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Wilms Tumor 1b defines a wound-specific sheath cell subpopulation associated with notochord repair
Regenerative therapy for degenerative spine disorders requires the identification of cells that can slow down and possibly reverse degenerative processes. Here, we identify an unanticipated wound-specific notochord sheath cell subpopulation that expresses Wilms Tumor (WT) 1b following injury in zebr...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5811212/ https://www.ncbi.nlm.nih.gov/pubmed/29405914 http://dx.doi.org/10.7554/eLife.30657 |
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author | Lopez-Baez, Juan Carlos Simpson, Daniel J LLeras Forero, Laura Zeng, Zhiqiang Brunsdon, Hannah Salzano, Angela Brombin, Alessandro Wyatt, Cameron Rybski, Witold Huitema, Leonie F A Dale, Rodney M Kawakami, Koichi Englert, Christoph Chandra, Tamir Schulte-Merker, Stefan Hastie, Nicholas D Patton, E Elizabeth |
author_facet | Lopez-Baez, Juan Carlos Simpson, Daniel J LLeras Forero, Laura Zeng, Zhiqiang Brunsdon, Hannah Salzano, Angela Brombin, Alessandro Wyatt, Cameron Rybski, Witold Huitema, Leonie F A Dale, Rodney M Kawakami, Koichi Englert, Christoph Chandra, Tamir Schulte-Merker, Stefan Hastie, Nicholas D Patton, E Elizabeth |
author_sort | Lopez-Baez, Juan Carlos |
collection | PubMed |
description | Regenerative therapy for degenerative spine disorders requires the identification of cells that can slow down and possibly reverse degenerative processes. Here, we identify an unanticipated wound-specific notochord sheath cell subpopulation that expresses Wilms Tumor (WT) 1b following injury in zebrafish. We show that localized damage leads to Wt1b expression in sheath cells, and that wt1b(+)cells migrate into the wound to form a stopper-like structure, likely to maintain structural integrity. Wt1b(+)sheath cells are distinct in expressing cartilage and vacuolar genes, and in repressing a Wt1b-p53 transcriptional programme. At the wound, wt1b(+)and entpd5(+) cells constitute separate, tightly-associated subpopulations. Surprisingly, wt1b expression at the site of injury is maintained even into adult stages in developing vertebrae, which form in an untypical manner via a cartilage intermediate. Given that notochord cells are retained in adult intervertebral discs, the identification of novel subpopulations may have important implications for regenerative spine disorder treatments. |
format | Online Article Text |
id | pubmed-5811212 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-58112122018-02-14 Wilms Tumor 1b defines a wound-specific sheath cell subpopulation associated with notochord repair Lopez-Baez, Juan Carlos Simpson, Daniel J LLeras Forero, Laura Zeng, Zhiqiang Brunsdon, Hannah Salzano, Angela Brombin, Alessandro Wyatt, Cameron Rybski, Witold Huitema, Leonie F A Dale, Rodney M Kawakami, Koichi Englert, Christoph Chandra, Tamir Schulte-Merker, Stefan Hastie, Nicholas D Patton, E Elizabeth eLife Stem Cells and Regenerative Medicine Regenerative therapy for degenerative spine disorders requires the identification of cells that can slow down and possibly reverse degenerative processes. Here, we identify an unanticipated wound-specific notochord sheath cell subpopulation that expresses Wilms Tumor (WT) 1b following injury in zebrafish. We show that localized damage leads to Wt1b expression in sheath cells, and that wt1b(+)cells migrate into the wound to form a stopper-like structure, likely to maintain structural integrity. Wt1b(+)sheath cells are distinct in expressing cartilage and vacuolar genes, and in repressing a Wt1b-p53 transcriptional programme. At the wound, wt1b(+)and entpd5(+) cells constitute separate, tightly-associated subpopulations. Surprisingly, wt1b expression at the site of injury is maintained even into adult stages in developing vertebrae, which form in an untypical manner via a cartilage intermediate. Given that notochord cells are retained in adult intervertebral discs, the identification of novel subpopulations may have important implications for regenerative spine disorder treatments. eLife Sciences Publications, Ltd 2018-02-06 /pmc/articles/PMC5811212/ /pubmed/29405914 http://dx.doi.org/10.7554/eLife.30657 Text en © 2018, Lopez-Baez et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Stem Cells and Regenerative Medicine Lopez-Baez, Juan Carlos Simpson, Daniel J LLeras Forero, Laura Zeng, Zhiqiang Brunsdon, Hannah Salzano, Angela Brombin, Alessandro Wyatt, Cameron Rybski, Witold Huitema, Leonie F A Dale, Rodney M Kawakami, Koichi Englert, Christoph Chandra, Tamir Schulte-Merker, Stefan Hastie, Nicholas D Patton, E Elizabeth Wilms Tumor 1b defines a wound-specific sheath cell subpopulation associated with notochord repair |
title | Wilms Tumor 1b defines a wound-specific sheath cell subpopulation associated with notochord repair |
title_full | Wilms Tumor 1b defines a wound-specific sheath cell subpopulation associated with notochord repair |
title_fullStr | Wilms Tumor 1b defines a wound-specific sheath cell subpopulation associated with notochord repair |
title_full_unstemmed | Wilms Tumor 1b defines a wound-specific sheath cell subpopulation associated with notochord repair |
title_short | Wilms Tumor 1b defines a wound-specific sheath cell subpopulation associated with notochord repair |
title_sort | wilms tumor 1b defines a wound-specific sheath cell subpopulation associated with notochord repair |
topic | Stem Cells and Regenerative Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5811212/ https://www.ncbi.nlm.nih.gov/pubmed/29405914 http://dx.doi.org/10.7554/eLife.30657 |
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