Evidence map›Paper›PMID 31914171›Full record

ArticleThe Journal of cell biology2020

Hemidesmosomes modulate force generation via focal adhesions.

Wei Wang, Alba Zuidema, Lisa Te Molder, Leila Nahidiazar, Liesbeth Hoekman, Thomas Schmidt, Stefano Coppola, Arnoud Sonnenberg

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed
9.4field-weighted citation impact, top 1% 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

59 citing papers in PubMed, 127 citations in OpenAlex.

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  7. Hemidesmosomes regulate epidermal differentiation during embryogenesis.bioRxiv : the preprint server for biology · 2025
    Article
  8. Review
  9. Challenges of Studying Amelogenesis in Gene-Targeted Mouse Models.International journal of molecular sciences · 2025
    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

8 authors at 2 institutions in 1 country.

Wei WangDivision of Cell Biology, The Netherlands Cancer Institute, Amsterdam, Netherlands.
Alba ZuidemaDivision of Cell Biology, The Netherlands Cancer Institute, Amsterdam, Netherlands.
Lisa Te MolderDivision of Cell Biology, The Netherlands Cancer Institute, Amsterdam, Netherlands.
Leila NahidiazarDivision of Cell Biology, The Netherlands Cancer Institute, Amsterdam, Netherlands.
Liesbeth HoekmanMass Spectrometry/Proteomics Facility, The Netherlands Cancer Institute, Amsterdam, Netherlands.
Thomas SchmidtPhysics of Life Processes, Huygens-Kamerlingh Onnes Laboratory, Leiden University, Leiden, Netherlands.
Stefano CoppolaPhysics of Life Processes, Huygens-Kamerlingh Onnes Laboratory, Leiden University, Leiden, Netherlands.
Arnoud SonnenbergDivision of Cell Biology, The Netherlands Cancer Institute, Amsterdam, Netherlands.
The Netherlands Cancer Institute · NLLeiden University · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hemidesmosomes are specialized cell-matrix adhesion structures that are associated with the keratin cytoskeleton. Although the adhesion function of hemidesmosomes has been extensively studied, their role in mechanosignaling and transduction remains largely unexplored. Here, we show that keratinocytes lacking hemidesmosomal integrin α6β4 exhibit increased focal adhesion formation, cell spreading, and traction-force generation. Moreover, disruption of the interaction between α6β4 and intermediate filaments or laminin-332 results in similar phenotypical changes. We further demonstrate that integrin α6β4 regulates the activity of the mechanosensitive transcriptional regulator YAP through inhibition of Rho-ROCK-MLC- and FAK-PI3K-dependent signaling pathways. Additionally, increased tension caused by impaired hemidesmosome assembly leads to a redistribution of integrin αVβ5 from clathrin lattices to focal adhesions. Our results reveal a novel role for hemidesmosomes as regulators of cellular mechanical forces and establish the existence of a mechanical coupling between adhesion complexes.

Indexed as

Adaptor Proteins, Signal TransducingCell Adhesion MoleculesCell-Matrix JunctionsCell MovementCells, CulturedCytoskeletonFocal AdhesionsHemidesmosomesHumansIntegrin alpha6beta4Intermediate FilamentsKalininKeratinocytesKeratinsMechanotransduction, Cellularrho-Associated KinasesAdaptor Proteins, Signal TransducingCell Adhesion MoleculesIntegrin alpha6beta4KalininKeratinsrho-Associated KinasesTranscription FactorsYAP1 protein, humanYAP-Signaling Proteins

Identifiers

PMID31914171
PMCPMC7041674
OpenAlexW3000247586

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.