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Single-cell analysis reveals distinct fibroblast plasticity during tenocyte regeneration in zebrafish
Despite their importance in tissue maintenance and repair, fibroblast diversity and plasticity remain poorly understood. Using single-cell RNA sequencing, we uncover distinct sclerotome-derived fibroblast populations in zebrafish, including progenitor-like perivascular/interstitial fibroblasts, and...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10651129/ https://www.ncbi.nlm.nih.gov/pubmed/37967180 http://dx.doi.org/10.1126/sciadv.adi5771 |
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author | Rajan, Arsheen M. Rosin, Nicole L. Labit, Elodie Biernaskie, Jeff Liao, Shan Huang, Peng |
author_facet | Rajan, Arsheen M. Rosin, Nicole L. Labit, Elodie Biernaskie, Jeff Liao, Shan Huang, Peng |
author_sort | Rajan, Arsheen M. |
collection | PubMed |
description | Despite their importance in tissue maintenance and repair, fibroblast diversity and plasticity remain poorly understood. Using single-cell RNA sequencing, we uncover distinct sclerotome-derived fibroblast populations in zebrafish, including progenitor-like perivascular/interstitial fibroblasts, and specialized fibroblasts such as tenocytes. To determine fibroblast plasticity in vivo, we develop a laser-induced tendon ablation and regeneration model. Lineage tracing reveals that laser-ablated tenocytes are quickly regenerated by preexisting fibroblasts. By combining single-cell clonal analysis and live imaging, we demonstrate that perivascular/interstitial fibroblasts actively migrate to the injury site, where they proliferate and give rise to new tenocytes. By contrast, perivascular fibroblast–derived pericytes or specialized fibroblasts, including tenocytes, exhibit no regenerative plasticity. Active Hedgehog (Hh) signaling is required for the proliferation of activated fibroblasts to ensure efficient tenocyte regeneration. Together, our work highlights the functional diversity of fibroblasts and establishes perivascular/interstitial fibroblasts as tenocyte progenitors that promote tendon regeneration in a Hh signaling–dependent manner. |
format | Online Article Text |
id | pubmed-10651129 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-106511292023-11-15 Single-cell analysis reveals distinct fibroblast plasticity during tenocyte regeneration in zebrafish Rajan, Arsheen M. Rosin, Nicole L. Labit, Elodie Biernaskie, Jeff Liao, Shan Huang, Peng Sci Adv Biomedicine and Life Sciences Despite their importance in tissue maintenance and repair, fibroblast diversity and plasticity remain poorly understood. Using single-cell RNA sequencing, we uncover distinct sclerotome-derived fibroblast populations in zebrafish, including progenitor-like perivascular/interstitial fibroblasts, and specialized fibroblasts such as tenocytes. To determine fibroblast plasticity in vivo, we develop a laser-induced tendon ablation and regeneration model. Lineage tracing reveals that laser-ablated tenocytes are quickly regenerated by preexisting fibroblasts. By combining single-cell clonal analysis and live imaging, we demonstrate that perivascular/interstitial fibroblasts actively migrate to the injury site, where they proliferate and give rise to new tenocytes. By contrast, perivascular fibroblast–derived pericytes or specialized fibroblasts, including tenocytes, exhibit no regenerative plasticity. Active Hedgehog (Hh) signaling is required for the proliferation of activated fibroblasts to ensure efficient tenocyte regeneration. Together, our work highlights the functional diversity of fibroblasts and establishes perivascular/interstitial fibroblasts as tenocyte progenitors that promote tendon regeneration in a Hh signaling–dependent manner. American Association for the Advancement of Science 2023-11-15 /pmc/articles/PMC10651129/ /pubmed/37967180 http://dx.doi.org/10.1126/sciadv.adi5771 Text en Copyright © 2023 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Biomedicine and Life Sciences Rajan, Arsheen M. Rosin, Nicole L. Labit, Elodie Biernaskie, Jeff Liao, Shan Huang, Peng Single-cell analysis reveals distinct fibroblast plasticity during tenocyte regeneration in zebrafish |
title | Single-cell analysis reveals distinct fibroblast plasticity during tenocyte regeneration in zebrafish |
title_full | Single-cell analysis reveals distinct fibroblast plasticity during tenocyte regeneration in zebrafish |
title_fullStr | Single-cell analysis reveals distinct fibroblast plasticity during tenocyte regeneration in zebrafish |
title_full_unstemmed | Single-cell analysis reveals distinct fibroblast plasticity during tenocyte regeneration in zebrafish |
title_short | Single-cell analysis reveals distinct fibroblast plasticity during tenocyte regeneration in zebrafish |
title_sort | single-cell analysis reveals distinct fibroblast plasticity during tenocyte regeneration in zebrafish |
topic | Biomedicine and Life Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10651129/ https://www.ncbi.nlm.nih.gov/pubmed/37967180 http://dx.doi.org/10.1126/sciadv.adi5771 |
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