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Cellular diversity of the regenerating caudal fin

Zebrafish faithfully regenerate their caudal fin after amputation. During this process, both differentiated cells and resident progenitors migrate to the wound site and undergo lineage-restricted, programmed cellular state transitions to populate the new regenerate. Until now, systematic characteriz...

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Autores principales: Hou, Yiran, Lee, Hyung Joo, Chen, Yujie, Ge, Jiaxin, Osman, Fujr Osman Ibrahim, McAdow, Anthony R., Mokalled, Mayssa H., Johnson, Stephen L., Zhao, Guoyan, Wang, Ting
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7423392/
https://www.ncbi.nlm.nih.gov/pubmed/32851162
http://dx.doi.org/10.1126/sciadv.aba2084
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author Hou, Yiran
Lee, Hyung Joo
Chen, Yujie
Ge, Jiaxin
Osman, Fujr Osman Ibrahim
McAdow, Anthony R.
Mokalled, Mayssa H.
Johnson, Stephen L.
Zhao, Guoyan
Wang, Ting
author_facet Hou, Yiran
Lee, Hyung Joo
Chen, Yujie
Ge, Jiaxin
Osman, Fujr Osman Ibrahim
McAdow, Anthony R.
Mokalled, Mayssa H.
Johnson, Stephen L.
Zhao, Guoyan
Wang, Ting
author_sort Hou, Yiran
collection PubMed
description Zebrafish faithfully regenerate their caudal fin after amputation. During this process, both differentiated cells and resident progenitors migrate to the wound site and undergo lineage-restricted, programmed cellular state transitions to populate the new regenerate. Until now, systematic characterizations of cells comprising the new regenerate and molecular definitions of their state transitions have been lacking. We hereby characterize the dynamics of gene regulatory programs during fin regeneration by creating single-cell transcriptome maps of both preinjury and regenerating fin tissues at 1/2/4 days post-amputation. We consistently identified epithelial, mesenchymal, and hematopoietic populations across all stages. We found common and cell type–specific cell cycle programs associated with proliferation. In addition to defining the processes of epithelial replenishment and mesenchymal differentiation, we also identified molecular signatures that could better distinguish epithelial and mesenchymal subpopulations in fish. The insights for natural cell state transitions during regeneration point to new directions for studying this regeneration model.
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spelling pubmed-74233922020-08-25 Cellular diversity of the regenerating caudal fin Hou, Yiran Lee, Hyung Joo Chen, Yujie Ge, Jiaxin Osman, Fujr Osman Ibrahim McAdow, Anthony R. Mokalled, Mayssa H. Johnson, Stephen L. Zhao, Guoyan Wang, Ting Sci Adv Research Articles Zebrafish faithfully regenerate their caudal fin after amputation. During this process, both differentiated cells and resident progenitors migrate to the wound site and undergo lineage-restricted, programmed cellular state transitions to populate the new regenerate. Until now, systematic characterizations of cells comprising the new regenerate and molecular definitions of their state transitions have been lacking. We hereby characterize the dynamics of gene regulatory programs during fin regeneration by creating single-cell transcriptome maps of both preinjury and regenerating fin tissues at 1/2/4 days post-amputation. We consistently identified epithelial, mesenchymal, and hematopoietic populations across all stages. We found common and cell type–specific cell cycle programs associated with proliferation. In addition to defining the processes of epithelial replenishment and mesenchymal differentiation, we also identified molecular signatures that could better distinguish epithelial and mesenchymal subpopulations in fish. The insights for natural cell state transitions during regeneration point to new directions for studying this regeneration model. American Association for the Advancement of Science 2020-08-12 /pmc/articles/PMC7423392/ /pubmed/32851162 http://dx.doi.org/10.1126/sciadv.aba2084 Text en Copyright © 2020 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/ 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 Research Articles
Hou, Yiran
Lee, Hyung Joo
Chen, Yujie
Ge, Jiaxin
Osman, Fujr Osman Ibrahim
McAdow, Anthony R.
Mokalled, Mayssa H.
Johnson, Stephen L.
Zhao, Guoyan
Wang, Ting
Cellular diversity of the regenerating caudal fin
title Cellular diversity of the regenerating caudal fin
title_full Cellular diversity of the regenerating caudal fin
title_fullStr Cellular diversity of the regenerating caudal fin
title_full_unstemmed Cellular diversity of the regenerating caudal fin
title_short Cellular diversity of the regenerating caudal fin
title_sort cellular diversity of the regenerating caudal fin
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7423392/
https://www.ncbi.nlm.nih.gov/pubmed/32851162
http://dx.doi.org/10.1126/sciadv.aba2084
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