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Generation of transgene-free human induced pluripotent stem cells from erythroblasts in feeder-free conditions

This protocol describes the generation and characterization of human induced pluripotent stem cells (hiPSCs) from erythroblasts. A key difference with classical protocols is the reprogramming of erythroblasts from a simple blood draw as opposed to fibroblasts/keratinocytes, which requires a biopsy....

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Detalles Bibliográficos
Autores principales: Perriot, Sylvain, Canales, Mathieu, Mathias, Amandine, Du Pasquier, Renaud
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9403557/
https://www.ncbi.nlm.nih.gov/pubmed/36035798
http://dx.doi.org/10.1016/j.xpro.2022.101620
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author Perriot, Sylvain
Canales, Mathieu
Mathias, Amandine
Du Pasquier, Renaud
author_facet Perriot, Sylvain
Canales, Mathieu
Mathias, Amandine
Du Pasquier, Renaud
author_sort Perriot, Sylvain
collection PubMed
description This protocol describes the generation and characterization of human induced pluripotent stem cells (hiPSCs) from erythroblasts. A key difference with classical protocols is the reprogramming of erythroblasts from a simple blood draw as opposed to fibroblasts/keratinocytes, which requires a biopsy. Moreover, working with erythroblasts ensures that no recombination of the TCR/BCR genes occurs, as opposed to T cells and whole peripheral blood mononuclear cells-based approaches. Last, this approach uses non-integrative episomes ensuring no integration of transgenes into the hiPSCs genome. For complete details on the use and execution of this protocol, please refer to Perriot et al. (2018).
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spelling pubmed-94035572022-08-26 Generation of transgene-free human induced pluripotent stem cells from erythroblasts in feeder-free conditions Perriot, Sylvain Canales, Mathieu Mathias, Amandine Du Pasquier, Renaud STAR Protoc Protocol This protocol describes the generation and characterization of human induced pluripotent stem cells (hiPSCs) from erythroblasts. A key difference with classical protocols is the reprogramming of erythroblasts from a simple blood draw as opposed to fibroblasts/keratinocytes, which requires a biopsy. Moreover, working with erythroblasts ensures that no recombination of the TCR/BCR genes occurs, as opposed to T cells and whole peripheral blood mononuclear cells-based approaches. Last, this approach uses non-integrative episomes ensuring no integration of transgenes into the hiPSCs genome. For complete details on the use and execution of this protocol, please refer to Perriot et al. (2018). Elsevier 2022-08-17 /pmc/articles/PMC9403557/ /pubmed/36035798 http://dx.doi.org/10.1016/j.xpro.2022.101620 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Protocol
Perriot, Sylvain
Canales, Mathieu
Mathias, Amandine
Du Pasquier, Renaud
Generation of transgene-free human induced pluripotent stem cells from erythroblasts in feeder-free conditions
title Generation of transgene-free human induced pluripotent stem cells from erythroblasts in feeder-free conditions
title_full Generation of transgene-free human induced pluripotent stem cells from erythroblasts in feeder-free conditions
title_fullStr Generation of transgene-free human induced pluripotent stem cells from erythroblasts in feeder-free conditions
title_full_unstemmed Generation of transgene-free human induced pluripotent stem cells from erythroblasts in feeder-free conditions
title_short Generation of transgene-free human induced pluripotent stem cells from erythroblasts in feeder-free conditions
title_sort generation of transgene-free human induced pluripotent stem cells from erythroblasts in feeder-free conditions
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9403557/
https://www.ncbi.nlm.nih.gov/pubmed/36035798
http://dx.doi.org/10.1016/j.xpro.2022.101620
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