Evidence map›Paper›PMID 40741726›Full record

ArticleJournal of cell science2025

Piezo1 balances membrane and cortex tension to stabilize intercellular junctions and maintain the epithelial barrier.

Ahsan Javed, Aki Stubb, Clémentine Villeneuve, Satu-Marja Myllymäki, Franziska Peters, Matthias Rübsam, Carien M Niessen, Leah C Biggs, Sara A Wickström

Abstract read
In one paragraph

Article in Journal of cell science, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Toxics · 2026
    Article
  4. 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

9 authors.

Ahsan JavedStem Cells and Metabolism Research Program, Faculty of Medicine, University of Helsinki, 00290 HelsinkiFinland.
Aki StubbStem Cells and Metabolism Research Program, Faculty of Medicine, University of Helsinki, 00290 HelsinkiFinland.
Clémentine VilleneuveStem Cells and Metabolism Research Program, Faculty of Medicine, University of Helsinki, 00290 HelsinkiFinland.
Satu-Marja MyllymäkiStem Cells and Metabolism Research Program, Faculty of Medicine, University of Helsinki, 00290 HelsinkiFinland.
Franziska PetersStem Cells and Metabolism Research Program, Faculty of Medicine, University of Helsinki, 00290 HelsinkiFinland.
Matthias RübsamDepartment Cell Biology of the Skin, Cologne Excellence Cluster on Cellular Stress Responses in Aging Associated Diseases (CECAD), Center for Molecular Medicine Cologne, University Hospital Cologne, University of Cologne, Joseph-Stelzmann-Str. 26, 50931 Cologne, Germany.ORCID 0000-0002-0012-2601
Carien M NiessenDepartment Cell Biology of the Skin, Cologne Excellence Cluster on Cellular Stress Responses in Aging Associated Diseases (CECAD), Center for Molecular Medicine Cologne, University Hospital Cologne, University of Cologne, Joseph-Stelzmann-Str. 26, 50931 Cologne, Germany.
Leah C BiggsStem Cells and Metabolism Research Program, Faculty of Medicine, University of Helsinki, 00290 HelsinkiFinland.ORCID 0000-0002-4990-8664
Sara A WickströmStem Cells and Metabolism Research Program, Faculty of Medicine, University of Helsinki, 00290 HelsinkiFinland.ORCID 0000-0001-6383-6292

Funding

Academy of Finland 317597Academy of Finland 332821Academy of Finland 346131BiomedicumEuropean Union's Horizon 2020 101032331H2020 Marie Skodowska-Curie Actions 101032331Helsinki Institute of Life ScienceHorizon 2020 Framework ProgrammeInstrumentarium Science FoundationMax-Planck-GesellschaftResearch Council of Finland 332821Sigrid Juselius Foundation
6 · The paper itself

Abstract

Formation of the skin barrier is essential for organismal survival and tissue homeostasis. Barrier formation requires positioning of functional tight junctions (TJs) to the most suprabasal viable layer of the epidermis through a mechanical circuit that is driven by generation of high tension at adherens junctions. However, what allows the sensing of tension build-up at these adhesions and how this tension is balanced to match the requirements of tissue mechanical properties is unclear. Here, we show that the mechanosensitive ion channel Piezo1 is essential for the maturation of intercellular junctions into functional continuous adhesions. Deletion of Piezo1 results in an imbalance of cell contractility and membrane tension, leading to a delay in adhesion maturation. Consequently, the requirement for Piezo1 activity can be bypassed by lowering contractility or elevating membrane tension. In vivo, Piezo1 function in adhesion integrity becomes essential only in aged mice where alterations in tissue mechanics lead to impaired tight junctions and barrier dysfunction. Collectively these studies reveal an essential function of Piezo1 in the timely establishment and maintenance of cell-cell junctions within a mechanically tensed epidermis.

Indexed as

Cell MembraneEpithelial CellsIntercellular JunctionsIon ChannelsTight JunctionsAdherens JunctionsAnimalsCell AdhesionEpidermisKeratinocytesMiceMice, KnockoutIon ChannelsPiezo1 protein, mouseCell–cell contactsEpidermisMechanotransductionPiezo1

Identifiers

PMID40741726
PMCPMC12450467

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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.