Evidence map›Paper›PMID 24431434›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2014

S6 kinase inhibits intrinsic axon regeneration capacity via AMP kinase in Caenorhabditis elegans.

Thomas Hubert, Zilu Wu, Andrew D Chisholm, Yishi Jin

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.3field-weighted citation impact, top 25% 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

24 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Axon Injury-Induced Autophagy Activation Is Impaired in aInternational journal of molecular sciences · 2020
    Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Functional Interactions BetweenG3 (Bethesda, Md.) · 2018
    Article
  12. Article
  13. Review
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  15. Article
  16. Review
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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 at 1 institution in 1 country.

Thomas HubertDivision of Biological Sciences, Section of Neurobiology, and Howard Hughes Medical Institute, University of California San Diego, La Jolla, California 92093.
Zilu Wu
Andrew D Chisholm
Yishi Jin
University of California, San Diego · US

Funding

Enhancing and expanding the CGC Strain CollectionP40OD010440 · OD · UNIVERSITY OF MINNESOTA · PI Aric L Daul, Ann E. Rougvie · 2012 to 2026
$7.5M
Development of a C. elegans model for axonal regenerationR01NS057317 · NINDS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI CHISHOLM, ANDREW D · 2009 to 2013
$1.5M
NIH HHS P40 OD010440NINDS NIH HHS R01 NS057317NINDS NIH HHS R01NS057317
6 · The paper itself

Abstract

The ability of axons to regrow after injury is determined by the complex interplay of intrinsic growth programs and external cues. In Caenorhabditis elegans mechanosensory neuron, axons exhibit robust regenerative regrowth following laser axotomy. By surveying conserved metabolic signaling pathways, we have identified the ribosomal S6 kinase RSKS-1 as a new cell-autonomous inhibitor of axon regeneration. RSKS-1 is not required for axonal development but inhibits axon regrowth after injury in multiple neuron types. Loss of function in rsks-1 results in more rapid growth cone formation after injury and accelerates subsequent axon extension. The enhanced regrowth of rsks-1 mutants is partly dependent on the DLK-1 MAPK cascade. An essential output of RSKS-1 in axon regrowth is the metabolic sensor AMP kinase, AAK-2. We further show that the antidiabetic drug phenformin, which activates AMP kinase, can promote axon regrowth. Our data reveal a new function for an S6 kinase acting through an AMP kinase in regenerative growth of injured axons.

Indexed as

Adenylate KinaseAMP-Activated Protein KinasesAnimalsAxonsCaenorhabditis elegansCaenorhabditis elegans ProteinsNerve RegenerationProtein Serine-Threonine KinasesRibosomal Protein S6 Kinases, 70-kDaTransgenesAAK-2 protein, C elegansAdenylate KinaseAMP-Activated Protein KinasesCaenorhabditis elegans ProteinsProtein Serine-Threonine KinasesRibosomal Protein S6 Kinases, 70-kDaRsks-1 protein, C elegansAMP kinaseCaenorhabditis elegansDLK kinaselaser axotomyribosomal S6 kinase

Identifiers

PMID24431434
PMCPMC3891956
OpenAlexW2020872204

What OpenQuestion holds

Textmetadata
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.