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The Mixture of Bisphenol-A and Its Substitutes Bisphenol-S and Bisphenol-F Exerts Obesogenic Activity on Human Adipose-Derived Stem Cells.
Reina-Pérez, Iris; Olivas-Martínez, Alicia; Mustieles, Vicente; Salamanca-Fernández, Elena; Molina-Molina, José Manuel; Olea, Nicolás; Fernández, Mariana F.
Affiliation
  • Reina-Pérez I; Centre for Biomedical Research & School of Medicine, Radiology and Physical Medicine Department, University of Granada, 18011 Granada, Spain.
  • Olivas-Martínez A; Instituto de Investigación Biosanitaria (ibs.GRANADA), 18012 Granada, Spain.
  • Mustieles V; Centre for Biomedical Research & School of Medicine, Radiology and Physical Medicine Department, University of Granada, 18011 Granada, Spain.
  • Salamanca-Fernández E; Instituto de Investigación Biosanitaria (ibs.GRANADA), 18012 Granada, Spain.
  • Molina-Molina JM; Centre for Biomedical Research & School of Medicine, Radiology and Physical Medicine Department, University of Granada, 18011 Granada, Spain.
  • Olea N; Instituto de Investigación Biosanitaria (ibs.GRANADA), 18012 Granada, Spain.
  • Fernández MF; CIBER de Epidemiología y Salud Pública (CIBERESP), 28029 Madrid, Spain.
Toxics ; 10(6)2022 May 27.
Article in En | MEDLINE | ID: mdl-35736896
ABSTRACT
Bisphenol A (BPA) and its substitutes, bisphenol F (BPF) and S (BPS), have previously shown in vitro obesogenic activity. This study was designed to investigate their combined effect on the adipogenic differentiation of human adipose-derived stem cells (hASCs). Cells were exposed for 14 days to an equimolar mixture of bisphenols (MIX) (range 10 nM-10 µM). Oil Red staining was used to measure intracellular lipid accumulation, quantitative real-time polymerase chain reaction (qRT-PCR) to study gene expression of adipogenic markers (PPARγ, C/EBPα, LPL, and FABP4), and Western Blot to determine their corresponding proteins. The MIX promoted intracellular lipid accumulation in a dose-dependent manner with a maximal response at 10 µM. Co-incubation with pure antiestrogen (ICI 182,780) inhibited lipid accumulation, suggesting that the effect was mediated by the estrogen receptor. The MIX also significantly altered the expression of PPARγ, C/EBPα, LPL, and FABP4 markers, observing a non-monotonic (U-shaped) dose-response, with maximal gene expression at 10 nM and 10 µM and lesser expression at 1 µM. This pattern was not observed when bisphenols were tested individually. Exposure to MIX (1-10 µM) also increased all encoded proteins except for FABP4, which showed no changes. Evaluation of the combined effect of relevant chemical mixtures is needed rather than single chemical testing.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Toxics Year: 2022 Document type: Article Affiliation country: Spain

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Toxics Year: 2022 Document type: Article Affiliation country: Spain