Nature Communications · 2024 · 31 citations · 75 references
Life SciencesNeurosciencePhysiologySensory NeuroscienceSensory PhysiologySignal TransductionAuditory NeurophysiologyAuditory PhysiologyAuditory SystemCochlear FunctionCochlear NeuroscienceInner Ear FunctionChannelsHair Cell BiologyInner Ear PhysiologyMammalian Hair CellsMechanoelectrical TransductionMechanotransduction In Hair CellsPiezo Channel FunctionPiezo Channel Mechanotransduction
The inner ear is the hub where hair cells (HCs) transduce sound, gravity, and head acceleration stimuli to the brain. Hearing and balance rely on mechanosensation, the fastest sensory signals transmitted to the brain. The mechanoelectrical transducer (MET) channel is the entryway for the sound-balance-brain interface, but the channel-complex composition is not entirely known. Here, we report that the mouse utilizes Piezo1 (Pz1) and Piezo2 (Pz2) isoforms as MET-complex components. The Pz channels, expressed in HC stereocilia, and cell lines are co-localized and co-assembled with MET complex partners. Mice expressing non-functional Pz1 and Pz2 at the ROSA26 locus have impaired auditory and vestibular traits that can only be explained if the Pzs are integral to the MET complex. We suggest that Pz subunits constitute part of the MET complex and that interactions with other MET complex components yield functional MET units to generate HC MET currents.
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Piezo1 and Piezo2 Are Essential Components of Distinct Mechanically Activated Cation Channels
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