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Capacity for stochastic self-renewal and differentiation in mammalian spermatogonial stem cells
Mammalian spermatogenesis is initiated and sustained by spermatogonial stem cells (SSCs) through self-renewal and differentiation. The basic question of whether SSCs have the potential to specify self-renewal and differentiation in a cell-autonomous manner has yet to be addressed. Here, we show that...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2779229/ https://www.ncbi.nlm.nih.gov/pubmed/19948499 http://dx.doi.org/10.1083/jcb.200907047 |
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author | Wu, Zhuoru Luby-Phelps, Katherine Bugde, Abhijit Molyneux, Laura A. Denard, Bray Li, Wen-Hong Süel, Gürol M. Garbers, David L. |
author_facet | Wu, Zhuoru Luby-Phelps, Katherine Bugde, Abhijit Molyneux, Laura A. Denard, Bray Li, Wen-Hong Süel, Gürol M. Garbers, David L. |
author_sort | Wu, Zhuoru |
collection | PubMed |
description | Mammalian spermatogenesis is initiated and sustained by spermatogonial stem cells (SSCs) through self-renewal and differentiation. The basic question of whether SSCs have the potential to specify self-renewal and differentiation in a cell-autonomous manner has yet to be addressed. Here, we show that rat SSCs in ex vivo culture conditions consistently give rise to two distinct types of progeny: new SSCs and differentiating germ cells, even when they have been exposed to virtually identical microenvironments. Quantitative experimental measurements and mathematical modeling indicates that fate decision is stochastic, with constant probability. These results reveal an unexpected ability in a mammalian SSC to specify both self-renewal and differentiation through a self-directed mechanism, and further suggest that this mechanism operates according to stochastic principles. These findings provide an experimental basis for autonomous and stochastic fate choice as an alternative strategy for SSC fate bifurcation, which may also be relevant to other stem cell types. |
format | Text |
id | pubmed-2779229 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-27792292010-05-16 Capacity for stochastic self-renewal and differentiation in mammalian spermatogonial stem cells Wu, Zhuoru Luby-Phelps, Katherine Bugde, Abhijit Molyneux, Laura A. Denard, Bray Li, Wen-Hong Süel, Gürol M. Garbers, David L. J Cell Biol Research Articles Mammalian spermatogenesis is initiated and sustained by spermatogonial stem cells (SSCs) through self-renewal and differentiation. The basic question of whether SSCs have the potential to specify self-renewal and differentiation in a cell-autonomous manner has yet to be addressed. Here, we show that rat SSCs in ex vivo culture conditions consistently give rise to two distinct types of progeny: new SSCs and differentiating germ cells, even when they have been exposed to virtually identical microenvironments. Quantitative experimental measurements and mathematical modeling indicates that fate decision is stochastic, with constant probability. These results reveal an unexpected ability in a mammalian SSC to specify both self-renewal and differentiation through a self-directed mechanism, and further suggest that this mechanism operates according to stochastic principles. These findings provide an experimental basis for autonomous and stochastic fate choice as an alternative strategy for SSC fate bifurcation, which may also be relevant to other stem cell types. The Rockefeller University Press 2009-11-16 /pmc/articles/PMC2779229/ /pubmed/19948499 http://dx.doi.org/10.1083/jcb.200907047 Text en © 2009 Wu et al. This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.jcb.org/misc/terms.shtml). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/). |
spellingShingle | Research Articles Wu, Zhuoru Luby-Phelps, Katherine Bugde, Abhijit Molyneux, Laura A. Denard, Bray Li, Wen-Hong Süel, Gürol M. Garbers, David L. Capacity for stochastic self-renewal and differentiation in mammalian spermatogonial stem cells |
title | Capacity for stochastic self-renewal and differentiation in mammalian spermatogonial stem cells |
title_full | Capacity for stochastic self-renewal and differentiation in mammalian spermatogonial stem cells |
title_fullStr | Capacity for stochastic self-renewal and differentiation in mammalian spermatogonial stem cells |
title_full_unstemmed | Capacity for stochastic self-renewal and differentiation in mammalian spermatogonial stem cells |
title_short | Capacity for stochastic self-renewal and differentiation in mammalian spermatogonial stem cells |
title_sort | capacity for stochastic self-renewal and differentiation in mammalian spermatogonial stem cells |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2779229/ https://www.ncbi.nlm.nih.gov/pubmed/19948499 http://dx.doi.org/10.1083/jcb.200907047 |
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