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Article
2 induce adipogenesis of NIH-3T3 cells with similar efficiency and kinetics
Departments of 1 Molecular Pharmacology and 2 Molecular Sciences, AstraZeneca Research and Development, Molndal; 3 Lund Strategic Research Center for Stem Cell Biology and Cell Therapy, Lund; and 4 Chalmers Technical University, Department of Mathematical Statistics, Goteborg, Sweden
ABSTRACT
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)
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
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
2 induce adipocyte differentiation with comparable kinetics and efficiency.
adipogenesis; early B cell factor; peroxisome proliferator-activated receptor-
2
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