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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

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Author
Pavlíková, NelaORCiD Profile - 0000-0001-7468-1505WoS Profile - W-7000-2018Scopus Profile - 35491148000
Šrámek, JanORCiD Profile - 0000-0003-0218-7238WoS Profile - W-7092-2018Scopus Profile - 55613662100
Jaček, MartinORCiD Profile - 0000-0001-9988-9281WoS Profile - S-2805-2016Scopus Profile - 16417317600
Kovář, JanORCiD Profile - 0000-0001-9432-8960WoS Profile - Y-7480-2018Scopus Profile - 55614006600
Němcová, VlastaORCiD Profile - 0000-0002-2296-3540WoS Profile - V-5924-2017Scopus Profile - 35218108300

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Publication date
2023
Published in
Environmental Toxicology and Pharmacology
Volume / Issue
104 (November)
ISBN / ISSN
ISSN: 1382-6689
ISBN / ISSN
eISSN: 1872-7077
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  • 3. Faculty of Medicine

This publication has a published version with DOI 10.1016/j.etap.2023.104299

Abstract
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.
Keywords
ATP citrate lyase, Beta-cells, Diabetes, Hexachlorocyclohexane, Insulin, Perilipin-2
Permanent link
https://hdl.handle.net/20.500.14178/2155
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WOS:001098194700001
SCOPUS:2-s2.0-85174464085
PUBMED:37865351
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Full text of this result is licensed under: Creative Commons Uveďte původ 4.0 International

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