition affected the LTA induced Ser536 phosphorylation and DNA-binding of NFkappaB. In conclusion, our results demonstrate that Btk and PI3K occupy important roles in TLR2-induced activation of macrophages, resulting in selective regulation of cytokines.en_GB
dc.description.sponsorshipJRC.I.2-Validation of biomedical testing methodsen_GB
dc.format.mediumOnlineen_GB
dc.languageENGen_GB
dc.publisherELSEVIER SCIENCE INCen_GB
dc.relation.ispartofseriesJRC35940en_GB
dc.titleBruton's Tyrosine Kinase together with PI 3-Kinase are part of Toll-like Receptor 2 Multiprotein Complex and mediate LTA induced Toll-like Receptor 2 responses in macrophages.en_GB
dc.typeArticles in periodicals and booksen_GB
JRC Directorate:Institute for Health and Consumer Protection Historical Collection

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