Zebrafish Spinal Cord Repair Is Accompanied by Transient Tissue Stiffening.


Journal

Biophysical journal
ISSN: 1542-0086
Titre abrégé: Biophys J
Pays: United States
ID NLM: 0370626

Informations de publication

Date de publication:
21 01 2020
Historique:
received: 13 06 2019
revised: 17 10 2019
accepted: 24 10 2019
pubmed: 25 12 2019
medline: 13 4 2021
entrez: 25 12 2019
Statut: ppublish

Résumé

Severe injury to the mammalian spinal cord results in permanent loss of function due to the formation of a glial-fibrotic scar. Both the chemical composition and the mechanical properties of the scar tissue have been implicated to inhibit neuronal regrowth and functional recovery. By contrast, adult zebrafish are able to repair spinal cord tissue and restore motor function after complete spinal cord transection owing to a complex cellular response that includes axon regrowth and is accompanied by neurogenesis. The mechanical mechanisms contributing to successful spinal cord repair in adult zebrafish are, however, currently unknown. Here, we employ atomic force microscopy-enabled nanoindentation to determine the spatial distributions of apparent elastic moduli of living spinal cord tissue sections obtained from uninjured zebrafish and at distinct time points after complete spinal cord transection. In uninjured specimens, spinal gray matter regions were stiffer than white matter regions. During regeneration after transection, the spinal cord tissues displayed a significant increase of the respective apparent elastic moduli that transiently obliterated the mechanical difference between the two types of matter before returning to baseline values after the completion of repair. Tissue stiffness correlated variably with cell number density, oligodendrocyte interconnectivity, axonal orientation, and vascularization. This work constitutes the first quantitative mapping of the spatiotemporal changes of spinal cord tissue stiffness in regenerating adult zebrafish and provides the tissue mechanical basis for future studies into the role of mechanosensing in spinal cord repair.

Identifiants

pubmed: 31870536
pii: S0006-3495(19)34352-8
doi: 10.1016/j.bpj.2019.10.044
pmc: PMC6976874
pii:
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

448-463

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2019. Published by Elsevier Inc.

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Auteurs

Stephanie Möllmert (S)

Biotechnology Center, Technische Universität Dresden, Dresden, Germany.

Maria A Kharlamova (MA)

Biotechnology Center, Technische Universität Dresden, Dresden, Germany.

Tobias Hoche (T)

Biotechnology Center, Technische Universität Dresden, Dresden, Germany.

Anna V Taubenberger (AV)

Biotechnology Center, Technische Universität Dresden, Dresden, Germany.

Shada Abuhattum (S)

Biotechnology Center, Technische Universität Dresden, Dresden, Germany; JPK Instruments, Berlin, Germany; Max Planck Institut for the Science of Light & Max-Planck Institut für Physik und Medizin, Erlangen, Germany.

Veronika Kuscha (V)

Center for Regenerative Therapies, Technische Universität Dresden, Dresden, Germany.

Thomas Kurth (T)

Center for Regenerative Therapies, Technische Universität Dresden, Dresden, Germany.

Michael Brand (M)

Center for Regenerative Therapies, Technische Universität Dresden, Dresden, Germany.

Jochen Guck (J)

Biotechnology Center, Technische Universität Dresden, Dresden, Germany; Max Planck Institut for the Science of Light & Max-Planck Institut für Physik und Medizin, Erlangen, Germany. Electronic address: jochen.guck@mpl.mpg.de.

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