Gene expression profile of adipocyte differentiation and its regulation by peroxisome proliferator-activated receptor-γ agonists

被引:158
作者
Gerhold, DL
Liu, F
Jiang, G
Li, Z
Xu, J
Lu, M
Sachs, JR
Bagchi, A
Fridman, A
Holder, DJ
Doebber, TW
Berger, J
Elbrecht, A
Moller, DE
Zhang, BB
机构
[1] Merck Res Labs, Dept Mol Endocrinol, Rahway, NJ 07065 USA
[2] Merck Res Labs, Dept Pharmacol, Rahway, NJ 07065 USA
[3] Merck Res Labs, Dept Comp Sci & Appl Math, Rahway, NJ 07065 USA
[4] Merck Res Labs, Dept Biometr Res, Rahway, NJ 07065 USA
[5] Merck Res Labs, Dept Biometr Res, West Point, PA USA
关键词
D O I
10.1210/en.143.6.2106
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
PPARgamma is an adipocyte-specific nuclear hormone receptor. Agonists of PPARgamma, such as thiazolidinediones (TZDs), promote adipocyte differentiation and have insulin-sensitizing effects in animals and diabetic patients. Affymetrix oligonucleotide arrays representing 6347 genes were employed to profile the gene expression responses of mature 3T3-L1 adipocytes and differentiating preadipocytes to a TZD PPARgamma agonist in vitro. The expression of 579 genes was significantly up- or down-regulated by more than 1.5-fold during differentiation and/or by treatment with TZD, and these genes were organized into 32 clusters that demonstrated concerted changes in expression of genes controlling cell growth or lipid metabolism. Quantitative PCR was employed to further characterize gene expression and led to the identification of beta-catenin as a new PPARgamma target gene. Both mRNA and protein levels for beta-catenin were down-regulated in 3T3-L1 adipocytes compared with fibroblasts and were further decreased by treatment of adipocytes with PPARgamma agonists. Treatment of db/db mice with a PPARgamma agonist also resulted in reduction of beta-catenin mRNA levels in adipose tissue. These results suggest that beta-catenin plays an important role in the regulation of adipogenesis. Thus, the transcriptional patterns revealed in this study further the understanding of adipogenesis process and the function of PPARgamma activation.
引用
收藏
页码:2106 / 2118
页数:13
相关论文
共 64 条
[41]   Negative regulation of β enolase gene transcription in embryonic muscle is dependent upon a zinc finger factor that binds to the G-rich box within the muscle-specific enhancer [J].
Passantino, R ;
Antona, V ;
Barbieri, G ;
Rubino, P ;
Melchionna, R ;
Cossu, G ;
Feo, S ;
Giallongo, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (01) :484-494
[43]   PPARγ is required for the differentiation of adipose tissue in vivo and in vitro [J].
Rosen, ED ;
Sarraf, P ;
Troy, AE ;
Bradwin, G ;
Moore, K ;
Milstone, DS ;
Spiegelman, BM ;
Mortensen, RM .
MOLECULAR CELL, 1999, 4 (04) :611-617
[44]   The short- and long-term effects of tumor necrosis factor-α and BRL 49653 on peroxisome proliferator-activated receptor (PPAR)γ2 gene expression and other adipocyte genes [J].
Rosenbaum, SE ;
Greenberg, AS .
MOLECULAR ENDOCRINOLOGY, 1998, 12 (08) :1150-1160
[45]   Inhibition of adipogenesis by Wnt signaling [J].
Ross, SE ;
Hemati, N ;
Longo, KA ;
Bennett, CN ;
Lucas, PC ;
Erickson, RL ;
MacDougald, OA .
SCIENCE, 2000, 289 (5481) :950-953
[46]  
RYSECK RP, 1991, CELL GROWTH DIFFER, V2, P225
[47]  
Sakanaka C, 2000, RECENT PROG HORM RES, V55, P225
[48]   ANGIOTENSINOGEN GENE-EXPRESSION IN 3T3-L1 CELLS [J].
SAYE, JA ;
CASSIS, LA ;
STURGILL, TW ;
LYNCH, KR ;
PEACH, MJ .
AMERICAN JOURNAL OF PHYSIOLOGY, 1989, 256 (02) :C448-C451
[49]   A NOVEL SERUM-PROTEIN SIMILAR TO C1Q, PRODUCED EXCLUSIVELY IN ADIPOCYTES [J].
SCHERER, PE ;
WILLIAMS, S ;
FOGLIANO, M ;
BALDINI, G ;
LODISH, HF .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (45) :26746-26749
[50]   Biochemical interactions in the wnt pathway [J].
Seidensticker, MJ ;
Behrens, J .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 2000, 1495 (02) :168-182