Evidence map›Paper›PMID 30863858›Full record

ArticleJournal of neuropathology and experimental neurology2019

Axotomy Induces Phasic Alterations in Luman/CREB3 Expression and Nuclear Localization in Injured and Contralateral Uninjured Sensory Neurons: Correlation With Intrinsic Axon Growth Capacity.

Jovan C D Hasmatali, Jolly De Guzman, Ruiling Zhai, Lisa Yang, Nikki A McLean, Catherine Hutchinson, Jayne M Johnston, Vikram Misra, Valerie M K Verge

Open access · bronzeAbstract read
In one paragraph

Article in Journal of neuropathology and experimental neurology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.9field-weighted citation impact, top 32% 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

12 citing papers in PubMed, 19 citations in OpenAlex.

  1. Beneficially Stressing the Peripheral Nervous System to Repair.International journal of molecular sciences · 2026
    Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Pinostrobin from Boesenbergia rotunda attenuates oxidative stress and promotes functional recovery in rat model of sciatic nerve crush injury.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2023
    Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Review
  12. Article
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

9 authors at 1 institution in 1 country.

Jovan C D HasmataliDepartment of Anatomy, Physiology and Pharmacology.
Jolly De GuzmanDepartment of Anatomy, Physiology and Pharmacology.
Ruiling ZhaiDepartment of Anatomy, Physiology and Pharmacology.
Lisa YangCameco MS Neuroscience Research Center.
Nikki A McLeanDepartment of Anatomy, Physiology and Pharmacology.
Catherine HutchinsonDepartment of Anatomy, Physiology and Pharmacology.
Jayne M JohnstonDepartment of Anatomy, Physiology and Pharmacology.
Vikram MisraDepartment of Veterinary Microbiology, University of Saskatchewan, Saskatoon, Saskatchewan, Canada.
Valerie M K VergeDepartment of Anatomy, Physiology and Pharmacology.
University of Saskatchewan · CA

Funding

CIHR 14238CIHR 74747
6 · The paper itself

Abstract

Luman/CREB3 is an important early retrograde axotomy signal regulating acute axon outgrowth in sensory neurons through the adaptive unfolded protein response. As the injury response is transcriptionally multiphasic, a spatiotemporal analysis of Luman/CREB3 localization in rat dorsal root ganglion (DRG) with unilateral L4-L6 spinal nerve injury was conducted to determine if Luman/CREB3 expression was similarly regulated. Biphasic alterations in Luman/CREB3 immunofluorescence and nuclear localization occurred in neurons ipsilateral to 1-hour, 1-day, 2-day, 4-day, and 1-week injury, with a largely parallel, but less avid response contralaterally. This biphasic response was not observed at the transcript level. To assess whether changes in neuronal Luman expression corresponded with an altered intrinsic capacity to grow an axon/neurite in vitro, injury-conditioned and contralateral uninjured DRG neurons underwent a 24-hour axon growth assay. Two-day injury-conditioned neurons exhibited maximal outgrowth capacity relative to naïve, declining at later injury-conditioned timepoints. Only neurons contralateral to 1-week injury exhibited significantly higher axon growth capacity than naïve. In conclusion, alterations in neuronal injury-associated Luman/CREB3 expression support that a multiphasic cell body response occurs and reveal a novel contralateral plasticity in axon growth capacity at 1-week post-injury. These adaptive responses have the potential to inform when repair or therapeutic intervention may be most effective.

Indexed as

AnimalsAxonsAxotomyCyclic AMP Response Element-Binding ProteinFunctional LateralityGanglia, SpinalMaleNerve RegenerationNeuritesPeripheral Nerve InjuriesRatsRats, WistarSensory Receptor CellsCREB3 protein, ratCyclic AMP Response Element-Binding ProteinAxotomyContralateralLZIPPeripheral nerve injuryUnfolded protein response

Identifiers

PMID30863858
PMCPMC6426154
OpenAlexW2921212820

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.