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@article{1588156,
author = {Svobodová, Jana and Procházková, Jiřina and Kabátková, Markéta and Krkoška, Martin and Šmerdová, Lenka and Líbalová, Helena and Topinka, Jan and Kléma, Jiří and Kozubík, Alois and Machala, Miroslav and Vondráček, Jan},
article_location = {OXFORD},
article_number = {2},
doi = {http://dx.doi.org/10.1093/toxsci/kfz202},
keywords = {aryl hydrocarbon receptor; HepaRG cells; cell proliferation; apoptosis; Hippo signaling},
language = {eng},
issn = {1096-6080},
journal = {TOXICOLOGICAL SCIENCES},
title = {2,3,7,8-Tetrachlorodibenzo-p-dioxin (TCDD) Disrupts Control of Cell Proliferation and Apoptosis in a Human Model of Adult Liver Progenitors.},
url = {http://dx.doi.org/10.1093/toxsci/kfz202},
volume = {172},
year = {2019}
}
TY - JOUR
ID - 1588156
AU - Svobodová, Jana - Procházková, Jiřina - Kabátková, Markéta - Krkoška, Martin - Šmerdová, Lenka - Líbalová, Helena - Topinka, Jan - Kléma, Jiří - Kozubík, Alois - Machala, Miroslav - Vondráček, Jan
PY - 2019
TI - 2,3,7,8-Tetrachlorodibenzo-p-dioxin (TCDD) Disrupts Control of Cell Proliferation and Apoptosis in a Human Model of Adult Liver Progenitors.
JF - TOXICOLOGICAL SCIENCES
VL - 172
IS - 2
SP - 368-384
EP - 368-384
PB - OXFORD UNIV PRESS
SN - 10966080
KW - aryl hydrocarbon receptor
KW - HepaRG cells
KW - cell proliferation
KW - apoptosis
KW - Hippo signaling
UR - http://dx.doi.org/10.1093/toxsci/kfz202
L2 - http://dx.doi.org/10.1093/toxsci/kfz202
N2 - The aryl hydrocarbon receptor (AhR) activation has been shown to alter proliferation, apoptosis, or differentiation of adult rat liver progenitors. Here, we investigated the impact of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD)-mediated AhR activation on a human model of bipotent liver progenitors, undifferentiated HepaRG cells. We used both intact undifferentiated HepaRG cells, and the cells with silenced Hippo pathway effectors, yes-associated protein 1 (YAP) and transcriptional coactivator with PDZ-binding motif (TAZ), which play key role(s) in tissue-specific progenitor cell self-renewal and expansion, such as in liver, cardiac, or respiratory progenitors. TCDD induced cell proliferation in confluent undifferentiated HepaRG cells; however, following YAP, and, in particular, double YAP/TAZ knockdown, TCDD promoted induction of apoptosis. These results suggested that, unlike in mature hepatocytes, or hepatocyte-like cells, activation of the AhR may sensitize undifferentiated HepaRG cells to apoptotic stimuli. Induction of apoptosis in cells with silenced YAP/TAZ was associated with upregulation of death ligand TRAIL, and seemed to involve both extrinsic and mitochondrial apoptosis pathways. Global gene expression analysis further suggested that TCDD significantly altered expression of constituents and/or transcriptional targets of signaling pathways participating in control of expansion or differentiation of liver progenitors, including EGFR, Wnt/beta-catenin, or tumor growth factor-beta signaling pathways. TCDD significantly upregulated cytosolic proapoptotic protein BMF (Bcl-2 modifying factor) in HepaRG cells, which could be linked with an enhanced sensitivity of TCDD-treated cells to apoptosis. Our results suggest that, in addition to promotion of cell proliferation and alteration of signaling pathways controlling expansion of human adult liver progenitors, AhR ligands may also sensitize human liver progenitor cells to apoptosis.
ER -
SVOBODOVÁ, Jana, Jiřina PROCHÁZKOVÁ, Markéta KABÁTKOVÁ, Martin KRKOŠKA, Lenka ŠMERDOVÁ, Helena LÍBALOVÁ, Jan TOPINKA, Jiří KLÉMA, Alois KOZUBÍK, Miroslav MACHALA and Jan VONDRÁČEK. 2,3,7,8-Tetrachlorodibenzo-p-dioxin (TCDD) Disrupts Control of Cell Proliferation and Apoptosis in a Human Model of Adult Liver Progenitors. \textit{TOXICOLOGICAL SCIENCES}. OXFORD: OXFORD UNIV PRESS, 2019, vol.~172, No~2, p.~368-384. ISSN~1096-6080. Available from: https://dx.doi.org/10.1093/toxsci/kfz202.
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