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
Hauptverfasser: 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
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container_title Nature methods
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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
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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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