| Literature DB >> 30201800 |
Rituparna Chakrabarti1,2,3,4, Susann Michanski1,2,3,5, Carolin Wichmann6,2,3.
Abstract
The afferent inner hair cell synapse harbors the synaptic ribbon, which ensures a constant vesicle supply. Synaptic vesicles (SVs) are arranged in morphologically discernable pools, linked via filaments to the ribbon or the presynaptic membrane. We propose that filaments play a major role in SV resupply and exocytosis at the ribbon. Using advanced electron microscopy, we demonstrate that SVs are organized in sub-pools defined by the filament number per vesicle and its connections. Upon stimulation, SVs increasingly linked to other vesicles and to the ribbon, whereas single-tethered SVs dominated at the membrane. Mutant mice for the hair cell protein otoferlin (pachanga, Otof Pga/Pga ) are profoundly deaf with reduced sustained release, serving as a model to investigate the SV replenishment at IHCs. Upon stimulation, multiple-tethered and docked vesicles (rarely observed in wild-type) accumulated at Otof Pga/Pga active zones due to an impairment downstream of docking. Conclusively, vesicles are organized in sub-pools at ribbon-type active zones by filaments to support vesicle supply, transport, and finally release.Entities:
Keywords: exocytosis; high‐pressure freezing; ribbon synapse; sub‐pools; synaptic vesicle tethering
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Year: 2018 PMID: 30201800 PMCID: PMC6216280 DOI: 10.15252/embr.201744937
Source DB: PubMed Journal: EMBO Rep ISSN: 1469-221X Impact factor: 8.807