Evidence map›Paper›PMID 31961897›Full record

ArticlePloS one2020

Targeting chondroitinase ABC to axons enhances the ability of chondroitinase to promote neurite outgrowth and sprouting.

Priscilla Day, Nuno Alves, Esther Daniell, Debayan Dasgupta, Rosalie Ogborne, Ashley Steeper, Mansoor Raza, Clare Ellis, James Fawcett, Roger Keynes and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.7field-weighted citation impact, top 18% of its field
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

13 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
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  7. Pathophysiology and Therapeutic Approaches for Spinal Cord Injury.International journal of molecular sciences · 2022
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 1 institution in 1 country.

Priscilla DayDepartment of Physiology Development and Neuroscience, University of Cambridge, Cambridge, United Kingdom.
Nuno AlvesJohn Van Geest Centre for Brain Repair, University of Cambridge, Cambridge, United Kingdom.
Esther DaniellDepartment of Physiology Development and Neuroscience, University of Cambridge, Cambridge, United Kingdom.
Debayan DasguptaDepartment of Physiology Development and Neuroscience, University of Cambridge, Cambridge, United Kingdom.
Rosalie OgborneDepartment of Physiology Development and Neuroscience, University of Cambridge, Cambridge, United Kingdom.ORCID 0000-0003-3327-6030
Ashley SteeperDepartment of Physiology Development and Neuroscience, University of Cambridge, Cambridge, United Kingdom.
Mansoor RazaDepartment of Physiology Development and Neuroscience, University of Cambridge, Cambridge, United Kingdom.
Clare EllisDepartment of Physiology Development and Neuroscience, University of Cambridge, Cambridge, United Kingdom.
James FawcettJohn Van Geest Centre for Brain Repair, University of Cambridge, Cambridge, United Kingdom.
Roger KeynesDepartment of Physiology Development and Neuroscience, University of Cambridge, Cambridge, United Kingdom.
Elizabeth MuirDepartment of Physiology Development and Neuroscience, University of Cambridge, Cambridge, United Kingdom.
University of Cambridge · GB

Funding

Medical Research Council MR/R004463/1Wellcome TrustWellcome Trust RG45123
6 · The paper itself

Abstract

backgroundThere is currently no effective treatment for promoting regeneration of injured nerves in patients who have sustained injury to the central nervous system such as spinal cord injury. Chondroitinase ABC is an enzyme, which promotes neurite outgrowth and regeneration. It has shown considerable promise as a therapy for these conditions. The aim of the study is to determine if targeting chondroitinase ABC expression to the neuronal axon can further enhance its ability to promote axon outgrowth. Long-distance axon regeneration has not yet been achieved, and would be a significant step in attaining functional recovery following spinal cord injury. METHODOLOGY/PRINCIPAL

findingsTo investigate this, neuronal cultures were transfected with constructs encoding axon-targeted chondroitinase, non-targeted chondroitinase or GFP, and the effects on neuron outgrowth and sprouting determined on substrates either permissive or inhibitory to neuron regeneration. The mechanisms underlying the observed effects were also explored. Targeting chondroitinase to the neuronal axon markedly enhances its ability to promote neurite outgrowth. The increase in neurite length is associated with an upregulation of β-integrin staining at the axonal cell surface. Staining for phosphofocal adhesion kinase, is also increased, indicating that the β-integrins are in an activated state. Expression of chondroitinase within the neurons also resulted in a decrease in expression of PTEN and RhoA, molecules which present a block to neurite outgrowth, thus identifying two of the pathways by which ChABC promotes neurite outgrowth. CONCLUSIONS / SIGNIFICANCE: The novel finding that targeting ChABC to the axon significantly enhances its ability to promote neurite extension, suggests that this may be an effective way of promoting long-distance axon regeneration following spinal cord injury. It could also potentially improve its efficacy in the treatment of other pathologies, where it has been shown to promote recovery, such as myocardial infarction, stroke and Parkinson's disease.

Indexed as

AnimalsAxonsChondroitin ABC LyaseGene Expression RegulationHumansNerve RegenerationNeuritesNeuronal OutgrowthNeuronsPTEN PhosphohydrolaseRecovery of FunctionrhoA GTP-Binding ProteinSpinal Cord InjuriesChondroitin ABC LyasePTEN PhosphohydrolaserhoA GTP-Binding Protein

Identifiers

PMID31961897
PMCPMC6974052
OpenAlexW3001325600

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.