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Functional compensation precedes recovery of tissue mass following acute liver injury

The liver plays a central role in metabolism, protein synthesis and detoxification. It possesses unique regenerative capacity upon injury. While many factors regulating cellular proliferation during liver repair have been identified, the mechanisms by which the injured liver maintains vital function...

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Autores principales: Walesky, Chad M., Kolb, Kellie E., Winston, Carolyn L., Henderson, Jake, Kruft, Benjamin, Fleming, Ira, Ko, Sungjin, Monga, Satdarshan P., Mueller, Florian, Apte, Udayan, Shalek, Alex K., Goessling, Wolfram
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7677389/
https://www.ncbi.nlm.nih.gov/pubmed/33214549
http://dx.doi.org/10.1038/s41467-020-19558-3
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author Walesky, Chad M.
Kolb, Kellie E.
Winston, Carolyn L.
Henderson, Jake
Kruft, Benjamin
Fleming, Ira
Ko, Sungjin
Monga, Satdarshan P.
Mueller, Florian
Apte, Udayan
Shalek, Alex K.
Goessling, Wolfram
author_facet Walesky, Chad M.
Kolb, Kellie E.
Winston, Carolyn L.
Henderson, Jake
Kruft, Benjamin
Fleming, Ira
Ko, Sungjin
Monga, Satdarshan P.
Mueller, Florian
Apte, Udayan
Shalek, Alex K.
Goessling, Wolfram
author_sort Walesky, Chad M.
collection PubMed
description The liver plays a central role in metabolism, protein synthesis and detoxification. It possesses unique regenerative capacity upon injury. While many factors regulating cellular proliferation during liver repair have been identified, the mechanisms by which the injured liver maintains vital functions prior to tissue recovery are unknown. Here, we identify a new phase of functional compensation following acute liver injury that occurs prior to cellular proliferation. By coupling single-cell RNA-seq with in situ transcriptional analyses in two independent murine liver injury models, we discover adaptive reprogramming to ensure expression of both injury response and core liver function genes dependent on macrophage-derived WNT/β-catenin signaling. Interestingly, transcriptional compensation is most prominent in non-proliferating cells, clearly delineating two temporally distinct phases of liver recovery. Overall, our work describes a mechanism by which the liver maintains essential physiological functions prior to cellular reconstitution and characterizes macrophage-derived WNT signals required for this compensation.
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spelling pubmed-76773892020-11-24 Functional compensation precedes recovery of tissue mass following acute liver injury Walesky, Chad M. Kolb, Kellie E. Winston, Carolyn L. Henderson, Jake Kruft, Benjamin Fleming, Ira Ko, Sungjin Monga, Satdarshan P. Mueller, Florian Apte, Udayan Shalek, Alex K. Goessling, Wolfram Nat Commun Article The liver plays a central role in metabolism, protein synthesis and detoxification. It possesses unique regenerative capacity upon injury. While many factors regulating cellular proliferation during liver repair have been identified, the mechanisms by which the injured liver maintains vital functions prior to tissue recovery are unknown. Here, we identify a new phase of functional compensation following acute liver injury that occurs prior to cellular proliferation. By coupling single-cell RNA-seq with in situ transcriptional analyses in two independent murine liver injury models, we discover adaptive reprogramming to ensure expression of both injury response and core liver function genes dependent on macrophage-derived WNT/β-catenin signaling. Interestingly, transcriptional compensation is most prominent in non-proliferating cells, clearly delineating two temporally distinct phases of liver recovery. Overall, our work describes a mechanism by which the liver maintains essential physiological functions prior to cellular reconstitution and characterizes macrophage-derived WNT signals required for this compensation. Nature Publishing Group UK 2020-11-19 /pmc/articles/PMC7677389/ /pubmed/33214549 http://dx.doi.org/10.1038/s41467-020-19558-3 Text en © The Author(s) 2020 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Walesky, Chad M.
Kolb, Kellie E.
Winston, Carolyn L.
Henderson, Jake
Kruft, Benjamin
Fleming, Ira
Ko, Sungjin
Monga, Satdarshan P.
Mueller, Florian
Apte, Udayan
Shalek, Alex K.
Goessling, Wolfram
Functional compensation precedes recovery of tissue mass following acute liver injury
title Functional compensation precedes recovery of tissue mass following acute liver injury
title_full Functional compensation precedes recovery of tissue mass following acute liver injury
title_fullStr Functional compensation precedes recovery of tissue mass following acute liver injury
title_full_unstemmed Functional compensation precedes recovery of tissue mass following acute liver injury
title_short Functional compensation precedes recovery of tissue mass following acute liver injury
title_sort functional compensation precedes recovery of tissue mass following acute liver injury
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7677389/
https://www.ncbi.nlm.nih.gov/pubmed/33214549
http://dx.doi.org/10.1038/s41467-020-19558-3
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