Regulation by glucocorticoids of angiotensinogen gene expression and secretion in adipose cells

被引:84
作者
Aubert, J [1 ]
Darimont, C [1 ]
Safonova, I [1 ]
Ailhaud, G [1 ]
Negrel, R [1 ]
机构
[1] UNIV NICE SOPHIA ANTIPOLIS, CTR BIOCHIM, CNRS, UMR 6543, F-06108 NICE 2, FRANCE
关键词
D O I
10.1042/bj3280701
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Adipose cells are an important source of angiotensinogen (AT). Its activation product, angiotensin II, stimulates in vitro and in vivo the production and release of prostacyclin which acts as a potent adipogenic signal in promoting the terminal differentiation of preadipocytes to adipocytes. Since glucocorticoids are known to promote adipose cell differentiation in vitro as well as in vivo, their role in the regulation of AT gene expression and secretion has been investigated in cultured Ob1771 mouse adipose cells. In contrast with liver cells, which are the major source of AT and the target of several hormones for the regulation of its expression, adipose cells are only responsive to glucocorticoids, which are able to up-regulate AT gene expression and AT secretion rapidly and dose-dependently. On exposure to glucocorticoids, accumulation of AT mRNA appears primarily to be due to transcriptional activation of the gene and is parallelled by secretion of the protein. Similar results on AT mRNA expression and AT secretion were obtained using explants of rat adipose tissue ex vivo demonstrating a major if not exclusive mechanism of regulation, of AT production by glucocorticoids in mature adipose cells. Together these results provide a potential link between glucocorticoids, AT, the growth of adipose tissue and increased blood pressure.
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收藏
页码:701 / 706
页数:6
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[1]   Evidence for a novel regulatory pathway activated by (carba)prostacyclin in preadipose and adipose cells [J].
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[2]   SPECIFIC CYTOPLASMIC GLUCOCORTICOID HORMONE RECEPTORS IN HEPATOMA TISSUE CULTURE CELLS [J].
BAXTER, JD ;
TOMKINS, GM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1971, 68 (05) :932-&
[3]   Mechanisms for inducible control of angiotensinogen gene transcription [J].
Brasier, AR ;
Li, JY .
HYPERTENSION, 1996, 27 (03) :465-475
[4]   TRANSCRIPTION FACTORS MODULATING ANGIOTENSINOGEN GENE-EXPRESSION IN HEPATOCYTES [J].
BRASIER, AR ;
LI, JY ;
COPLAND, A .
KIDNEY INTERNATIONAL, 1994, 46 (06) :1564-1566
[5]   CIRCULATING AND TISSUE ANGIOTENSIN SYSTEMS [J].
CAMPBELL, DJ .
JOURNAL OF CLINICAL INVESTIGATION, 1987, 79 (01) :1-6
[6]   CELLULAR-LOCALIZATION OF ANGIOTENSINOGEN GENE-EXPRESSION IN BROWN ADIPOSE-TISSUE AND MESENTERY - QUANTIFICATION OF MESSENGER-RIBONUCLEIC-ACID ABUNDANCE USING HYBRIDIZATION INSITU [J].
CAMPBELL, DJ ;
HABENER, JF .
ENDOCRINOLOGY, 1987, 121 (05) :1616-1626
[7]   THE SITE OF ANGIOTENSIN PRODUCTION [J].
CAMPBELL, DJ .
JOURNAL OF HYPERTENSION, 1985, 3 (03) :199-207
[8]   LOCATION AND REGULATION OF RAT ANGIOTENSINOGEN MESSENGER-RNA [J].
CASSIS, LA ;
SAYE, J ;
PEACH, MJ .
HYPERTENSION, 1988, 11 (06) :591-596
[9]   LOCALIZATION OF ANGIOTENSINOGEN MESSENGER-RNA IN RAT AORTA [J].
CASSIS, LA ;
LYNCH, KR ;
PEACH, MJ .
CIRCULATION RESEARCH, 1988, 62 (06) :1259-1262
[10]   AUTOCRINE CONTROL OF ADIPOSE CELL-DIFFERENTIATION BY PROSTACYCLIN AND PGF2-ALPHA [J].
CATALIOTO, RM ;
GAILLARD, D ;
MACLOUF, J ;
AILHAUD, G ;
NEGREL, R .
BIOCHIMICA ET BIOPHYSICA ACTA, 1991, 1091 (03) :364-369