Evidence map›Paper›PMID 36795747›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2023

The energetics of rapid cellular mechanotransduction.

Michael N Young, Michael J Sindoni, Amanda H Lewis, Stefan Zauscher, Jörg Grandl

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Piezo2 tension sensitivity and its modulation by alternative splicing.bioRxiv : the preprint server for biology · 2026
    Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Review
  13. Piezo1 in Digestive System Function and Dysfunction.International journal of molecular sciences · 2023
    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

5 authors.

Michael N YoungDepartment of Neurobiology, Duke University Medical Center, Durham, NC 27710.ORCID 0000-0003-3051-5171
Michael J SindoniDepartment of Neurobiology, Duke University Medical Center, Durham, NC 27710.ORCID 0000-0002-6752-1420
Amanda H LewisDepartment of Neurobiology, Duke University Medical Center, Durham, NC 27710.
Stefan ZauscherDepartment of Mechanical Engineering and Materials Science, Duke University, Durham, NC 27710.ORCID 0000-0002-2290-7178
Jörg GrandlDepartment of Neurobiology, Duke University Medical Center, Durham, NC 27710.ORCID 0000-0001-7179-7609

Funding

Mechanisms of Disease associated with mechanically-activated Piezo ion channelsR01NS110552 · NINDS · DUKE UNIVERSITY · PI GRANDL, JORG · 2020 to 2024
$1.8M
NINDS NIH HHS R01 NS110552
6 · The paper itself

Abstract

Cells throughout the human body detect mechanical forces. While it is known that the rapid (millisecond) detection of mechanical forces is mediated by force-gated ion channels, a detailed quantitative understanding of cells as sensors of mechanical energy is still lacking. Here, we combine atomic force microscopy with patch-clamp electrophysiology to determine the physical limits of cells expressing the force-gated ion channels (FGICs) Piezo1, Piezo2, TREK1, and TRAAK. We find that, depending on the ion channel expressed, cells can function either as proportional or nonlinear transducers of mechanical energy and detect mechanical energies as little as ~100 fJ, with a resolution of up to ~1 fJ. These specific energetic values depend on cell size, channel density, and cytoskeletal architecture. We also make the surprising discovery that cells can transduce forces either nearly instantaneously (<1 ms) or with a substantial time delay (~10 ms). Using a chimeric experimental approach and simulations, we show how such delays can emerge from channel-intrinsic properties and the slow diffusion of tension in the membrane. Overall, our experiments reveal the capabilities and limits of cellular mechanosensing and provide insights into molecular mechanisms that different cell types may employ to specialize for their distinct physiological roles.

Indexed as

Ion ChannelsMechanotransduction, CellularCytoskeletonHumansIon ChannelsPIEZO1 protein, humanforce-gated ion channelmechanotransductionmechanotransmission

Identifiers

PMID36795747
PMCPMC9974467

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.