Assessment and Comparison of Early Developmental Toxicity of Six Per- and Polyfluoroalkyl Substances with Human Embryonic Stem Cell Models.
Miaomiao ZhaoNuoya YinRenjun YangShichang LiShuxian ZhangFrancesco FaiolaPublished in: Environmental science & technology (2024)
Per- and polyfluoroalkyl substances (PFAS) are extensively utilized in varieties of products and tend to accumulate in the human body including umbilical cord blood and embryos/fetuses. In this study, we conducted an assessment and comparison of the potential early developmental toxicity of perfluorooctanoic acid (PFOA), undecafluorohexanoic acid (PFHxA), heptafluorobutyric acid, perfluorooctanesulfonate (PFOS), perfluorohexanesulfonate, and perfluorobutyric acid at noncytotoxic concentrations relevant to human exposure using models based on human embryonic stem cells in both three-dimensional embryoid body (EB) and monolayer differentiation configurations. All six compounds influenced the determination of cell fate by disrupting the expression of associated markers in both models and, in some instances, even led to alterations in the formation of cystic EBs. The expression of cilia-related gene IFT122 was significantly inhibited. Additionally, PFOS and PFOA inhibited ciliogenesis, while PFOA specifically reduced the cilia length. Transcriptome analysis revealed that PFOS altered 1054 genes and disrupted crucial signaling pathways such as WNT and TGF-β, which play integral roles in cilia transduction and are critical for early embryonic development. These results provide precise and comprehensive insights into the potential adverse health effects of these six PFAS compounds directly concerning early human embryonic development.
Keyphrases
- endothelial cells
- stem cells
- induced pluripotent stem cells
- pluripotent stem cells
- poor prognosis
- umbilical cord
- mesenchymal stem cells
- oxidative stress
- emergency department
- public health
- mental health
- signaling pathway
- genome wide
- high resolution
- drinking water
- multidrug resistant
- single cell
- bone marrow
- transforming growth factor
- long non coding rna
- human health
- solid phase extraction
- simultaneous determination
- tandem mass spectrometry
- genome wide analysis