Evidence map›Paper›PMID 31823869›Full record

ReviewNeural regeneration research2020

Heterogeneity in the regenerative abilities of central nervous system axons within species: why do some neurons regenerate better than others?

William Rodemer, Jianli Hu, Michael E Selzer, Michael I Shifman

Abstract readReview
In one paragraph

Review in Neural regeneration research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
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

10 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Calcium in Neuronal and Glial Response to Axotomy.International journal of molecular sciences · 2021
    Review
  10. 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

4 authors.

William RodemerShriners Hospitals Pediatric Research Center (Center for Neural Repair and Rehabilitation), the Lewis Katz School of Medicine at Temple University, Philadelphia, PA, USA.
Jianli HuShriners Hospitals Pediatric Research Center (Center for Neural Repair and Rehabilitation), the Lewis Katz School of Medicine at Temple University, Philadelphia, PA, USA.
Michael E SelzerShriners Hospitals Pediatric Research Center (Center for Neural Repair and Rehabilitation); Department of Neurology, the Lewis Katz School of Medicine at Temple University, Philadelphia, PA, USA.
Michael I ShifmanShriners Hospitals Pediatric Research Center (Center for Neural Repair and Rehabilitation), the Lewis Katz School of Medicine at Temple University, Philadelphia, PA, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Some neurons, especially in mammalian peripheral nervous system or in lower vertebrate or in vertebrate central nervous system (CNS) regenerate after axotomy, while most mammalian CNS neurons fail to regenerate. There is an emerging consensus that neurons have different intrinsic regenerative capabilities, which theoretically could be manipulated therapeutically to improve regeneration. Population-based comparisons between "good regenerating" and "bad regenerating" neurons in the CNS and peripheral nervous system of most vertebrates yield results that are inconclusive or difficult to interpret. At least in part, this reflects the great diversity of cells in the mammalian CNS. Using mammalian nervous system imposes several methodical limitations. First, the small sizes and large numbers of neurons in the CNS make it very difficult to distinguish regenerating neurons from non-regenerating ones. Second, the lack of identifiable neurons makes it impossible to correlate biochemical changes in a neuron with axonal damage of the same neuron, and therefore, to dissect the molecular mechanisms of regeneration on the level of single neurons. This review will survey the reported responses to axon injury and the determinants of axon regeneration, emphasizing non-mammalian model organisms, which are often under-utilized, but in which the data are especially easy to interpret.

Indexed as

axonal regenerationidentifiable neuronsintrinsic factorslampreyMauthner cellMüller cellneuronal deathnon-mammalian model organismsspinal cord injuryzebrafish

Identifiers

PMID31823869
PMCPMC7034288

What OpenQuestion holds

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LicenceCC BY-NC-SA
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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.