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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...

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Autores principales: Rajan, Arsheen M., Rosin, Nicole L., Labit, Elodie, Biernaskie, Jeff, Liao, Shan, Huang, Peng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2023
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.
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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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