Purinergic signaling in cochlear supporting cells reduces hair cell excitability by increasing the extracellular space

Neurons in developing sensory pathways exhibit spontaneous bursts of electrical activity that are critical for survival, maturation and circuit refinement. In the auditory system, intrinsically generated activity arises within the cochlea, but the molecular mechanisms that initiate this activity rem...

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Main Authors: Travis A Babola, Calvin J Kersbergen, Han Chin Wang, Dwight E Bergles
Format: Article
Language:English
Published: eLife Sciences Publications Ltd 2020-01-01
Series:eLife
Subjects:
Online Access:https://elifesciences.org/articles/52160
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spelling doaj-fba236a8e3b7490197f0b91cd05f6f9e2021-05-05T20:42:48ZengeLife Sciences Publications LtdeLife2050-084X2020-01-01910.7554/eLife.52160Purinergic signaling in cochlear supporting cells reduces hair cell excitability by increasing the extracellular spaceTravis A Babola0https://orcid.org/0000-0003-4440-5029Calvin J Kersbergen1Han Chin Wang2Dwight E Bergles3https://orcid.org/0000-0002-7133-7378The Solomon Snyder Department of Neuroscience, Johns Hopkins University, Baltimore, United StatesThe Solomon Snyder Department of Neuroscience, Johns Hopkins University, Baltimore, United StatesThe Solomon Snyder Department of Neuroscience, Johns Hopkins University, Baltimore, United StatesThe Solomon Snyder Department of Neuroscience, Johns Hopkins University, Baltimore, United States; Department of Otolaryngology Head and Neck Surgery, Johns Hopkins University, Baltimore, United States; Kavli Neuroscience Discovery Institute, Johns Hopkins University, Baltimore, United StatesNeurons in developing sensory pathways exhibit spontaneous bursts of electrical activity that are critical for survival, maturation and circuit refinement. In the auditory system, intrinsically generated activity arises within the cochlea, but the molecular mechanisms that initiate this activity remain poorly understood. We show that burst firing of mouse inner hair cells prior to hearing onset requires P2RY1 autoreceptors expressed by inner supporting cells. P2RY1 activation triggers K+ efflux and depolarization of hair cells, as well as osmotic shrinkage of supporting cells that dramatically increased the extracellular space and speed of K+ redistribution. Pharmacological inhibition or genetic disruption of P2RY1 suppressed neuronal burst firing by reducing K+ release, but unexpectedly enhanced their tonic firing, as water resorption by supporting cells reduced the extracellular space, leading to K+ accumulation. These studies indicate that purinergic signaling in supporting cells regulates hair cell excitability by controlling the volume of the extracellular space.https://elifesciences.org/articles/52160cochleapurinergiccalciumhair cellP2Y1potassium
collection DOAJ
language English
format Article
sources DOAJ
author Travis A Babola
Calvin J Kersbergen
Han Chin Wang
Dwight E Bergles
spellingShingle Travis A Babola
Calvin J Kersbergen
Han Chin Wang
Dwight E Bergles
Purinergic signaling in cochlear supporting cells reduces hair cell excitability by increasing the extracellular space
eLife
cochlea
purinergic
calcium
hair cell
P2Y1
potassium
author_facet Travis A Babola
Calvin J Kersbergen
Han Chin Wang
Dwight E Bergles
author_sort Travis A Babola
title Purinergic signaling in cochlear supporting cells reduces hair cell excitability by increasing the extracellular space
title_short Purinergic signaling in cochlear supporting cells reduces hair cell excitability by increasing the extracellular space
title_full Purinergic signaling in cochlear supporting cells reduces hair cell excitability by increasing the extracellular space
title_fullStr Purinergic signaling in cochlear supporting cells reduces hair cell excitability by increasing the extracellular space
title_full_unstemmed Purinergic signaling in cochlear supporting cells reduces hair cell excitability by increasing the extracellular space
title_sort purinergic signaling in cochlear supporting cells reduces hair cell excitability by increasing the extracellular space
publisher eLife Sciences Publications Ltd
series eLife
issn 2050-084X
publishDate 2020-01-01
description Neurons in developing sensory pathways exhibit spontaneous bursts of electrical activity that are critical for survival, maturation and circuit refinement. In the auditory system, intrinsically generated activity arises within the cochlea, but the molecular mechanisms that initiate this activity remain poorly understood. We show that burst firing of mouse inner hair cells prior to hearing onset requires P2RY1 autoreceptors expressed by inner supporting cells. P2RY1 activation triggers K+ efflux and depolarization of hair cells, as well as osmotic shrinkage of supporting cells that dramatically increased the extracellular space and speed of K+ redistribution. Pharmacological inhibition or genetic disruption of P2RY1 suppressed neuronal burst firing by reducing K+ release, but unexpectedly enhanced their tonic firing, as water resorption by supporting cells reduced the extracellular space, leading to K+ accumulation. These studies indicate that purinergic signaling in supporting cells regulates hair cell excitability by controlling the volume of the extracellular space.
topic cochlea
purinergic
calcium
hair cell
P2Y1
potassium
url https://elifesciences.org/articles/52160
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AT calvinjkersbergen purinergicsignalingincochlearsupportingcellsreduceshaircellexcitabilitybyincreasingtheextracellularspace
AT hanchinwang purinergicsignalingincochlearsupportingcellsreduceshaircellexcitabilitybyincreasingtheextracellularspace
AT dwightebergles purinergicsignalingincochlearsupportingcellsreduceshaircellexcitabilitybyincreasingtheextracellularspace
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