Evidence map›Paper›PMID 27452696›Full record

ArticleNature communications2016

Plexins function in epithelial repair in both Drosophila and zebrafish.

Sa Kan Yoo, Heath G Pascoe, Telmo Pereira, Shu Kondo, Antonio Jacinto, Xuewu Zhang, Iswar K Hariharan

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
2.7field-weighted citation impact, top 11% 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

36 citing papers in PubMed, 51 citations in OpenAlex.

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  11. Imaginal Disc Regeneration: Something Old, Something New.Cold Spring Harbor perspectives in biology · 2022
    Review
  12. Review
  13. Article
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  17. Article
  18. Article
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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

7 authors at 5 institutions in 3 countries.

Sa Kan YooDepartment of Molecular and Cell Biology, University of California, Berkeley, California 94720, USA.
Heath G PascoeDepartment of Pharmacology, University of Texas Southwestern Medical Center, Dallas, Texas 75390, USA.
Telmo PereiraInstituto de Medicina Molecular, Faculdade de Medicina da Universidade de Lisboa, 1649-028 Lisboa, Portugal.
Shu KondoGenetic Strains Research Center, National Institute of Genetics, 1111 Yata, Mishima, Shizuoka 411-8540, Japan.
Antonio JacintoCEDOC, Chronic Diseases Research Centre, NOVA Medical School, Universidade NOVA de Lisboa, 130, 1169-056 Lisboa, Portugal.
Xuewu ZhangDepartment of Pharmacology, University of Texas Southwestern Medical Center, Dallas, Texas 75390, USA.
Iswar K HariharanDepartment of Molecular and Cell Biology, University of California, Berkeley, California 94720, USA.
The University of Texas Southwestern Medical Center · USUniversity of California, Berkeley · USNational Institute of Genetics · JPUniversidade Nova de Lisboa · PTUniversity of Lisbon · PT

Funding

DIVISION OF CELL &MOLECULAR BIOLOGY TRAINING PROGRAMT32GM008203 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI COBB, MELANIE H. · 1987 to 2018
$7.0M
Signaling and Regulation Mechanisms of PlexinR01GM088197 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI ZHANG, XUEWU · 2009 to 2017
$2.8M
Identifying novel strategies to promote tissue regenerationR01GM085576 · NIGMS · UNIVERSITY OF CALIFORNIA BERKELEY · PI HARIHARAN, ISWAR K. · 2008 to 2016
$2.4M
European Research CouncilNIGMS NIH HHS R01 GM085576NIGMS NIH HHS R01 GM088197NIGMS NIH HHS T32 GM008203
6 · The paper itself

Abstract

In most multicellular organisms, homeostasis is contingent upon maintaining epithelial integrity. When unanticipated insults breach epithelial barriers, dormant programmes of tissue repair are immediately activated. However, many of the mechanisms that repair damaged epithelia remain poorly characterized. Here we describe a role for Plexin A (PlexA), a protein with particularly well-characterized roles in axonal pathfinding, in the healing of damaged epithelia in Drosophila. Semaphorins, which are PlexA ligands, also regulate tissue repair. We show that Drosophila PlexA has GAP activity for the Rap1 GTPase, which is known to regulate the stability of adherens junctions. Our observations suggest that the inhibition of Rap1 activity by PlexA in damaged Drosophila epithelia allows epithelial remodelling, thus facilitating wound repair. We also demonstrate a role for Plexin A1, a zebrafish orthologue of Drosophila PlexA, in epithelial repair in zebrafish tail fins. Thus, plexins function in epithelial wound healing in diverse taxa.

Indexed as

Wound HealingActinsAdherens JunctionsAnimal FinsAnimalsCell Adhesion MoleculesDrosophila melanogasterEpithelial CellsEpitheliumNerve Tissue ProteinsRNA InterferenceSignal TransductionZebrafishActinsCell Adhesion MoleculesNerve Tissue Proteinsplexin

Identifiers

PMID27452696
PMCPMC4962468
OpenAlexW2483338484

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.