Gene expression analysis suggests that EBF-1 and PPARγ2 induce adipogenesis of NIH-3T3 cells with similar efficiency and kinetics

被引:47
作者
Åkerblad, P [1 ]
Månsson, R
Lagergren, A
Westerlund, S
Basta, B
Lind, U
Thelin, A
Gisler, R
Liberg, D
Nelander, S
Bamberg, K
Sigvardsson, M
机构
[1] AstraZeneca R&D Molndal, Dept Mol Pharmacol, S-43183 Molndal, Sweden
[2] AstraZeneca R&D Molndal, Dept Mol Sci, Molndal, Sweden
[3] Chalmers Univ Technol, Dept Math Stat, Gothenburg, Sweden
[4] Lund Strateg Res Ctr Stem Cell Biol & Cell Therap, Lund, Sweden
关键词
adipogenesis; early B cell factor; peroxisome proliferator-activated receptor-gamma 2;
D O I
10.1152/physiolgenomics.00015.2005
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Differentiation of multipotent mesenchymal stem cells into lipid-accumulating adipocytes is a physiological process induced by transcription factors in combination with hormonal stimulation. We have used Affymetrix microarrays to compare the adipogenic differentiation pathways of NIH-3T3 fibroblasts induced to undergo in vitro differentiation by ectopic expression of early B cell factor (EBF)-1 or peroxisome proliferator-activated receptor (PPAR)gamma 2. These experiments revealed that commitment to the adipogenic pathway in the NIH-3T3 cells was not reflected in gene expression until 4 days after induction of differentiation. Furthermore, gene expression patterns at the earlier time points after stimulation indicated that EBF-1 and PPAR gamma 2 induced different sets of genes, while the similarities increased upon differentiation, and that several genes linked to adipocyte differentiation were also transiently induced in the vector-transduced cells. These data suggest that the initial activation of genes associated with adipocyte development is independent of commitment to the adipogenic pathway and that EBF-1 and PPAR gamma 2 induce adipocyte differentiation with comparable kinetics and efficiency.
引用
收藏
页码:206 / 216
页数:11
相关论文
共 28 条
[1]   Early B-cell factor (O/E-1) is a promoter of adipogenesis and involved in control of genes important for terminal adipocyte differentiation [J].
Åkerblad, P ;
Lind, U ;
Liberg, D ;
Bamberg, K ;
Sigvardsson, M .
MOLECULAR AND CELLULAR BIOLOGY, 2002, 22 (22) :8015-8025
[2]   REGULATED EXPRESSION OF 3 C/EBP ISOFORMS DURING ADIPOSE CONVERSION OF 3T3-L1 CELLS [J].
CAO, ZD ;
UMEK, RM ;
MCKNIGHT, SL .
GENES & DEVELOPMENT, 1991, 5 (09) :1538-1552
[3]   Molecular regulation of adipocyte differentiation [J].
Cowherd, RM ;
Lyle, RE ;
McGehee, RE .
SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY, 1999, 10 (01) :3-10
[4]   Olf-1/Early B cell factor is a regulator of glut4 gene expression in 3T3-L1 adipocytes [J].
Dowell, P ;
Cooke, DW .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (03) :1712-1718
[5]  
Elberg G, 2000, J BIOL CHEM, V275, P27815
[6]   The organization, promoter analysis, and expression of the human PPAR gamma gene [J].
Fajas, L ;
Auboeuf, D ;
Raspe, E ;
Schoonjans, K ;
Lefebvre, AM ;
Saladin, R ;
Najib, J ;
Laville, M ;
Fruchart, JC ;
Deeb, S ;
VidalPuig, A ;
Flier, J ;
Briggs, MR ;
Staels, B ;
Vidal, H ;
Auwerx, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (30) :18779-18789
[7]   CLONING AND FUNCTIONAL-CHARACTERIZATION OF EARLY B-CELL FACTOR, A REGULATOR OF LYMPHOCYTE-SPECIFIC GENE-EXPRESSION [J].
HAGMAN, J ;
BELANGER, C ;
TRAVIS, A ;
TURCK, CW ;
GROSSCHEDL, R .
GENES & DEVELOPMENT, 1993, 7 (05) :760-773
[8]   ADD1/SREBP1 promotes adipocyte differentiation and gene expression linked to fatty acid metabolism [J].
Kim, JB ;
Spiegelman, BM .
GENES & DEVELOPMENT, 1996, 10 (09) :1096-1107
[9]   Model-based analysis of oligonucleotide arrays: Expression index computation and outlier detection [J].
Li, C ;
Wong, WH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (01) :31-36
[10]   CCAAT/ENHANCER BINDING-PROTEIN-ALPHA IS SUFFICIENT TO INITIATE THE 3T3-L1 ADIPOCYTE DIFFERENTIATION PROGRAM [J].
LIN, FT ;
LANE, MD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (19) :8757-8761