GLUCOCORTICOIDS STIMULATE THE EXPRESSION OF PROSTAGLANDIN ENDOPEROXIDE-H SYNTHASE-2 IN AMNION CELLS

被引:97
作者
ZAKAR, T [1 ]
HIRST, JJ [1 ]
MIJOVIC, JE [1 ]
OLSON, DM [1 ]
机构
[1] UNIV ALBERTA, DEPT PHYSIOL, EDMONTON, AB, CANADA
关键词
D O I
10.1210/en.136.4.1610
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Corticosteroids increase the production of prostaglandin E(2) (PGE(2)) and the activity of prostaglandin endoperoxide H synthase (PGHS) in cultured amnion cells, although they inhibit prostanoid biosynthesis in numerous other cell types. This suggests that glucocorticoids control the level of PGHS in amnion cells by a hitherto unexplored, positive regulatory mechanism. We have tested the possibility that corticosteroids act by stimulating the expression of messenger RNAs (mRNAs) encoding one or both isoforms of PGHS. Ribonuclease protection assays were used to determine the levels of PGHS-1 and -2 mRNAs and, for reference, alpha-actin mRNA levels in confluent primary cultures of human amnion cells. In untreated cultures, PGHS-1 and -2 mRNA levels were low, often not reaching the level of detection. Dexamethasone (DEX) treatment for 4 h resulted in a measurable level of PGHS-2 mRNA, which increased further 10-fold and 20-fold after incubation with the glucocorticoid for 8 h and 16 h, respectively. The stimulation was dependent on DEX concentration, and was concomitant with an increase in the capacity of the cells to metabolize arachidonic acid to PGE(2). PGHS-1 mRNA levels remained low in DEX-treated cells, while the gamma-actin message level showed no change. Estradiol and progesterone had no influence on PGHS-2 mRNA expression, but cortisol increased the PGHS-2 mRNA abundance. The glucocorticoid antagonist RU486 blocked the effect of DEX. Conditioned media of DEX-treated cells did not contain steroid-induced factor(s) stimulating PGE(2) production. inhibition of protein synthesis by cycloheximide potentiated the effect of DEX, and raised the abundance of PGHS-1, PGHS-2, and gamma-actin mRNAs in untreated cells. DEX did not affect the stability of the PGHS-2 mRNA. These results show that glucocorticoids promote PGE, synthesis by amnion cells by stimulating the expression of PGHS-2 mRNA in a receptor-dependent, selective, and immediate fashion.
引用
收藏
页码:1610 / 1619
页数:10
相关论文
共 50 条
[1]   HYDROCORTISONE HAS A BIPHASIC EFFECT ON RAT GASTRIC-MUCOSAL PROSTAGLANDIN GENERATION INVIVO - INHIBITION AT LOW-DOSES, STIMULATION AT HIGH-DOSES [J].
AVUNDUK, C ;
EASTWOOD, GL ;
POLAKOWSKI, N ;
BURSTEIN, S .
PROSTAGLANDINS LEUKOTRIENES AND ESSENTIAL FATTY ACIDS, 1992, 45 (04) :329-332
[2]   CORTICOSTEROIDS SUPPRESS CYCLOOXYGENASE MESSENGER-RNA LEVELS AND PROSTANOID SYNTHESIS IN CULTURED VASCULAR CELLS [J].
BAILEY, JM ;
MAKHEJA, AN ;
PASH, J ;
VERMA, M .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1988, 157 (03) :1159-1163
[3]   THE STEROID ANTAGONIST RU486 EXERTS DIFFERENT EFFECTS ON THE GLUCOCORTICOID AND PROGESTERONE RECEPTORS [J].
BECK, CA ;
ESTES, PA ;
BONA, BJ ;
MUROCACHO, CA ;
NORDEEN, SK ;
EDWARDS, DP .
ENDOCRINOLOGY, 1993, 133 (02) :728-740
[4]   ACTION OF CORTICOSTEROIDS IN REGULATION OF PROSTAGLANDIN BIOSYNTHESIS IN CULTURED FIBROBLASTS [J].
CHANDRABOSE, KA ;
LAPETINA, EG ;
SCHMITGES, CJ ;
SIEGEL, MI ;
CUATRECASAS, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1978, 75 (01) :214-217
[5]   ISOLATION OF BIOLOGICALLY-ACTIVE RIBONUCLEIC-ACID FROM SOURCES ENRICHED IN RIBONUCLEASE [J].
CHIRGWIN, JM ;
PRZYBYLA, AE ;
MACDONALD, RJ ;
RUTTER, WJ .
BIOCHEMISTRY, 1979, 18 (24) :5294-5299
[6]   SERUM AND GLUCOCORTICOID REGULATION OF GENE-TRANSCRIPTION AND EXPRESSION OF THE PROSTAGLANDIN-H SYNTHASE-1 AND PROSTAGLANDIN-H SYNTHASE-2 ISOZYMES [J].
DEWITT, DL ;
MEADE, EA .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1993, 306 (01) :94-102
[7]   GLUCOCORTICOIDS AND PROSTAGLANDIN SYNTHESIS - WE CANNOT SEE THE WOOD FOR THE TREES [J].
DUVAL, D ;
FREYSSBEGUIN, M .
PROSTAGLANDINS LEUKOTRIENES AND ESSENTIAL FATTY ACIDS, 1992, 45 (02) :85-112
[8]   PROSTAGLANDIN-G/H SYNTHASE ISOENZYME-2 EXPRESSION IN FIBROBLASTS - REGULATION BY DEXAMETHASONE, MITOGENS, AND ONCOGENES [J].
EVETT, GE ;
XIE, WL ;
CHIPMAN, JG ;
ROBERTSON, DL ;
SIMMONS, DL .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1993, 306 (01) :169-177
[9]  
FLETCHER BS, 1992, J BIOL CHEM, V267, P4338
[10]  
FLOWER RJ, 1985, AGENTS ACTIONS, V17, P255