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TNF signaling and macrophages govern fin regeneration in zebrafish larvae

Macrophages are essential for appendage regeneration after amputation in regenerative species. The molecular mechanisms through which macrophages orchestrate blastema formation and regeneration are still unclear. Here, we use the genetically tractable and transparent zebrafish larvae to study the fu...

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Autores principales: Nguyen-Chi, Mai, Laplace-Builhé, Béryl, Travnickova, Jana, Luz-Crawford, Patricia, Tejedor, Gautier, Lutfalla, Georges, Kissa, Karima, Jorgensen, Christian, Djouad, Farida
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5596562/
https://www.ncbi.nlm.nih.gov/pubmed/28796253
http://dx.doi.org/10.1038/cddis.2017.374
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author Nguyen-Chi, Mai
Laplace-Builhé, Béryl
Travnickova, Jana
Luz-Crawford, Patricia
Tejedor, Gautier
Lutfalla, Georges
Kissa, Karima
Jorgensen, Christian
Djouad, Farida
author_facet Nguyen-Chi, Mai
Laplace-Builhé, Béryl
Travnickova, Jana
Luz-Crawford, Patricia
Tejedor, Gautier
Lutfalla, Georges
Kissa, Karima
Jorgensen, Christian
Djouad, Farida
author_sort Nguyen-Chi, Mai
collection PubMed
description Macrophages are essential for appendage regeneration after amputation in regenerative species. The molecular mechanisms through which macrophages orchestrate blastema formation and regeneration are still unclear. Here, we use the genetically tractable and transparent zebrafish larvae to study the functions of polarized macrophage subsets during caudal fin regeneration. After caudal fin amputation, we show an early and transient accumulation of pro-inflammatory macrophages concomitant with the accumulation of non-inflammatory macrophages which, in contrast to pro-inflammatory macrophages, remain associated to the fin until the end of the regeneration. Chemical and genetic depletion of macrophages suggested that early recruited macrophages that express TNFα are critical for blastema formation. Combining parabiosis and morpholino knockdown strategies, we show that TNFα/TNFR1 signaling pathway is required for the fin regeneration. Our study reveals that TNFR1 has a necessary and direct role in blastema cell activation suggesting that macrophage subset balance provides the accurate TNFα signal to prime regeneration in zebrafish.
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spelling pubmed-55965622017-09-14 TNF signaling and macrophages govern fin regeneration in zebrafish larvae Nguyen-Chi, Mai Laplace-Builhé, Béryl Travnickova, Jana Luz-Crawford, Patricia Tejedor, Gautier Lutfalla, Georges Kissa, Karima Jorgensen, Christian Djouad, Farida Cell Death Dis Original Article Macrophages are essential for appendage regeneration after amputation in regenerative species. The molecular mechanisms through which macrophages orchestrate blastema formation and regeneration are still unclear. Here, we use the genetically tractable and transparent zebrafish larvae to study the functions of polarized macrophage subsets during caudal fin regeneration. After caudal fin amputation, we show an early and transient accumulation of pro-inflammatory macrophages concomitant with the accumulation of non-inflammatory macrophages which, in contrast to pro-inflammatory macrophages, remain associated to the fin until the end of the regeneration. Chemical and genetic depletion of macrophages suggested that early recruited macrophages that express TNFα are critical for blastema formation. Combining parabiosis and morpholino knockdown strategies, we show that TNFα/TNFR1 signaling pathway is required for the fin regeneration. Our study reveals that TNFR1 has a necessary and direct role in blastema cell activation suggesting that macrophage subset balance provides the accurate TNFα signal to prime regeneration in zebrafish. Nature Publishing Group 2017-08 2017-08-10 /pmc/articles/PMC5596562/ /pubmed/28796253 http://dx.doi.org/10.1038/cddis.2017.374 Text en Copyright © 2017 The Author(s) http://creativecommons.org/licenses/by/4.0/ Cell Death and Disease is an open-access journal published by Nature Publishing Group. This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Original Article
Nguyen-Chi, Mai
Laplace-Builhé, Béryl
Travnickova, Jana
Luz-Crawford, Patricia
Tejedor, Gautier
Lutfalla, Georges
Kissa, Karima
Jorgensen, Christian
Djouad, Farida
TNF signaling and macrophages govern fin regeneration in zebrafish larvae
title TNF signaling and macrophages govern fin regeneration in zebrafish larvae
title_full TNF signaling and macrophages govern fin regeneration in zebrafish larvae
title_fullStr TNF signaling and macrophages govern fin regeneration in zebrafish larvae
title_full_unstemmed TNF signaling and macrophages govern fin regeneration in zebrafish larvae
title_short TNF signaling and macrophages govern fin regeneration in zebrafish larvae
title_sort tnf signaling and macrophages govern fin regeneration in zebrafish larvae
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5596562/
https://www.ncbi.nlm.nih.gov/pubmed/28796253
http://dx.doi.org/10.1038/cddis.2017.374
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