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dc.contributor.authorDUNNE, AISLINGen
dc.contributor.authorO'NEILL, LUKEen
dc.date.accessioned2015-12-11T16:04:50Z
dc.date.available2015-12-11T16:04:50Z
dc.date.issued2014en
dc.date.submitted2014en
dc.identifier.citationWochal, P., Rathinam, V.A.K., Dunne, A., (...), Fitzgerald, K.A., O'Neill, L.A.J., TRIL is involved in cytokine production in the brain following escherichia coli infection, Journal of Immunology, 193, 4, 2014, 1911-1919en
dc.identifier.otherYen
dc.descriptionPUBLISHEDen
dc.description.abstractTLR4 interactor with leucine-rich repeats (TRIL) is a brain-enriched accessory protein that is important in TLR3 and TLR4 signaling. In this study, we generated Tril(-/-) mice and examined TLR responses in vitro and in vivo. We found a role for TRIL in both TLR4 and TLR3 signaling in mixed glial cells, consistent with the high level of expression of TRIL in these cells. We also found that TRIL is a modulator of the innate immune response to LPS challenge and Escherichia coli infection in vivo. Tril(-/-) mice produce lower levels of multiple proinflammatory cytokines and chemokines specifically within the brain after E. coli and LPS challenge. Collectively, these data uncover TRIL as a mediator of innate immune responses within the brain, where it enhances neuronal cytokine responses to infection.en
dc.format.extent1911-1919en
dc.relation.ispartofseriesJournal of Immunologyen
dc.relation.ispartofseries193en
dc.relation.ispartofseries4en
dc.rightsYen
dc.subjectTRILen
dc.titleTRIL is involved in cytokine production in the brain following escherichia coli infectionen
dc.typeJournal Articleen
dc.type.supercollectionscholarly_publicationsen
dc.type.supercollectionrefereed_publicationsen
dc.identifier.peoplefinderurlhttp://people.tcd.ie/laoneillen
dc.identifier.peoplefinderurlhttp://people.tcd.ie/aidunneen
dc.identifier.rssinternalid100546en
dc.identifier.doihttp://dx.doi.org/10.4049/jimmunol.1302392en
dc.rights.ecaccessrightsopenAccess
dc.identifier.urihttp://hdl.handle.net/2262/75303


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