Fyn regulates the duration of TCR engagement needed for commitment to effector function

被引:55
作者
Filby, Andrew
Seddon, Benedict
Kleczkowska, Joanna
Salmond, Robert
Tomlinson, Peter
Smida, Michal
Lindquist, Jonathan A.
Schraven, Burkhart
Zamoyska, Rose
机构
[1] Natl Inst Med Res, Div Mol Immunol, London NW7 1AA, England
[2] Natl Inst Med Res, MRC, Div Immune Cell Biol, London NW7 1AA, England
[3] Otto Von Guericke Univ, Inst Immunol, Magdeburg, Germany
基金
英国医学研究理事会;
关键词
D O I
10.4049/jimmunol.179.7.4635
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
In naive T cells, engagement of the TCR with agonist peptide:MHC molecules leads to phosphorylation of key intracellular signaling intermediates within seconds and this peaks within minutes. However, the cell does not commit to proliferation and IL-2 cytokine production unless receptor contact is sustained for several hours. The biochemical basis for this transition to full activation may underlie how T cells receive survival signals while maintaining tolerance, and is currently not well understood. We show here that for CD8 T cells commitment to proliferation and cytokine production requires sustained activation of the Src family kinase Lck and is opposed by the action of Fyn. Thus, in the absence of Fyn, commitment to activation occurs more rapidly, the cells produce more IL-2, and undergo more rounds of division. Our data demonstrate a role for Fyn in modulating the response to Ag in primary T cells.
引用
收藏
页码:4635 / 4644
页数:10
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