Methoxychlor and Vinclozolin Induce Rapid Changes in Intercellular and Intracellular Signaling in Liver Progenitor Cells
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem, Research Support, N.I.H., Extramural
Grantová podpora
R01 ES013268
NIEHS NIH HHS - United States
PubMed
27413106
PubMed Central
PMC5013879
DOI
10.1093/toxsci/kfw114
PII: kfw114
Knihovny.cz E-zdroje
- Klíčová slova
- endocrine disruptors, epigenetic toxicity, gap junctional intercellular communication, mitogen-activated protein kinases, non-genomic signaling., phosphatidylcholine-specific phospholipase C,
- MeSH
- androgenní receptory metabolismus MeSH
- buněčné linie MeSH
- insekticidy toxicita MeSH
- játra cytologie účinky léků metabolismus MeSH
- kmenové buňky účinky léků metabolismus MeSH
- konexin 43 metabolismus MeSH
- krysa rodu Rattus MeSH
- MAP kinasový signální systém účinky léků MeSH
- methoxychlor toxicita MeSH
- mezerový spoj účinky léků MeSH
- mezibuněčná komunikace účinky léků MeSH
- mitogenem aktivované proteinkinasy p38 metabolismus MeSH
- oxazoly toxicita MeSH
- potkani inbrední F344 MeSH
- receptory pro estrogeny metabolismus MeSH
- signální transdukce účinky léků MeSH
- zvířata MeSH
- Check Tag
- krysa rodu Rattus MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Research Support, N.I.H., Extramural MeSH
- Názvy látek
- androgenní receptory MeSH
- insekticidy MeSH
- konexin 43 MeSH
- methoxychlor MeSH
- mitogenem aktivované proteinkinasy p38 MeSH
- oxazoly MeSH
- receptory pro estrogeny MeSH
- vinclozolin MeSH Prohlížeč
Methoxychlor (MXC) and vinclozolin (VIN) are well-recognized endocrine disrupting chemicals known to alter epigenetic regulations and transgenerational inheritance; however, non-endocrine disruption endpoints are also important. Thus, we determined the effects of MXC and VIN on the dysregulation of gap junctional intercellular communication (GJIC) and activation of mitogen-activated protein kinases (MAPKs) in WB-F344 rat liver epithelial cells. Both chemicals induced a rapid dysregulation of GJIC at non-cytotoxic doses, with 30 min EC50 values for GJIC inhibition being 10 µM for MXC and 126 µM for VIN. MXC inhibited GJIC for at least 24 h, while VIN effects were transient and GJIC recovered after 4 h. VIN induced rapid hyperphosphorylation and internalization of gap junction protein connexin43, and both chemicals also activated MAPK ERK1/2 and p38. Effects on GJIC were not prevented by MEK1/2 inhibitor, but by an inhibitor of phosphatidylcholine-specific phospholipase C (PC-PLC), resveratrol, and in the case of VIN, also, by a p38 inhibitor. Estrogen (ER) and androgen receptor (AR) modulators (estradiol, ICI 182,780, HPTE, testosterone, flutamide, VIN M2) did not attenuate MXC or VIN effects on GJIC. Our data also indicate that the effects were elicited by the parental compounds of MXC and VIN. Our study provides new evidence that MXC and VIN dysregulate GJIC via mechanisms involving rapid activation of PC-PLC occurring independently of ER- or AR-dependent genomic signaling. Such alterations of rapid intercellular and intracellular signaling events involved in regulations of gene expression, tissue development, function and homeostasis, could also contribute to transgenerational epigenetic effects of endocrine disruptors.
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Applicability of Scrape Loading-Dye Transfer Assay for Non-Genotoxic Carcinogen Testing