| Literature DB >> 30867284 |
Susann Michanski1,2, Katharina Smaluch2,3,4, Anna Maria Steyer5,6, Rituparna Chakrabarti1,2, Cristian Setz2,3,4,7,8, David Oestreicher3,4,7, Christian Fischer9, Wiebke Möbius5,6, Tobias Moser2,3,6,8,10, Christian Vogl11,3,4,8, Carolin Wichmann12,2,8.
Abstract
Ribbon synapses of cochlear inner hair cells (IHCs) undergo molecular assembly and extensive functional and structural maturation before hearing onset. Here, we characterized the nanostructure of IHC synapses from late prenatal mouse embryo stages (embryonic days 14-18) into adulthood [postnatal day (P)48] using electron microscopy and tomography as well as optical nanoscopy of apical turn organs of Corti. We find that synaptic ribbon precursors arrive at presynaptic active zones (AZs) after afferent contacts have been established. These ribbon precursors contain the proteins RIBEYE and piccolino, tether synaptic vesicles and their delivery likely involves active, microtubule-based transport pathways. Synaptic contacts undergo a maturational transformation from multiple small to one single, large AZ. This maturation is characterized by the fusion of ribbon precursors with membrane-anchored ribbons that also appear to fuse with each other. Such fusion events are most frequently encountered around P12 and hence, coincide with hearing onset in mice. Thus, these events likely underlie the morphological and functional maturation of the AZ. Moreover, the postsynaptic densities appear to undergo a similar refinement alongside presynaptic maturation. Blockwise addition of ribbon material by fusion as found during AZ maturation might represent a general mechanism for modulating ribbon size.Entities:
Keywords: presynaptic development; ribbon synapse maturation; synaptic heterogeneity; synaptogenesis
Mesh:
Year: 2019 PMID: 30867284 PMCID: PMC6442603 DOI: 10.1073/pnas.1812029116
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205