Cargando…
Wnt signaling controls pro-regenerative Collagen XII in functional spinal cord regeneration in zebrafish
The inhibitory extracellular matrix in a spinal lesion site is a major impediment to axonal regeneration in mammals. In contrast, the extracellular matrix in zebrafish allows substantial axon re-growth, leading to recovery of movement. However, little is known about regulation and composition of the...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5526933/ https://www.ncbi.nlm.nih.gov/pubmed/28743881 http://dx.doi.org/10.1038/s41467-017-00143-0 |
_version_ | 1783252878891155456 |
---|---|
author | Wehner, Daniel Tsarouchas, Themistoklis M. Michael, Andria Haase, Christa Weidinger, Gilbert Reimer, Michell M. Becker, Thomas Becker, Catherina G. |
author_facet | Wehner, Daniel Tsarouchas, Themistoklis M. Michael, Andria Haase, Christa Weidinger, Gilbert Reimer, Michell M. Becker, Thomas Becker, Catherina G. |
author_sort | Wehner, Daniel |
collection | PubMed |
description | The inhibitory extracellular matrix in a spinal lesion site is a major impediment to axonal regeneration in mammals. In contrast, the extracellular matrix in zebrafish allows substantial axon re-growth, leading to recovery of movement. However, little is known about regulation and composition of the growth-promoting extracellular matrix. Here we demonstrate that activity of the Wnt/β-catenin pathway in fibroblast-like cells in the lesion site is pivotal for axon re-growth and functional recovery. Wnt/β-catenin signaling induces expression of col12a1a/b and deposition of Collagen XII, which is necessary for axons to actively navigate the non-neural lesion site environment. Overexpression of col12a1a rescues the effects of Wnt/β-catenin pathway inhibition and is sufficient to accelerate regeneration. We demonstrate that in a vertebrate of high regenerative capacity, Wnt/β-catenin signaling controls the composition of the lesion site extracellular matrix and we identify Collagen XII as a promoter of axonal regeneration. These findings imply that the Wnt/β-catenin pathway and Collagen XII may be targets for extracellular matrix manipulations in non-regenerating species. |
format | Online Article Text |
id | pubmed-5526933 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55269332017-07-31 Wnt signaling controls pro-regenerative Collagen XII in functional spinal cord regeneration in zebrafish Wehner, Daniel Tsarouchas, Themistoklis M. Michael, Andria Haase, Christa Weidinger, Gilbert Reimer, Michell M. Becker, Thomas Becker, Catherina G. Nat Commun Article The inhibitory extracellular matrix in a spinal lesion site is a major impediment to axonal regeneration in mammals. In contrast, the extracellular matrix in zebrafish allows substantial axon re-growth, leading to recovery of movement. However, little is known about regulation and composition of the growth-promoting extracellular matrix. Here we demonstrate that activity of the Wnt/β-catenin pathway in fibroblast-like cells in the lesion site is pivotal for axon re-growth and functional recovery. Wnt/β-catenin signaling induces expression of col12a1a/b and deposition of Collagen XII, which is necessary for axons to actively navigate the non-neural lesion site environment. Overexpression of col12a1a rescues the effects of Wnt/β-catenin pathway inhibition and is sufficient to accelerate regeneration. We demonstrate that in a vertebrate of high regenerative capacity, Wnt/β-catenin signaling controls the composition of the lesion site extracellular matrix and we identify Collagen XII as a promoter of axonal regeneration. These findings imply that the Wnt/β-catenin pathway and Collagen XII may be targets for extracellular matrix manipulations in non-regenerating species. Nature Publishing Group UK 2017-07-25 /pmc/articles/PMC5526933/ /pubmed/28743881 http://dx.doi.org/10.1038/s41467-017-00143-0 Text en © The Author(s) 2017 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 Wehner, Daniel Tsarouchas, Themistoklis M. Michael, Andria Haase, Christa Weidinger, Gilbert Reimer, Michell M. Becker, Thomas Becker, Catherina G. Wnt signaling controls pro-regenerative Collagen XII in functional spinal cord regeneration in zebrafish |
title | Wnt signaling controls pro-regenerative Collagen XII in functional spinal cord regeneration in zebrafish |
title_full | Wnt signaling controls pro-regenerative Collagen XII in functional spinal cord regeneration in zebrafish |
title_fullStr | Wnt signaling controls pro-regenerative Collagen XII in functional spinal cord regeneration in zebrafish |
title_full_unstemmed | Wnt signaling controls pro-regenerative Collagen XII in functional spinal cord regeneration in zebrafish |
title_short | Wnt signaling controls pro-regenerative Collagen XII in functional spinal cord regeneration in zebrafish |
title_sort | wnt signaling controls pro-regenerative collagen xii in functional spinal cord regeneration in zebrafish |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5526933/ https://www.ncbi.nlm.nih.gov/pubmed/28743881 http://dx.doi.org/10.1038/s41467-017-00143-0 |
work_keys_str_mv | AT wehnerdaniel wntsignalingcontrolsproregenerativecollagenxiiinfunctionalspinalcordregenerationinzebrafish AT tsarouchasthemistoklism wntsignalingcontrolsproregenerativecollagenxiiinfunctionalspinalcordregenerationinzebrafish AT michaelandria wntsignalingcontrolsproregenerativecollagenxiiinfunctionalspinalcordregenerationinzebrafish AT haasechrista wntsignalingcontrolsproregenerativecollagenxiiinfunctionalspinalcordregenerationinzebrafish AT weidingergilbert wntsignalingcontrolsproregenerativecollagenxiiinfunctionalspinalcordregenerationinzebrafish AT reimermichellm wntsignalingcontrolsproregenerativecollagenxiiinfunctionalspinalcordregenerationinzebrafish AT beckerthomas wntsignalingcontrolsproregenerativecollagenxiiinfunctionalspinalcordregenerationinzebrafish AT beckercatherinag wntsignalingcontrolsproregenerativecollagenxiiinfunctionalspinalcordregenerationinzebrafish |