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Disruption of adaptor protein 2μ (AP‐2μ) in cochlear hair cells impairs vesicle reloading of synaptic release sites and hearing
Authors:Zhizi Jing  Andreas Neef  Natalia H Revelo  Hanan Al‐Moyed  Sandra Meese  Sonja M Wojcik  Iliana Panou  Haydar Bulut  Peter Schu  Ralf Ficner  Ellen Reisinger  Silvio O Rizzoli  Jakob Neef  Nicola Strenzke  Volker Haucke  Tobias Moser
Institution:1. Collaborative Research Center 889, University of G?ttingen, G?ttingen, Germany;2. Auditory Systems Physiology Group, InnerEarLab, Department of Otolaryngology, University Medical Center G?ttingen, G?ttingen, Germany;3. Bernstein Group Biophysics of Neural Computation, Max Planck Institute for Dynamics and Self‐Organization, G?ttingen, Germany;4. Department of Neuro‐ and Sensory Physiology, University Medical Center G?ttingen, G?ttingen, Germany;5. Molecular Architecture of Synapses Group, Institute for Auditory Neuroscience and InnerEarLab, University Medical Center G?ttingen, G?ttingen, Germany;6. Department of Molecular Structural Biology, Institute for Microbiology and Genetics, University of G?ttingen, G?ttingen, Germany;7. Department of Molecular Neurobiology, Max Planck Institute of Experimental Medicine, G?ttingen, Germany;8. Institute for Auditory Neuroscience and InnerEarLab, University Medical Center G?ttingen, G?ttingen, Germany;9. Leibniz Institut für Molekulare Pharmakologie (FMP), Berlin, Germany;10. Department of Cellular Biochemistry, University Medical Center G?ttingen, G?ttingen, Germany;11. Molecular Biology of Cochlear Neurotransmission Group, InnerEarLab, Department of Otolaryngology, University Medical Center G?ttingen, G?ttingen, Germany;12. Center for Nanoscale Microscopy and Molecular Physiology of the Brain, University of G?ttingen, G?ttingen, Germany;13. Synaptic Nanophysiology Group, Max Planck Institute for Biophysical Chemistry, G?ttingen, Germany;14. NeuroCure Cluster of Excellence & Collaborative Research Center 958, Freie Universit?t Berlin, Berlin, Germany
Abstract:Active zones (AZs) of inner hair cells (IHCs) indefatigably release hundreds of vesicles per second, requiring each release site to reload vesicles at tens per second. Here, we report that the endocytic adaptor protein 2μ (AP‐2μ) is required for release site replenishment and hearing. We show that hair cell‐specific disruption of AP‐2μ slows IHC exocytosis immediately after fusion of the readily releasable pool of vesicles, despite normal abundance of membrane‐proximal vesicles and intact endocytic membrane retrieval. Sound‐driven postsynaptic spiking was reduced in a use‐dependent manner, and the altered interspike interval statistics suggested a slowed reloading of release sites. Sustained strong stimulation led to accumulation of endosome‐like vacuoles, fewer clathrin‐coated endocytic intermediates, and vesicle depletion of the membrane‐distal synaptic ribbon in AP‐2μ‐deficient IHCs, indicating a further role of AP‐2μ in clathrin‐dependent vesicle reformation on a timescale of many seconds. Finally, we show that AP‐2 sorts its IHC‐cargo otoferlin. We propose that binding of AP‐2 to otoferlin facilitates replenishment of release sites, for example, via speeding AZ clearance of exocytosed material, in addition to a role of AP‐2 in synaptic vesicle reformation.
Keywords:active zone  endocytosis  release site clearance  synaptic ribbon  vesicle reformation
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