Abstract
Mammalian transmembrane channel-like proteins 1 and 2 (TMC1 and TMC2) have emerged as very promising candidate mechanotransduction channels in hair cells. However, controversy persists because the heterogeneously expressed TMC1/2 in cultured cells lack evidence of mechanical gating, primarily due to their absence from the plasma membrane. By employing domain swapping with OSCA1.1 and subsequent point mutations, we successfully identified membrane-localized mouse TMC1/2 mutants, demonstrating that they are mechanically gated in heterologous cells. Further, whole-genome CRISPRi screening enabled wild-type human TMC1/2 localization in the plasma membrane, where they responded robustly to poking stimuli. In addition, wild-type human TMC1/2 showed stretch-activated currents and clear single-channel current activities. Deafness-related TMC1 mutations altered the reversal potential of TMC1, indicating that TMC1/2 are pore-forming mechanotransduction channels. In summary, our study provides evidence that human TMC1/2 are pore-forming, mechanically activated ion channels, supporting their roles as mechanotransduction channels in hair cells.
| Original language | English |
|---|---|
| Pages (from-to) | 411-425.e4 |
| Journal | Neuron |
| Volume | 113 |
| Issue number | 3 |
| DOIs | |
| Publication status | Published - 5 Feb 2025 |
| Externally published | Yes |
Bibliographical note
Publisher Copyright:© 2024 The Authors
Keywords
- TMC1
- TMC1/2
- auditory and vestibular
- hair cells
- hearing
- mechanically activated ion channels
- mechanically gated ion channels
- mechanoelectrical transduction
- mechanosensitive ion channels
- mechanosensory transduction channels
- transmembrane channel-like 1