Regulation of erythropoietin gene expression in fetal sheep by glucocorticoids

被引:25
作者
Lim, GB
Dodic, M
Earnest, L
Jeyaseelan, K
Wintour, EM
机构
[1] UNIV MELBOURNE, HOWARD FLOREY INST EXPTL PHYSIOL & MED, PARKVILLE, VIC 3052, AUSTRALIA
[2] NATL UNIV SINGAPORE, DEPT BIOCHEM, SINGAPORE 117548, SINGAPORE
关键词
D O I
10.1210/en.137.5.1658
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Erythropoietin (Epo) gene expression in ovine fetal liver and kidneys was measured by competitive RT-PCR in situations in which fetal glucocorticoid status was altered. Bilateral adrenalectomy at 120 +/- 0.3 days gestation (term is 145-150 days) caused a significant (P < 0.05) 5-fold increase in renal Epo messenger RNA(mrna) levels at 145 +/- 1 days compared to those in age-matched controls. With cortisol replacement in adrenalectomized fetuses, renal Epo mRNA levels dropped to 17% of this value (P < 0.05). Cortisol infusion (230 mu g/h for 48 h) at 108 +/- 1 day decreased renal Epo gene expression significantly (P < 0.01) to 23% of the control value; dexamethasone treatment of the ewe at midgestation (0.76 mg/h for 48 h) also decreased fetal, but not adult, renal Epo mRNA levels (to 12% of control value; P < 0.01), Fetal and maternal liver Epo mRNA levels were unaffected by glucocorticoid status at any stage of pregnancy. Thus, glucocorticoids can influence fetal renal, but not maternal, Epo gene expression. In the presence of high concentrations of fetal glucocorticoids, plasma Epo values were consistently 4-5 mU/ml, close to the sensitivity of the assay, whereas in seven adrenalectomized fetuses, the plasma Epo value was 9.1 +/- 1.4 mU/ml.
引用
收藏
页码:1658 / 1663
页数:6
相关论文
共 43 条
[1]  
BAUER C, 1989, ANNU REV PHYSIOL, V51, P845, DOI 10.1146/annurev.physiol.51.1.845
[2]   CONTROL OF IGF-II MESSENGER-RNA LEVELS BY GLUCOCORTICOIDS IN THE NEONATAL RAT [J].
BECK, F ;
SAMANI, NJ ;
SENIOR, P ;
BYRNE, S ;
MORGAN, K ;
GEBHARD, R ;
BRAMMAR, WJ .
JOURNAL OF MOLECULAR ENDOCRINOLOGY, 1988, 1 (03) :R5-R8
[3]   THE EFFECT OF BILATERAL FETAL ADRENALECTOMY ON FLUID BALANCE IN THE OVINE FETUS [J].
BENSON, CA ;
WINTOUR, EM .
JOURNAL OF PHYSIOLOGY-LONDON, 1995, 489 (01) :235-241
[4]   HYPOXIC INDUCTION OF THE HUMAN ERYTHROPOIETIN GENE - COOPERATION BETWEEN THE PROMOTER AND ENHANCER, EACH OF WHICH CONTAINS STEROID-RECEPTOR RESPONSE ELEMENTS [J].
BLANCHARD, KL ;
ACQUAVIVA, AM ;
GALSON, DL ;
BUNN, HF .
MOLECULAR AND CELLULAR BIOLOGY, 1992, 12 (12) :5373-5385
[5]   INHIBITION OF MOUSE GATA-1 FUNCTION BY THE GLUCOCORTICOID RECEPTOR - POSSIBLE MECHANISM OF STEROID INHIBITION OF ERYTHROLEUKEMIA CELL-DIFFERENTIATION [J].
CHANG, TJ ;
SCHER, BM ;
WAXMAN, S ;
SCHER, W .
MOLECULAR ENDOCRINOLOGY, 1993, 7 (04) :528-542
[6]   DEXAMETHASONE INHIBITS ALPHA-FETOPROTEIN GENE-EXPRESSION IN DEVELOPING MOUSE-LIVER [J].
COMMER, P ;
SCHWARTZ, C ;
TRACY, S ;
TAMAOKI, T ;
CHIU, JF .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1979, 89 (04) :1294-1299
[7]   ERYTHROPOIETIN GENE-EXPRESSION IN FETAL AND ADULT SHEEP KIDNEY [J].
DARBY, IA ;
EVANS, BA ;
FU, P ;
LIM, GB ;
MORITZ, KM ;
WINTOUR, EM .
BRITISH JOURNAL OF HAEMATOLOGY, 1995, 89 (02) :266-270
[8]   EFFECTS OF PROLONGED (48-H) INFUSION OF CORTISOL ON BLOOD-PRESSURE, RENAL-FUNCTION AND FETAL FLUIDS IN THE IMMATURE OVINE FETUS [J].
DODIC, M ;
WINTOUR, EM .
CLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY, 1994, 21 (12) :971-980
[9]   ERYTHROPOIETIN - OXYGEN-DEPENDENT CONTROL OF ERYTHROPOIESIS AND ITS FAILURE IN RENAL-DISEASE [J].
ECKARDT, KU .
NEPHRON, 1994, 67 (01) :7-23
[10]   AGE-DEPENDENT EXPRESSION OF THE ERYTHROPOIETIN GENE IN RAT-LIVER AND KIDNEYS [J].
ECKARDT, KU ;
RATCLIFFE, PJ ;
TAN, CC ;
BAUER, C ;
KURTZ, A .
JOURNAL OF CLINICAL INVESTIGATION, 1992, 89 (03) :753-760