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The plasticizer BBP selectively inhibits epigenetic regulator sirtuins.
- Source :
-
Toxicology [Toxicology] 2015 Dec 02; Vol. 338, pp. 130-41. Date of Electronic Publication: 2015 Oct 28. - Publication Year :
- 2015
-
Abstract
- The plasticizer benzyl butyl phthalate (BBP) is a well-known endocrine disruptor. Widespread human exposure to phthalates has raised substantial public concern due to its detrimental health effects. However, molecular mechanisms of the phthalates effect require elucidation. In this study, we analyzed: 1) the binding interaction of several phthalates and persistent organic pollutants with epigenetic regulator sirtuins and 2) the effect of BBP on the sirtuins in HepG2 cells. AutoDock molecular docking analysis showed that BBP binds to Sirt1 and Sirt3 proteins similarly to the native ligands with shortest binding free energies (ΔGb) of -7.35 and -8.3 kcal/mol, respectively; and inhibition constants (Ki) of 4.07 μM and 0.82 μM, respectively. Furthermore, BBP was superimposed onto the co-crystallized ligands within the least root-mean-square deviation (RMSD) of 0.96Å and 1.55Å for Sirt1 and Sirt3, respectively, and bound into the sites with a sufficient number of hydrogen bonds, implying the best fit compared to other sirtuins. In HepG2 cells, BBP significantly down-regulated Sirt1 and Sirt3 (p<0.05) gene expression at a concentration as low as 10nM; other sirtuins remained unaffected. Consistent with decreased gene expression, Sirt1 and Sirt3 protein levels were significantly decreased at 48 h (p<0.05). In addition, mitochondrial biogenesis regulators PGC-1α, NRF-1, and NRF-2, were decreased (p<0.05). SiRNA studies showed that BBP did not regulate PGC-1α via sirtuin and BBP requires sirtuin's presence to regulate NRF-1 or NRF-2. BBP significantly increased ROS production (p<0.05) and ROS may be chiefly regulated by NRF-1 and NRF-2 in HepG2 cells under Sirt1 and Sirt3 silenced condition. This is the first report to demonstrate that BBP selectively disrupts specific sirtuins in HepG2 cells. In conclusion, our study suggests that BBP can impair two vital epigenetic regulators and mitochondrial biogenesis regulators in liver cells.<br /> (Published by Elsevier Ireland Ltd.)
- Subjects :
- Binding Sites
Crystallography
Dose-Response Relationship, Drug
Endocrine Disruptors metabolism
Gene Expression Regulation
Hep G2 Cells
Hepatocytes enzymology
Hepatocytes pathology
Histone Deacetylase Inhibitors metabolism
Humans
Hydrogen Bonding
Ligands
Mitochondria, Liver drug effects
Mitochondria, Liver enzymology
Mitochondria, Liver pathology
Molecular Docking Simulation
NF-E2-Related Factor 2 genetics
NF-E2-Related Factor 2 metabolism
Nuclear Respiratory Factor 1 genetics
Nuclear Respiratory Factor 1 metabolism
Organelle Biogenesis
Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha
Phthalic Acids metabolism
Plasticizers metabolism
Protein Binding
Protein Conformation
RNA Interference
Reactive Oxygen Species metabolism
Sirtuin 1 genetics
Sirtuin 1 metabolism
Sirtuin 3 genetics
Sirtuin 3 metabolism
Transcription Factors genetics
Transcription Factors metabolism
Transfection
Endocrine Disruptors toxicity
Epigenesis, Genetic drug effects
Hepatocytes drug effects
Histone Deacetylase Inhibitors toxicity
Phthalic Acids toxicity
Plasticizers toxicity
Sirtuin 1 antagonists & inhibitors
Sirtuin 3 antagonists & inhibitors
Subjects
Details
- Language :
- English
- ISSN :
- 1879-3185
- Volume :
- 338
- Database :
- MEDLINE
- Journal :
- Toxicology
- Publication Type :
- Academic Journal
- Accession number :
- 26520405
- Full Text :
- https://doi.org/10.1016/j.tox.2015.10.004