Isolation of human iPS cells using EOS lentiviral vectors to select for pluripotency
Lentiviral vectors that express a fluorescent reporter and a selectable marker in pluripotent cells improve and simplify isolation of induced pluripotent stem cell lines in mouse and human. Induced pluripotent stem (iPS) cells may be of use in regenerative medicine. However, the low efficiency of re...
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Veröffentlicht in: | Nature methods 2009-05, Vol.6 (5), p.370-376 |
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creator | Hotta, Akitsu Cheung, Aaron Y L Farra, Natalie Vijayaragavan, Kausalia Séguin, Cheryle A Draper, Jonathan S Pasceri, Peter Maksakova, Irina A Mager, Dixie L Rossant, Janet Bhatia, Mickie Ellis, James |
description | Lentiviral vectors that express a fluorescent reporter and a selectable marker in pluripotent cells improve and simplify isolation of induced pluripotent stem cell lines in mouse and human.
Induced pluripotent stem (iPS) cells may be of use in regenerative medicine. However, the low efficiency of reprogramming is a major impediment to the generation of patient-specific iPS cell lines. Here we report the first selection system for the isolation of human iPS cells. We developed the EOS (Early Transposon promoter and
Oct-4
(
Pou5f1
) and
Sox2
enhancers) lentiviral vector to specifically express in mouse and human embryonic stem cells but not in primary fibroblasts. The bicistronic EOS vector marked emerging mouse and human iPS cell colonies with EGFP, and we used puromycin selection to aid the isolation of iPS cell lines that expressed endogenous pluripotency markers. These lines differentiated into cell types from all three germ layers. Reporter expression was extinguished upon differentiation and therefore monitored the residual pluripotent cells that form teratomas. Finally, we used EOS selection to establish Rett syndrome–specific mouse and human iPS cell lines with known mutations in
MECP2
. |
doi_str_mv | 10.1038/nmeth.1325 |
format | Article |
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Induced pluripotent stem (iPS) cells may be of use in regenerative medicine. However, the low efficiency of reprogramming is a major impediment to the generation of patient-specific iPS cell lines. Here we report the first selection system for the isolation of human iPS cells. We developed the EOS (Early Transposon promoter and
Oct-4
(
Pou5f1
) and
Sox2
enhancers) lentiviral vector to specifically express in mouse and human embryonic stem cells but not in primary fibroblasts. The bicistronic EOS vector marked emerging mouse and human iPS cell colonies with EGFP, and we used puromycin selection to aid the isolation of iPS cell lines that expressed endogenous pluripotency markers. These lines differentiated into cell types from all three germ layers. Reporter expression was extinguished upon differentiation and therefore monitored the residual pluripotent cells that form teratomas. Finally, we used EOS selection to establish Rett syndrome–specific mouse and human iPS cell lines with known mutations in
MECP2
.</description><identifier>ISSN: 1548-7091</identifier><identifier>EISSN: 1548-7105</identifier><identifier>DOI: 10.1038/nmeth.1325</identifier><identifier>PMID: 19404254</identifier><language>eng</language><publisher>New York: Nature Publishing Group US</publisher><subject>Analysis ; Animals ; Bioinformatics ; Biological Microscopy ; Biological Techniques ; Biomedical and Life Sciences ; Biomedical Engineering/Biotechnology ; Cell Dedifferentiation - genetics ; Cell Differentiation - drug effects ; Cell physiology ; Cell Separation - methods ; Cellular biology ; DNA Transposable Elements - genetics ; Embryo, Mammalian - cytology ; Embryonic Stem Cells - cytology ; Embryonic Stem Cells - metabolism ; Enhancer Elements, Genetic - genetics ; Fibroblasts - cytology ; Fibroblasts - metabolism ; Gene expression ; Genes, Reporter - genetics ; Genetic Vectors - genetics ; Green Fluorescent Proteins - genetics ; Green Fluorescent Proteins - metabolism ; Humans ; Lentivirus - genetics ; Life Sciences ; Methods ; Methyl-CpG-Binding Protein 2 - genetics ; Mice ; Mice, Inbred NOD ; Mice, Mutant Strains ; Mice, SCID ; Mutation ; Nuclear reprogramming ; Physiological aspects ; Pluripotent Stem Cells - cytology ; Pluripotent Stem Cells - metabolism ; Promoter Regions, Genetic - genetics ; Promoters (Genetics) ; Proteomics ; Research methodology ; Rett Syndrome - genetics ; Rett Syndrome - pathology ; Stem cells ; Teratoma - pathology ; Transposons</subject><ispartof>Nature methods, 2009-05, Vol.6 (5), p.370-376</ispartof><rights>Springer Nature America, Inc. 2009</rights><rights>COPYRIGHT 2009 Nature Publishing Group</rights><rights>Copyright Nature Publishing Group May 2009</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c512t-daf60e9c951001b4e6b95432e7962eb9283a521b5d138311892ee84cc320f5ee3</citedby><cites>FETCH-LOGICAL-c512t-daf60e9c951001b4e6b95432e7962eb9283a521b5d138311892ee84cc320f5ee3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1038/nmeth.1325$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1038/nmeth.1325$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19404254$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hotta, Akitsu</creatorcontrib><creatorcontrib>Cheung, Aaron Y L</creatorcontrib><creatorcontrib>Farra, Natalie</creatorcontrib><creatorcontrib>Vijayaragavan, Kausalia</creatorcontrib><creatorcontrib>Séguin, Cheryle A</creatorcontrib><creatorcontrib>Draper, Jonathan S</creatorcontrib><creatorcontrib>Pasceri, Peter</creatorcontrib><creatorcontrib>Maksakova, Irina A</creatorcontrib><creatorcontrib>Mager, Dixie L</creatorcontrib><creatorcontrib>Rossant, Janet</creatorcontrib><creatorcontrib>Bhatia, Mickie</creatorcontrib><creatorcontrib>Ellis, James</creatorcontrib><title>Isolation of human iPS cells using EOS lentiviral vectors to select for pluripotency</title><title>Nature methods</title><addtitle>Nat Methods</addtitle><addtitle>Nat Methods</addtitle><description>Lentiviral vectors that express a fluorescent reporter and a selectable marker in pluripotent cells improve and simplify isolation of induced pluripotent stem cell lines in mouse and human.
Induced pluripotent stem (iPS) cells may be of use in regenerative medicine. However, the low efficiency of reprogramming is a major impediment to the generation of patient-specific iPS cell lines. Here we report the first selection system for the isolation of human iPS cells. We developed the EOS (Early Transposon promoter and
Oct-4
(
Pou5f1
) and
Sox2
enhancers) lentiviral vector to specifically express in mouse and human embryonic stem cells but not in primary fibroblasts. The bicistronic EOS vector marked emerging mouse and human iPS cell colonies with EGFP, and we used puromycin selection to aid the isolation of iPS cell lines that expressed endogenous pluripotency markers. These lines differentiated into cell types from all three germ layers. Reporter expression was extinguished upon differentiation and therefore monitored the residual pluripotent cells that form teratomas. Finally, we used EOS selection to establish Rett syndrome–specific mouse and human iPS cell lines with known mutations in
MECP2
.</description><subject>Analysis</subject><subject>Animals</subject><subject>Bioinformatics</subject><subject>Biological Microscopy</subject><subject>Biological Techniques</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedical Engineering/Biotechnology</subject><subject>Cell Dedifferentiation - genetics</subject><subject>Cell Differentiation - drug effects</subject><subject>Cell physiology</subject><subject>Cell Separation - methods</subject><subject>Cellular biology</subject><subject>DNA Transposable Elements - genetics</subject><subject>Embryo, Mammalian - cytology</subject><subject>Embryonic Stem Cells - cytology</subject><subject>Embryonic Stem Cells - metabolism</subject><subject>Enhancer Elements, Genetic - genetics</subject><subject>Fibroblasts - cytology</subject><subject>Fibroblasts - metabolism</subject><subject>Gene expression</subject><subject>Genes, Reporter - genetics</subject><subject>Genetic Vectors - genetics</subject><subject>Green Fluorescent 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of human iPS cells using EOS lentiviral vectors to select for pluripotency</title><author>Hotta, Akitsu ; Cheung, Aaron Y L ; Farra, Natalie ; Vijayaragavan, Kausalia ; Séguin, Cheryle A ; Draper, Jonathan S ; Pasceri, Peter ; Maksakova, Irina A ; Mager, Dixie L ; Rossant, Janet ; Bhatia, Mickie ; Ellis, James</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c512t-daf60e9c951001b4e6b95432e7962eb9283a521b5d138311892ee84cc320f5ee3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Analysis</topic><topic>Animals</topic><topic>Bioinformatics</topic><topic>Biological Microscopy</topic><topic>Biological Techniques</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedical Engineering/Biotechnology</topic><topic>Cell Dedifferentiation - genetics</topic><topic>Cell Differentiation - drug effects</topic><topic>Cell physiology</topic><topic>Cell Separation - methods</topic><topic>Cellular biology</topic><topic>DNA Transposable Elements - genetics</topic><topic>Embryo, Mammalian - cytology</topic><topic>Embryonic Stem Cells - cytology</topic><topic>Embryonic Stem Cells - metabolism</topic><topic>Enhancer Elements, Genetic - genetics</topic><topic>Fibroblasts - cytology</topic><topic>Fibroblasts - metabolism</topic><topic>Gene expression</topic><topic>Genes, Reporter - genetics</topic><topic>Genetic Vectors - genetics</topic><topic>Green Fluorescent Proteins - genetics</topic><topic>Green Fluorescent Proteins - metabolism</topic><topic>Humans</topic><topic>Lentivirus - genetics</topic><topic>Life Sciences</topic><topic>Methods</topic><topic>Methyl-CpG-Binding Protein 2 - genetics</topic><topic>Mice</topic><topic>Mice, Inbred NOD</topic><topic>Mice, Mutant Strains</topic><topic>Mice, SCID</topic><topic>Mutation</topic><topic>Nuclear reprogramming</topic><topic>Physiological aspects</topic><topic>Pluripotent Stem Cells - 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Central Basic</collection><collection>Genetics Abstracts</collection><jtitle>Nature methods</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hotta, Akitsu</au><au>Cheung, Aaron Y L</au><au>Farra, Natalie</au><au>Vijayaragavan, Kausalia</au><au>Séguin, Cheryle A</au><au>Draper, Jonathan S</au><au>Pasceri, Peter</au><au>Maksakova, Irina A</au><au>Mager, Dixie L</au><au>Rossant, Janet</au><au>Bhatia, Mickie</au><au>Ellis, James</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Isolation of human iPS cells using EOS lentiviral vectors to select for pluripotency</atitle><jtitle>Nature methods</jtitle><stitle>Nat Methods</stitle><addtitle>Nat Methods</addtitle><date>2009-05-01</date><risdate>2009</risdate><volume>6</volume><issue>5</issue><spage>370</spage><epage>376</epage><pages>370-376</pages><issn>1548-7091</issn><eissn>1548-7105</eissn><abstract>Lentiviral vectors that express a fluorescent reporter and a selectable marker in pluripotent cells improve and simplify isolation of induced pluripotent stem cell lines in mouse and human.
Induced pluripotent stem (iPS) cells may be of use in regenerative medicine. However, the low efficiency of reprogramming is a major impediment to the generation of patient-specific iPS cell lines. Here we report the first selection system for the isolation of human iPS cells. We developed the EOS (Early Transposon promoter and
Oct-4
(
Pou5f1
) and
Sox2
enhancers) lentiviral vector to specifically express in mouse and human embryonic stem cells but not in primary fibroblasts. The bicistronic EOS vector marked emerging mouse and human iPS cell colonies with EGFP, and we used puromycin selection to aid the isolation of iPS cell lines that expressed endogenous pluripotency markers. These lines differentiated into cell types from all three germ layers. Reporter expression was extinguished upon differentiation and therefore monitored the residual pluripotent cells that form teratomas. Finally, we used EOS selection to establish Rett syndrome–specific mouse and human iPS cell lines with known mutations in
MECP2
.</abstract><cop>New York</cop><pub>Nature Publishing Group US</pub><pmid>19404254</pmid><doi>10.1038/nmeth.1325</doi><tpages>7</tpages></addata></record> |
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subjects | Analysis Animals Bioinformatics Biological Microscopy Biological Techniques Biomedical and Life Sciences Biomedical Engineering/Biotechnology Cell Dedifferentiation - genetics Cell Differentiation - drug effects Cell physiology Cell Separation - methods Cellular biology DNA Transposable Elements - genetics Embryo, Mammalian - cytology Embryonic Stem Cells - cytology Embryonic Stem Cells - metabolism Enhancer Elements, Genetic - genetics Fibroblasts - cytology Fibroblasts - metabolism Gene expression Genes, Reporter - genetics Genetic Vectors - genetics Green Fluorescent Proteins - genetics Green Fluorescent Proteins - metabolism Humans Lentivirus - genetics Life Sciences Methods Methyl-CpG-Binding Protein 2 - genetics Mice Mice, Inbred NOD Mice, Mutant Strains Mice, SCID Mutation Nuclear reprogramming Physiological aspects Pluripotent Stem Cells - cytology Pluripotent Stem Cells - metabolism Promoter Regions, Genetic - genetics Promoters (Genetics) Proteomics Research methodology Rett Syndrome - genetics Rett Syndrome - pathology Stem cells Teratoma - pathology Transposons |
title | Isolation of human iPS cells using EOS lentiviral vectors to select for pluripotency |
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