Evidence map›Paper›PMID 27984580›Full record

ArticlePLoS genetics2016

The C. elegans Discoidin Domain Receptor DDR-2 Modulates the Met-like RTK-JNK Signaling Pathway in Axon Regeneration.

Naoki Hisamoto, Yuki Nagamori, Tatsuhiro Shimizu, Strahil I Pastuhov, Kunihiro Matsumoto

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

18 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. An expanded GCaMP reporter toolkit for functional imaging inbioRxiv : the preprint server for biology · 2023
    Article
  9. Article
  10. Review
  11. Article
  12. The Journal of neuroscience : the official journal of the Society for Neuroscience · 2021
    Article
  13. [Research progress on intrinsic signaling pathways in axon regeneration].Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences · 2020
    Review
  14. Article
  15. Genetics · 2019
    Article
  16. The Journal of neuroscience : the official journal of the Society for Neuroscience · 2019
    Article
  17. Article
  18. 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

5 authors at 1 institution in 1 country.

Naoki HisamotoDivision of Biological Science, Graduate School of Science, Nagoya University, Chikusa-ku, Nagoya, Japan.
Yuki NagamoriDivision of Biological Science, Graduate School of Science, Nagoya University, Chikusa-ku, Nagoya, Japan.ORCID http://orcid.org/0000-0002-0013-4047
Tatsuhiro ShimizuDivision of Biological Science, Graduate School of Science, Nagoya University, Chikusa-ku, Nagoya, Japan.
Strahil I PastuhovDivision of Biological Science, Graduate School of Science, Nagoya University, Chikusa-ku, Nagoya, Japan.ORCID http://orcid.org/0000-0002-5871-7149
Kunihiro MatsumotoDivision of Biological Science, Graduate School of Science, Nagoya University, Chikusa-ku, Nagoya, Japan.
Nagoya University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The ability of specific neurons to regenerate their axons after injury is governed by cell-intrinsic regeneration pathways. However, the signaling pathways that orchestrate axon regeneration are not well understood. In Caenorhabditis elegans, initiation of axon regeneration is positively regulated by SVH-2 Met-like growth factor receptor tyrosine kinase (RTK) signaling through the JNK MAPK pathway. Here we show that SVH-4/DDR-2, an RTK containing a discoidin domain that is activated by collagen, and EMB-9 collagen type IV regulate the regeneration of neurons following axon injury. The scaffold protein SHC-1 interacts with both DDR-2 and SVH-2. Furthermore, we demonstrate that overexpression of svh-2 and shc-1 suppresses the delay in axon regeneration observed in ddr-2 mutants, suggesting that DDR-2 functions upstream of SVH-2 and SHC-1. These results suggest that DDR-2 modulates the SVH-2-JNK pathway via SHC-1. We thus identify two different RTK signaling networks that play coordinated roles in the regulation of axonal regeneration.

Indexed as

Adaptor Proteins, Signal TransducingAnimalsAxonsCaenorhabditis elegansCaenorhabditis elegans ProteinsDiscoidin DomainDiscoidin Domain Receptor 2JNK Mitogen-Activated Protein KinasesNerve RegenerationNeuronsReceptor Protein-Tyrosine KinasesSignal TransductionAdaptor Proteins, Signal TransducingCaenorhabditis elegans ProteinsDiscoidin Domain Receptor 2JNK Mitogen-Activated Protein KinasesReceptor Protein-Tyrosine KinasesSHC-1 protein, C elegansSVH-2 protein, C elegans

Identifiers

PMID27984580
PMCPMC5161311
OpenAlexW2562988173

What OpenQuestion holds

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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.