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Fibroblast dedifferentiation as a determinant of successful regeneration
Limb regeneration, while observed lifelong in salamanders, is restricted in post-metamorphic Xenopus laevis frogs. Whether this loss is due to systemic factors or an intrinsic incapability of cells to form competent stem cells has been unclear. Here, we use genetic fate mapping to establish that con...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8140481/ https://www.ncbi.nlm.nih.gov/pubmed/34004152 http://dx.doi.org/10.1016/j.devcel.2021.04.016 |
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author | Lin, Tzi-Yang Gerber, Tobias Taniguchi-Sugiura, Yuka Murawala, Prayag Hermann, Sarah Grosser, Lidia Shibata, Eri Treutlein, Barbara Tanaka, Elly M. |
author_facet | Lin, Tzi-Yang Gerber, Tobias Taniguchi-Sugiura, Yuka Murawala, Prayag Hermann, Sarah Grosser, Lidia Shibata, Eri Treutlein, Barbara Tanaka, Elly M. |
author_sort | Lin, Tzi-Yang |
collection | PubMed |
description | Limb regeneration, while observed lifelong in salamanders, is restricted in post-metamorphic Xenopus laevis frogs. Whether this loss is due to systemic factors or an intrinsic incapability of cells to form competent stem cells has been unclear. Here, we use genetic fate mapping to establish that connective tissue (CT) cells form the post-metamorphic frog blastema, as in the case of axolotls. Using heterochronic transplantation into the limb bud and single-cell transcriptomic profiling, we show that axolotl CT cells dedifferentiate and integrate to form lineages, including cartilage. In contrast, frog blastema CT cells do not fully re-express the limb bud progenitor program, even when transplanted into the limb bud. Correspondingly, transplanted cells contribute to extraskeletal CT, but not to the developing cartilage. Furthermore, using single-cell RNA-seq analysis we find that embryonic and adult frog cartilage differentiation programs are molecularly distinct. This work defines intrinsic restrictions in CT dedifferentiation as a limitation in adult regeneration. |
format | Online Article Text |
id | pubmed-8140481 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-81404812021-05-26 Fibroblast dedifferentiation as a determinant of successful regeneration Lin, Tzi-Yang Gerber, Tobias Taniguchi-Sugiura, Yuka Murawala, Prayag Hermann, Sarah Grosser, Lidia Shibata, Eri Treutlein, Barbara Tanaka, Elly M. Dev Cell Article Limb regeneration, while observed lifelong in salamanders, is restricted in post-metamorphic Xenopus laevis frogs. Whether this loss is due to systemic factors or an intrinsic incapability of cells to form competent stem cells has been unclear. Here, we use genetic fate mapping to establish that connective tissue (CT) cells form the post-metamorphic frog blastema, as in the case of axolotls. Using heterochronic transplantation into the limb bud and single-cell transcriptomic profiling, we show that axolotl CT cells dedifferentiate and integrate to form lineages, including cartilage. In contrast, frog blastema CT cells do not fully re-express the limb bud progenitor program, even when transplanted into the limb bud. Correspondingly, transplanted cells contribute to extraskeletal CT, but not to the developing cartilage. Furthermore, using single-cell RNA-seq analysis we find that embryonic and adult frog cartilage differentiation programs are molecularly distinct. This work defines intrinsic restrictions in CT dedifferentiation as a limitation in adult regeneration. Cell Press 2021-05-17 /pmc/articles/PMC8140481/ /pubmed/34004152 http://dx.doi.org/10.1016/j.devcel.2021.04.016 Text en © 2021 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Lin, Tzi-Yang Gerber, Tobias Taniguchi-Sugiura, Yuka Murawala, Prayag Hermann, Sarah Grosser, Lidia Shibata, Eri Treutlein, Barbara Tanaka, Elly M. Fibroblast dedifferentiation as a determinant of successful regeneration |
title | Fibroblast dedifferentiation as a determinant of successful regeneration |
title_full | Fibroblast dedifferentiation as a determinant of successful regeneration |
title_fullStr | Fibroblast dedifferentiation as a determinant of successful regeneration |
title_full_unstemmed | Fibroblast dedifferentiation as a determinant of successful regeneration |
title_short | Fibroblast dedifferentiation as a determinant of successful regeneration |
title_sort | fibroblast dedifferentiation as a determinant of successful regeneration |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8140481/ https://www.ncbi.nlm.nih.gov/pubmed/34004152 http://dx.doi.org/10.1016/j.devcel.2021.04.016 |
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