Cargando…
The presynaptic ribbon maintains vesicle populations at the hair cell afferent fiber synapse
The ribbon is the structural hallmark of cochlear inner hair cell (IHC) afferent synapses, yet its role in information transfer to spiral ganglion neurons (SGNs) remains unclear. We investigated the ribbon’s contribution to IHC synapse formation and function using KO mice lacking RIBEYE. Despite los...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5794257/ https://www.ncbi.nlm.nih.gov/pubmed/29328021 http://dx.doi.org/10.7554/eLife.30241 |
_version_ | 1783297089698004992 |
---|---|
author | Becker, Lars Schnee, Michael E Niwa, Mamiko Sun, Willy Maxeiner, Stephan Talaei, Sara Kachar, Bechara Rutherford, Mark A Ricci, Anthony J |
author_facet | Becker, Lars Schnee, Michael E Niwa, Mamiko Sun, Willy Maxeiner, Stephan Talaei, Sara Kachar, Bechara Rutherford, Mark A Ricci, Anthony J |
author_sort | Becker, Lars |
collection | PubMed |
description | The ribbon is the structural hallmark of cochlear inner hair cell (IHC) afferent synapses, yet its role in information transfer to spiral ganglion neurons (SGNs) remains unclear. We investigated the ribbon’s contribution to IHC synapse formation and function using KO mice lacking RIBEYE. Despite loss of the entire ribbon structure, synapses retained their spatiotemporal development and KO mice had a mild hearing deficit. IHCs of KO had fewer synaptic vesicles and reduced exocytosis in response to brief depolarization; a high stimulus level rescued exocytosis in KO. SGNs exhibited a lack of sustained excitatory postsynaptic currents (EPSCs). We observed larger postsynaptic glutamate receptor plaques, potentially compensating for the reduced EPSC rate in KO. Surprisingly, large-amplitude EPSCs were maintained in KO, while a small population of low-amplitude slower EPSCs was increased in number. The ribbon facilitates signal transduction at physiological stimulus levels by retaining a larger residency pool of synaptic vesicles. |
format | Online Article Text |
id | pubmed-5794257 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-57942572018-02-05 The presynaptic ribbon maintains vesicle populations at the hair cell afferent fiber synapse Becker, Lars Schnee, Michael E Niwa, Mamiko Sun, Willy Maxeiner, Stephan Talaei, Sara Kachar, Bechara Rutherford, Mark A Ricci, Anthony J eLife Neuroscience The ribbon is the structural hallmark of cochlear inner hair cell (IHC) afferent synapses, yet its role in information transfer to spiral ganglion neurons (SGNs) remains unclear. We investigated the ribbon’s contribution to IHC synapse formation and function using KO mice lacking RIBEYE. Despite loss of the entire ribbon structure, synapses retained their spatiotemporal development and KO mice had a mild hearing deficit. IHCs of KO had fewer synaptic vesicles and reduced exocytosis in response to brief depolarization; a high stimulus level rescued exocytosis in KO. SGNs exhibited a lack of sustained excitatory postsynaptic currents (EPSCs). We observed larger postsynaptic glutamate receptor plaques, potentially compensating for the reduced EPSC rate in KO. Surprisingly, large-amplitude EPSCs were maintained in KO, while a small population of low-amplitude slower EPSCs was increased in number. The ribbon facilitates signal transduction at physiological stimulus levels by retaining a larger residency pool of synaptic vesicles. eLife Sciences Publications, Ltd 2018-01-12 /pmc/articles/PMC5794257/ /pubmed/29328021 http://dx.doi.org/10.7554/eLife.30241 Text en http://creativecommons.org/publicdomain/zero/1.0/ http://creativecommons.org/publicdomain/zero/1.0/This is an open-access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication (http://creativecommons.org/publicdomain/zero/1.0/) . |
spellingShingle | Neuroscience Becker, Lars Schnee, Michael E Niwa, Mamiko Sun, Willy Maxeiner, Stephan Talaei, Sara Kachar, Bechara Rutherford, Mark A Ricci, Anthony J The presynaptic ribbon maintains vesicle populations at the hair cell afferent fiber synapse |
title | The presynaptic ribbon maintains vesicle populations at the hair cell afferent fiber synapse |
title_full | The presynaptic ribbon maintains vesicle populations at the hair cell afferent fiber synapse |
title_fullStr | The presynaptic ribbon maintains vesicle populations at the hair cell afferent fiber synapse |
title_full_unstemmed | The presynaptic ribbon maintains vesicle populations at the hair cell afferent fiber synapse |
title_short | The presynaptic ribbon maintains vesicle populations at the hair cell afferent fiber synapse |
title_sort | presynaptic ribbon maintains vesicle populations at the hair cell afferent fiber synapse |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5794257/ https://www.ncbi.nlm.nih.gov/pubmed/29328021 http://dx.doi.org/10.7554/eLife.30241 |
work_keys_str_mv | AT beckerlars thepresynapticribbonmaintainsvesiclepopulationsatthehaircellafferentfibersynapse AT schneemichaele thepresynapticribbonmaintainsvesiclepopulationsatthehaircellafferentfibersynapse AT niwamamiko thepresynapticribbonmaintainsvesiclepopulationsatthehaircellafferentfibersynapse AT sunwilly thepresynapticribbonmaintainsvesiclepopulationsatthehaircellafferentfibersynapse AT maxeinerstephan thepresynapticribbonmaintainsvesiclepopulationsatthehaircellafferentfibersynapse AT talaeisara thepresynapticribbonmaintainsvesiclepopulationsatthehaircellafferentfibersynapse AT kacharbechara thepresynapticribbonmaintainsvesiclepopulationsatthehaircellafferentfibersynapse AT rutherfordmarka thepresynapticribbonmaintainsvesiclepopulationsatthehaircellafferentfibersynapse AT riccianthonyj thepresynapticribbonmaintainsvesiclepopulationsatthehaircellafferentfibersynapse AT beckerlars presynapticribbonmaintainsvesiclepopulationsatthehaircellafferentfibersynapse AT schneemichaele presynapticribbonmaintainsvesiclepopulationsatthehaircellafferentfibersynapse AT niwamamiko presynapticribbonmaintainsvesiclepopulationsatthehaircellafferentfibersynapse AT sunwilly presynapticribbonmaintainsvesiclepopulationsatthehaircellafferentfibersynapse AT maxeinerstephan presynapticribbonmaintainsvesiclepopulationsatthehaircellafferentfibersynapse AT talaeisara presynapticribbonmaintainsvesiclepopulationsatthehaircellafferentfibersynapse AT kacharbechara presynapticribbonmaintainsvesiclepopulationsatthehaircellafferentfibersynapse AT rutherfordmarka presynapticribbonmaintainsvesiclepopulationsatthehaircellafferentfibersynapse AT riccianthonyj presynapticribbonmaintainsvesiclepopulationsatthehaircellafferentfibersynapse |