Evidence map›Paper›PMID 25216747›Full record

ArticleBrain : a journal of neurology2014

c-Jun activation in Schwann cells protects against loss of sensory axons in inherited neuropathy.

Janina Hantke, Lucy Carty, Laura J Wagstaff, Mark Turmaine, Daniel K Wilton, Susanne Quintes, Martin Koltzenburg, Frank Baas, Rhona Mirsky, Kristján R Jessen

Abstract read
In one paragraph

Article in Brain : a journal of neurology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
2.1field-weighted citation impact, top 15% 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

53 citing papers in PubMed, 73 citations in OpenAlex.

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  12. Testing SIPA1L2 as a modifier of CMT1A using mouse models.Journal of neuropathology and experimental neurology · 2024
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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

10 authors at 2 institutions in 2 countries.

Janina Hantke1 Department of Cell and Developmental Biology, University College London (UCL), Gower Street, London WC1E 6BT, UK.
Lucy Carty1 Department of Cell and Developmental Biology, University College London (UCL), Gower Street, London WC1E 6BT, UK.
Laura J Wagstaff1 Department of Cell and Developmental Biology, University College London (UCL), Gower Street, London WC1E 6BT, UK.
Mark Turmaine1 Department of Cell and Developmental Biology, University College London (UCL), Gower Street, London WC1E 6BT, UK.
Daniel K Wilton1 Department of Cell and Developmental Biology, University College London (UCL), Gower Street, London WC1E 6BT, UK.
Susanne Quintes1 Department of Cell and Developmental Biology, University College London (UCL), Gower Street, London WC1E 6BT, UK.
Martin Koltzenburg2 UCL Institute of Neurology, Queen Square, London WC1N 3BG, UK.
Frank Baas3 Department of Genome Analysis, Academic Medical Centre, Amsterdam, The Netherlands.
Rhona Mirsky1 Department of Cell and Developmental Biology, University College London (UCL), Gower Street, London WC1E 6BT, UK.
Kristján R Jessen1 Department of Cell and Developmental Biology, University College London (UCL), Gower Street, London WC1E 6BT, UK k.jessen@ucl.ac.uk.
University College London · GBAcademic Medical Center · NL

Funding

Medical Research Council G0600967Medical Research Council G0802497Wellcome Trust 074665Wellcome Trust 091119
6 · The paper itself

Abstract

Charcot-Marie-Tooth disease type 1A is the most frequent inherited peripheral neuropathy. It is generally due to heterozygous inheritance of a partial chromosomal duplication resulting in over-expression of PMP22. A key feature of Charcot-Marie-Tooth disease type 1A is secondary death of axons. Prevention of axonal loss is therefore an important target of clinical intervention. We have previously identified a signalling mechanism that promotes axon survival and prevents neuron death in mechanically injured peripheral nerves. This work suggested that Schwann cells respond to injury by activating/enhancing trophic support for axons through a mechanism that depends on upregulation of the transcription factor c-Jun in Schwann cells, resulting in the sparing of axons that would otherwise die. As c-Jun orchestrates Schwann cell support for distressed neurons after mechanical injury, we have now asked: do Schwann cells also activate a c-Jun dependent neuron-supportive programme in inherited demyelinating disease? We tested this by using the C3 mouse model of Charcot-Marie-Tooth disease type 1A. In line with our previous findings in humans with Charcot-Marie-Tooth disease type 1A, we found that Schwann cell c-Jun was elevated in (uninjured) nerves of C3 mice. We determined the impact of this c-Jun activation by comparing C3 mice with double mutant mice, namely C3 mice in which c-Jun had been conditionally inactivated in Schwann cells (C3/Schwann cell-c-Jun(-/-) mice), using sensory-motor tests and electrophysiological measurements, and by counting axons in proximal and distal nerves. The results indicate that c-Jun elevation in the Schwann cells of C3 nerves serves to prevent loss of myelinated sensory axons, particularly in distal nerves, improve behavioural symptoms, and preserve F-wave persistence. This suggests that Schwann cells have two contrasting functions in Charcot-Marie-Tooth disease type 1A: on the one hand they are the genetic source of the disease, on the other, they respond to it by mounting a c-Jun-dependent response that significantly reduces its impact. Because axonal death is a central feature of much nerve pathology it will be important to establish whether an axon-supportive Schwann cell response also takes place in other conditions. Amplification of this axon-supportive mechanism constitutes a novel target for clinical intervention that might be useful in Charcot-Marie-Tooth disease type 1A and other neuropathies that involve axon loss.

Indexed as

AnimalsAxonsBehavior, AnimalCharcot-Marie-Tooth DiseaseDemyelinating DiseasesDisease Models, AnimalMiceMice, Inbred C3HMice, KnockoutMotor NeuronsProto-Oncogene Proteins c-junSchwann CellsProto-Oncogene Proteins c-junaxonal degenerationdemyelinating diseaseneural repairneuron-glial interactionneuropathy

Identifiers

PMID25216747
PMCPMC4208468
OpenAlexW1971830677

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.