Evidence map›Paper›PMID 29301867›Full record

ArticleThe Journal of cell biology2018

Protease signaling regulates apical cell extrusion, cell contacts, and proliferation in epithelia.

Antonino Schepis, Adrian Barker, Yoga Srinivasan, Eaman Balouch, Yaowu Zheng, Ian Lam, Hilary Clay, Chung-Der Hsiao, Shaun R Coughlin

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

12 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
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  9. Trypsin-Like Proteases and Their Role in Muco-Obstructive Lung Diseases.International journal of molecular sciences · 2021
    Review
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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

9 authors at 2 institutions in 2 countries.

Antonino SchepisCardiovascular Research Institute, University of California, San Francisco, San Francisco, CA.
Adrian BarkerCardiovascular Research Institute, University of California, San Francisco, San Francisco, CA.
Yoga SrinivasanCardiovascular Research Institute, University of California, San Francisco, San Francisco, CA.
Eaman BalouchCardiovascular Research Institute, University of California, San Francisco, San Francisco, CA.
Yaowu ZhengCardiovascular Research Institute, University of California, San Francisco, San Francisco, CA.
Ian LamCardiovascular Research Institute, University of California, San Francisco, San Francisco, CA.
Hilary ClayCardiovascular Research Institute, University of California, San Francisco, San Francisco, CA.
Chung-Der HsiaoDepartment of Bioscience Technology, Chung Yuan Christian University, Chung-Li, Taiwan.
Shaun R CoughlinCardiovascular Research Institute, University of California, San Francisco, San Francisco, CA shaun.coughlin@ucsf.edu.ORCID 0000-0003-2337-2002
University of California, San Francisco · USChung Yuan Christian University · TW

Funding

MOLECULAR AND CELLULAR BASIS OF CARDIOVASCULAR DISEASET32HL007731 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Brian L Black · 1992 to 2026
$12.4M
MOLECULAR GENETICS OF CARDIAC CELL DIFFERENTIATIONR01HL054737 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI COUGHLIN, SHAUN R. · 1996 to 2015
$5.4M
Structure-Function and Roles of Protease-Activated ReceptorsR35HL135755 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI COUGHLIN, SHAUN R. · 2017 to 2017
$396k
NHLBI NIH HHS R01 HL054737NHLBI NIH HHS R35 HL135755NHLBI NIH HHS T32 HL007731
6 · The paper itself

Abstract

Mechanisms that sense and regulate epithelial morphogenesis, integrity, and homeostasis are incompletely understood. Protease-activated receptor 2 (Par2), the Par2-activating membrane-tethered protease matriptase, and its inhibitor, hepatocyte activator inhibitor 1 (Hai1), are coexpressed in most epithelia and may make up a local signaling system that regulates epithelial behavior. We explored the role of Par2b in matriptase-dependent skin abnormalities in Hai1a-deficient zebrafish embryos. We show an unexpected role for Par2b in regulation of epithelial apical cell extrusion, roles in regulating proliferation that were opposite in distinct but adjacent epithelial monolayers, and roles in regulating cell-cell junctions, mobility, survival, and expression of genes involved in tissue remodeling and inflammation. The epidermal growth factor receptor Erbb2 and matrix metalloproteinases, the latter induced by Par2b, may contribute to some matriptase- and Par2b-dependent phenotypes and be permissive for others. Our results suggest that local protease-activated receptor signaling can coordinate cell behaviors known to contribute to epithelial morphogenesis and homeostasis.

Indexed as

AnimalsCell ProliferationEpithelial CellsHomeostasisMorphogenesisReceptor, PAR-2Serine EndopeptidasesSignal TransductionZebrafishZebrafish ProteinsmatriptaseReceptor, PAR-2Serine EndopeptidasesZebrafish Proteins

Identifiers

PMID29301867
PMCPMC5839797
OpenAlexW2781640270

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.