Fast recovery of disrupted tip links induced by mechanical displacement of hair bundles

• Published in: Proceedings of the National Academy of Sciences - PNAS 2020-12, Vol.117 (48), p.30722-30727
• Main Authors: Alonso, R. G., Tobin, M., Martin, P., Hudspeth, A. J.
• Format: Article
• Language: English
• Subjects: Action Potentials; Animals; Biological Physics; Biological Sciences; Biomarkers; Bundles; Bundling; Cadherin 23; Cadherins; Calcium; Calcium - metabolism; Calcium Chelating Agents - pharmacology; Calcium ions; Cellular Biology; Chelating agents; Chelation; Cochlea; Cochlea - physiology; Cognitive science; Dimers; Electrophysiological Phenomena; Hair; Hair Cells, Auditory - physiology; Human health and pathology; Life Sciences; Links; Mechanical Phenomena; Mechanical stimuli; Mechanotransduction, Cellular; Neuroscience; Physics; Protocadherin; Rats; Recovery; Saccule; Sensory Organs; Signal transduction; Stereocilia - metabolism; Stiffness; Stimulation; Subcellular Processes; Vibrations
• ISSN: 0027-8424; 1091-6490
• DOI: 10.1073/pnas.2016858117

Hearing and balance rely on the capacity of mechanically sensitive hair bundles to transduce vibrations into electrical signals that are forwarded to the brain. Hair bundles possess tip links that interconnect the mechanosensitive stereocilia and convey force to the transduction channels. A dimer of dimers, each of these links comprises two molecules of protocadherin 15 (PCDH15) joined to two of cadherin 23 (CDH23). The “handshake” that conjoins the four molecules can be disrupted in vivo by intense stimulation and in vitro by exposure to Ca2+ chelators. Using hair bundles from the rat’s cochlea and the bullfrog’s sacculus, we observed that extensive recovery of mechanoelectrical transduction, hair bundle stiffness, and spontaneous bundle oscillation can occur within seconds after Ca2+ chelation, especially if hair bundles are deflected toward their short edges. Investigating the phenomenon in a two-compartment ionic environment that mimics natural conditions, we combined iontophoretic application of a Ca2+ chelator to selectively disrupt the tip links of individual frog hair bundles with displacement clamping to control hair bundle motion and measure forces. Our observations suggest that, after the normal Ca2+ concentration has been restored, mechanical stimulation facilitates the reconstitution of functional tip links.