-
Something wrong with this record ?
2,3,7,8-Tetrachlorodibenzo-p-dioxin (TCDD) Disrupts Control of Cell Proliferation and Apoptosis in a Human Model of Adult Liver Progenitors
J. Svobodová, J. Procházková, M. Kabátková, M. Krkoška, L. Šmerdová, H. Líbalová, J. Topinka, J. Kléma, A. Kozubík, M. Machala, J. Vondráček,
Language English Country United States
Document type Journal Article, Research Support, Non-U.S. Gov't
NLK
Free Medical Journals
from 1996 to 1 year ago
Open Access Digital Library
from 1996-01-01
Medline Complete (EBSCOhost)
from 1998-01-01 to 1 year ago
PubMed
31536130
DOI
10.1093/toxsci/kfz202
Knihovny.cz E-resources
- 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
- Signal Transduction MeSH
- Trans-Activators genetics MeSH
- Transfection MeSH
- Transcription Factors genetics MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
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
References provided by Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc20025469
- 003
- CZ-PrNML
- 005
- 20201222155219.0
- 007
- ta
- 008
- 201125s2019 xxu f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1093/toxsci/kfz202 $2 doi
- 035 __
- $a (PubMed)31536130
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xxu
- 100 1_
- $a Svobodová, Jana $u Department of Cytokinetics, Institute of Biophysics of the Czech Academy of Sciences, Brno 61265, Czech Republic. Department of Experimental Biology, Faculty of Science, Masaryk University, Brno 61137, Czech Republic.
- 245 10
- $a 2,3,7,8-Tetrachlorodibenzo-p-dioxin (TCDD) Disrupts Control of Cell Proliferation and Apoptosis in a Human Model of Adult Liver Progenitors / $c J. Svobodová, J. Procházková, M. Kabátková, M. Krkoška, L. Šmerdová, H. Líbalová, J. Topinka, J. Kléma, A. Kozubík, M. Machala, J. Vondráček,
- 520 9_
- $a 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.
- 650 _2
- $a adaptorové proteiny signální transdukční $x genetika $7 D048868
- 650 _2
- $a apoptóza $x účinky léků $x genetika $7 D017209
- 650 _2
- $a buněčné linie $7 D002460
- 650 _2
- $a proliferace buněk $x účinky léků $x genetika $7 D049109
- 650 _2
- $a exprese genu $x účinky léků $7 D015870
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a játra $x účinky léků $x patologie $7 D008099
- 650 12
- $a biologické modely $7 D008954
- 650 _2
- $a polychlorované dibenzodioxiny $x toxicita $7 D000072317
- 650 _2
- $a malá interferující RNA $x genetika $7 D034741
- 650 _2
- $a receptory aromatických uhlovodíků $x metabolismus $7 D018336
- 650 _2
- $a signální transdukce $7 D015398
- 650 _2
- $a kmenové buňky $x účinky léků $x patologie $7 D013234
- 650 _2
- $a trans-aktivátory $x genetika $7 D015534
- 650 _2
- $a transkripční faktory $x genetika $7 D014157
- 650 _2
- $a transfekce $7 D014162
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Procházková, Jiřina $u Department of Chemistry and Toxicology, Veterinary Research Institute, Brno 62100, Czech Republic.
- 700 1_
- $a Kabátková, Markéta $u Department of Cytokinetics, Institute of Biophysics of the Czech Academy of Sciences, Brno 61265, Czech Republic.
- 700 1_
- $a Krkoška, Martin $u Department of Cytokinetics, Institute of Biophysics of the Czech Academy of Sciences, Brno 61265, Czech Republic. Department of Experimental Biology, Faculty of Science, Masaryk University, Brno 61137, Czech Republic.
- 700 1_
- $a Šmerdová, Lenka $u Department of Cytokinetics, Institute of Biophysics of the Czech Academy of Sciences, Brno 61265, Czech Republic.
- 700 1_
- $a Líbalová, Helena $u Department of Genetic Ecotoxicology, Institute of Experimental Medicine of the Czech Academy of Sciences, Prague 14220, Czech Republic.
- 700 1_
- $a Topinka, Jan $u Department of Genetic Ecotoxicology, Institute of Experimental Medicine of the Czech Academy of Sciences, Prague 14220, Czech Republic.
- 700 1_
- $a Kléma, Jiří $u Department of Computer Science, Czech Technical University, Prague 12135, Czech Republic.
- 700 1_
- $a Kozubík, Alois $u Department of Cytokinetics, Institute of Biophysics of the Czech Academy of Sciences, Brno 61265, Czech Republic.
- 700 1_
- $a Machala, Miroslav $u Department of Chemistry and Toxicology, Veterinary Research Institute, Brno 62100, Czech Republic.
- 700 1_
- $a Vondráček, Jan $u Department of Cytokinetics, Institute of Biophysics of the Czech Academy of Sciences, Brno 61265, Czech Republic.
- 773 0_
- $w MED00007104 $t Toxicological sciences : an official journal of the Society of Toxicology $x 1096-0929 $g Roč. 172, č. 2 (2019), s. 368-384
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/31536130 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20201125 $b ABA008
- 991 __
- $a 20201222155215 $b ABA008
- 999 __
- $a ok $b bmc $g 1599614 $s 1116155
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2019 $b 172 $c 2 $d 368-384 $e 20191201 $i 1096-0929 $m Toxicological sciences $n Toxicol Sci $x MED00007104
- LZP __
- $a Pubmed-20201125