LHFPL5 is required for maximal activation of the mechanotransduction channel in cochlear hair cells

Mechanoelectrical transduction (MET) channels in cochlear hair cells are gated by tip links through a mechanism that is poorly defined. LHFPL5 interacts with the tip-link component PCDH15 and the MET-channel component TMC1, suggesting that LHFPL5 regulates channel activation by mechanical force. To test this hypothesis, we analyzed MET in hair cells from mice expressing an LHFPL5 mutant protein lacking three N-terminal amino acids. These mutant mice suffer from recessive deafness, and MET is drastically impaired in cochlear hair cells. The resting open probability of the MET channels is increased in the mutants, while unitary channel conductance, adaptation, and tonotopic channel properties remain unaltered. Unlike in other LHFPL5 mutants, MET channel proteins are still present at normal levels in stereocilia of mutant mice. We conclude that LHFPL5 is required for maximal mechanical activation of MET channels in cochlear hair cells thereby affecting the hair bundle sensitivity to mechanical stimulation and thus the sound sensitivity of the auditory sense organ.

Authors

Institutions

Publication Details

Journal
Proceedings of the National Academy of Sciences
Published
2025-11-04
DOI
https://doi.org/10.1073/pnas.2505627122
Primary Topic
Hearing, Cochlea, Tinnitus, Genetics
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

LHFPL5 is required for maximal activation of the mechanotransduction channel in cochlear hair cells

José P. Llongueras, Xufeng Qiu, Christopher L. Cunningham, Ulrich Mueller et al.
Proceedings of the National Academy of Sciences
Hearing, Cochlea, Tinnitus, Genetics
article

LHFPL5 is required for maximal activation of the mechanotransduction channel in cochlear hair cells

José P. Llongueras, Xufeng Qiu, Christopher L. Cunningham, Ulrich Mueller, Lili Yin
article en

Abstract

Mechanoelectrical transduction (MET) channels in cochlear hair cells are gated by tip links through a mechanism that is poorly defined. LHFPL5 interacts with the tip-link component PCDH15 and the MET-channel component TMC1, suggesting that LHFPL5 regulates channel activation by mechanical force. To test this hypothesis, we analyzed MET in hair cells from mice expressing an LHFPL5 mutant protein lacking three N-terminal amino acids. These mutant mice suffer from recessive deafness, and MET is drastically impaired in cochlear hair cells. The resting open probability of the MET channels is increased in the mutants, while unitary channel conductance, adaptation, and tonotopic channel properties remain unaltered. Unlike in other LHFPL5 mutants, MET channel proteins are still present at normal levels in stereocilia of mutant mice. We conclude that LHFPL5 is required for maximal mechanical activation of MET channels in cochlear hair cells thereby affecting the hair bundle sensitivity to mechanical stimulation and thus the sound sensitivity of the auditory sense organ.

Proceedings of the National Academy of SciencesVol. 122(45)
Johns Hopkins University (US), University of Pittsburgh (US), Johns Hopkins Medicine (US)
Openalex Percentile: Top 68%
Hearing, Cochlea, Tinnitus, Genetics
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.