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dc.contributor.authorErnst, M
dc.contributor.authorInglese, M
dc.contributor.authorScholz, GM
dc.contributor.authorHarder, KW
dc.contributor.authorClay, FJ
dc.contributor.authorBozinovski, S
dc.contributor.authorWaring, P
dc.contributor.authorDarwiche, R
dc.contributor.authorKay, T
dc.contributor.authorSly, P
dc.contributor.authorCollins, R
dc.contributor.authorTurner, D
dc.contributor.authorHibbs, ML
dc.contributor.authorAnderson, GP
dc.contributor.authorDunn, AR
dc.date.available2014-05-21T19:19:59Z
dc.date.issued2002-09-02
dc.identifierhttp://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000177984700004&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=d4d813f4571fa7d6246bdc0dfeca3a1c
dc.identifier.citationErnst, M., Inglese, M., Scholz, G. M., Harder, K. W., Clay, F. J., Bozinovski, S., Waring, P., Darwiche, R., Kay, T., Sly, P., Collins, R., Turner, D., Hibbs, M. L., Anderson, G. P. & Dunn, A. R. (2002). Constitutive activation of the Src family kinase Hck results in spontaneous pulmonary inflammation and an enhanced innate immune response. JOURNAL OF EXPERIMENTAL MEDICINE, 196 (5), pp.589-604. https://doi.org/10.1084/jem.20020873.
dc.identifier.issn0022-1007
dc.identifier.urihttp://hdl.handle.net/11343/26121
dc.descriptionC1 - Journal Articles Refereed
dc.description.abstractTo identify the physiological role of Hck, a functionally redundant member of the Src family of tyrosine kinases expressed in myelomonocytic cells, we generated Hck(F/F) "knock-in" mice which carry a targeted tyrosine (Y) to phenylalanine (F) substitution of the COOH-terminal, negative regulatory Y(499)-residue in the Hck protein. Unlike their Hck(-/-) "loss-of-function" counterparts, Hck(F/F) "gain-of-function" mice spontaneously acquired a lung pathology characterized by extensive eosinophilic and mononuclear cell infiltration within the lung parenchyma, alveolar airspaces, and around blood vessels, as well as marked epithelial mucus metaplasia in conducting airways. Lungs from Hck(F/F) mice showed areas of mild emphysema and pulmonary fibrosis, which together with inflammation resulted in altered lung function and respiratory distress in aging mice. When challenged transnasally with lipopolysaccharide (LPS), Hck(F/F) mice displayed an exaggerated pulmonary innate immune response, characterized by excessive release of matrix metalloproteinases and tumor necrosis factor (TNF)alpha. Similarly, Hck(F/F) mice were highly sensitive to endotoxemia after systemic administration of LPS, and macrophages and neutrophils derived from Hck(F/F) mice exhibited enhanced effector functions in vitro (e.g., nitric oxide and TNFalpha production, chemotaxis, and degranulation). Based on the demonstrated functional association of Hck with leukocyte integrins, we propose that constitutive activation of Hck may mimic adhesion-dependent priming of leukocytes. Thus, our observations collectively suggest an enhanced innate immune response in Hck(F/F) mice thereby skewing innate immunity from a reversible physiological host defense response to one causing irreversible tissue damage.
dc.languageEnglish
dc.publisherROCKEFELLER UNIV PRESS
dc.subjectTumor Immunology ; Cancer and Related Disorders
dc.titleConstitutive activation of the Src family kinase Hck results in spontaneous pulmonary inflammation and an enhanced innate immune response
dc.typeJournal Article
dc.identifier.doi10.1084/jem.20020873
melbourne.peerreviewPeer Reviewed
melbourne.affiliationThe University of Melbourne
melbourne.affiliation.departmentSurgery - Royal Melbourne And Western Hospital
melbourne.source.titleJOURNAL OF EXPERIMENTAL MEDICINE
melbourne.source.volume196
melbourne.source.issue5
melbourne.source.pages589-604
dc.research.coderfcd320206
dc.research.codeseo1998730108
dc.rights.licenseCC BY-NC-SA
melbourne.publicationid10700
melbourne.elementsid253099
melbourne.openaccess.pmchttp://www.ncbi.nlm.nih.gov/pmc/articles/PMC2193996
melbourne.contributor.authorErnst, Matthias
melbourne.contributor.authorScholz, Glen
melbourne.contributor.authorBozinovski, Steven
melbourne.contributor.authorWaring, Paul
melbourne.contributor.authorKay, Thomas
melbourne.contributor.authorAnderson, Gary
melbourne.contributor.authorDunn, Ashley
melbourne.contributor.authorClay, Fiona
dc.identifier.eissn1540-9538
melbourne.conference.locationUnited States
melbourne.accessrightsAccess this item via the Open Access location


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