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Identification of an integrated stress and growth response signaling switch that directs vertebrate intestinal regeneration

BACKGROUND: Snakes exhibit extreme intestinal regeneration following months-long fasts that involves unparalleled increases in metabolism, function, and tissue growth, but the specific molecular control of this process is unknown. Understanding the mechanisms that coordinate these regenerative pheno...

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Autores principales: Westfall, Aundrea K., Perry, Blair W., Kamal, Abu H. M., Hales, Nicole R., Kay, Jarren C., Sapkota, Madhab, Schield, Drew R., Pellegrino, Mark W., Secor, Stephen M., Chowdhury, Saiful M., Castoe, Todd A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8725436/
https://www.ncbi.nlm.nih.gov/pubmed/34983392
http://dx.doi.org/10.1186/s12864-021-08226-5
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author Westfall, Aundrea K.
Perry, Blair W.
Kamal, Abu H. M.
Hales, Nicole R.
Kay, Jarren C.
Sapkota, Madhab
Schield, Drew R.
Pellegrino, Mark W.
Secor, Stephen M.
Chowdhury, Saiful M.
Castoe, Todd A.
author_facet Westfall, Aundrea K.
Perry, Blair W.
Kamal, Abu H. M.
Hales, Nicole R.
Kay, Jarren C.
Sapkota, Madhab
Schield, Drew R.
Pellegrino, Mark W.
Secor, Stephen M.
Chowdhury, Saiful M.
Castoe, Todd A.
author_sort Westfall, Aundrea K.
collection PubMed
description BACKGROUND: Snakes exhibit extreme intestinal regeneration following months-long fasts that involves unparalleled increases in metabolism, function, and tissue growth, but the specific molecular control of this process is unknown. Understanding the mechanisms that coordinate these regenerative phenotypes provides valuable opportunities to understand critical pathways that may control vertebrate regeneration and novel perspectives on vertebrate regenerative capacities. RESULTS: Here, we integrate a comprehensive set of phenotypic, transcriptomic, proteomic, and phosphoproteomic data from boa constrictors to identify the mechanisms that orchestrate shifts in metabolism, nutrient uptake, and cellular stress to direct phases of the regenerative response. We identify specific temporal patterns of metabolic, stress response, and growth pathway activation that direct regeneration and provide evidence for multiple key central regulatory molecules kinases that integrate these signals, including major conserved pathways like mTOR signaling and the unfolded protein response. CONCLUSION: Collectively, our results identify a novel switch-like role of stress responses in intestinal regeneration that forms a primary regulatory hub facilitating organ regeneration and could point to potential pathways to understand regenerative capacity in vertebrates. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-021-08226-5.
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spelling pubmed-87254362022-01-06 Identification of an integrated stress and growth response signaling switch that directs vertebrate intestinal regeneration Westfall, Aundrea K. Perry, Blair W. Kamal, Abu H. M. Hales, Nicole R. Kay, Jarren C. Sapkota, Madhab Schield, Drew R. Pellegrino, Mark W. Secor, Stephen M. Chowdhury, Saiful M. Castoe, Todd A. BMC Genomics Research Article BACKGROUND: Snakes exhibit extreme intestinal regeneration following months-long fasts that involves unparalleled increases in metabolism, function, and tissue growth, but the specific molecular control of this process is unknown. Understanding the mechanisms that coordinate these regenerative phenotypes provides valuable opportunities to understand critical pathways that may control vertebrate regeneration and novel perspectives on vertebrate regenerative capacities. RESULTS: Here, we integrate a comprehensive set of phenotypic, transcriptomic, proteomic, and phosphoproteomic data from boa constrictors to identify the mechanisms that orchestrate shifts in metabolism, nutrient uptake, and cellular stress to direct phases of the regenerative response. We identify specific temporal patterns of metabolic, stress response, and growth pathway activation that direct regeneration and provide evidence for multiple key central regulatory molecules kinases that integrate these signals, including major conserved pathways like mTOR signaling and the unfolded protein response. CONCLUSION: Collectively, our results identify a novel switch-like role of stress responses in intestinal regeneration that forms a primary regulatory hub facilitating organ regeneration and could point to potential pathways to understand regenerative capacity in vertebrates. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-021-08226-5. BioMed Central 2022-01-04 /pmc/articles/PMC8725436/ /pubmed/34983392 http://dx.doi.org/10.1186/s12864-021-08226-5 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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
Westfall, Aundrea K.
Perry, Blair W.
Kamal, Abu H. M.
Hales, Nicole R.
Kay, Jarren C.
Sapkota, Madhab
Schield, Drew R.
Pellegrino, Mark W.
Secor, Stephen M.
Chowdhury, Saiful M.
Castoe, Todd A.
Identification of an integrated stress and growth response signaling switch that directs vertebrate intestinal regeneration
title Identification of an integrated stress and growth response signaling switch that directs vertebrate intestinal regeneration
title_full Identification of an integrated stress and growth response signaling switch that directs vertebrate intestinal regeneration
title_fullStr Identification of an integrated stress and growth response signaling switch that directs vertebrate intestinal regeneration
title_full_unstemmed Identification of an integrated stress and growth response signaling switch that directs vertebrate intestinal regeneration
title_short Identification of an integrated stress and growth response signaling switch that directs vertebrate intestinal regeneration
title_sort identification of an integrated stress and growth response signaling switch that directs vertebrate intestinal regeneration
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8725436/
https://www.ncbi.nlm.nih.gov/pubmed/34983392
http://dx.doi.org/10.1186/s12864-021-08226-5
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