Targets for pollutants in rat and human pancreatic beta-cells: The effect of prolonged exposure to sub-lethal concentrations of hexachlorocyclohexane isomers on the expression of function- and survival-related proteins
Language English Country Netherlands Media print-electronic
Document type Journal Article
PubMed
37865351
DOI
10.1016/j.etap.2023.104299
PII: S1382-6689(23)00241-7
Knihovny.cz E-resources
- Keywords
- ATP citrate lyase, Beta-cells, Diabetes, Hexachlorocyclohexane, Insulin, Perilipin-2,
- MeSH
- Hexachlorocyclohexane * toxicity metabolism MeSH
- Isomerism MeSH
- Rats MeSH
- Environmental Pollutants * toxicity MeSH
- Humans MeSH
- Animals MeSH
- Check Tag
- Rats MeSH
- Humans MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- alpha-hexachlorocyclohexane MeSH Browser
- beta-hexachlorocyclohexane MeSH Browser
- Hexachlorocyclohexane * MeSH
- Environmental Pollutants * MeSH
Decades after most countries banned hexachlorocyclohexane, HCH isomers still pollute the environment. Many studies described HCH as a pro-diabetic factor; nevertheless, the effect of HCH isomers on pancreatic beta-cells remains unexplored. This study investigated the effects of a one-month exposure to α-HCH, β-HCH, and γ-HCH on protein expression in human (NES2Y) and rat (INS1E) pancreatic beta-cell lines. α-HCH and γ-HCH increased proinsulin and insulin levels in INS1E cells, while β-HCH showed the opposite trend. α-HCH altered the expression of PKA, ATF3, and PLIN2. β-HCH affected the expression of GLUT1, GLUT2, PKA, ATF3, p-eIF2α, ATP-CL, and PLIN2. γ-HCH altered the expression of PKA, ATF3, PLIN2, PLIN5, and IDH1. From the tested proteins, PKA, ATF3, and PLIN-2 were the most sensitive to HCH exposure and have the potential to be used as biomarkers.
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