Current concepts in cochlear ribbon synapse formation.
cochlea
hair cell
ribbon synapse
spiral ganglion neuron
synaptopathy
Journal
Synapse (New York, N.Y.)
ISSN: 1098-2396
Titre abrégé: Synapse
Pays: United States
ID NLM: 8806914
Informations de publication
Date de publication:
05 2019
05 2019
Historique:
received:
29
08
2018
revised:
20
12
2018
accepted:
21
12
2018
pubmed:
29
12
2018
medline:
22
4
2020
entrez:
29
12
2018
Statut:
ppublish
Résumé
In mammals, hair cells and spiral ganglion neurons (SGNs) in the cochlea together are sophisticated "sensorineural" structures that transduce auditory information from the outside world into the brain. Hair cells and SGNs are joined by glutamatergic ribbon-type synapses composed of a molecular machinery rivaling in complexity the mechanoelectric transduction components found at the apical side of the hair cell. The cochlear hair cell ribbon synapse has received much attention lately because of recent and important findings related to its damage (sometimes termed "synaptopathy") as a result of noise overexposure. During development, ribbon synapses between type I SGNs and inner hair cells form in the time window between birth and hearing onset and is a process coordinated with type I SGN myelination, spontaneous activity, synaptic pruning, and innervation by efferents. In this review, we highlight new findings regarding the diversity of type I SGNs and inner hair cell synapses, and the molecular mechanisms of selective hair cell targeting. Also discussed are cell adhesion molecules and protein constituents of the ribbon synapse, and how these factors participate in ribbon synapse formation. We also note interesting new insights into the morphological development of type II SGNs, and the potential for cochlear macrophages as important players in protecting SGNs. We also address recent studies demonstrating that the structural and physiological profiles of the type I SGNs do not reach full maturity until weeks after hearing onset, suggesting a protracted development that is likely modulated by activity.
Identifiants
pubmed: 30592086
doi: 10.1002/syn.22087
pmc: PMC6573016
mid: NIHMS1035278
doi:
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
e22087Subventions
Organisme : NIDCD NIH HHS
ID : F31 DC015946
Pays : United States
Organisme : NIDCD NIH HHS
ID : DC0022756
Pays : United States
Organisme : NIDCD NIH HHS
ID : R00 DC013107
Pays : United States
Organisme : NIDCD NIH HHS
ID : R01 DC016595
Pays : United States
Informations de copyright
© 2018 Wiley Periodicals, Inc.
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