2016
Methoxychlor and Vinclozolin Induce Rapid Changes in Intercellular and Intracellular Signaling in Liver Progenitor Cells
BABICA, Pavel, Rimma ZURABIAN, Esha R. KUMAR, Rajus CHOPRA, Maxwell J. MIANECKI et. al.Základní údaje
Originální název
Methoxychlor and Vinclozolin Induce Rapid Changes in Intercellular and Intracellular Signaling in Liver Progenitor Cells
Autoři
BABICA, Pavel (203 Česká republika, garant, domácí), Rimma ZURABIAN (840 Spojené státy), Esha R. KUMAR (840 Spojené státy), Rajus CHOPRA (840 Spojené státy), Maxwell J. MIANECKI (840 Spojené státy), Joon-Suk PARK (410 Korejská republika), Libor JAŠA (203 Česká republika, domácí), James E. TROSKO (840 Spojené státy) a Brad L. UPHAM (840 Spojené státy)
Vydání
Toxicological sciences, OXFORD, OXFORD UNIV PRESS, 2016, 1096-6080
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
30304 Public and environmental health
Stát vydavatele
Velká Británie a Severní Irsko
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Impakt faktor
Impact factor: 4.081
Kód RIV
RIV/00216224:14310/16:00093526
Organizační jednotka
Přírodovědecká fakulta
UT WoS
000386475700016
Klíčová slova anglicky
gap junctional intercellular communication; endocrine disruptors; mitogen-activated protein kinases; phosphatidylcholine-specific phospholipase C; epigenetic toxicity; non-genomic signaling
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 2. 3. 2017 12:13, Mgr. Michaela Hylsová, Ph.D.
Anotace
V originále
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 A mu M for MXC and 126 A mu M 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.
Návaznosti
LM2015051, projekt VaV |
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LO1214, projekt VaV |
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