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Inhibition of Antigen-Specific T Cell Proliferation and Cytokine Production by Protein Kinase A Type I
Author(s) -
Einar Martin Aandahl,
Walter J. Moretto,
Patrick Haslett,
Torkel Vang,
Tone Bryn,
Kjetil Taskén,
Douglas F. Nixon
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.169.2.802
Subject(s) - protein kinase a , t cell , microbiology and biotechnology , effector , immune system , cytokine , biology , zap70 , il 2 receptor , cd8 , chemistry , kinase , immunology
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.

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