Evidence map›Paper›PMID 42247293›Full record

ArticleCell reports2026

Piezo2 tension sensitivity and its modulation by alternative splicing.

Michael Sindoni, William Sharp, Jörg Grandl

Abstract read
In one paragraph

Article in Cell reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors.

Michael SindoniDepartment of Neurobiology, Duke University Medical Center, Durham, NC 27710, USA.
William SharpDepartment of Biology, Duke University, Durham, NC 27708, USA.
Jörg GrandlDepartment of Neurobiology, Duke University Medical Center, Durham, NC 27710, USA. Electronic address: grandl@neuro.duke.edu.

Funding

Mechanisms of Disease associated with mechanically-activated Piezo ion channelsR01NS110552 · NINDS · DUKE UNIVERSITY · PI GRANDL, JORG · 2020 to 2024
$1.8M
Biophysical characterization of the human force-gated ion channel Piezo2F31NS139449 · NINDS · DUKE UNIVERSITY · PI SINDONI, MICHAEL JAMES · 2024 to 2025
$84k
NINDS NIH HHS F31 NS139449NINDS NIH HHS R01 NS110552
6 · The paper itself

Abstract

Piezo2 is a force-gated ion channel that functions as a sensor of mechanical touch, proprioception, lung inflation, and gut transit. Human Piezo2 contains seven domains that are alternatively spliced in a tissue-specific fashion resulting in the expression of at least 22 distinct variants. Despite the relevance of Piezo2 in human physiology, its sensitivity to membrane tension, and how this fundamental biophysical property is affected by alternative splicing, are unknown. Here, we use cell-attached pressure-clamp electrophysiology combined with differential interference contrast microscopy to quantify the response of Piezo2 to membrane tension and identify the alternatively spliced exon 35 as a domain sufficient to confer high sensitivity to membrane tension and cellular indentation. We further show that physiological variants of Piezo2 sense mechanical forces with distinct sensitivities and dynamic ranges. Together, our findings rationalize how Piezo2 variants may fulfill distinct physiological functions required for somatosensation and interoception.

Indexed as

Alternative SplicingIon ChannelsAnimalsExonsHEK293 CellsHumansMechanotransduction, CellularIon ChannelsPIEZO2 protein, humanalternative splicingCP: molecular biologyCP: neuroscienceforce gated ion channelmechanotransductionPiezo1Piezo2

Identifiers

PMID42247293
PMCPMC13382605

What Socratic holds

Textmetadata
LicenceTDM
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 Socratic graph.