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Molecular and Cellular Biology, February 2001, p. 771-780, Vol. 21, No. 3
0270-7306/01/$04.00+0 DOI: 10.1128/MCB.21.3.771-780.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Dexamethasone Destabilizes Cyclooxygenase 2 mRNA by
Inhibiting Mitogen-Activated Protein Kinase p38
Marina
Lasa,
Matthew
Brook,
Jeremy
Saklatvala, and
Andrew R.
Clark*
Kennedy Institute of Rheumatology Division,
Imperial College School of Medicine, Hammersmith, London W6 8LH,
United Kingdom
Received 24 August 2000/Returned for modification 12 October
2000/Accepted 8 November 2000
The stability of cyclooxygenase 2 (Cox-2) mRNA is regulated
positively by proinflammatory stimuli acting through mitogen-activated protein kinase (MAPK) p38 and negatively by anti-inflammatory glucocorticoids such as dexamethasone. A tetracycline-regulated reporter system was used to investigate mechanisms of regulation of
Cox-2 mRNA stability. Dexamethasone was found to destabilize
-globin-Cox-2 reporter mRNAs by inhibiting p38. This inhibition occurred at the level of p38 itself: stabilization of reporter mRNA by
a kinase upstream of p38 was blocked by dexamethasone, while
stabilization by a kinase downstream of p38 was insensitive to
dexamethasone. Inhibition of p38 activity by dexamethasone was observed
in a variety of cell types treated with different activating stimuli.
Furthermore, inhibition of p38 was antagonized by the
anti-glucocorticoid RU486 and was delayed and actinomycin D sensitive,
suggesting that ongoing glucocorticoid receptor-dependent transcription
is required.
*
Corresponding author. Mailing address: Kennedy
Institute of Rheumatology Division, Imperial College School of
Medicine, 1 Aspenlea Rd., Hammersmith, London W6 8LH, United Kingdom.
Phone: (0044) 20 8383 4430. Fax: (0044) 20 8383 4499. E-mail:
andy.clark{at}ic.ac.uk.
Molecular and Cellular Biology, February 2001, p. 771-780, Vol. 21, No. 3
0270-7306/01/$04.00+0 DOI: 10.1128/MCB.21.3.771-780.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
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