Source:http://linkedlifedata.com/resource/pubmed/id/19098901
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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
2
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| pubmed:dateCreated |
2009-2-3
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| pubmed:abstractText |
In adults, stem cells are responsible for the maintenance of many actively renewing tissues, such as haematopoietic, skin, gut and germinal tissues. These stem cells can self-renew or be committed to becoming progenitors. Stem-cell commitment is thought to be irreversible but in male and female Drosophila melanogaster, it was shown recently that differentiating germ cells can revert to functional stem cells that can restore germinal lineage. Whether progenitors are also able to generate stem cells in mammals remains unknown. Here we show that purified mouse spermatogonial progenitors committed to differentiation can generate functional germinal stem cells that can repopulate germ-cell-depleted testes when transplanted into adult mice. We found that GDNF, a key regulator of the stem-cell niche, and FGF2 are able to reprogram in vitro spermatogonial progenitors for reverse differentiation. This study supports the emerging concept that the stem-cell identity is not restricted in adults to a definite pool of cells that self-renew, but that stemness could be acquired by differentiating progenitors after tissue injury and throughout life.
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| pubmed:commentsCorrections | |
| pubmed:language |
eng
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| pubmed:journal | |
| pubmed:citationSubset |
IM
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| pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Fibroblast Growth Factor 2,
http://linkedlifedata.com/resource/pubmed/chemical/Glial Cell Line-Derived...,
http://linkedlifedata.com/resource/pubmed/chemical/Green Fluorescent Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/enhanced green fluorescent protein
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| pubmed:status |
MEDLINE
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| pubmed:month |
Feb
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| pubmed:issn |
1476-4679
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| pubmed:author | |
| pubmed:issnType |
Electronic
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| pubmed:volume |
11
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| pubmed:owner |
NLM
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| pubmed:authorsComplete |
Y
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| pubmed:pagination |
190-6
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| pubmed:meshHeading |
pubmed-meshheading:19098901-Animals,
pubmed-meshheading:19098901-Cell Dedifferentiation,
pubmed-meshheading:19098901-Cell Differentiation,
pubmed-meshheading:19098901-Cell Lineage,
pubmed-meshheading:19098901-Cell Proliferation,
pubmed-meshheading:19098901-Fibroblast Growth Factor 2,
pubmed-meshheading:19098901-Germ Cells,
pubmed-meshheading:19098901-Glial Cell Line-Derived Neurotrophic Factor,
pubmed-meshheading:19098901-Green Fluorescent Proteins,
pubmed-meshheading:19098901-Male,
pubmed-meshheading:19098901-Mice,
pubmed-meshheading:19098901-Mice, Inbred C57BL,
pubmed-meshheading:19098901-Mice, Transgenic,
pubmed-meshheading:19098901-Regeneration,
pubmed-meshheading:19098901-Spermatogonia,
pubmed-meshheading:19098901-Stem Cell Transplantation,
pubmed-meshheading:19098901-Stem Cells,
pubmed-meshheading:19098901-Testis
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| pubmed:year |
2009
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| pubmed:articleTitle |
Mouse differentiating spermatogonia can generate germinal stem cells in vivo.
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| pubmed:affiliation |
Laboratoire Gamétogenèse, Apoptose et Génotoxicité, INSERM U566, Institut de Radiobiologie Cellulaire et Moléculaire, Direction des Sciences du Vivant, CEA, 92265 Fontenay aux Roses, France.
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| pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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