Evidence map›Paper›PMID 30001326›Full record

ArticlePLoS genetics2018

BMP signaling downstream of the Highwire E3 ligase sensitizes nociceptors.

Ken Honjo, W Daniel Tracey

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.8field-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

14 citing papers in PubMed, 17 citations in OpenAlex.

  1. The nociceptor primary cilium.Brain : a journal of neurology · 2026
    Review
  2. Article
  3. Review
  4. Nociception inCold Spring Harbor protocols · 2025
    Article
  5. Article
  6. Article
  7. Article
  8. Frontiers in physiology · 2022
    Review
  9. Biology open · 2021
    Article
  10. Role of the Ubiquitin System in Chronic Pain.Frontiers in molecular neuroscience · 2021
    Review
  11. Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  12. Article
  13. Article
  14. 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

2 authors at 2 institutions in 2 countries.

Ken HonjoFaculty of Life and Environmental Sciences, University of Tsukuba, Tsukuba, Ibaraki, Japan.ORCID 0000-0001-7804-2436
W Daniel TraceyDepartment of Biology, Indiana University, Bloomington, Indiana, United States of America.ORCID 0000-0003-4666-8199
Indiana University Bloomington · USUniversity of Tsukuba · JP

Funding

A Genome-Wide Analysis of Nociception Molecules, from Expression to FunctionR01GM086458 · NIGMS · TRUSTEES OF INDIANA UNIVERSITY · PI TRACEY, WILLIAM D · 2011 to 2020
$2.6M
NIGMS NIH HHS R01 GM086458
6 · The paper itself

Abstract

A comprehensive understanding of the molecular machinery important for nociception is essential to improving the treatment of pain. Here, we show that the BMP signaling pathway regulates nociception downstream of the E3 ubiquitin ligase highwire (hiw). hiw loss of function in nociceptors caused antagonistic and pleiotropic phenotypes with simultaneous insensitivity to noxious heat but sensitized responses to optogenetic activation of nociceptors. Thus, hiw functions to both positively and negatively regulate nociceptors. We find that a sensory reception-independent sensitization pathway was associated with BMP signaling. BMP signaling in nociceptors was up-regulated in hiw mutants, and nociceptor-specific expression of hiw rescued all nociception phenotypes including the increased BMP signaling. Blocking the transcriptional output of the BMP pathway with dominant negative Mad suppressed nociceptive hypersensitivity that was induced by interfering with hiw. The up-regulated BMP signaling phenotype in hiw genetic mutants could not be suppressed by mutation in wallenda suggesting that hiw regulates BMP in nociceptors via a wallenda independent pathway. In a newly established Ca2+ imaging preparation, we observed that up-regulated BMP signaling caused a significantly enhanced Ca2+ signal in the axon terminals of nociceptors that were stimulated by noxious heat. This response likely accounts for the nociceptive hypersensitivity induced by elevated BMP signaling in nociceptors. Finally, we showed that 24-hour activation of BMP signaling in nociceptors was sufficient to sensitize nociceptive responses to optogenetically-triggered nociceptor activation without altering nociceptor morphology. Overall, this study demonstrates the previously unrevealed roles of the Hiw-BMP pathway in the regulation of nociception and provides the first direct evidence that up-regulated BMP signaling physiologically sensitizes responses of nociceptors and nociception behaviors.

Indexed as

AnimalsAnimals, Genetically ModifiedBehavior, AnimalBone Morphogenetic ProteinsDrosophila melanogasterDrosophila ProteinsFemaleMaleMAP Kinase Kinase KinasesModels, AnimalNerve Tissue ProteinsNociceptionNociceptorsPresynaptic TerminalsSignal TransductionUp-RegulationBone Morphogenetic ProteinsDrosophila ProteinsHIW protein, DrosophilaMAP Kinase Kinase KinasesNerve Tissue Proteinswnd protein, Drosophila

Identifiers

PMID30001326
PMCPMC6042685
OpenAlexW2953354754

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.