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A protocol to assess cell cycle and apoptosis in human and mouse pluripotent cells

Embryonic stem cells (ESC) and induced pluripotent stem cells (iPSCs) present a great opportunity to treat and model human disease as a cell replacement therapy. There is a growing pressure to understand better the signal transduction pathways regulating pluripotency and self-renewal of these specia...

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Detalles Bibliográficos
Autores principales: Edel, Michael J, Menchon, Cristina, Vaquero, Jose Miguel Andres, Izpisua Belmonte, Juan Carlos
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3101157/
https://www.ncbi.nlm.nih.gov/pubmed/21481269
http://dx.doi.org/10.1186/1478-811X-9-8
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author Edel, Michael J
Menchon, Cristina
Vaquero, Jose Miguel Andres
Izpisua Belmonte, Juan Carlos
author_facet Edel, Michael J
Menchon, Cristina
Vaquero, Jose Miguel Andres
Izpisua Belmonte, Juan Carlos
author_sort Edel, Michael J
collection PubMed
description Embryonic stem cells (ESC) and induced pluripotent stem cells (iPSCs) present a great opportunity to treat and model human disease as a cell replacement therapy. There is a growing pressure to understand better the signal transduction pathways regulating pluripotency and self-renewal of these special cells in order to deliver a safe and reliable cell based therapy in the near future. Many signal transduction pathways converge on two major cell functions associated with self-renewal and pluripotency: control of the cell cycle and apoptosis, although a standard method is lacking across the field. Here we present a detailed protocol to assess the cell cycle and apoptosis of ESC and iPSCs as a single reference point offering an easy to use standard approach across the field.
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spelling pubmed-31011572011-05-25 A protocol to assess cell cycle and apoptosis in human and mouse pluripotent cells Edel, Michael J Menchon, Cristina Vaquero, Jose Miguel Andres Izpisua Belmonte, Juan Carlos Cell Commun Signal Methodology Embryonic stem cells (ESC) and induced pluripotent stem cells (iPSCs) present a great opportunity to treat and model human disease as a cell replacement therapy. There is a growing pressure to understand better the signal transduction pathways regulating pluripotency and self-renewal of these special cells in order to deliver a safe and reliable cell based therapy in the near future. Many signal transduction pathways converge on two major cell functions associated with self-renewal and pluripotency: control of the cell cycle and apoptosis, although a standard method is lacking across the field. Here we present a detailed protocol to assess the cell cycle and apoptosis of ESC and iPSCs as a single reference point offering an easy to use standard approach across the field. BioMed Central 2011-04-11 /pmc/articles/PMC3101157/ /pubmed/21481269 http://dx.doi.org/10.1186/1478-811X-9-8 Text en Copyright ©2011 Edel 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 Methodology
Edel, Michael J
Menchon, Cristina
Vaquero, Jose Miguel Andres
Izpisua Belmonte, Juan Carlos
A protocol to assess cell cycle and apoptosis in human and mouse pluripotent cells
title A protocol to assess cell cycle and apoptosis in human and mouse pluripotent cells
title_full A protocol to assess cell cycle and apoptosis in human and mouse pluripotent cells
title_fullStr A protocol to assess cell cycle and apoptosis in human and mouse pluripotent cells
title_full_unstemmed A protocol to assess cell cycle and apoptosis in human and mouse pluripotent cells
title_short A protocol to assess cell cycle and apoptosis in human and mouse pluripotent cells
title_sort protocol to assess cell cycle and apoptosis in human and mouse pluripotent cells
topic Methodology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3101157/
https://www.ncbi.nlm.nih.gov/pubmed/21481269
http://dx.doi.org/10.1186/1478-811X-9-8
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