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Regeneration and reprogramming compared

BACKGROUND: Dedifferentiation occurs naturally in mature cell types during epimorphic regeneration in fish and some amphibians. Dedifferentiation also occurs in the induction of pluripotent stem cells when a set of transcription factors (Oct4, Sox2, Klf4 and c-Myc) is over expressed in mature cell t...

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Autores principales: Christen, Bea, Robles, Vanesa, Raya, Marina, Paramonov, Ida, Belmonte, Juan Carlos Izpisúa
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2826312/
https://www.ncbi.nlm.nih.gov/pubmed/20089153
http://dx.doi.org/10.1186/1741-7007-8-5
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author Christen, Bea
Robles, Vanesa
Raya, Marina
Paramonov, Ida
Belmonte, Juan Carlos Izpisúa
author_facet Christen, Bea
Robles, Vanesa
Raya, Marina
Paramonov, Ida
Belmonte, Juan Carlos Izpisúa
author_sort Christen, Bea
collection PubMed
description BACKGROUND: Dedifferentiation occurs naturally in mature cell types during epimorphic regeneration in fish and some amphibians. Dedifferentiation also occurs in the induction of pluripotent stem cells when a set of transcription factors (Oct4, Sox2, Klf4 and c-Myc) is over expressed in mature cell types. RESULTS: We hypothesised that there are parallels between dedifferentiation or reprogramming of somatic cells to induced pluripotent stem cells and the natural process of dedifferentiation during epimorphic regeneration. We analysed expression levels of the most commonly used pluripotency associated factors in regenerating and non-regenerating tissue and compared them with levels in a pluripotent reference cell. We found that some of the pluripotency associated factors (oct4/pou5f1, sox2, c-myc, klf4, tert, sall4, zic3, dppa2/4 and fut1, a homologue of ssea1) were expressed before and during regeneration and that at least two of these factors (oct4, sox2) were also required for normal fin regeneration in the zebrafish. However these factors were not upregulated during regeneration as would be expected if blastema cells acquired pluripotency. CONCLUSIONS: By comparing cells from the regeneration blastema with embryonic pluripotent reference cells we found that induced pluripotent stem and blastema cells do not share pluripotency. However, during blastema formation some of the key reprogramming factors are both expressed and are also required for regeneration to take place. We therefore propose a link between partially reprogrammed induced pluripotent stem cells and the half way state of blastema cells and suggest that a common mechanism might be regulating these two processes.
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spelling pubmed-28263122010-02-23 Regeneration and reprogramming compared Christen, Bea Robles, Vanesa Raya, Marina Paramonov, Ida Belmonte, Juan Carlos Izpisúa BMC Biol Research article BACKGROUND: Dedifferentiation occurs naturally in mature cell types during epimorphic regeneration in fish and some amphibians. Dedifferentiation also occurs in the induction of pluripotent stem cells when a set of transcription factors (Oct4, Sox2, Klf4 and c-Myc) is over expressed in mature cell types. RESULTS: We hypothesised that there are parallels between dedifferentiation or reprogramming of somatic cells to induced pluripotent stem cells and the natural process of dedifferentiation during epimorphic regeneration. We analysed expression levels of the most commonly used pluripotency associated factors in regenerating and non-regenerating tissue and compared them with levels in a pluripotent reference cell. We found that some of the pluripotency associated factors (oct4/pou5f1, sox2, c-myc, klf4, tert, sall4, zic3, dppa2/4 and fut1, a homologue of ssea1) were expressed before and during regeneration and that at least two of these factors (oct4, sox2) were also required for normal fin regeneration in the zebrafish. However these factors were not upregulated during regeneration as would be expected if blastema cells acquired pluripotency. CONCLUSIONS: By comparing cells from the regeneration blastema with embryonic pluripotent reference cells we found that induced pluripotent stem and blastema cells do not share pluripotency. However, during blastema formation some of the key reprogramming factors are both expressed and are also required for regeneration to take place. We therefore propose a link between partially reprogrammed induced pluripotent stem cells and the half way state of blastema cells and suggest that a common mechanism might be regulating these two processes. BioMed Central 2010-01-20 /pmc/articles/PMC2826312/ /pubmed/20089153 http://dx.doi.org/10.1186/1741-7007-8-5 Text en Copyright ©2010 Christen et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 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 cited.
spellingShingle Research article
Christen, Bea
Robles, Vanesa
Raya, Marina
Paramonov, Ida
Belmonte, Juan Carlos Izpisúa
Regeneration and reprogramming compared
title Regeneration and reprogramming compared
title_full Regeneration and reprogramming compared
title_fullStr Regeneration and reprogramming compared
title_full_unstemmed Regeneration and reprogramming compared
title_short Regeneration and reprogramming compared
title_sort regeneration and reprogramming compared
topic Research article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2826312/
https://www.ncbi.nlm.nih.gov/pubmed/20089153
http://dx.doi.org/10.1186/1741-7007-8-5
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