Evidence map›Paper›PMID 33306674›Full record

ArticlePLoS genetics2020

Autocrine insulin pathway signaling regulates actin dynamics in cell wound repair.

Mitsutoshi Nakamura, Jeffrey M Verboon, Tessa E Allen, Maria Teresa Abreu-Blanco, Raymond Liu, Andrew N M Dominguez, Jeffrey J Delrow, Susan M Parkhurst

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.7field-weighted citation impact, top 34% 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

8 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Early Endosomes Act as Local Exocytosis Hubs to Repair Endothelial Membrane Damage.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2023
    Article
  7. Review
  8. Review
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

8 authors at 1 institution in 1 country.

Mitsutoshi NakamuraBasic Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, WA, United States of America.ORCID 0000-0001-7879-3176
Jeffrey M VerboonBasic Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, WA, United States of America.
Tessa E AllenBasic Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, WA, United States of America.ORCID 0000-0002-5929-116X
Maria Teresa Abreu-BlancoBasic Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, WA, United States of America.ORCID 0000-0003-0074-4563
Raymond LiuBasic Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, WA, United States of America.ORCID 0000-0002-4739-8293
Andrew N M DominguezBasic Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, WA, United States of America.ORCID 0000-0001-9608-3522
Jeffrey J DelrowGenomics Shared Resource, Fred Hutchinson Cancer Research Center, Seattle, WA, United States of America.ORCID 0000-0003-1020-3154
Susan M ParkhurstBasic Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, WA, United States of America.ORCID 0000-0001-5806-9930
Fred Hutch Cancer Center · US

Funding

Translational Bioimaging Core Shared ResourceP30CA015704 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Eric Collisson · 1985 to 2026
$296.4M
Molecular and Cellular Mechanisms of Wound RepairR01GM111635 · NIGMS · FRED HUTCHINSON CANCER RESEARCH CENTER · PI PARKHURST, SUSAN M · 2015 to 2025
$4.8M
NCI NIH HHS P30 CA015704NIGMS NIH HHS R01 GM111635
6 · The paper itself

Abstract

Cells are exposed to frequent mechanical and/or chemical stressors that can compromise the integrity of the plasma membrane and underlying cortical cytoskeleton. The molecular mechanisms driving the immediate repair response launched to restore the cell cortex and circumvent cell death are largely unknown. Using microarrays and drug-inhibition studies to assess gene expression, we find that initiation of cell wound repair in the Drosophila model is dependent on translation, whereas transcription is required for subsequent steps. We identified 253 genes whose expression is up-regulated (80) or down-regulated (173) in response to laser wounding. A subset of these genes were validated using RNAi knockdowns and exhibit aberrant actomyosin ring assembly and/or actin remodeling defects. Strikingly, we find that the canonical insulin signaling pathway controls actin dynamics through the actin regulators Girdin and Chickadee (profilin), and its disruption leads to abnormal wound repair. Our results provide new insight for understanding how cell wound repair proceeds in healthy individuals and those with diseases involving wound healing deficiencies.

Indexed as

Autocrine CommunicationSignal TransductionWound HealingActinsAnimalsDrosophila melanogasterDrosophila ProteinsInsulinIntracellular Signaling Peptides and ProteinsProfilinsTranscriptomeActinschic protein, DrosophilaDrosophila ProteinsGirdin protein, DrosophilaInsulinIntracellular Signaling Peptides and ProteinsProfilins

Identifiers

PMID33306674
PMCPMC7758051
OpenAlexW3112480809

What Socratic 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 Socratic graph.