Inhibition of antigen-specific T cell proliferation and cytokine production by protein kinase a type I

被引:79
作者
Aandahl, EM
Moretto, WJ
Haslett, PA
Vang, T
Bryn, T
Tasken, K
Nixon, DF
机构
[1] Univ Calif San Francisco, Gladstone Inst Virol & Immunol, San Francisco, CA 94141 USA
[2] Univ Oslo, Dept Med Biochem, Oslo, Norway
[3] Rockefeller Univ, Cellular Physiol & Immunol Lab, New York, NY 10021 USA
关键词
D O I
10.4049/jimmunol.169.2.802
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
cAMP inhibits biochemical events leading to T cell activation by triggering of an inhibitory protein kinase A (PKA)-C-terminal Src kinase pathway assembled in lipid rafts. In this study, we demonstrate that activation of PKA type I by Sp-8-bromo-cAMPS (a cAMP agonist) has profound inhibitory effects on Ag-specific immune responses in peripheral effector T cells. Activation of PKA type I inhibits both cytokine production and proliferative responses in both CD4(+) and CD8(+) T cells in a concentration-dependent manner. The observed effects of cAMP appeared to occur endogenously in T cells and were not dependent on APC. The inhibition of responses was not due to apoptosis of specific T cells and was reversible by a PKA type I-selective cAMP antagonist. This supports the notion of PKA type I as a key enzyme in the negative regulation of immune responses and a potential target for inhibiting autoreactive T cells.
引用
收藏
页码:802 / 808
页数:7
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