Evidence map›Paper›PMID 26255846›Full record

ArticleCurrent biology : CB2015

Integrin Adhesions Suppress Syncytium Formation in the Drosophila Larval Epidermis.

Yan Wang, Marco Antunes, Aimee E Anderson, Julie L Kadrmas, Antonio Jacinto, Michael J Galko

Open access · bronzeAbstract read
In one paragraph

Article in Current biology : CB, 2015. 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
1.6field-weighted citation impact, top 19% 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, 35 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Size compensation inFrontiers in cell and developmental biology · 2023
    Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. Polyploidy in Tissue Repair and Regeneration.Cold Spring Harbor perspectives in biology · 2021
    Review
  11. The Journal of experimental biology · 2021
    Article
  12. Article
  13. Article
  14. A Drosophila Model to Study Wound-induced Polyploidization.Journal of visualized experiments : JoVE · 2020
    Article
  15. Article
  16. An assay for chemical nociception inPhilosophical transactions of the Royal Society of London. Series B, Biological sciences · 2019
    Article
  17. Growth Factor Signaling Regulates Mechanical Nociception in Flies and Vertebrates.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2019
    Article
  18. Article
  19. Article
  20. Polyploidy in tissue homeostasis and regeneration.Development (Cambridge, England) · 2018
    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

6 authors at 4 institutions in 2 countries.

Yan WangDepartment of Genetics, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Marco AntunesCEDOC-Faculdade de Ciências Médicas, Universidade Nova de Lisboa Campo Mártires da Pátria, 130, 1169-056 Lisboa, Portugal; Instituto de Medicina Molecular Faculdade de Medicina da Universidade de Lisboa Edificio Egas Moniz, Av Prof Egas Moniz, 1649-028 Lisboa, Portugal.
Aimee E AndersonDepartment of Genetics, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Julie L KadrmasDepartment of Oncological Sciences, Huntsman Cancer Institute, University of Utah, Salt Lake City, UT 84112, USA.
Antonio JacintoCEDOC-Faculdade de Ciências Médicas, Universidade Nova de Lisboa Campo Mártires da Pátria, 130, 1169-056 Lisboa, Portugal; Instituto de Medicina Molecular Faculdade de Medicina da Universidade de Lisboa Edificio Egas Moniz, Av Prof Egas Moniz, 1649-028 Lisboa, Portugal; Instituto Gulbenkian de Ciência, Rua da Quinta Grande 6, 2780-156 Oeiras, Portugal.
Michael J GalkoDepartment of Genetics, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA; Genes and Development Graduate Program, The University of Texas Graduate School of Biomedical Sciences, Houston, TX 77030, USA. Electronic address: mjgalko@mdanderson.org.
The University of Texas MD Anderson Cancer Center · USUniversidade Nova de Lisboa · PTUniversity of Lisbon · PTUniversity of Utah · US

Funding

Genetic control of postembryonic wound healing in DrosophilaR01GM083031 · NIGMS · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI GALKO, MICHAEL J · 2008 to 2016
$2.9M
Mechanisms for regulation of cell adhesion and migrationR01GM084103 · NIGMS · UNIVERSITY OF UTAH · PI KADRMAS, JULIE L · 2009 to 2013
$1.4M
NIGMS NIH HHS R01 GM083031NIGMS NIH HHS R01 GM084103
6 · The paper itself

Abstract

Integrins are critical for barrier epithelial architecture. Integrin loss in vertebrate skin leads to blistering and wound healing defects. However, how integrins and associated proteins maintain the regular morphology of epithelia is not well understood. We found that targeted knockdown of the integrin focal adhesion (FA) complex components β-integrin, PINCH, and integrin-linked kinase (ILK) caused formation of multinucleate epidermal cells within the Drosophila larval epidermis. This phenotype was specific to the integrin FA complex and not due to secondary effects on polarity or junctional structures. The multinucleate cells resembled the syncytia caused by physical wounding. Live imaging of wound-induced syncytium formation in the pupal epidermis suggested direct membrane breakdown leading to cell-cell fusion and consequent mixing of cytoplasmic contents. Activation of Jun N-terminal kinase (JNK) signaling, which occurs upon wounding, also correlated with syncytium formation induced by PINCH knockdown. Further, ectopic JNK activation directly caused epidermal syncytium formation. No mode of syncytium formation, including that induced by wounding, genetic loss of FA proteins, or local JNK hyperactivation, involved misregulation of mitosis or apoptosis. Finally, the mechanism of epidermal syncytium formation following JNK hyperactivation and wounding appeared to be direct disassembly of FA complexes. In conclusion, the loss-of-function phenotype of integrin FA components in the larval epidermis resembles a wound. Integrin FA loss in mouse and human skin also causes a wound-like appearance. Our results reveal a novel and unexpected role for proper integrin-based adhesion in suppressing larval epidermal cell-cell fusion--a role that may be conserved in other epithelia.

Indexed as

AnimalsDrosophilaDrosophila ProteinsEpidermisGene Knockdown TechniquesGiant CellsIntegrin beta ChainsLarvaProtein Serine-Threonine KinasesPupaScaffold Protein ILKTranscription FactorsDrosophila ProteinsIntegrin beta ChainsProtein Serine-Threonine KinasesScaffold Protein ILKstck protein, DrosophilaTranscription Factors

Identifiers

PMID26255846
PMCPMC4558245
OpenAlexW1828486192

What OpenQuestion holds

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Registered trials

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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.