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- Title
Identification of mechanisms of action of bisphenol a-induced human preadipocyte differentiation by transcriptional profiling.
- Authors
Boucher, Jonathan G.; Husain, Mainul; Rowan‐Carroll, Andrea; Williams, Andrew; Yauk, Carole L.; Atlas, Ella
- Abstract
Objective Exposure to the endocrine-disrupting chemical bisphenol A (BPA) is correlated with obesity and adipogenesis of human preadipocytes. However, the mechanism of action of BPA-induced human adipogenesis remains to be determined. Methods Primary human preadipocytes were differentiated in the presence of 50 µM BPA or 1 µM dexamethasone (DEX) for 48 hours. Potential mechanisms of BPA-induced adipogenesis were evaluated using gene expression microarray analysis. Results Microarray analysis revealed 373 differentially expressed genes following BPA treatment, including upregulation of sterol regulatory element binding factor 1 ( SREBF1), a key regulator of lipid metabolism. For DEX-treated preadipocytes, 2167 genes were differentially expressed, including upregulation of the adipogenic marker lipoprotein lipase. Ingenuity Pathway Analysis was used to identify functional annotations of the gene expression changes associated with response to BPA and DEX. BPA exposure was associated with expression changes in the genes involved in triacylglycerol accumulation while DEX was linked to triacylglycerol and fatty acid metabolism. The analysis also revealed enrichment of genes following BPA exposure in the thyroid-receptor/retinoic X receptor (TR/RXR) and mammalian target of rapamycin (mTOR) signaling pathways. Conclusions Our data suggest that potential mechanisms of action of BPA-induced adipogenesis involve SREBF1, the TR/RXR, and the mTOR pathways.
- Subjects
BISPHENOL A; OBESITY; ADIPOGENESIS; DEXAMETHASONE; GENE expression
- Publication
Obesity (19307381), 2014, Vol 22, Issue 11, p2333
- ISSN
1930-7381
- Publication type
Article
- DOI
10.1002/oby.20848