Evidence map›Paper›PMID 24719025›Full record

ArticleDisease models & mechanisms2014

Precise control of miR-125b levels is required to create a regeneration-permissive environment after spinal cord injury: a cross-species comparison between salamander and rat.

Juan Felipe Diaz Quiroz, Eve Tsai, Matthew Coyle, Tina Sehm, Karen Echeverri

Open access · goldAbstract readComparative Study
In one paragraph

Article in Disease models & mechanisms, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

42 citing papers in PubMed, 68 citations in OpenAlex.

  1. Article
  2. The endocannabinoid system regulates both ependymoglial and neuronal cell responses to a tail amputation in the axolotl.Developmental dynamics : an official publication of the American Association of Anatomists · 2026
    Article
  3. Review
  4. MicroRNAs in Tissue Regeneration: Lessons from Animal Models.International journal of molecular sciences · 2025
    Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. Now that We Got There, What Next?Methods in molecular biology (Clifton, N.J.) · 2023
    Article
  15. Article
  16. Article
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  18. Article
  19. Article
  20. Review
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

5 authors at 4 institutions in 3 countries.

Juan Felipe Diaz QuirozUniversity of Minnesota, Department of Genetics, Cell Biology and Development, Stem Cell Institute, 2001 6th St SE, Minneapolis, MN 55455, USA.
Eve TsaiOttawa Hospital Research Institute, Ottowa, ON K1H 8L6, Canada.
Matthew CoyleOttawa Hospital Research Institute, Ottowa, ON K1H 8L6, Canada.
Tina SehmUniversity of Erlangen-Nürnberg, Department of Neurosurgery, 91054 Erlangen, Germany.
Karen EcheverriUniversity of Minnesota, Department of Genetics, Cell Biology and Development, Stem Cell Institute, 2001 6th St SE, Minneapolis, MN 55455, USA. echev020@umn.edu.
University of Minnesota · USFriedrich-Alexander-Universität Erlangen-Nürnberg · DEOttawa Hospital · CAOttawa Hospital Research Institute

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Most spinal cord injuries lead to permanent paralysis in mammals. By contrast, the remarkable regenerative abilities of salamanders enable full functional recovery even from complete spinal cord transections. The molecular differences underlying this evolutionary divergence between mammals and amphibians are poorly understood. We focused on upstream regulators of gene expression as primary entry points into this question. We identified a group of microRNAs (miRNAs) that are conserved between the Mexican axolotl salamander (Ambystoma mexicanum) and mammals but show marked cross-species differences in regulation patterns following spinal cord injury. We found that precise post-injury levels of one of these miRNAs (miR-125b) is essential for functional recovery, and guides correct regeneration of axons through the lesion site in a process involving the direct downstream target Sema4D in axolotls. Translating these results to a mammalian model, we increased miR-125b levels in the rat through mimic treatments following spinal cord transection. These treatments downregulated Sema4D and other glial-scar-related genes, and enhanced the animal's functional recovery. Our study identifies a key regulatory molecule conserved between salamander and mammal, and shows that the expression of miR-125b and Sema4D must be carefully controlled in the right cells at the correct level to promote regeneration. We also show that these molecular components of the salamander's regeneration-permissive environment can be experimentally harnessed to improve treatment outcomes for mammalian spinal cord injuries.

Indexed as

RegenerationAnimalsAxonsCaudataMicroRNAsRatsSpecies SpecificitySpinal Cord InjuriesMicroRNAsAxolotlmicroRNAsRegenerationSpinal cord injury

Identifiers

PMID24719025
PMCPMC4036468
OpenAlexW2110648073

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.