Evidence map›Paper›PMID 31870536›Full record

ArticleBiophysical journal2020

Zebrafish Spinal Cord Repair Is Accompanied by Transient Tissue Stiffening.

Stephanie Möllmert, Maria A Kharlamova, Tobias Hoche, Anna V Taubenberger, Shada Abuhattum, Veronika Kuscha, Thomas Kurth, Michael Brand, Jochen Guck

Abstract read
In one paragraph

Article in Biophysical journal, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

24 citing papers in PubMed.

  1. Article
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  4. From Biophysics to Biomedical Physics.ACS bio & med chem Au · 2025
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  11. Can't handle the stress? Mechanobiology and disease.Trends in molecular medicine · 2022
    Review
  12. Open biology · 2022
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  16. Pressure Drives Rapid Burst-Like Coordinated Cellular Motion from 3D Cancer Aggregates.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2022
    Article
  17. Mathematical models of neuronal growth.Biomechanics and modeling in mechanobiology · 2022
    Review
  18. Article
  19. Review
  20. Cardiac regenerative capacity: an evolutionary afterthought?Cellular and molecular life sciences : CMLS · 2021
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Stephanie MöllmertBiotechnology Center, Technische Universität Dresden, Dresden, Germany.
Maria A KharlamovaBiotechnology Center, Technische Universität Dresden, Dresden, Germany.
Tobias HocheBiotechnology Center, Technische Universität Dresden, Dresden, Germany.
Anna V TaubenbergerBiotechnology Center, Technische Universität Dresden, Dresden, Germany.
Shada AbuhattumBiotechnology 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 KuschaCenter for Regenerative Therapies, Technische Universität Dresden, Dresden, Germany.
Thomas KurthCenter for Regenerative Therapies, Technische Universität Dresden, Dresden, Germany.
Michael BrandCenter for Regenerative Therapies, Technische Universität Dresden, Dresden, Germany.
Jochen GuckBiotechnology 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.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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.

Indexed as

Mechanical PhenomenaZebrafishAnimalsBiomechanical PhenomenaSpinal CordSpinal Cord Regeneration

Identifiers

PMID31870536
PMCPMC6976874

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.