Lentiviral transduction of CD34(+) cells induces genome-wide epigenetic modifications
Epigenetic modifications may occur during in vitro manipulations of stem cells but these effects have remained unexplored in the context of cell and gene therapy protocols. In an experimental model of ex vivo gene modification for hematopoietic gene therapy, human CD34(+) cells were cultured shortly...
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creator | Yamagata, Yoshiaki Parietti, Véronique Stockholm, Daniel Corre, Guillaume Poinsignon, Catherine Touleimat, Nizar Delafoy, Damien Besse, Céline Tost, Jörg Galy, Anne Paldi, András |
description | Epigenetic modifications may occur during in vitro manipulations of stem cells but these effects have remained unexplored in the context of cell and gene therapy protocols. In an experimental model of ex vivo gene modification for hematopoietic gene therapy, human CD34(+) cells were cultured shortly in the presence of cytokines then with a gene transfer lentiviral vector (LV) expected to transduce cells but to have otherwise limited biological effects on the cells. At the end of the culture, the population of cells remained largely similar at the phenotypic level but some epigenetic changes were evident. Exposure of CD34(+) cells to cytokines increased nuclear expression of epigenetic regulators SIRT1 or DNMT1 and caused genome-wide DNA methylation changes. Surprisingly, the LV caused additional and distinct effects. Large-scale genomic DNA methylation analysis showed that balanced methylation changes occurred in about 200 genes following culture of CD34(+) cells in the presence of cytokines but 900 genes were modified following addition of the LV, predominantly increasing CpG methylation. Epigenetic effects resulting from ex vivo culture and from the use of LV may constitute previously unsuspected sources of biological effects in stem cells and may provide new biomarkers to rationally optimize gene and cell therapy protocols. |
doi_str_mv | 10.1371/journal.pone.0048943 |
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In an experimental model of ex vivo gene modification for hematopoietic gene therapy, human CD34(+) cells were cultured shortly in the presence of cytokines then with a gene transfer lentiviral vector (LV) expected to transduce cells but to have otherwise limited biological effects on the cells. At the end of the culture, the population of cells remained largely similar at the phenotypic level but some epigenetic changes were evident. Exposure of CD34(+) cells to cytokines increased nuclear expression of epigenetic regulators SIRT1 or DNMT1 and caused genome-wide DNA methylation changes. Surprisingly, the LV caused additional and distinct effects. Large-scale genomic DNA methylation analysis showed that balanced methylation changes occurred in about 200 genes following culture of CD34(+) cells in the presence of cytokines but 900 genes were modified following addition of the LV, predominantly increasing CpG methylation. Epigenetic effects resulting from ex vivo culture and from the use of LV may constitute previously unsuspected sources of biological effects in stem cells and may provide new biomarkers to rationally optimize gene and cell therapy protocols.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0048943</identifier><identifier>PMID: 23145033</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Antigens, CD34 - genetics ; Antigens, CD34 - metabolism ; Biochemistry, Molecular Biology ; Biological effects ; Biology ; Biomarkers ; Biotechnology ; CD34 antigen ; Cell culture ; Cell division ; Cells, Cultured ; Cellular Biology ; CpG islands ; Cytokines ; Cytokines - metabolism ; Deoxyribonucleic acid ; DNA ; DNA (Cytosine-5-)-Methyltransferase 1 ; DNA (Cytosine-5-)-Methyltransferases - genetics ; DNA (Cytosine-5-)-Methyltransferases - metabolism ; DNA methylation ; DNA Methylation - genetics ; DNMT1 protein ; Embryos ; Epigenesis, Genetic ; Epigenetics ; Epigenomics ; Fetal Blood - metabolism ; Gene expression ; Gene therapy ; Genes ; Genetic modification ; Genetic Therapy - methods ; Genetic Vectors - genetics ; Genetics ; Genome - genetics ; Genomes ; Hematopoietic Stem Cells - metabolism ; Humans ; Immunology ; Lentivirus - genetics ; Lentivirus - metabolism ; Life Sciences ; Proteins ; Quantitative Methods ; Regulators ; SIRT1 protein ; Sirtuin 1 - genetics ; Sirtuin 1 - metabolism ; Stem cells ; Transduction, Genetic - methods ; Vectors (Biology)</subject><ispartof>PloS one, 2012-11, Vol.7 (11), p.e48943-e48943</ispartof><rights>2012 Yamagata et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><rights>2012 Yamagata et al 2012 Yamagata et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c560t-4f30dcbcdee79a8ef0593f47b466fd465b6783198bd49e19ce233a66c4a91a643</citedby><cites>FETCH-LOGICAL-c560t-4f30dcbcdee79a8ef0593f47b466fd465b6783198bd49e19ce233a66c4a91a643</cites><orcidid>0000-0003-4446-7625 ; 0000-0002-5069-5256 ; 0000-0002-1953-1931 ; 0000-0002-0153-4392 ; 0000-0002-0755-8336</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3492239/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3492239/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,315,728,781,785,865,886,2103,2929,23871,27929,27930,53796,53798</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23145033$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://univ-evry.hal.science/hal-02177572$$DView record in HAL$$Hfree_for_read</backlink></links><search><contributor>Wagner, Wolfgang</contributor><creatorcontrib>Yamagata, Yoshiaki</creatorcontrib><creatorcontrib>Parietti, Véronique</creatorcontrib><creatorcontrib>Stockholm, Daniel</creatorcontrib><creatorcontrib>Corre, Guillaume</creatorcontrib><creatorcontrib>Poinsignon, Catherine</creatorcontrib><creatorcontrib>Touleimat, Nizar</creatorcontrib><creatorcontrib>Delafoy, Damien</creatorcontrib><creatorcontrib>Besse, Céline</creatorcontrib><creatorcontrib>Tost, Jörg</creatorcontrib><creatorcontrib>Galy, Anne</creatorcontrib><creatorcontrib>Paldi, András</creatorcontrib><title>Lentiviral transduction of CD34(+) cells induces genome-wide epigenetic modifications</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>Epigenetic modifications may occur during in vitro manipulations of stem cells but these effects have remained unexplored in the context of cell and gene therapy protocols. In an experimental model of ex vivo gene modification for hematopoietic gene therapy, human CD34(+) cells were cultured shortly in the presence of cytokines then with a gene transfer lentiviral vector (LV) expected to transduce cells but to have otherwise limited biological effects on the cells. At the end of the culture, the population of cells remained largely similar at the phenotypic level but some epigenetic changes were evident. Exposure of CD34(+) cells to cytokines increased nuclear expression of epigenetic regulators SIRT1 or DNMT1 and caused genome-wide DNA methylation changes. Surprisingly, the LV caused additional and distinct effects. Large-scale genomic DNA methylation analysis showed that balanced methylation changes occurred in about 200 genes following culture of CD34(+) cells in the presence of cytokines but 900 genes were modified following addition of the LV, predominantly increasing CpG methylation. Epigenetic effects resulting from ex vivo culture and from the use of LV may constitute previously unsuspected sources of biological effects in stem cells and may provide new biomarkers to rationally optimize gene and cell therapy protocols.</description><subject>Antigens, CD34 - genetics</subject><subject>Antigens, CD34 - metabolism</subject><subject>Biochemistry, Molecular Biology</subject><subject>Biological effects</subject><subject>Biology</subject><subject>Biomarkers</subject><subject>Biotechnology</subject><subject>CD34 antigen</subject><subject>Cell culture</subject><subject>Cell division</subject><subject>Cells, Cultured</subject><subject>Cellular Biology</subject><subject>CpG islands</subject><subject>Cytokines</subject><subject>Cytokines - metabolism</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>DNA (Cytosine-5-)-Methyltransferase 1</subject><subject>DNA (Cytosine-5-)-Methyltransferases - genetics</subject><subject>DNA (Cytosine-5-)-Methyltransferases - metabolism</subject><subject>DNA methylation</subject><subject>DNA Methylation - genetics</subject><subject>DNMT1 protein</subject><subject>Embryos</subject><subject>Epigenesis, Genetic</subject><subject>Epigenetics</subject><subject>Epigenomics</subject><subject>Fetal Blood - metabolism</subject><subject>Gene expression</subject><subject>Gene therapy</subject><subject>Genes</subject><subject>Genetic modification</subject><subject>Genetic Therapy - methods</subject><subject>Genetic Vectors - genetics</subject><subject>Genetics</subject><subject>Genome - genetics</subject><subject>Genomes</subject><subject>Hematopoietic Stem Cells - metabolism</subject><subject>Humans</subject><subject>Immunology</subject><subject>Lentivirus - genetics</subject><subject>Lentivirus - metabolism</subject><subject>Life Sciences</subject><subject>Proteins</subject><subject>Quantitative Methods</subject><subject>Regulators</subject><subject>SIRT1 protein</subject><subject>Sirtuin 1 - genetics</subject><subject>Sirtuin 1 - metabolism</subject><subject>Stem cells</subject><subject>Transduction, Genetic - methods</subject><subject>Vectors (Biology)</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>DOA</sourceid><recordid>eNptUk1v1DAQjRCIlsI_QBCJSyuUxfY4dnxBqpaPVlqJCz1bjj3ZepXES5ws4t_jsGnVVpxsz7z3ZuZ5suwtJSsKkn7ahWnoTbvahx5XhPBKcXiWnVIFrBCMwPMH95PsVYw7QkqohHiZnTCgvCQAp9nNBvvRH_xg2nwcTB_dZEcf-jw0-foL8POPF7nFto2571MKY77FPnRY_PYOc9z79MTR27wLzjfempkcX2cvGtNGfLOcZ9nNt68_11fF5sf36_XlprClIGPBGyDO1tYhSmUqbEipoOGy5kI0jouyFrICqqracYVUWWQARgjLjaJGcDjL3h91922IenEkagpMSICylAlxfUS4YHZ6P_jODH90MF7_C4Rhq82Q-m9Rl1xWyjCqVF1x2lCTemLSVTW6iiW_ktbnpdpUd-hsci7Z9kj0cab3t3obDhq4YgxUErg4Ctw-oV1dbvQcI4xKWUp2oAl7vhQbwq8J46g7H-efMD2GKc1IS6qo5HTu68MT6P-d4EeUHUKMAzb3HVCi5426Y-l5o_SyUYn27uHQ96S7FYK_nBDIDQ</recordid><startdate>20121107</startdate><enddate>20121107</enddate><creator>Yamagata, Yoshiaki</creator><creator>Parietti, Véronique</creator><creator>Stockholm, Daniel</creator><creator>Corre, Guillaume</creator><creator>Poinsignon, Catherine</creator><creator>Touleimat, Nizar</creator><creator>Delafoy, Damien</creator><creator>Besse, Céline</creator><creator>Tost, Jörg</creator><creator>Galy, Anne</creator><creator>Paldi, András</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QO</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TG</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>7X8</scope><scope>1XC</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0003-4446-7625</orcidid><orcidid>https://orcid.org/0000-0002-5069-5256</orcidid><orcidid>https://orcid.org/0000-0002-1953-1931</orcidid><orcidid>https://orcid.org/0000-0002-0153-4392</orcidid><orcidid>https://orcid.org/0000-0002-0755-8336</orcidid></search><sort><creationdate>20121107</creationdate><title>Lentiviral transduction of CD34(+) cells induces genome-wide epigenetic modifications</title><author>Yamagata, Yoshiaki ; Parietti, Véronique ; Stockholm, Daniel ; Corre, Guillaume ; Poinsignon, Catherine ; Touleimat, Nizar ; Delafoy, Damien ; Besse, Céline ; Tost, Jörg ; Galy, Anne ; Paldi, András</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c560t-4f30dcbcdee79a8ef0593f47b466fd465b6783198bd49e19ce233a66c4a91a643</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Antigens, CD34 - genetics</topic><topic>Antigens, CD34 - metabolism</topic><topic>Biochemistry, Molecular Biology</topic><topic>Biological effects</topic><topic>Biology</topic><topic>Biomarkers</topic><topic>Biotechnology</topic><topic>CD34 antigen</topic><topic>Cell culture</topic><topic>Cell division</topic><topic>Cells, Cultured</topic><topic>Cellular Biology</topic><topic>CpG islands</topic><topic>Cytokines</topic><topic>Cytokines - metabolism</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>DNA (Cytosine-5-)-Methyltransferase 1</topic><topic>DNA (Cytosine-5-)-Methyltransferases - genetics</topic><topic>DNA (Cytosine-5-)-Methyltransferases - metabolism</topic><topic>DNA methylation</topic><topic>DNA Methylation - genetics</topic><topic>DNMT1 protein</topic><topic>Embryos</topic><topic>Epigenesis, Genetic</topic><topic>Epigenetics</topic><topic>Epigenomics</topic><topic>Fetal Blood - metabolism</topic><topic>Gene expression</topic><topic>Gene therapy</topic><topic>Genes</topic><topic>Genetic modification</topic><topic>Genetic Therapy - 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In an experimental model of ex vivo gene modification for hematopoietic gene therapy, human CD34(+) cells were cultured shortly in the presence of cytokines then with a gene transfer lentiviral vector (LV) expected to transduce cells but to have otherwise limited biological effects on the cells. At the end of the culture, the population of cells remained largely similar at the phenotypic level but some epigenetic changes were evident. Exposure of CD34(+) cells to cytokines increased nuclear expression of epigenetic regulators SIRT1 or DNMT1 and caused genome-wide DNA methylation changes. Surprisingly, the LV caused additional and distinct effects. Large-scale genomic DNA methylation analysis showed that balanced methylation changes occurred in about 200 genes following culture of CD34(+) cells in the presence of cytokines but 900 genes were modified following addition of the LV, predominantly increasing CpG methylation. 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subjects | Antigens, CD34 - genetics Antigens, CD34 - metabolism Biochemistry, Molecular Biology Biological effects Biology Biomarkers Biotechnology CD34 antigen Cell culture Cell division Cells, Cultured Cellular Biology CpG islands Cytokines Cytokines - metabolism Deoxyribonucleic acid DNA DNA (Cytosine-5-)-Methyltransferase 1 DNA (Cytosine-5-)-Methyltransferases - genetics DNA (Cytosine-5-)-Methyltransferases - metabolism DNA methylation DNA Methylation - genetics DNMT1 protein Embryos Epigenesis, Genetic Epigenetics Epigenomics Fetal Blood - metabolism Gene expression Gene therapy Genes Genetic modification Genetic Therapy - methods Genetic Vectors - genetics Genetics Genome - genetics Genomes Hematopoietic Stem Cells - metabolism Humans Immunology Lentivirus - genetics Lentivirus - metabolism Life Sciences Proteins Quantitative Methods Regulators SIRT1 protein Sirtuin 1 - genetics Sirtuin 1 - metabolism Stem cells Transduction, Genetic - methods Vectors (Biology) |
title | Lentiviral transduction of CD34(+) cells induces genome-wide epigenetic modifications |
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