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An anti-inflammatory activation sequence governs macrophage transcriptional dynamics during tissue injury in zebrafish

Macrophages are essential for tissue repair and regeneration. Yet, the molecular programs, as well as the timing of their activation during and after tissue injury are poorly defined. Using a high spatio-temporal resolution single cell analysis of macrophages coupled with live imaging after sensory...

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Autores principales: Denans, Nicolas, Tran, Nhung T. T., Swall, Madeleine E., Diaz, Daniel C., Blanck, Jillian, Piotrowski, Tatjana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9489698/
https://www.ncbi.nlm.nih.gov/pubmed/36127326
http://dx.doi.org/10.1038/s41467-022-33015-3
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author Denans, Nicolas
Tran, Nhung T. T.
Swall, Madeleine E.
Diaz, Daniel C.
Blanck, Jillian
Piotrowski, Tatjana
author_facet Denans, Nicolas
Tran, Nhung T. T.
Swall, Madeleine E.
Diaz, Daniel C.
Blanck, Jillian
Piotrowski, Tatjana
author_sort Denans, Nicolas
collection PubMed
description Macrophages are essential for tissue repair and regeneration. Yet, the molecular programs, as well as the timing of their activation during and after tissue injury are poorly defined. Using a high spatio-temporal resolution single cell analysis of macrophages coupled with live imaging after sensory hair cell death in zebrafish, we find that the same population of macrophages transitions through a sequence of three major anti-inflammatory activation states. Macrophages first show a signature of glucocorticoid activation, then IL-10 signaling and finally the induction of oxidative phosphorylation by IL-4/Polyamine signaling. Importantly, loss-of-function of glucocorticoid and IL-10 signaling shows that each step of the sequence is independently activated. Lastly, we show that IL-10 and IL-4 signaling act synergistically to promote synaptogenesis between hair cells and efferent neurons during regeneration. Our results show that macrophages, in addition to a switch from M1 to M2, sequentially and independently transition though three anti-inflammatory pathways in vivo during tissue injury in a regenerating organ.
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spelling pubmed-94896982022-09-22 An anti-inflammatory activation sequence governs macrophage transcriptional dynamics during tissue injury in zebrafish Denans, Nicolas Tran, Nhung T. T. Swall, Madeleine E. Diaz, Daniel C. Blanck, Jillian Piotrowski, Tatjana Nat Commun Article Macrophages are essential for tissue repair and regeneration. Yet, the molecular programs, as well as the timing of their activation during and after tissue injury are poorly defined. Using a high spatio-temporal resolution single cell analysis of macrophages coupled with live imaging after sensory hair cell death in zebrafish, we find that the same population of macrophages transitions through a sequence of three major anti-inflammatory activation states. Macrophages first show a signature of glucocorticoid activation, then IL-10 signaling and finally the induction of oxidative phosphorylation by IL-4/Polyamine signaling. Importantly, loss-of-function of glucocorticoid and IL-10 signaling shows that each step of the sequence is independently activated. Lastly, we show that IL-10 and IL-4 signaling act synergistically to promote synaptogenesis between hair cells and efferent neurons during regeneration. Our results show that macrophages, in addition to a switch from M1 to M2, sequentially and independently transition though three anti-inflammatory pathways in vivo during tissue injury in a regenerating organ. Nature Publishing Group UK 2022-09-20 /pmc/articles/PMC9489698/ /pubmed/36127326 http://dx.doi.org/10.1038/s41467-022-33015-3 Text en © The Author(s) 2022 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 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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Denans, Nicolas
Tran, Nhung T. T.
Swall, Madeleine E.
Diaz, Daniel C.
Blanck, Jillian
Piotrowski, Tatjana
An anti-inflammatory activation sequence governs macrophage transcriptional dynamics during tissue injury in zebrafish
title An anti-inflammatory activation sequence governs macrophage transcriptional dynamics during tissue injury in zebrafish
title_full An anti-inflammatory activation sequence governs macrophage transcriptional dynamics during tissue injury in zebrafish
title_fullStr An anti-inflammatory activation sequence governs macrophage transcriptional dynamics during tissue injury in zebrafish
title_full_unstemmed An anti-inflammatory activation sequence governs macrophage transcriptional dynamics during tissue injury in zebrafish
title_short An anti-inflammatory activation sequence governs macrophage transcriptional dynamics during tissue injury in zebrafish
title_sort anti-inflammatory activation sequence governs macrophage transcriptional dynamics during tissue injury in zebrafish
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9489698/
https://www.ncbi.nlm.nih.gov/pubmed/36127326
http://dx.doi.org/10.1038/s41467-022-33015-3
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