Evidence map›Paper›PMID 15647476›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2005

Axonal protein synthesis and degradation are necessary for efficient growth cone regeneration.

Poonam Verma, Sabrina Chierzi, Amanda M Codd, Douglas S Campbell, Ronald L Meyer, Christine E Holt, James W Fawcett

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 200 papers.

0numbers the graph read from it
0cells of the map it votes in
200citing papers in PubMed
8.4field-weighted citation impact, top 1% 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

200 citing papers in PubMed, 407 citations in OpenAlex.

  1. Article
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  4. Article
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  7. Review
  8. Review
  9. Review
  10. Genes in Axonal Regeneration.Molecular neurobiology · 2024
    Review
  11. Review
  12. Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Integrin-Driven Axon Regeneration in the Spinal Cord Activates a Distinctive CNS Regeneration Program.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2023
    Article
  18. Review
  19. Spatial patterns of the cap-binding complex eIF4F in human melanoma cells.Computational and structural biotechnology journal · 2023
    Article
  20. Unleashing Intrinsic Growth Pathways in Regenerating Peripheral Neurons.International journal of molecular sciences · 2022
    Review

140 more citing papers are in PubMed but not listed here.

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

7 authors at 3 institutions in 2 countries.

Poonam VermaCambridge University Centre for Brain Repair, Cambridge CB2 2PY, United Kingdom.
Sabrina Chierzi
Amanda M Codd
Douglas S Campbell
Ronald L Meyer
Christine E Holt
James W Fawcett
University of Cambridge · GBUniversity of California, Irvine · USUniversity of California, San Francisco · US

Funding

Wellcome Trust 070568
6 · The paper itself

Abstract

Axonal regeneration can occur within hours of injury, the first step being the formation of a new growth cone. For sensory and retinal axons, regenerative ability in vivo correlates with the potential to form a new growth cone after axotomy in vitro. We show that this ability to regenerate a new growth cone depends on local protein synthesis and degradation within the axon. Axotomy in vitro leads to a fourfold to sixfold increase in 3H-leucine incorporation in both neurones and axons, starting within 10 min and peaking 1 h after axotomy. Application of protein synthesis inhibitors (cycloheximide and anisomycin) to cut axons, including axons whose cell bodies were removed, or proteasome inhibitors (lactacystin and N-acetyl-Nor-Leu-Leu-Al) all result in a reduction in the proportion of transected axons able to reform growth cones. Similar inhibition of growth cone formation was observed on addition of target of rapamycin (TOR), p38 MAPK (mitogen-activated protein kinase), and caspase-3 inhibitors. Comparing retinal and sensory axons of different developmental stages, levels of ribosomal protein P0 and phosphorylated translation initiation factor are high in sensory axons, lower in embryonic axons, and absent in adult retinal axons. Conditioning lesions, which increase the regenerative ability of sensory axons, lead to increases in intra-axonal protein synthetic and degradative machinery both in vitro and in vivo. Collectively, these findings suggest that local protein synthesis and degradation, controlled by various TOR-, p38 MAPK-, and caspase-dependent pathways, underlie growth cone initiation after axotomy.

Indexed as

AgingAnimalsAxonsAxotomyCaspase 3Caspase InhibitorsCaspasesCells, CulturedFemaleGanglia, SpinalGrowth ConesNerve RegenerationNerve Tissue ProteinsNeurons, Afferentp38 Mitogen-Activated Protein KinasesProteasome Endopeptidase ComplexCasp3 protein, ratCaspase 3Caspase InhibitorsCaspasesmTOR protein, ratNerve Tissue Proteinsp38 Mitogen-Activated Protein KinasesProteasome Endopeptidase ComplexProteasome InhibitorsProtein Kinase InhibitorsProtein KinasesProtein Synthesis InhibitorsTOR Serine-Threonine Kinases

Identifiers

PMID15647476
PMCPMC3687202
OpenAlexW2158021569

What OpenQuestion holds

Textmetadata
LicenceTDM
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.