Abstract

Transmembrane channel like protein 1 (TMC1) is likely to be a pore-forming subunit of the transduction channel of cochlear hair cells that is mechanically gated by tension on tip links in the stereocilia bundle. To localise TMC1 precisely, we labelled mice cochleae of different ages using custom-made polyclonal antibodies to TMC1 for light and transmission electron microscopy (TEM). Immunofluorescence revealed stereocilia labelling at P9 but not at P3 in apical hair cells. Immunogold labelling for TEM confirmed that labelling was absent at P3, and showed weak labelling at P6 with no stereocilia tip labelling, increasing at P9, with specific tip labelling on shorter stereocilia and some throughout the bundle. At P12 and P21, labelling was refined mostly to stereocilia tips. Quantification showed that labelling overall reached maximum by P12, labelling per tip was relatively constant from P9 to P21, but percent tips labelled was reduced from 16% to 8%. Tmc1−/− showed no labelling. Thus TMC1 occurs at the lower end of the tip link, supporting its presence in the MET complex and likely the channel. Tip localisation from P9 onwards coincides with lipoma HMGIC fusion partner-like 5 (LHFPL5), a protein that may be involved in acquiring/maintaining TMC1 localisation.

Highlights

  • Hair cells of the cochlea have an apical hair bundle containing a highly sensitive mechanoelectrical transduction (MET) apparatus that enables them to detect mechanical stimulation caused by sound

  • Gradients in the MET channel conductance occur at P5 along the tonotopic axis of the cochlear spiral that have been attributed to changes in the number of Transmembrane channel like protein 1 (TMC1) molecules at stereocilia tips, based on experiments using mCherry-TMC1 expression[20]

  • TMC proteins interact with PCDH1521 and TMC1 knockouts affect the distribution of LHFPL522

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Summary

Introduction

Hair cells of the cochlea have an apical hair bundle containing a highly sensitive mechanoelectrical transduction (MET) apparatus that enables them to detect mechanical stimulation caused by sound. Associated with the lower end of the tip link, i.e. with PCDH15, are proteins such as lipoma HMGIC fusion partner-like 5 (LHFPL54,5), transmembrane protein of the inner ear (TMIE6), two likely channel components, transmembrane-like channel 1 (TMC1) and TMC27–9, and calcium sensitive integrin-binding protein 2 (CIB210), amongst others. Mutations in these proteins are associated with deafness in mice models and humans, for example mutations in mice with hearing loss such as deafness (dn)[11] and Beethoven www.nature.com/scientificreports/. The same type of data do not yet exist for TMC1

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