CRE-mediated transcriptional activation is involved in cAMP protection of 
T-cell receptor-induced apoptosis but not in cAMP potentiation of 
glucocorticoid-mediated programmed cell death

Igaz, M; Refojo, D; Costas, MA; Holsboer, F; Arzt, E

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CRE-mediated transcriptional activation is involved in cAMP protection of T-cell receptor-induced apoptosis but not in cAMP potentiation of glucocorticoid-mediated programmed cell death

MPS-Authors

Igaz, M
Max Planck Institute of Psychiatry, Max Planck Society;

Refojo, D
Max Planck Institute of Psychiatry, Max Planck Society;

Costas, MA
Max Planck Institute of Psychiatry, Max Planck Society;

Holsboer, F
Max Planck Institute of Psychiatry, Max Planck Society;

Arzt, E
Max Planck Institute of Psychiatry, Max Planck Society;

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引用

Igaz, M., Refojo, D., Costas, M., Holsboer, F., & Arzt, E. (2002). CRE-mediated transcriptional activation is involved in cAMP protection of T-cell receptor-induced apoptosis but not in cAMP potentiation of glucocorticoid-mediated programmed cell death. Biochimica et Biophysica Acta-Molecular Cell Research, 1542(1-3), 139-148.

引用: https://hdl.handle.net/11858/00-001M-0000-000E-A261-B

要旨

Apoptosis of thymic cells induced by glucocorticoids (GC) and T-cell receptor (TCR) engagement are mutually antagonistic. We demonstrate that cAMP enhances GC and antagonizes TCR (anti- CD3) apoptosis on the same cell (DO-11.10 and 2B4.11 T-cell hybridomas). We analyzed the activity of several transcription factors in this cAMP dual, stimulus-dependent, regulatory action. Anti-CD3 increases kB-activity which is inhibited by CPTcAMP or dexamethasone (DEX), supporting the proapoptotic role of NFkB on TCR-induced apoptosis. Anti-CD3 not only increases kB- but diminishes GC response element (GRE)-activity induced by DEX, suggesting that TCR-mediated blockade of GC- induced apoptosis involves not only the proposed antiapoptotic action of NF-kB on GC, but also the inhibition of GRE-regulated proapoptotic genes. To test the involvement of CRE-driven transcription in the cAMP dual apoptotic regulation, cells were transfected with a CRE decoy DNA oligomer. Blockade of CRE transactivation with decoy targeting of CRE completely blocked the protection of TCR-induced apoptosis by cAMP, while it did not modify the enhancement by cAMP on GC-induced apoptosis. We show that CRE-binding factors have a definite role in T-cell apoptosis: they are involved in cAMP protection of TCR- but not in cAMP potentiation of GC-induced apoptosis. (C) 2002 Elsevier Science B.V. All rights reserved