Evidence map›Paper›PMID 34109380›Full record

ArticleDevelopment (Cambridge, England)2021

Regulation of UNC-40/DCC and UNC-6/Netrin by DAF-16 promotes functional rewiring of the injured axon.

Atrayee Basu, Sibaram Behera, Smriti Bhardwaj, Shirshendu Dey, Anindya Ghosh-Roy

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in Development (Cambridge, England), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.1field-weighted citation impact, top 26% 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

6 citing papers in PubMed, 17 citations in OpenAlex.

  1. The conserved fibroblast growth factor receptor-based signaling is required for dendrite regeneration.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  2. Exercise-Induced Differential Transcriptional Output of AMPK Signaling Improves Axon Regeneration and Functional Recovery.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. The regulatory landscape of neurite development inFrontiers in molecular neuroscience · 2022
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

Atrayee BasuDepartment of Cellular and Molecular Neuroscience, National Brain Research Centre, Manesar, Nainwal Mode, Gurgaon, Haryana 122051, India.ORCID 0000-0001-6056-7138
Sibaram BeheraDepartment of Cellular and Molecular Neuroscience, National Brain Research Centre, Manesar, Nainwal Mode, Gurgaon, Haryana 122051, India.
Smriti BhardwajDepartment of Cellular and Molecular Neuroscience, National Brain Research Centre, Manesar, Nainwal Mode, Gurgaon, Haryana 122051, India.ORCID 0000-0003-1930-9457
Shirshendu DeyFluorescence Microscopy Division, Bruker India Scientific PvT Ltd, International Trade Tower, Nehru Place, New Delhi 110019, India.
Anindya Ghosh-RoyDepartment of Cellular and Molecular Neuroscience, National Brain Research Centre, Manesar, Nainwal Mode, Gurgaon, Haryana 122051, India.ORCID 0000-0002-3428-4588
National Brain Research Centre · IN

Funding

Enhancing and expanding the CGC Strain CollectionP40OD010440 · OD · UNIVERSITY OF MINNESOTA · PI Ann E. Rougvie · 2012 to 2026
$7.5M
DBT/Wellcome Trust India Alliance IA/I/13/1/500874NIH HHS P40 OD010440Wellcome Trust
6 · The paper itself

Abstract

The adult nervous system has a limited capacity to regenerate after accidental damage. Post-injury functional restoration requires proper targeting of the injured axon to its postsynaptic cell. Although the initial response to axonal injury has been studied in great detail, it is rather unclear what controls the re-establishment of a functional connection. Using the posterior lateral microtubule neuron in Caenorhabditis elegans, we found that after axotomy, the regrowth from the proximal stump towards the ventral side and accumulation of presynaptic machinery along the ventral nerve cord correlated to the functional recovery. We found that the loss of insulin receptor DAF-2 promoted 'ventral targeting' in a DAF-16-dependent manner. We further showed that coordinated activities of DAF-16 in neuron and muscle promoted 'ventral targeting'. In response to axotomy, expression of the Netrin receptor UNC-40 was upregulated in the injured neuron in a DAF-16-dependent manner. In contrast, the DAF-2-DAF-16 axis contributed to the age-related decline in Netrin expression in muscle. Therefore, our study revealed an important role for insulin signaling in regulating the axon guidance molecules during the functional rewiring process.

Indexed as

AnimalsAxon GuidanceAxonsCaenorhabditis elegansCaenorhabditis elegans ProteinsCell Adhesion MoleculesForkhead Transcription FactorsGene Expression RegulationMicrotubulesNerve Growth FactorsNerve Tissue ProteinsNetrin ReceptorsNetrinsNeuronsSignal TransductionCaenorhabditis elegans ProteinsCell Adhesion Moleculesdaf-16 protein, C elegansForkhead Transcription FactorsNerve Growth FactorsNerve Tissue ProteinsNetrin ReceptorsNetrinsUNC-40 protein, C elegansUNC-6 protein, C elegansAxon regenerationCaenorhabditis elegansDAF-16Functional restorationPLM neuronUNC-40

Identifiers

PMID34109380
PMCPMC8217708
OpenAlexW3166648860

What Socratic 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 Socratic graph.