Evidence map›Paper›PMID 24840036›Full record

ArticlePloS one2014

CaMKK-CaMK1a, a new post-traumatic signalling pathway induced in mouse somatosensory neurons.

Lucie Elzière, Chamroeun Sar, Stéphanie Ventéo, Steeve Bourane, Sylvie Puech, Corinne Sonrier, Hassan Boukhadaoui, Agnès Fichard, Alexandre Pattyn, Jean Valmier and 2 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.7field-weighted citation impact, top 29% 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

8 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Article
  3. Calcium in Neuronal and Glial Response to Axotomy.International journal of molecular sciences · 2021
    Review
  4. Article
  5. Article
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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

12 authors at 3 institutions in 2 countries.

Lucie ElzièreInstitute for Neurosciences of Montpellier, I.N.S.E.R.M. U1051, Montpellier, France.
Chamroeun SarInstitute for Neurosciences of Montpellier, I.N.S.E.R.M. U1051, Montpellier, France.
Stéphanie VentéoInstitute for Neurosciences of Montpellier, I.N.S.E.R.M. U1051, Montpellier, France.
Steeve BouraneMolecular Neurobiology Laboratory, The Salk Institute, La Jolla, California, United States of America.
Sylvie PuechInstitute for Neurosciences of Montpellier, I.N.S.E.R.M. U1051, Montpellier, France.
Corinne SonrierInstitute for Neurosciences of Montpellier, I.N.S.E.R.M. U1051, Montpellier, France.
Hassan BoukhadaouiInstitute for Neurosciences of Montpellier, I.N.S.E.R.M. U1051, Montpellier, France.
Agnès FichardInstitute for Neurosciences of Montpellier, I.N.S.E.R.M. U1051, Montpellier, France; Department BioMV, University of Montpellier II, Montpellier, France.
Alexandre PattynInstitute for Neurosciences of Montpellier, I.N.S.E.R.M. U1051, Montpellier, France.
Jean ValmierInstitute for Neurosciences of Montpellier, I.N.S.E.R.M. U1051, Montpellier, France; Department BioMV, University of Montpellier II, Montpellier, France.
Patrick CarrollInstitute for Neurosciences of Montpellier, I.N.S.E.R.M. U1051, Montpellier, France.
Ilana MéchalyInstitute for Neurosciences of Montpellier, I.N.S.E.R.M. U1051, Montpellier, France; Department BioMV, University of Montpellier II, Montpellier, France.
Institute for Neurosciences of Montpellier · FRSalk Institute for Biological Studies · USUniversité de Montpellier · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neurons innervating peripheral tissues display complex responses to peripheral nerve injury. These include the activation and suppression of a variety of signalling pathways that together influence regenerative growth and result in more or less successful functional recovery. However, these responses can be offset by pathological consequences including neuropathic pain. Calcium signalling plays a major role in the different steps occurring after nerve damage. As part of our studies to unravel the roles of injury-induced molecular changes in dorsal root ganglia (DRG) neurons during their regeneration, we show that the calcium calmodulin kinase CaMK1a is markedly induced in mouse DRG neurons in several models of mechanical peripheral nerve injury, but not by inflammation. Intrathecal injection of NRTN or GDNF significantly prevents the post-traumatic induction of CaMK1a suggesting that interruption of target derived factors might be a starter signal in this de novo induction. Inhibition of CaMK signalling in injured DRG neurons by pharmacological means or treatment with CaMK1a siRNA resulted in decreased velocity of neurite growth in vitro. Altogether, the results suggest that CaMK1a induction is part of the intrinsic regenerative response of DRG neurons to peripheral nerve injury, and is thus a potential target for therapeutic intervention to improve peripheral nerve regeneration.

Indexed as

AnimalsAxotomyCalcium-Calmodulin-Dependent Protein Kinase Type 1Calcium SignalingGanglia, SpinalImmunohistochemistryIn Situ HybridizationMiceNerve RegenerationNeuritesNeuronsReal-Time Polymerase Chain ReactionSciatic NerveCalcium-Calmodulin-Dependent Protein Kinase Type 1

Identifiers

PMID24840036
PMCPMC4026325
OpenAlexW2074308857

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.