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Genetic reporter analysis reveals an expandable reservoir of OCT4+ cells in adult skin

The transcription factor Oct4 (Pou5f1) is a critical regulator of pluripotency in embryonic and induced pluripotent stem cells. Therefore, Oct4 expression might identify somatic stem cell populations with inherent multipotent potential or a propensity for facilitated reprogramming. However, analysis...

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Autores principales: Limbourg, Anne, Schnabel, Sabine, Lozanovski, Vladimir J, Napp, L Christian, Ha, Teng-Cheong, Maetzig, Tobias, Bauersachs, Johann, Naim, Hassan Y, Schambach, Axel, Limbourg, Florian P
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4230759/
https://www.ncbi.nlm.nih.gov/pubmed/25408888
http://dx.doi.org/10.1186/2045-9769-3-9
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author Limbourg, Anne
Schnabel, Sabine
Lozanovski, Vladimir J
Napp, L Christian
Ha, Teng-Cheong
Maetzig, Tobias
Bauersachs, Johann
Naim, Hassan Y
Schambach, Axel
Limbourg, Florian P
author_facet Limbourg, Anne
Schnabel, Sabine
Lozanovski, Vladimir J
Napp, L Christian
Ha, Teng-Cheong
Maetzig, Tobias
Bauersachs, Johann
Naim, Hassan Y
Schambach, Axel
Limbourg, Florian P
author_sort Limbourg, Anne
collection PubMed
description The transcription factor Oct4 (Pou5f1) is a critical regulator of pluripotency in embryonic and induced pluripotent stem cells. Therefore, Oct4 expression might identify somatic stem cell populations with inherent multipotent potential or a propensity for facilitated reprogramming. However, analysis of Oct4 expression is confounded by Oct4 pseudogenes or non-pluripotency-related isoforms. Systematic analysis of a transgenic Oct4-EGFP reporter mouse identified testis and skin as two principle sources of Oct4 (+) cells in postnatal mice. While the prevalence of GFP(+) cells in testis rapidly declined with age, the skin-resident GFP(+) population expanded in a cyclical fashion. These cells were identified as epidermal stem cells dwelling in the stem cell niche of the hair follicle, which endogenously expressed all principle reprogramming factors at low levels. Interestingly, skin wounding or non-traumatic hair removal robustly expanded the GFP(+) epidermal cell pool not only locally, but also in uninjured skin areas, demonstrating the existence of a systemic response. Thus, the epithelial stem cell niche of the hair follicle harbors an expandable pool of Oct4+ stem cells, which might be useful for therapeutic cell transfer or facilitated reprogramming. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi: 10.1186/2045-9769-3-9) contains supplementary material, which is available to authorized users.
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spelling pubmed-42307592014-11-18 Genetic reporter analysis reveals an expandable reservoir of OCT4+ cells in adult skin Limbourg, Anne Schnabel, Sabine Lozanovski, Vladimir J Napp, L Christian Ha, Teng-Cheong Maetzig, Tobias Bauersachs, Johann Naim, Hassan Y Schambach, Axel Limbourg, Florian P Cell Regen Short Report The transcription factor Oct4 (Pou5f1) is a critical regulator of pluripotency in embryonic and induced pluripotent stem cells. Therefore, Oct4 expression might identify somatic stem cell populations with inherent multipotent potential or a propensity for facilitated reprogramming. However, analysis of Oct4 expression is confounded by Oct4 pseudogenes or non-pluripotency-related isoforms. Systematic analysis of a transgenic Oct4-EGFP reporter mouse identified testis and skin as two principle sources of Oct4 (+) cells in postnatal mice. While the prevalence of GFP(+) cells in testis rapidly declined with age, the skin-resident GFP(+) population expanded in a cyclical fashion. These cells were identified as epidermal stem cells dwelling in the stem cell niche of the hair follicle, which endogenously expressed all principle reprogramming factors at low levels. Interestingly, skin wounding or non-traumatic hair removal robustly expanded the GFP(+) epidermal cell pool not only locally, but also in uninjured skin areas, demonstrating the existence of a systemic response. Thus, the epithelial stem cell niche of the hair follicle harbors an expandable pool of Oct4+ stem cells, which might be useful for therapeutic cell transfer or facilitated reprogramming. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi: 10.1186/2045-9769-3-9) contains supplementary material, which is available to authorized users. BioMed Central 2014-06-14 /pmc/articles/PMC4230759/ /pubmed/25408888 http://dx.doi.org/10.1186/2045-9769-3-9 Text en © Limbourg et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Short Report
Limbourg, Anne
Schnabel, Sabine
Lozanovski, Vladimir J
Napp, L Christian
Ha, Teng-Cheong
Maetzig, Tobias
Bauersachs, Johann
Naim, Hassan Y
Schambach, Axel
Limbourg, Florian P
Genetic reporter analysis reveals an expandable reservoir of OCT4+ cells in adult skin
title Genetic reporter analysis reveals an expandable reservoir of OCT4+ cells in adult skin
title_full Genetic reporter analysis reveals an expandable reservoir of OCT4+ cells in adult skin
title_fullStr Genetic reporter analysis reveals an expandable reservoir of OCT4+ cells in adult skin
title_full_unstemmed Genetic reporter analysis reveals an expandable reservoir of OCT4+ cells in adult skin
title_short Genetic reporter analysis reveals an expandable reservoir of OCT4+ cells in adult skin
title_sort genetic reporter analysis reveals an expandable reservoir of oct4+ cells in adult skin
topic Short Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4230759/
https://www.ncbi.nlm.nih.gov/pubmed/25408888
http://dx.doi.org/10.1186/2045-9769-3-9
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