Cargando…

Efferent Control of the Electrical and Mechanical Properties of Hair Cells in the Bullfrog's Sacculus

BACKGROUND: Hair cells in the auditory, vestibular, and lateral-line systems respond to mechanical stimulation and transmit information to afferent nerve fibers. The sensitivity of mechanoelectrical transduction is modulated by the efferent pathway, whose activity usually reduces the responsiveness...

Descripción completa

Detalles Bibliográficos
Autores principales: Castellano-Muñoz, Manuel, Israel, Samuel H., Hudspeth, A. J.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2966443/
https://www.ncbi.nlm.nih.gov/pubmed/21048944
http://dx.doi.org/10.1371/journal.pone.0013777
_version_ 1782189583442640896
author Castellano-Muñoz, Manuel
Israel, Samuel H.
Hudspeth, A. J.
author_facet Castellano-Muñoz, Manuel
Israel, Samuel H.
Hudspeth, A. J.
author_sort Castellano-Muñoz, Manuel
collection PubMed
description BACKGROUND: Hair cells in the auditory, vestibular, and lateral-line systems respond to mechanical stimulation and transmit information to afferent nerve fibers. The sensitivity of mechanoelectrical transduction is modulated by the efferent pathway, whose activity usually reduces the responsiveness of hair cells. The basis of this effect remains unknown. METHODOLOGY AND PRINCIPAL FINDINGS: We employed immunocytological, electrophysiological, and micromechanical approaches to characterize the anatomy of efferent innervation and the effect of efferent activity on the electrical and mechanical properties of hair cells in the bullfrog's sacculus. We found that efferent fibers form extensive synaptic terminals on all macular and extramacular hair cells. Macular hair cells expressing the Ca(2+)-buffering protein calretinin contain half as many synaptic ribbons and are innervated by twice as many efferent terminals as calretinin-negative hair cells. Efferent activity elicits inhibitory postsynaptic potentials in hair cells and thus inhibits their electrical resonance. In hair cells that exhibit spiking activity, efferent stimulation suppresses the generation of action potentials. Finally, efferent activity triggers a displacement of the hair bundle's resting position. CONCLUSIONS AND SIGNIFICANCE: The hair cells of the bullfrog's sacculus receive a rich efferent innervation with the heaviest projection to calretinin-containing cells. Stimulation of efferent axons desensitizes the hair cells and suppresses their spiking activity. Although efferent activation influences mechanoelectrical transduction, the mechanical effects on hair bundles are inconsistent.
format Text
id pubmed-2966443
institution National Center for Biotechnology Information
language English
publishDate 2010
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-29664432010-11-03 Efferent Control of the Electrical and Mechanical Properties of Hair Cells in the Bullfrog's Sacculus Castellano-Muñoz, Manuel Israel, Samuel H. Hudspeth, A. J. PLoS One Research Article BACKGROUND: Hair cells in the auditory, vestibular, and lateral-line systems respond to mechanical stimulation and transmit information to afferent nerve fibers. The sensitivity of mechanoelectrical transduction is modulated by the efferent pathway, whose activity usually reduces the responsiveness of hair cells. The basis of this effect remains unknown. METHODOLOGY AND PRINCIPAL FINDINGS: We employed immunocytological, electrophysiological, and micromechanical approaches to characterize the anatomy of efferent innervation and the effect of efferent activity on the electrical and mechanical properties of hair cells in the bullfrog's sacculus. We found that efferent fibers form extensive synaptic terminals on all macular and extramacular hair cells. Macular hair cells expressing the Ca(2+)-buffering protein calretinin contain half as many synaptic ribbons and are innervated by twice as many efferent terminals as calretinin-negative hair cells. Efferent activity elicits inhibitory postsynaptic potentials in hair cells and thus inhibits their electrical resonance. In hair cells that exhibit spiking activity, efferent stimulation suppresses the generation of action potentials. Finally, efferent activity triggers a displacement of the hair bundle's resting position. CONCLUSIONS AND SIGNIFICANCE: The hair cells of the bullfrog's sacculus receive a rich efferent innervation with the heaviest projection to calretinin-containing cells. Stimulation of efferent axons desensitizes the hair cells and suppresses their spiking activity. Although efferent activation influences mechanoelectrical transduction, the mechanical effects on hair bundles are inconsistent. Public Library of Science 2010-10-29 /pmc/articles/PMC2966443/ /pubmed/21048944 http://dx.doi.org/10.1371/journal.pone.0013777 Text en Castellano-Muñoz et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Castellano-Muñoz, Manuel
Israel, Samuel H.
Hudspeth, A. J.
Efferent Control of the Electrical and Mechanical Properties of Hair Cells in the Bullfrog's Sacculus
title Efferent Control of the Electrical and Mechanical Properties of Hair Cells in the Bullfrog's Sacculus
title_full Efferent Control of the Electrical and Mechanical Properties of Hair Cells in the Bullfrog's Sacculus
title_fullStr Efferent Control of the Electrical and Mechanical Properties of Hair Cells in the Bullfrog's Sacculus
title_full_unstemmed Efferent Control of the Electrical and Mechanical Properties of Hair Cells in the Bullfrog's Sacculus
title_short Efferent Control of the Electrical and Mechanical Properties of Hair Cells in the Bullfrog's Sacculus
title_sort efferent control of the electrical and mechanical properties of hair cells in the bullfrog's sacculus
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2966443/
https://www.ncbi.nlm.nih.gov/pubmed/21048944
http://dx.doi.org/10.1371/journal.pone.0013777
work_keys_str_mv AT castellanomunozmanuel efferentcontroloftheelectricalandmechanicalpropertiesofhaircellsinthebullfrogssacculus
AT israelsamuelh efferentcontroloftheelectricalandmechanicalpropertiesofhaircellsinthebullfrogssacculus
AT hudspethaj efferentcontroloftheelectricalandmechanicalpropertiesofhaircellsinthebullfrogssacculus