Evidence map›Paper›PMID 30726731›Full record

ArticleCell reports2019

Retracted: Macrophage-Derived Slit3 Controls Cell Migration and Axon Pathfinding in the Peripheral Nerve Bridge.

Xin-Peng Dun, Lauren Carr, Patricia K Woodley, Riordan W Barry, Louisa K Drake, Thomas Mindos, Sheridan L Roberts, Alison C Lloyd, David B Parkinson

RetractedOpen access · goldAbstract readRetracted Publication
In one paragraph

Article in Cell reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
5.5field-weighted citation impact, top 3% 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

50 citing papers in PubMed, 73 citations in OpenAlex.

  1. Peripheral nerve repair: innovations and future directions.Journal of translational medicine · 2026
    Review
  2. Article
  3. Article
  4. Cell Heterogeneity and Variability in Peripheral Nerve after Injury.International journal of molecular sciences · 2024
    Review
  5. Review
  6. Review
  7. SLIT3-mediated fibroblast signaling: a promising target for antifibrotic therapies.American journal of physiology. Heart and circulatory physiology · 2023
    Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 4 institutions in 2 countries.

Xin-Peng DunFaculty of Medicine and Dentistry, Plymouth University, Plymouth, Devon, UK; School of Pharmacy, Hubei University of Science and Technology, Xian-Ning City, Hubei, China; The Co-innovation Center of Neuroregeneration, Nantong University, Jiangsu Province, China. Electronic address: xin-peng.dun@plymouth.ac.uk.
Lauren CarrFaculty of Medicine and Dentistry, Plymouth University, Plymouth, Devon, UK.
Patricia K WoodleyFaculty of Medicine and Dentistry, Plymouth University, Plymouth, Devon, UK.
Riordan W BarryUniversity of Bath, Bath, UK.
Louisa K DrakeUniversity of Bath, Bath, UK.
Thomas MindosFaculty of Medicine and Dentistry, Plymouth University, Plymouth, Devon, UK.
Sheridan L RobertsFaculty of Medicine and Dentistry, Plymouth University, Plymouth, Devon, UK.
Alison C LloydMRC Laboratory for Molecular Cell Biology, University College London, London, UK.
David B ParkinsonFaculty of Medicine and Dentistry, Plymouth University, Plymouth, Devon, UK.
University of Plymouth · GBUniversity of Bath · GBMRC Laboratory for Molecular Cell Biology · GBNantong University · CN

Funding

Cancer Research UK 11244Cancer Research UK 17135Medical Research Council MR/N009169/1Medical Research Council MR/R023816/1Wellcome TrustWellcome Trust 088228/Z/09/Z
6 · The paper itself

Abstract

Slit-Robo signaling has been characterized as a repulsive signal for precise axon pathfinding and cell migration during embryonic development. Here, we describe a role for Sox2 in the regulation of Robo1 in Schwann cells and for Slit3-Robo1 signaling in controlling axon guidance within the newly formed nerve bridge following peripheral nerve transection injury. In particular, we show that macrophages form the outermost layer of the nerve bridge and secrete high levels of Slit3, while migratory Schwann cells and fibroblasts inside the nerve bridge express the Robo1 receptor. In line with this pattern of Slit3 and Robo1 expression, we observed multiple axon regeneration and cell migration defects in the nerve bridge of Sox2-, Slit3-, and Robo1-mutant mice. Our findings have revealed important functions for macrophages in the peripheral nervous system, utilizing Slit3-Robo1 signaling to control correct peripheral nerve bridge formation and precise axon targeting to the distal nerve stump following injury.

Indexed as

Axon GuidanceNerve RegenerationAnimalsCell MovementCells, CulturedFemaleFibroblastsMacrophagesMaleMembrane ProteinsMiceMice, Inbred C57BLMutationNerve Tissue ProteinsPeripheral NervesRatsMembrane ProteinsNerve Tissue ProteinsReceptors, ImmunologicRoundabout ProteinsSlit3 protein, mouseSox2 protein, mouseSOXB1 Transcription Factorsfibroblastinjurymacrophagesmigrationperipheral nerveregenerationRobo1Schwann cellSlit3Sox2

Identifiers

PMID30726731
PMCPMC6367597
OpenAlexW2913784856

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.