Evidence map›Paper›PMID 29217640›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2017

Lipid bilayer mediates ion-channel cooperativity in a model of hair-cell mechanotransduction.

Francesco Gianoli, Thomas Risler, Andrei S Kozlov

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.3field-weighted citation impact, top 13% 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

25 citing papers in PubMed, 38 citations in OpenAlex.

  1. PIPbioRxiv : the preprint server for biology · 2026
    Article
  2. Article
  3. Electrical Control of the Transduction Channels' Gating Force in Mechanosensory Hair Cells.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  4. Article
  5. Review
  6. Review
  7. Ectopic mouse TMC1 and TMC2 alone form mechanosensitive channels that are potently modulated by TMIE.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  8. Article
  9. Article
  10. The conductance and organization of the TMC1-containing mechanotransducer channel complex in auditory hair cells.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  11. Mechanotransduction in mammalian sensory hair cells.Molecular and cellular neurosciences · 2022
    Review
  12. Article
  13. Review
  14. Article
  15. Dimensions of a Living Cochlear Hair Bundle.Frontiers in cell and developmental biology · 2021
    Article
  16. Article
  17. Article
  18. Modulation of Function, Structure and Clustering of KInternational journal of molecular sciences · 2020
    Review
  19. Article
  20. 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

3 authors at 2 institutions in 2 countries.

Francesco GianoliDepartment of Bioengineering, Imperial College London, London SW7 2AZ, United Kingdom.
Thomas RislerLaboratoire Physico Chimie Curie, Institut Curie, PSL Research University, CNRS, 75005 Paris, France; a.kozlov@imperial.ac.uk thomas.risler@curie.fr.ORCID 0000-0003-1677-4636
Andrei S KozlovDepartment of Bioengineering, Imperial College London, London SW7 2AZ, United Kingdom; a.kozlov@imperial.ac.uk thomas.risler@curie.fr.
Imperial College London · GBCentre National de la Recherche Scientifique · FR

Funding

Wellcome TrustWellcome Trust 108034/Z/15/Z
6 · The paper itself

Abstract

Mechanoelectrical transduction in the inner ear is a biophysical process underlying the senses of hearing and balance. The key players involved in this process are mechanosensitive ion channels. They are located in the stereocilia of hair cells and opened by the tension in specialized molecular springs, the tip links, connecting adjacent stereocilia. When channels open, the tip links relax, reducing the hair-bundle stiffness. This gating compliance makes hair cells especially sensitive to small stimuli. The classical explanation for the gating compliance is that the conformational rearrangement of a single channel directly shortens the tip link. However, to reconcile theoretical models based on this mechanism with experimental data, an unrealistically large structural change of the channel is required. Experimental evidence indicates that each tip link is a dimeric molecule, associated on average with two channels at its lower end. It also indicates that the lipid bilayer modulates channel gating, although it is not clear how. Here, we design and analyze a model of mechanotransduction where each tip link attaches to two channels, mobile within the membrane. Their states and positions are coupled by membrane-mediated elastic forces arising from the interaction between the channels' hydrophobic cores and that of the lipid bilayer. This coupling induces cooperative opening and closing of the channels. The model reproduces the main properties of hair-cell mechanotransduction using only realistic parameters constrained by experimental evidence. This work provides an insight into the fundamental role that membrane-mediated ion-channel cooperativity can play in sensory physiology.

Indexed as

Ion Channel GatingMechanotransduction, CellularAlgorithmsCalciumHair Cells, AuditoryIon ChannelsKineticsLipid BilayersModels, BiologicalCalciumIon ChannelsLipid Bilayersauditory systemcooperativityhair celllipid bilayermechanotransduction channels

Identifiers

PMID29217640
PMCPMC5754792
OpenAlexW2771807434

What OpenQuestion holds

Textmetadata
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.