Cargando…

Dynamic control of proinflammatory cytokines Il-1β and Tnf-α by macrophages in zebrafish spinal cord regeneration

Spinal cord injury leads to a massive response of innate immune cells in non-regenerating mammals, but also in successfully regenerating zebrafish. However, the role of the immune response in successful regeneration is poorly defined. Here we show that inhibiting inflammation reduces and promoting i...

Descripción completa

Detalles Bibliográficos
Autores principales: Tsarouchas, Themistoklis M., Wehner, Daniel, Cavone, Leonardo, Munir, Tahimina, Keatinge, Marcus, Lambertus, Marvin, Underhill, Anna, Barrett, Thomas, Kassapis, Elias, Ogryzko, Nikolay, Feng, Yi, van Ham, Tjakko J., Becker, Thomas, Becker, Catherina G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6220182/
https://www.ncbi.nlm.nih.gov/pubmed/30405119
http://dx.doi.org/10.1038/s41467-018-07036-w
_version_ 1783368776491728896
author Tsarouchas, Themistoklis M.
Wehner, Daniel
Cavone, Leonardo
Munir, Tahimina
Keatinge, Marcus
Lambertus, Marvin
Underhill, Anna
Barrett, Thomas
Kassapis, Elias
Ogryzko, Nikolay
Feng, Yi
van Ham, Tjakko J.
Becker, Thomas
Becker, Catherina G.
author_facet Tsarouchas, Themistoklis M.
Wehner, Daniel
Cavone, Leonardo
Munir, Tahimina
Keatinge, Marcus
Lambertus, Marvin
Underhill, Anna
Barrett, Thomas
Kassapis, Elias
Ogryzko, Nikolay
Feng, Yi
van Ham, Tjakko J.
Becker, Thomas
Becker, Catherina G.
author_sort Tsarouchas, Themistoklis M.
collection PubMed
description Spinal cord injury leads to a massive response of innate immune cells in non-regenerating mammals, but also in successfully regenerating zebrafish. However, the role of the immune response in successful regeneration is poorly defined. Here we show that inhibiting inflammation reduces and promoting it accelerates axonal regeneration in spinal-lesioned zebrafish larvae. Mutant analyses show that peripheral macrophages, but not neutrophils or microglia, are necessary for repair. Macrophage-less irf8 mutants show prolonged inflammation with elevated levels of Tnf-α and Il-1β. Inhibiting Tnf-α does not rescue axonal growth in irf8 mutants, but impairs it in wildtype animals, indicating a pro-regenerative role of Tnf-α. In contrast, decreasing Il-1β levels or number of Il-1β(+) neutrophils rescue functional regeneration in irf8 mutants. However, during early regeneration, interference with Il-1β function impairs regeneration in irf8 and wildtype animals. Hence, inflammation is dynamically controlled by macrophages to promote functional spinal cord regeneration in zebrafish.
format Online
Article
Text
id pubmed-6220182
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-62201822018-11-08 Dynamic control of proinflammatory cytokines Il-1β and Tnf-α by macrophages in zebrafish spinal cord regeneration Tsarouchas, Themistoklis M. Wehner, Daniel Cavone, Leonardo Munir, Tahimina Keatinge, Marcus Lambertus, Marvin Underhill, Anna Barrett, Thomas Kassapis, Elias Ogryzko, Nikolay Feng, Yi van Ham, Tjakko J. Becker, Thomas Becker, Catherina G. Nat Commun Article Spinal cord injury leads to a massive response of innate immune cells in non-regenerating mammals, but also in successfully regenerating zebrafish. However, the role of the immune response in successful regeneration is poorly defined. Here we show that inhibiting inflammation reduces and promoting it accelerates axonal regeneration in spinal-lesioned zebrafish larvae. Mutant analyses show that peripheral macrophages, but not neutrophils or microglia, are necessary for repair. Macrophage-less irf8 mutants show prolonged inflammation with elevated levels of Tnf-α and Il-1β. Inhibiting Tnf-α does not rescue axonal growth in irf8 mutants, but impairs it in wildtype animals, indicating a pro-regenerative role of Tnf-α. In contrast, decreasing Il-1β levels or number of Il-1β(+) neutrophils rescue functional regeneration in irf8 mutants. However, during early regeneration, interference with Il-1β function impairs regeneration in irf8 and wildtype animals. Hence, inflammation is dynamically controlled by macrophages to promote functional spinal cord regeneration in zebrafish. Nature Publishing Group UK 2018-11-07 /pmc/articles/PMC6220182/ /pubmed/30405119 http://dx.doi.org/10.1038/s41467-018-07036-w Text en © The Author(s) 2018 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
Tsarouchas, Themistoklis M.
Wehner, Daniel
Cavone, Leonardo
Munir, Tahimina
Keatinge, Marcus
Lambertus, Marvin
Underhill, Anna
Barrett, Thomas
Kassapis, Elias
Ogryzko, Nikolay
Feng, Yi
van Ham, Tjakko J.
Becker, Thomas
Becker, Catherina G.
Dynamic control of proinflammatory cytokines Il-1β and Tnf-α by macrophages in zebrafish spinal cord regeneration
title Dynamic control of proinflammatory cytokines Il-1β and Tnf-α by macrophages in zebrafish spinal cord regeneration
title_full Dynamic control of proinflammatory cytokines Il-1β and Tnf-α by macrophages in zebrafish spinal cord regeneration
title_fullStr Dynamic control of proinflammatory cytokines Il-1β and Tnf-α by macrophages in zebrafish spinal cord regeneration
title_full_unstemmed Dynamic control of proinflammatory cytokines Il-1β and Tnf-α by macrophages in zebrafish spinal cord regeneration
title_short Dynamic control of proinflammatory cytokines Il-1β and Tnf-α by macrophages in zebrafish spinal cord regeneration
title_sort dynamic control of proinflammatory cytokines il-1β and tnf-α by macrophages in zebrafish spinal cord regeneration
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6220182/
https://www.ncbi.nlm.nih.gov/pubmed/30405119
http://dx.doi.org/10.1038/s41467-018-07036-w
work_keys_str_mv AT tsarouchasthemistoklism dynamiccontrolofproinflammatorycytokinesil1bandtnfabymacrophagesinzebrafishspinalcordregeneration
AT wehnerdaniel dynamiccontrolofproinflammatorycytokinesil1bandtnfabymacrophagesinzebrafishspinalcordregeneration
AT cavoneleonardo dynamiccontrolofproinflammatorycytokinesil1bandtnfabymacrophagesinzebrafishspinalcordregeneration
AT munirtahimina dynamiccontrolofproinflammatorycytokinesil1bandtnfabymacrophagesinzebrafishspinalcordregeneration
AT keatingemarcus dynamiccontrolofproinflammatorycytokinesil1bandtnfabymacrophagesinzebrafishspinalcordregeneration
AT lambertusmarvin dynamiccontrolofproinflammatorycytokinesil1bandtnfabymacrophagesinzebrafishspinalcordregeneration
AT underhillanna dynamiccontrolofproinflammatorycytokinesil1bandtnfabymacrophagesinzebrafishspinalcordregeneration
AT barrettthomas dynamiccontrolofproinflammatorycytokinesil1bandtnfabymacrophagesinzebrafishspinalcordregeneration
AT kassapiselias dynamiccontrolofproinflammatorycytokinesil1bandtnfabymacrophagesinzebrafishspinalcordregeneration
AT ogryzkonikolay dynamiccontrolofproinflammatorycytokinesil1bandtnfabymacrophagesinzebrafishspinalcordregeneration
AT fengyi dynamiccontrolofproinflammatorycytokinesil1bandtnfabymacrophagesinzebrafishspinalcordregeneration
AT vanhamtjakkoj dynamiccontrolofproinflammatorycytokinesil1bandtnfabymacrophagesinzebrafishspinalcordregeneration
AT beckerthomas dynamiccontrolofproinflammatorycytokinesil1bandtnfabymacrophagesinzebrafishspinalcordregeneration
AT beckercatherinag dynamiccontrolofproinflammatorycytokinesil1bandtnfabymacrophagesinzebrafishspinalcordregeneration