The Src Family Kinase Fyn Mediates Signals Induced by TCR Antagonists
Author(s) -
Qizhi Tang,
Sumit K. Subudhi,
Kammi Henriksen,
Catherine Long,
Franklin Vives,
Jeffrey A. Bluestone
Publication year - 2002
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.168.9.4480
Subject(s) - fyn , t cell receptor , microbiology and biotechnology , cd3 , tyrosine kinase , src family kinase , tyrosine protein kinase csk , phosphorylation , t cell , proto oncogene tyrosine protein kinase src , signal transduction , biology , chemistry , antigen , cd8 , immunology , sh2 domain , immune system
FcR nonbinding anti-CD3 epsilon mAbs elicit partial TCR signaling that leads to T cell unresponsiveness and tolerance in vivo. In this study, the membrane-proximal events that promote T cell inactivation by FcR nonbinding anti-CD3 mAbs were examined. In the context of FcR nonbinding anti-CD3, TCR complexes did not aggregate and failed to translocate into glycolipid-enriched membrane microdomains. Furthermore, FcR nonbinding anti-CD3 mAbs induced tyrosine phosphorylation of the Fyn substrate Cbl, but not the ZAP-70 substrate linker for activation of T cells. Overexpression of Fyn, but not Lck, restored the mitogenicity of FcR nonbinding anti-CD3 in primary T cells. Taken together, these results suggest that Fyn mediates the partial signaling induced by TCR antagonists.
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