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Microcarrier-Based Expansion of Adult Murine Side Population Stem Cells
The lack of reliable methods to efficiently isolate and propagate stem cell populations is a significant obstacle to the advancement of cell-based therapies for human diseases. One isolation technique is based on efflux of the fluorophore Hoechst 33342. Using fluorescence-activated cell sorting (FAC...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3557248/ https://www.ncbi.nlm.nih.gov/pubmed/23383102 http://dx.doi.org/10.1371/journal.pone.0055187 |
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author | Pacak, Christina A. Eddy, Mau-Thek Woodhull, Lindsey Wang, Kai-Roy Alpatov, Ivan Fullen, Shelby Dowd, Rory P. Choi, Yeong-Hoon Cowan, Douglas B. |
author_facet | Pacak, Christina A. Eddy, Mau-Thek Woodhull, Lindsey Wang, Kai-Roy Alpatov, Ivan Fullen, Shelby Dowd, Rory P. Choi, Yeong-Hoon Cowan, Douglas B. |
author_sort | Pacak, Christina A. |
collection | PubMed |
description | The lack of reliable methods to efficiently isolate and propagate stem cell populations is a significant obstacle to the advancement of cell-based therapies for human diseases. One isolation technique is based on efflux of the fluorophore Hoechst 33342. Using fluorescence-activated cell sorting (FACS), a sub-population containing adult stem cells has been identified in a multitude of tissues in every mammalian species examined. These rare cells are referred to as the ‘side population’ or SP due to a distinctive FACS profile that results from weak staining by Hoechst dye. Although the SP contains multi-potent cells capable of differentiating toward hematopoietic and mesenchymal lineages; there is currently no method to efficiently expand them. Here, we describe a spinner-flask culture system containing C2C12 myoblasts attached to spherical microcarriers that act to support the growth of non-adherent, post-natal murine skeletal muscle and bone marrow SP cells. Using FACS and hemocytometry, we show expansion of unfractionated EGFP(+) SP cells over 6 wks. A significant number of these cells retain characteristics of freshly-isolated, unfractionated SP cells with respect to protein expression and dye efflux capacity. Expansion of the SP will permit further study of these heterogeneous cells and determine their therapeutic potential for regenerative and reparative therapies. |
format | Online Article Text |
id | pubmed-3557248 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-35572482013-02-04 Microcarrier-Based Expansion of Adult Murine Side Population Stem Cells Pacak, Christina A. Eddy, Mau-Thek Woodhull, Lindsey Wang, Kai-Roy Alpatov, Ivan Fullen, Shelby Dowd, Rory P. Choi, Yeong-Hoon Cowan, Douglas B. PLoS One Research Article The lack of reliable methods to efficiently isolate and propagate stem cell populations is a significant obstacle to the advancement of cell-based therapies for human diseases. One isolation technique is based on efflux of the fluorophore Hoechst 33342. Using fluorescence-activated cell sorting (FACS), a sub-population containing adult stem cells has been identified in a multitude of tissues in every mammalian species examined. These rare cells are referred to as the ‘side population’ or SP due to a distinctive FACS profile that results from weak staining by Hoechst dye. Although the SP contains multi-potent cells capable of differentiating toward hematopoietic and mesenchymal lineages; there is currently no method to efficiently expand them. Here, we describe a spinner-flask culture system containing C2C12 myoblasts attached to spherical microcarriers that act to support the growth of non-adherent, post-natal murine skeletal muscle and bone marrow SP cells. Using FACS and hemocytometry, we show expansion of unfractionated EGFP(+) SP cells over 6 wks. A significant number of these cells retain characteristics of freshly-isolated, unfractionated SP cells with respect to protein expression and dye efflux capacity. Expansion of the SP will permit further study of these heterogeneous cells and determine their therapeutic potential for regenerative and reparative therapies. Public Library of Science 2013-01-28 /pmc/articles/PMC3557248/ /pubmed/23383102 http://dx.doi.org/10.1371/journal.pone.0055187 Text en © 2013 Pacak et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Pacak, Christina A. Eddy, Mau-Thek Woodhull, Lindsey Wang, Kai-Roy Alpatov, Ivan Fullen, Shelby Dowd, Rory P. Choi, Yeong-Hoon Cowan, Douglas B. Microcarrier-Based Expansion of Adult Murine Side Population Stem Cells |
title | Microcarrier-Based Expansion of Adult Murine Side Population Stem Cells |
title_full | Microcarrier-Based Expansion of Adult Murine Side Population Stem Cells |
title_fullStr | Microcarrier-Based Expansion of Adult Murine Side Population Stem Cells |
title_full_unstemmed | Microcarrier-Based Expansion of Adult Murine Side Population Stem Cells |
title_short | Microcarrier-Based Expansion of Adult Murine Side Population Stem Cells |
title_sort | microcarrier-based expansion of adult murine side population stem cells |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3557248/ https://www.ncbi.nlm.nih.gov/pubmed/23383102 http://dx.doi.org/10.1371/journal.pone.0055187 |
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