The steroidogenic acute regulatory protein is induced by angiotensin II and K+ in H295R adrenocortical cells

被引:120
作者
Clark, BJ
Pezzi, V
Stocco, DM
Rainey, WE
机构
[1] TEXAS TECH UNIV,HLTH SCI CTR,DEPT BIOCHEM & CELL BIOL,LUBBOCK,TX 79430
[2] UNIV CALABRIA,CTR HLTH,I-87036 ARCAVACATA,CS,ITALY
[3] UNIV TEXAS,SW MED CTR,DEPT OBSTET & GYNECOL,DALLAS,TX 75235
关键词
StAR; steroidogenesis; adrenal; angiotensin; potassium;
D O I
10.1016/0303-7207(95)03683-0
中图分类号
Q2 [细胞生物学];
学科分类号
071009 [细胞生物学]; 090102 [作物遗传育种];
摘要
Adrenal steroid hormone biosynthesis can be activated by the protein kinase A pathway by ACTH, the protein kinase C pathway by angiotensin II (AII), or by increasing intracellular Ca2+ levels by AII or K+. Although their mechanisms of action are not known, each of these pathways is dependent upon the de novo synthesis of a protein that is required for the acute production of steroids. We have recently proposed the steroidogenic acute regulatory (StAR) protein as this required protein, therefore, we examined the effect of different agonists on StAR's expression in H295R human adrenocortical carcinoma cells. (Bu)(2)cAMP, AII, K+, BAYK8644 (a calcium channel agonist) and TPA are all shown to induce StAR. Aldosterone synthesis was stimulated by all the agonists with the exception of TPA, indicating that AII-stimulated steroid production is mediated by increases in intracellular calcium. Thus, these data suggest that regulation of StAR expression may represent mechanism for divergent pathways to acutely control adrenal steroidogenesis.
引用
收藏
页码:215 / 219
页数:5
相关论文
共 20 条
[1]
HUMAN NCI-H295 ADRENOCORTICAL CARCINOMA-CELLS - A MODEL FOR ANGIOTENSIN-II-RESPONSIVE ALDOSTERONE SECRETION [J].
BIRD, IM ;
HANLEY, NA ;
WORD, RA ;
MATHIS, JM ;
MCCARTHY, JL ;
MASON, JI ;
RAINEY, WE .
ENDOCRINOLOGY, 1993, 133 (04) :1555-1561
[2]
EFFECT OF DIFFERENT STEROIDOGENIC STIMULI ON PROTEIN-PHOSPHORYLATION AND STEROIDOGENESIS IN MA-10 MOUSE LEYDIG TUMOR-CELLS [J].
CHAUDHARY, LR ;
STOCCO, DM .
BIOCHIMICA ET BIOPHYSICA ACTA, 1991, 1094 (02) :175-184
[3]
CLARK BJ, 1994, J BIOL CHEM, V269, P28314
[4]
CLARK BJ, 1995, IN PRESS MOL ENDOCRI
[5]
IDENTIFICATION OF THE CYCLOHEXIMIDE-SENSITIVE SITE IN ANGIOTENSIN-STIMULATED ALDOSTERONE SYNTHESIS [J].
ELLIOTT, ME ;
GOODFRIEND, TL .
BIOCHEMICAL PHARMACOLOGY, 1984, 33 (09) :1519-1524
[6]
BOVINE ADRENAL GLOMERULOSA AND FASCICULATA CELLS EXHIBIT 28.5-KILODALTON PROTEINS SENSITIVE TO ANGIOTENSIN, OTHER AGONISTS, AND ATRIAL-NATRIURETIC-PEPTIDE [J].
ELLIOTT, ME ;
GOODFRIEND, TL ;
JEFCOATE, CR .
ENDOCRINOLOGY, 1993, 133 (04) :1669-1677
[7]
FERGUSON JJ, 1963, J BIOL CHEM, V238, P2754
[8]
STUDIES ON ROLE OF PROTEIN SYNTHESIS IN REGULATION OF CORTICOSTERONE PRODUCTION BY ADRENOCORTICOTROPIC HORMONE IN VIVO [J].
GARREN, LD ;
NEY, RL ;
DAVIS, WW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1965, 53 (06) :1443-&
[9]
COMPARISON OF PROTEIN-PHOSPHORYLATION PATTERNS PRODUCED IN ADRENAL-CELLS BY ACTIVATION OF CAMP-DEPENDENT PROTEIN-KINASE AND CA-DEPENDENT PROTEIN-KINASE [J].
HARTIGAN, JA ;
GREEN, EG ;
MORTENSEN, RM ;
MENACHERY, A ;
WILLIAMS, GH ;
ORMEJOHNSON, NR .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1995, 53 (1-6) :95-101
[10]
ACTH REGULATION OF CHOLESTEROL MOVEMENT IN ISOLATED ADRENAL-CELLS [J].
JEFCOATE, CR ;
DIBARTOLOMEIS, MJ ;
WILLIAMS, CA ;
MCNAMARA, BC .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1987, 27 (4-6) :721-729