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Differences in the Epigenetic Regulation of Cytochrome P450 Genes between Human Embryonic Stem Cell-Derived Hepatocytes and Primary Hepatocytes
by
Chun, Hang-Suk
, Song, Chang-Woo
, Yoon, Seokjoo
, Kim, Hyemin
, Kim, Ji Woo
, Park, Han-Jin
, Choi, Young-Jun
, Im, Ilkyun
, Han, Yong-Mahn
in
Cell Differentiation
/ Cell Line
/ Chromatin
/ Chromatin - metabolism
/ Chromatin - ultrastructure
/ Combinatorial analysis
/ CpG Islands
/ CYP1A2 protein
/ CYP2D6 protein
/ Cytochrome
/ Cytochrome P-450
/ Cytochrome P-450 CYP1A1 - genetics
/ Cytochrome P-450 CYP1A1 - metabolism
/ Cytochrome P-450 CYP1A2 - genetics
/ Cytochrome P-450 CYP1A2 - metabolism
/ Cytochrome P-450 CYP1B1 - genetics
/ Cytochrome P-450 CYP1B1 - metabolism
/ Cytochrome P-450 CYP2D6 - genetics
/ Cytochrome P-450 CYP2D6 - metabolism
/ Cytochrome P-450 CYP2E1 - genetics
/ Cytochrome P-450 CYP2E1 - metabolism
/ Cytochrome P450
/ Demethylation
/ Deoxyribonucleic acid
/ DNA
/ DNA Methylation
/ DNA Modification Methylases - genetics
/ DNA Modification Methylases - metabolism
/ Embryonic stem cells
/ Enzymes
/ Epigenesis, Genetic
/ Epigenetic inheritance
/ Gene expression
/ Gene regulation
/ Genes
/ Hepatocytes
/ Hepatocytes - cytology
/ Hepatocytes - metabolism
/ Hepatotoxicity
/ Histone Deacetylases - genetics
/ Histone Deacetylases - metabolism
/ Histones - genetics
/ Histones - metabolism
/ Human Embryonic Stem Cells - cytology
/ Human Embryonic Stem Cells - metabolism
/ Humans
/ Inhibition
/ Liver
/ Methylation
/ Organ Specificity
/ Pluripotency
/ Primary Cell Culture
/ Protein Processing, Post-Translational
/ Rodents
/ Science
/ Signal Transduction
/ Stem cells
/ Toxicity
/ Toxicity testing
/ Transcription
/ Transcription, Genetic
2015
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Differences in the Epigenetic Regulation of Cytochrome P450 Genes between Human Embryonic Stem Cell-Derived Hepatocytes and Primary Hepatocytes
by
Chun, Hang-Suk
, Song, Chang-Woo
, Yoon, Seokjoo
, Kim, Hyemin
, Kim, Ji Woo
, Park, Han-Jin
, Choi, Young-Jun
, Im, Ilkyun
, Han, Yong-Mahn
in
Cell Differentiation
/ Cell Line
/ Chromatin
/ Chromatin - metabolism
/ Chromatin - ultrastructure
/ Combinatorial analysis
/ CpG Islands
/ CYP1A2 protein
/ CYP2D6 protein
/ Cytochrome
/ Cytochrome P-450
/ Cytochrome P-450 CYP1A1 - genetics
/ Cytochrome P-450 CYP1A1 - metabolism
/ Cytochrome P-450 CYP1A2 - genetics
/ Cytochrome P-450 CYP1A2 - metabolism
/ Cytochrome P-450 CYP1B1 - genetics
/ Cytochrome P-450 CYP1B1 - metabolism
/ Cytochrome P-450 CYP2D6 - genetics
/ Cytochrome P-450 CYP2D6 - metabolism
/ Cytochrome P-450 CYP2E1 - genetics
/ Cytochrome P-450 CYP2E1 - metabolism
/ Cytochrome P450
/ Demethylation
/ Deoxyribonucleic acid
/ DNA
/ DNA Methylation
/ DNA Modification Methylases - genetics
/ DNA Modification Methylases - metabolism
/ Embryonic stem cells
/ Enzymes
/ Epigenesis, Genetic
/ Epigenetic inheritance
/ Gene expression
/ Gene regulation
/ Genes
/ Hepatocytes
/ Hepatocytes - cytology
/ Hepatocytes - metabolism
/ Hepatotoxicity
/ Histone Deacetylases - genetics
/ Histone Deacetylases - metabolism
/ Histones - genetics
/ Histones - metabolism
/ Human Embryonic Stem Cells - cytology
/ Human Embryonic Stem Cells - metabolism
/ Humans
/ Inhibition
/ Liver
/ Methylation
/ Organ Specificity
/ Pluripotency
/ Primary Cell Culture
/ Protein Processing, Post-Translational
/ Rodents
/ Science
/ Signal Transduction
/ Stem cells
/ Toxicity
/ Toxicity testing
/ Transcription
/ Transcription, Genetic
2015
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Differences in the Epigenetic Regulation of Cytochrome P450 Genes between Human Embryonic Stem Cell-Derived Hepatocytes and Primary Hepatocytes
by
Chun, Hang-Suk
, Song, Chang-Woo
, Yoon, Seokjoo
, Kim, Hyemin
, Kim, Ji Woo
, Park, Han-Jin
, Choi, Young-Jun
, Im, Ilkyun
, Han, Yong-Mahn
in
Cell Differentiation
/ Cell Line
/ Chromatin
/ Chromatin - metabolism
/ Chromatin - ultrastructure
/ Combinatorial analysis
/ CpG Islands
/ CYP1A2 protein
/ CYP2D6 protein
/ Cytochrome
/ Cytochrome P-450
/ Cytochrome P-450 CYP1A1 - genetics
/ Cytochrome P-450 CYP1A1 - metabolism
/ Cytochrome P-450 CYP1A2 - genetics
/ Cytochrome P-450 CYP1A2 - metabolism
/ Cytochrome P-450 CYP1B1 - genetics
/ Cytochrome P-450 CYP1B1 - metabolism
/ Cytochrome P-450 CYP2D6 - genetics
/ Cytochrome P-450 CYP2D6 - metabolism
/ Cytochrome P-450 CYP2E1 - genetics
/ Cytochrome P-450 CYP2E1 - metabolism
/ Cytochrome P450
/ Demethylation
/ Deoxyribonucleic acid
/ DNA
/ DNA Methylation
/ DNA Modification Methylases - genetics
/ DNA Modification Methylases - metabolism
/ Embryonic stem cells
/ Enzymes
/ Epigenesis, Genetic
/ Epigenetic inheritance
/ Gene expression
/ Gene regulation
/ Genes
/ Hepatocytes
/ Hepatocytes - cytology
/ Hepatocytes - metabolism
/ Hepatotoxicity
/ Histone Deacetylases - genetics
/ Histone Deacetylases - metabolism
/ Histones - genetics
/ Histones - metabolism
/ Human Embryonic Stem Cells - cytology
/ Human Embryonic Stem Cells - metabolism
/ Humans
/ Inhibition
/ Liver
/ Methylation
/ Organ Specificity
/ Pluripotency
/ Primary Cell Culture
/ Protein Processing, Post-Translational
/ Rodents
/ Science
/ Signal Transduction
/ Stem cells
/ Toxicity
/ Toxicity testing
/ Transcription
/ Transcription, Genetic
2015
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Differences in the Epigenetic Regulation of Cytochrome P450 Genes between Human Embryonic Stem Cell-Derived Hepatocytes and Primary Hepatocytes
Journal Article
Differences in the Epigenetic Regulation of Cytochrome P450 Genes between Human Embryonic Stem Cell-Derived Hepatocytes and Primary Hepatocytes
2015
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Overview
Human pluripotent stem cell-derived hepatocytes have the potential to provide in vitro model systems for drug discovery and hepatotoxicity testing. However, these cells are currently unsuitable for drug toxicity and efficacy testing because of their limited expression of genes encoding drug-metabolizing enzymes, especially cytochrome P450 (CYP) enzymes. Transcript levels of major CYP genes were much lower in human embryonic stem cell-derived hepatocytes (hESC-Hep) than in human primary hepatocytes (hPH). To verify the mechanism underlying this reduced expression of CYP genes, including CYP1A1, CYP1A2, CYP1B1, CYP2D6, and CYP2E1, we investigated their epigenetic regulation in terms of DNA methylation and histone modifications in hESC-Hep and hPH. CpG islands of CYP genes were hypermethylated in hESC-Hep, whereas they had an open chromatin structure, as represented by hypomethylation of CpG sites and permissive histone modifications, in hPH. Inhibition of DNA methyltransferases (DNMTs) during hepatic maturation induced demethylation of the CpG sites of CYP1A1 and CYP1A2, leading to the up-regulation of their transcription. Combinatorial inhibition of DNMTs and histone deacetylases (HDACs) increased the transcript levels of CYP1A1, CYP1A2, CYP1B1, and CYP2D6. Our findings suggest that limited expression of CYP genes in hESC-Hep is modulated by epigenetic regulatory factors such as DNMTs and HDACs.
Publisher
Public Library of Science,Public Library of Science (PLoS)
Subject
/ Cytochrome P-450 CYP1A1 - genetics
/ Cytochrome P-450 CYP1A1 - metabolism
/ Cytochrome P-450 CYP1A2 - genetics
/ Cytochrome P-450 CYP1A2 - metabolism
/ Cytochrome P-450 CYP1B1 - genetics
/ Cytochrome P-450 CYP1B1 - metabolism
/ Cytochrome P-450 CYP2D6 - genetics
/ Cytochrome P-450 CYP2D6 - metabolism
/ Cytochrome P-450 CYP2E1 - genetics
/ Cytochrome P-450 CYP2E1 - metabolism
/ DNA
/ DNA Modification Methylases - genetics
/ DNA Modification Methylases - metabolism
/ Enzymes
/ Genes
/ Histone Deacetylases - genetics
/ Histone Deacetylases - metabolism
/ Human Embryonic Stem Cells - cytology
/ Human Embryonic Stem Cells - metabolism
/ Humans
/ Liver
/ Protein Processing, Post-Translational
/ Rodents
/ Science
/ Toxicity
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