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Stem cell topography splits growth and homeostatic functions in the fish gill
While lower vertebrates contain adult stem cells (aSCs) that maintain homeostasis and drive un-exhaustive organismal growth, mammalian aSCs display mainly the homeostatic function. Here, we use lineage analysis in the medaka fish gill to address aSCs and report separate stem cell populations for hom...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6534379/ https://www.ncbi.nlm.nih.gov/pubmed/31090541 http://dx.doi.org/10.7554/eLife.43747 |
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author | Stolper, Julian Ambrosio, Elizabeth Mayela Danciu, Diana-Patricia Buono, Lorena Elliott, David A Naruse, Kiyoshi Martínez-Morales, Juan R Marciniak-Czochra, Anna Centanin, Lazaro |
author_facet | Stolper, Julian Ambrosio, Elizabeth Mayela Danciu, Diana-Patricia Buono, Lorena Elliott, David A Naruse, Kiyoshi Martínez-Morales, Juan R Marciniak-Czochra, Anna Centanin, Lazaro |
author_sort | Stolper, Julian |
collection | PubMed |
description | While lower vertebrates contain adult stem cells (aSCs) that maintain homeostasis and drive un-exhaustive organismal growth, mammalian aSCs display mainly the homeostatic function. Here, we use lineage analysis in the medaka fish gill to address aSCs and report separate stem cell populations for homeostasis and growth. These aSCs are fate-restricted during the entire post-embryonic life and even during re-generation paradigms. We use chimeric animals to demonstrate that p53 mediates growth coordination among fate-restricted aSCs, suggesting a hierarchical organisation among lineages in composite organs like the fish gill. Homeostatic and growth aSCs are clonal but differ in their topology; modifications in tissue architecture can convert the homeostatic zone into a growth zone, indicating a leading role for the physical niche defining stem cell output. We hypothesise that physical niches are main players to restrict aSCs to a homeostatic function in animals with fixed adult size. |
format | Online Article Text |
id | pubmed-6534379 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-65343792019-05-28 Stem cell topography splits growth and homeostatic functions in the fish gill Stolper, Julian Ambrosio, Elizabeth Mayela Danciu, Diana-Patricia Buono, Lorena Elliott, David A Naruse, Kiyoshi Martínez-Morales, Juan R Marciniak-Czochra, Anna Centanin, Lazaro eLife Developmental Biology While lower vertebrates contain adult stem cells (aSCs) that maintain homeostasis and drive un-exhaustive organismal growth, mammalian aSCs display mainly the homeostatic function. Here, we use lineage analysis in the medaka fish gill to address aSCs and report separate stem cell populations for homeostasis and growth. These aSCs are fate-restricted during the entire post-embryonic life and even during re-generation paradigms. We use chimeric animals to demonstrate that p53 mediates growth coordination among fate-restricted aSCs, suggesting a hierarchical organisation among lineages in composite organs like the fish gill. Homeostatic and growth aSCs are clonal but differ in their topology; modifications in tissue architecture can convert the homeostatic zone into a growth zone, indicating a leading role for the physical niche defining stem cell output. We hypothesise that physical niches are main players to restrict aSCs to a homeostatic function in animals with fixed adult size. eLife Sciences Publications, Ltd 2019-05-16 /pmc/articles/PMC6534379/ /pubmed/31090541 http://dx.doi.org/10.7554/eLife.43747 Text en © 2019, Stolper 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 | Developmental Biology Stolper, Julian Ambrosio, Elizabeth Mayela Danciu, Diana-Patricia Buono, Lorena Elliott, David A Naruse, Kiyoshi Martínez-Morales, Juan R Marciniak-Czochra, Anna Centanin, Lazaro Stem cell topography splits growth and homeostatic functions in the fish gill |
title | Stem cell topography splits growth and homeostatic functions in the fish gill |
title_full | Stem cell topography splits growth and homeostatic functions in the fish gill |
title_fullStr | Stem cell topography splits growth and homeostatic functions in the fish gill |
title_full_unstemmed | Stem cell topography splits growth and homeostatic functions in the fish gill |
title_short | Stem cell topography splits growth and homeostatic functions in the fish gill |
title_sort | stem cell topography splits growth and homeostatic functions in the fish gill |
topic | Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6534379/ https://www.ncbi.nlm.nih.gov/pubmed/31090541 http://dx.doi.org/10.7554/eLife.43747 |
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