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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...

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Autores principales: Lin, Tzi-Yang, Gerber, Tobias, Taniguchi-Sugiura, Yuka, Murawala, Prayag, Hermann, Sarah, Grosser, Lidia, Shibata, Eri, Treutlein, Barbara, Tanaka, Elly M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2021
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.
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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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