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Differentially expressed chaperone genes reveal a stress response required for unidirectional regeneration in the basal chordate Ciona
BACKGROUND: Unidirectional regeneration in the basal chordate Ciona intestinalis involves the proliferation of adult stem cells residing in the branchial sac vasculature and the migration of progenitor cells to the site of distal injury. However, after the Ciona body is bisected, regeneration occurs...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10294541/ https://www.ncbi.nlm.nih.gov/pubmed/37365564 http://dx.doi.org/10.1186/s12915-023-01633-y |
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author | Jeffery, William R. Li, Bo Ng, Mandy Li, Lianwei Gorički, Špela Ma, Li |
author_facet | Jeffery, William R. Li, Bo Ng, Mandy Li, Lianwei Gorički, Špela Ma, Li |
author_sort | Jeffery, William R. |
collection | PubMed |
description | BACKGROUND: Unidirectional regeneration in the basal chordate Ciona intestinalis involves the proliferation of adult stem cells residing in the branchial sac vasculature and the migration of progenitor cells to the site of distal injury. However, after the Ciona body is bisected, regeneration occurs in the proximal but not in the distal fragments, even if the latter include a part of the branchial sac with stem cells. A transcriptome was sequenced and assembled from the isolated branchial sacs of regenerating animals, and the information was used to provide insights into the absence of regeneration in distal body fragments. RESULTS: We identified 1149 differentially expressed genes, which were separated into two major modules by weighted gene correlation network analysis, one consisting of mostly upregulated genes correlated with regeneration and the other consisting of only downregulated genes associated with metabolism and homeostatic processes. The hsp70, dnaJb4, and bag3 genes were among the highest upregulated genes and were predicted to interact in an HSP70 chaperone system. The upregulation of HSP70 chaperone genes was verified and their expression confirmed in BS vasculature cells previously identified as stem and progenitor cells. siRNA-mediated gene knockdown showed that hsp70 and dnaJb4, but not bag3, are required for progenitor cell targeting and distal regeneration. However, neither hsp70 nor dnaJb4 were strongly expressed in the branchial sac vasculature of distal fragments, implying the absence of a stress response. Heat shock treatment of distal body fragments activated hsp70 and dnaJb4 expression indicative of a stress response, induced cell proliferation in branchial sac vasculature cells, and promoted distal regeneration. CONCLUSIONS: The chaperone system genes hsp70, dnaJb4, and bag3 are significantly upregulated in the branchial sac vasculature following distal injury, defining a stress response that is essential for regeneration. The stress response is absent from distal fragments, but can be induced by a heat shock, which activates cell division in the branchial sac vasculature and promotes distal regeneration. This study demonstrates the importance of a stress response for stem cell activation and regeneration in a basal chordate, which may have implications for understanding the limited regenerative activities in other animals, including vertebrates. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12915-023-01633-y. |
format | Online Article Text |
id | pubmed-10294541 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-102945412023-06-28 Differentially expressed chaperone genes reveal a stress response required for unidirectional regeneration in the basal chordate Ciona Jeffery, William R. Li, Bo Ng, Mandy Li, Lianwei Gorički, Špela Ma, Li BMC Biol Research Article BACKGROUND: Unidirectional regeneration in the basal chordate Ciona intestinalis involves the proliferation of adult stem cells residing in the branchial sac vasculature and the migration of progenitor cells to the site of distal injury. However, after the Ciona body is bisected, regeneration occurs in the proximal but not in the distal fragments, even if the latter include a part of the branchial sac with stem cells. A transcriptome was sequenced and assembled from the isolated branchial sacs of regenerating animals, and the information was used to provide insights into the absence of regeneration in distal body fragments. RESULTS: We identified 1149 differentially expressed genes, which were separated into two major modules by weighted gene correlation network analysis, one consisting of mostly upregulated genes correlated with regeneration and the other consisting of only downregulated genes associated with metabolism and homeostatic processes. The hsp70, dnaJb4, and bag3 genes were among the highest upregulated genes and were predicted to interact in an HSP70 chaperone system. The upregulation of HSP70 chaperone genes was verified and their expression confirmed in BS vasculature cells previously identified as stem and progenitor cells. siRNA-mediated gene knockdown showed that hsp70 and dnaJb4, but not bag3, are required for progenitor cell targeting and distal regeneration. However, neither hsp70 nor dnaJb4 were strongly expressed in the branchial sac vasculature of distal fragments, implying the absence of a stress response. Heat shock treatment of distal body fragments activated hsp70 and dnaJb4 expression indicative of a stress response, induced cell proliferation in branchial sac vasculature cells, and promoted distal regeneration. CONCLUSIONS: The chaperone system genes hsp70, dnaJb4, and bag3 are significantly upregulated in the branchial sac vasculature following distal injury, defining a stress response that is essential for regeneration. The stress response is absent from distal fragments, but can be induced by a heat shock, which activates cell division in the branchial sac vasculature and promotes distal regeneration. This study demonstrates the importance of a stress response for stem cell activation and regeneration in a basal chordate, which may have implications for understanding the limited regenerative activities in other animals, including vertebrates. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12915-023-01633-y. BioMed Central 2023-06-26 /pmc/articles/PMC10294541/ /pubmed/37365564 http://dx.doi.org/10.1186/s12915-023-01633-y Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Article Jeffery, William R. Li, Bo Ng, Mandy Li, Lianwei Gorički, Špela Ma, Li Differentially expressed chaperone genes reveal a stress response required for unidirectional regeneration in the basal chordate Ciona |
title | Differentially expressed chaperone genes reveal a stress response required for unidirectional regeneration in the basal chordate Ciona |
title_full | Differentially expressed chaperone genes reveal a stress response required for unidirectional regeneration in the basal chordate Ciona |
title_fullStr | Differentially expressed chaperone genes reveal a stress response required for unidirectional regeneration in the basal chordate Ciona |
title_full_unstemmed | Differentially expressed chaperone genes reveal a stress response required for unidirectional regeneration in the basal chordate Ciona |
title_short | Differentially expressed chaperone genes reveal a stress response required for unidirectional regeneration in the basal chordate Ciona |
title_sort | differentially expressed chaperone genes reveal a stress response required for unidirectional regeneration in the basal chordate ciona |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10294541/ https://www.ncbi.nlm.nih.gov/pubmed/37365564 http://dx.doi.org/10.1186/s12915-023-01633-y |
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