Evidence map›Paper›PMID 42234740›Full record

ArticleScience advances2026

Lipid composition and mechanical force underlie multi-modal regulation of Piezo1 gating.

George Vaisey, Roderick MacKinnon

Abstract read
In one paragraph

Article in Science advances, 2026. 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. Article
  3. Review
  4. MDFIC2 is a sensory neuron-specific PIEZO channel auxiliary subunit.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
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

2 authors.

George VaiseyLaboratory of Molecular Neurobiology and Biophysics, Howard Hughes Medical Institute, The Rockefeller University, New York, NY 10065, USA.ORCID 0000-0002-8359-1314
Roderick MacKinnonLaboratory of Molecular Neurobiology and Biophysics, Howard Hughes Medical Institute, The Rockefeller University, New York, NY 10065, USA.ORCID 0000-0001-7605-4679

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Piezo1 ion channels are widely expressed cellular mechanosensors. They adopt an intrinsically curved shape when closed and are thought to open when mechanical forces applied to the membrane favor a more flattened conformation. In previous studies, Piezo1 channels in lipid vesicles adopted a somewhat flattened conformation mediated by membrane curvature; however, the ion conduction pore remained closed. In line with the closed pore, Piezo1 channels do not open and conduct ions in the kind of lipids that were used in the structural studies. Here, we show first that Piezo1 channels in cell-derived membranes retain the ability to open and conduct ions under mechanical force, and second, that in cell-derived membrane vesicles, they adopt a more completely flattened disk shape associated with large conformational changes within and around the ion conduction pathway. These conformational changes occurring in cell-derived lipid membranes suggest that mechanical force is necessary but insufficient, and that a specific membrane-derived cofactor complements mechanical force to activate Piezo1.

Indexed as

Ion Channel GatingIon ChannelsLipidsAnimalsCell MembraneHumansMechanotransduction, CellularIon ChannelsLipidsPIEZO1 protein, humanPiezo1 protein, mouse

Identifiers

PMID42234740
PMCPMC13232553

What Socratic holds

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LicenceCC BY
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Registered trials

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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 Socratic graph.