2,3,7,8-Tetrachlorodibenzo-p-dioxin (TCDD) Disrupts Control of Cell Proliferation and Apoptosis in a Human Model of Adult Liver Progenitors
Jazyk angličtina Země Spojené státy americké Médium print
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
31536130
DOI
10.1093/toxsci/kfz202
PII: 5571722
Knihovny.cz E-zdroje
- Klíčová slova
- HepaRG cells, Hippo signaling, apoptosis, aryl hydrocarbon receptor, cell proliferation,
- MeSH
- adaptorové proteiny signální transdukční genetika MeSH
- apoptóza účinky léků genetika MeSH
- biologické modely * MeSH
- buněčné linie MeSH
- exprese genu účinky léků MeSH
- játra účinky léků patologie MeSH
- kmenové buňky účinky léků patologie MeSH
- lidé MeSH
- malá interferující RNA genetika MeSH
- polychlorované dibenzodioxiny toxicita MeSH
- proliferace buněk účinky léků genetika MeSH
- receptory aromatických uhlovodíků metabolismus MeSH
- signální proteiny YAP MeSH
- signální transdukce MeSH
- trans-aktivátory genetika MeSH
- transfekce MeSH
- transkripční faktory genetika MeSH
- transkripční koaktivátor s motivem vázajícím se na PDZ MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- adaptorové proteiny signální transdukční MeSH
- malá interferující RNA MeSH
- polychlorované dibenzodioxiny MeSH
- receptory aromatických uhlovodíků MeSH
- signální proteiny YAP MeSH
- trans-aktivátory MeSH
- transkripční faktory MeSH
- transkripční koaktivátor s motivem vázajícím se na PDZ MeSH
- WWTR1 protein, human MeSH Prohlížeč
- YAP1 protein, human MeSH Prohlížeč
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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