Bisphenol A (BPA) and its analogues are chemicals used in the production of plastics and epoxy resins, but due to their toxic effects, their use is strictly regulated. They act as endocrine-disrupting chemicals, as they interfere with hormone function – particularly sex hormones – through which they cause various biological effects, including immunomodulatory ones. Because on their impact on sex hormones, we investigated whether there are differences in immune responses between genders following exposure to selected bisphenols.
We selected seven bisphenols for investigation: BPA, BPE, BPAF, BPAP, BPPH, TMBPF, and TCBPA. As an in vitro model, we used lymphoblastoid cell lines (LCLs) from healthy, unrelated donors – specifically, five female and five male LCLs.
First, we determined cytotoxicity of the selected compounds using the MTS assay and calculated the IC50 values. Based on the average IC50 values determined in ten LCL cell lines, the following IC50 values were obtained for the bispenols studied (from least to most cytotoxic): BPE (IC50 = 156,8 μM), TCBPA (IC50 = 124,7 μM), BPA (IC50 = 89,3 μM), BPAP (IC50 = 59,0 μM), BPAF (IC50 = 31,8 μM), BPPH (IC50 = 31,8 μM) and TMBPF (IC50 = 9,2 μM). Correlation analysis between IC₅₀ values and log P indicated that increased lipophilicity was associated with enhanced cytotoxic activity. A correlation analysis of IC50 values of bisphenols across ten tested LCLs revealed the highest correlation between BPAF and TCBPA. The average IC50 values were higher in LCLs derived from male donors compared to those from female donors.
Evaluation of the immunomodulatory properties of the selected bisphenols using cytokine release assays revealed that their effects were dose-dependent. The most pronounced immunomodulatory effects were observed for BPA, BPAF, TMBPF, and BPPH at higher, 10 μM concentration. The bisphenols caused a minor impact on cytokine secretion at 100 nM concentration. We observed sex-specific immunomodulatory effects of tested bisfenols, indicating that bisphenols may act more immunosuppressive in male cells.
In conclusion, bisphenols exhibited varying degrees of cytotoxicity and immunomodulatory activity, with effects depending on both the chemical structure of the compound and its concentration. We observed sex-specific trends in the response to bisphenols in LCL cells, indicating a potential role of sex in bisphenol-induced immunotoxicity.
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