Chlorpyrifos and its metabolites alter gene expression at non-cytotoxic concentrations in D3 mouse embryonic stem cells under in vitro differentiation: Considerations for embryotoxic risk assessment |
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Authors: | Carmen Estevan Eugenio VilanovaMiguel A. Sogorb |
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Affiliation: | Instituto de Bioingeniería, Universidad Miguel Hernández de Elche, Spain |
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Abstract: | The effects of organophosphate insecticide chlorpyrifos (CPF) on development are currently under discussion. CPF and its metabolites, chlorpyrifos-oxon (CPO) and 3,5,6-trichloro-2-pyridinol (TClP), were more cytotoxic for D3 mouse embryonic stem cells than for differentiated fibroblasts 3T3 cells. Exposure to 10 μM CPF and TClP and 100 μM CPO for 12 h significantly altered the in vitro expression of biomarkers of differentiation in D3 cells. Similarly, exposure to 20 μM CPF and 25 μM CPO and TClP for 3 days also altered the expression of the biomarkers in the same model. These exposures caused no significant reduction in D3 viability with mild inhibition of acetylcholinesterase and neuropathy target esterase by CPF and severe inhibition by CPO. We conclude that certain in vivo exposure scenarios are possible, which cause inhibition of acetylcholinesterase but without clinical symptoms that reach high enough systemic CPF concentrations able to alter the expression of genes involved in cellular differentiation with potentially hazard effects on development. Conversely, the risk for embryotoxicity by CPO and TClP was very low because the required exposure would induce severe cholinergic syndrome. |
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Keywords: | Ache, acetylcholinesterase (gene) AChE, acetylcholinesterase (protein) Afp, α-fetoprotein CPF, chlorpyrifos (O,O-diethyl O-(3,5,6-trichloro-2-pyridinyl) phosphorothioate) CPO, chlorpyrifos-oxon (O,O-diethyl O-(3,5,6-trichloro-2-pyridinyl) phosphate) DEPC, diethylpyrocarbonate DMEM, Dulbecco's Modified Eagle's Medium ECx, concentration needed to cause a reduction in cell viability of X% EST, Embryonic Stem cell Test Flk1, foetal liver kinase 1 IC50, concentration needed to inhibit the enzymatic activity by 50% LIF, leukaemia inhibition factor Mhc, myosin heavy chain MTT, 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazoliumbromide Nanog, nanog homeobox Nefm, neurofilament medium polypeptide Nes, nestin NTE, neuropathy target esterase OP, organophosphorus compound PBS, phosphate buffered saline Pnpla6, patatin-like phospholipase domain containing 6 PV, phenyl valerate qRT-PCR, quantitative real-time PCR TClP, 3,5,6-trichloro-2-pyridinol TLV, Threshold Limit Value |
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