Molecular differences caused by differentiation of 3T3-L1 preadipocytes in the presence of either dehydroepiandrosterone (DHEA) or 7-oxo-DHEA

被引:29
作者
Gomez, FE
Miyazaki, M
Kim, YC
Marwah, P
Lardy, HA [1 ]
Ntambi, JM
Fox, BG
机构
[1] Univ Wisconsin, Coll Agr & Life Sci, Dept Biochem, Madison, WI 53706 USA
[2] Univ Wisconsin, Coll Agr & Life Sci, Dept Nutr Sci, Madison, WI 53706 USA
关键词
D O I
10.1021/bi012177r
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
The effects of dehydroepiandrosterone (DHEA) and 7-oxo-DHEA on the cell size, adiposity, and fatty acid composition of differentiating 3T3-L1 preadipocyte cells are correlated with stearoyl-CoA desaturase (SCD) expression (mRNA and protein levels) and enzyme activity. Fluorescence-activated cell sorting shows that preadipocyte cells treated with methylisobutylxanthine, dexamethasone, and insulin (MDT) plus DHEA comprise a population distribution of predominantly large cells with reduced adiposity. In contrast, cells treated with MDT plus 7-oxo-DHEA comprise a population distribution of almost equal proportions of small and large cells that have an adiposity equivalent to cells differentiated with MDT alone. The cells treated with MDT plus DHEA have significantly reduced levels of total fatty acid, mainly due to a dramatic reduction in the level of palmitoleic (Delta(9)-16:1) acid. The cells treated with MDT plus 7-oxo-DHEA have a significantly increased level of total fat, primarily due to increased levels of Delta(9)-16:1 and palmitic (16:0) acids. At the molecular level, the DHEA-treated cells contain lowered amounts of SCD1 mRNA and antibody-detectable desaturase protein, while 7-oxo-DHEA-treated cells contained elevated levels of SCD1 mRNA and protein. Inhibition of differentiation in DHEA-treated cells was also suggested by a reduction in the mRNA level of the adipogenic gene aP2. At the level of microsomal enzymatic activity, SCD activity was decreased in DHEA-treated cells while the SCD activity was increased in 7-oxo-DHEA-treated cells. The changes in mRNA levels and enzyme activity were concentration-dependent and appeared as early as day 3 of the differentiation protocol. The results show that DHEA and 7-oxo-DHEA have distinct modes of action with respect to the complex transcriptional cascade required for differentiation. Furthermore, differences in the insulin-stimulated uptake of 2-deoxyglucose and in the activity of carnitine palmitoyl transferase observed from either DHEA- or 7-oxo-DHEA-treated cells support the ability of DHEA to produce a thermogenic effect in differentiating preadipocytes, while 7-oxo-DHEA promotes differentiation without other changes typical of thermogenesis.
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页码:5473 / 5482
页数:10
相关论文
共 65 条
[1]   Thiazolidinediones but not metformin directly inhibit the steroidogenic enzymes P450c17 and 3β-hydroxysteroid dehydrogenase [J].
Arlt, W ;
Auchus, RJ ;
Miller, WL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (20) :16767-16771
[2]   Dehydroepiandrosterone (DHEA), DHEA sulfate, and aging:: Contribution of the DHEAge Study to a sociobiomedical issue [J].
Baulieu, EE ;
Thomas, G ;
Legrain, S ;
Lahlou, N ;
Roger, M ;
Debuire, B ;
Faucounau, V ;
Girard, L ;
Hervy, MP ;
Latour, F ;
Leaud, MC ;
Mokrane, A ;
Pitti-Ferrandi, H ;
Trivalle, C ;
de Lacharrière, O ;
Nouveau, S ;
Rakoto-Arison, B ;
Souberbielle, JC ;
Raison, J ;
Le Bouc, Y ;
Raynaud, A ;
Girerd, X ;
Forette, F .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (08) :4279-4284
[3]   Cloning and characterization of the human stearoyl-CoA desaturase gene promoter:: Transcriptional activation by sterol regulatory element binding protein and repression by polyunsaturated fatty acids and cholesterol [J].
Bené, H ;
Lasky, D ;
Ntambi, JM .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2001, 284 (05) :1194-1198
[4]  
BERNLOHR DA, 1985, J BIOL CHEM, V260, P5563
[5]   RAPID SPECTROPHOTOMETRIC ASSAY FOR CARNITINE PALMITOYLTRANSFERASE [J].
BIEBER, LL ;
ABRAHAM, T ;
HELMRATH, T .
ANALYTICAL BIOCHEMISTRY, 1972, 50 (02) :509-&
[6]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[7]   Immunological properties of dehydroepiandrosterone, its conjugates, and metabolites [J].
Bradlow, HL ;
Murphy, J ;
Byrne, JJ .
NEUROENDOCRINE IMMUNE BASIS OF THE RHEUMATIC DISEASES, 1999, 876 :91-101
[8]   PPAR gamma and the molecular control of adipogenesis [J].
Brun, RP ;
Spiegelman, BM .
JOURNAL OF ENDOCRINOLOGY, 1997, 155 (02) :217-218
[9]   THE EFFECT OF DEHYDROEPIANDROSTERONE ON LIVER METABOLITES [J].
CASAZZA, JP ;
SCHAFFER, WT ;
VEECH, RL .
JOURNAL OF NUTRITION, 1986, 116 (02) :304-310
[10]  
Davidson M, 2000, CLIN INVEST MED, V23, P300