AI Article Synopsis

  • Bisphenol A (BPA) and its substitutes, BPF and BPS, demonstrated in vitro effects that promote fat cell development when tested on human stem cells, particularly through a mixture (MIX) of these chemicals.
  • The MIX led to increased lipid accumulation in a dose-dependent manner, with the strongest effect at 10 µM, while the use of an antiestrogen indicated that estrogen receptors played a key role in this process.
  • The study found that the combined bisphenols altered the expression of important adipogenic markers in a non-linear fashion, suggesting that evaluating the effects of chemical mixtures is critical for understanding their impacts compared to testing individual substances.

Article 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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9229358PMC
http://dx.doi.org/10.3390/toxics10060287DOI Listing

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