Evidence map›Paper›PMID 34494554›Full record

ArticleJCI insight2021

GRHL3 activates FSCN1 to relax cell-cell adhesions between migrating keratinocytes during wound reepithelialization.

Ghaidaa Kashgari, Sanan Venkatesh, Samuel Refuerzo, Brandon Pham, Anita Bayat, Rachel Herndon Klein, Raul Ramos, Albert Paul Ta, Maksim V Plikus, Ping H Wang and 1 more

Open access · goldAbstract read
In one paragraph

Article in JCI insight, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.8field-weighted citation impact, top 13% 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

16 citing papers in PubMed, 28 citations in OpenAlex.

  1. Review
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  13. Functions of the RIP kinase family members in the skin.Cellular and molecular life sciences : CMLS · 2023
    Review
  14. Review
  15. Review
  16. Grainyhead-like (Grhl) Target Genes in Development and Cancer.International journal of molecular sciences · 2022
    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

11 authors at 1 institution in 1 country.

Ghaidaa KashgariDepartment of Biological Chemistry, School of Medicine.
Sanan VenkateshDepartment of Biological Chemistry, School of Medicine.
Samuel RefuerzoDepartment of Biological Chemistry, School of Medicine.
Brandon PhamDepartment of Biological Chemistry, School of Medicine.
Anita BayatDepartment of Biological Chemistry, School of Medicine.
Rachel Herndon KleinDepartment of Biological Chemistry, School of Medicine.
Raul RamosDepartment of Developmental & Cell Biology, School of Biological Sciences, and.
Albert Paul TaDepartment of Medicine, Division of Endocrinology, School of Medicine, University of California, Irvine (UCI), California, USA.
Maksim V PlikusDepartment of Developmental & Cell Biology, School of Biological Sciences, and.
Ping H WangDepartment of Medicine, Division of Endocrinology, School of Medicine, University of California, Irvine (UCI), California, USA.
Bogi AndersenDepartment of Biological Chemistry, School of Medicine.
University of California, Irvine · US

Funding

Univ.of Calif., Irvine Cancer Center Support GrantP30CA062203 · NCI · UNIVERSITY OF CALIFORNIA-IRVINE · PI Melanie Funes · 1994 to 2026
$57.9M
Transcriptional Co-Regulators in EpidermisR01AR044882 · NIAMS · UNIVERSITY OF CALIFORNIA SAN DIEGO · PI Bogi Andersen · 1998 to 2026
$9.0M
UCI P30 Skin Center Systems Biology CoreP30AR075047 · NIAMS · UNIVERSITY OF CALIFORNIA-IRVINE · PI ANDERSEN, BOGI, GANESAN, ANAND K · 2019 to 2025
$5.1M
NCI NIH HHS P30 CA062203NIAMS NIH HHS P30 AR075047NIAMS NIH HHS R01 AR044882
6 · The paper itself

Abstract

The migrating keratinocyte wound front is required for skin wound closure. Despite significant advances in wound healing research, we do not fully understand the molecular mechanisms that orchestrate collective keratinocyte migration. Here, we show that, in the wound front, the epidermal transcription factor Grainyhead like-3 (GRHL3) mediates decreased expression of the adherens junction protein E-cadherin; this results in relaxed adhesions between suprabasal keratinocytes, thus promoting collective cell migration and wound closure. Wound fronts from mice lacking GRHL3 in epithelial cells (Grhl3-cKO) have lower expression of Fascin-1 (FSCN1), a known negative regulator of E-cadherin. Assay for Transposase-Accessible Chromatin using sequencing (ATAC-seq) on wounded keratinocytes shows decreased wound-induced chromatin accessibility near the Fscn1 gene in Grhl3-cKO mice, a region enriched for GRHL3 motifs. These data reveal a wound-induced GRHL3/FSCN1/E-cadherin pathway that regulates keratinocyte-keratinocyte adhesion during wound-front migration; this pathway is activated in acute human wounds and is altered in diabetic wounds in mice, suggesting translational relevance.

Indexed as

Gene Expression RegulationWound HealingAnimalsCarrier ProteinsCell AdhesionCell LineCell MovementDisease Models, AnimalDNA-Binding ProteinsEpidermisKeratinocytesMiceMicrofilament ProteinsRNATranscription FactorsCarrier ProteinsDNA-Binding ProteinsFSCN1 protein, humanGrhl3 protein, mouseMicrofilament ProteinsRNATranscription FactorsCell migration/adhesionDermatologyGeneticsSkin

Identifiers

PMID34494554
PMCPMC8492311
OpenAlexW3197680611

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.