2,3,7,8-Tetrachlorodibenzo-p-dioxin (TCDD) Disrupts Control of Cell Proliferation and Apoptosis in a Human Model of Adult Liver Progenitors
Language English Country United States Media print
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
31536130
DOI
10.1093/toxsci/kfz202
PII: 5571722
Knihovny.cz E-resources
- Keywords
- HepaRG cells, Hippo signaling, apoptosis, aryl hydrocarbon receptor, cell proliferation,
- MeSH
- Adaptor Proteins, Signal Transducing genetics MeSH
- Apoptosis drug effects genetics MeSH
- Models, Biological * MeSH
- Cell Line MeSH
- Gene Expression drug effects MeSH
- Liver drug effects pathology MeSH
- Stem Cells drug effects pathology MeSH
- Humans MeSH
- RNA, Small Interfering genetics MeSH
- Polychlorinated Dibenzodioxins toxicity MeSH
- Cell Proliferation drug effects genetics MeSH
- Receptors, Aryl Hydrocarbon metabolism MeSH
- YAP-Signaling Proteins MeSH
- Signal Transduction MeSH
- Trans-Activators genetics MeSH
- Transfection MeSH
- Transcription Factors genetics MeSH
- Transcriptional Coactivator with PDZ-Binding Motif Proteins MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Adaptor Proteins, Signal Transducing MeSH
- RNA, Small Interfering MeSH
- Polychlorinated Dibenzodioxins MeSH
- Receptors, Aryl Hydrocarbon MeSH
- YAP-Signaling Proteins MeSH
- Trans-Activators MeSH
- Transcription Factors MeSH
- Transcriptional Coactivator with PDZ-Binding Motif Proteins MeSH
- WWTR1 protein, human MeSH Browser
- YAP1 protein, human MeSH Browser
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/β-catenin, or tumor growth factor-β 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.
Department of Chemistry and Toxicology Veterinary Research Institute Brno 62100 Czech Republic
Department of Computer Science Czech Technical University Prague 12135 Czech Republic
Department of Experimental Biology Faculty of Science Masaryk University Brno 61137 Czech Republic
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