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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2020
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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. |
format | Online Article Text |
id | pubmed-7423392 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
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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