Abstract

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.

Details

Title
Wnt signaling controls pro-regenerative Collagen XII in functional spinal cord regeneration in zebrafish
Author
Wehner, Daniel 1   VIAFID ORCID Logo  ; Tsarouchas, Themistoklis M 1 ; Andria, Michael 1 ; Haase, Christa 2 ; Weidinger, Gilbert 3   VIAFID ORCID Logo  ; Reimer, Michell M 4 ; Becker, Thomas 1 ; Becker, Catherina G 1 

 Centre for Neuroregeneration, University of Edinburgh, Edinburgh, UK 
 Institute for Immunology, TechnischeUniversität Dresden, Dresden, Germany 
 Institute of Biochemistry and Molecular Biology, Ulm University, Ulm, Germany 
 Technische Universität Dresden, DFG-Center of Regenerative Therapies Dresden, Cluster of Excellence at the TU Dresden, Dresden, Germany 
Pages
1-17
Publication year
2017
Publication date
Jul 2017
Publisher
Nature Publishing Group
e-ISSN
20411723
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
1923279071
Copyright
© 2017. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.