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Interferon α activates the tyrosine kinase Lyn in haemopoietic cells
Authors:Shahab Uddin,Isabella M. Grumbach,Taolin YI,Oscar R. Colamonici,&   Leonidas C. Platanias
Affiliation:Section of Hematology-Oncology, Department of Medicine, University of Illinois at Chicago and West Side Veterans Affairs Hospital, Chicago, Illinois, U.S.A.,;Department of Cancer Biology, The Cleveland Clinic Foundation Research Institute, Cleveland, Ohio, U.S.A.,;Department of Pathology, University of Tennessee, Memphis, Tennessee, U.S.A.
Abstract:
We investigated whether the src-family tyrosine kinase Lyn is involved in the generation of interferon α (IFNα) signals in haemopoietic cells. In vitro kinase assays using IFNα-sensitive cells of B-cell origin demonstrated the presence of IFNα-dependent kinase activity in anti-Lyn immunoprecipitates. Further studies demonstrated that Lyn associates via its src homology 2 (SH2) domain with the Janus family tyrosine kinase Tyk-2. This interaction was IFNα-dependent and involved direct binding of the SH2 domain of Lyn to the IFNα-activated form of Tyk-2. Thus, during binding of IFNα to its receptor in malignant haemopoietic cells, Lyn is engaged in an IFNα-signalling pathway, probably downstream of Tyk-2.
Keywords:interferon    tyrosine kinases    signal transduction
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