Rat Merkel cells are mechanoreceptors and osmoreceptors.

Merkel cells (MCs) associated with nerve terminals constitute MC-neurite complexes, which are involved in slowly-adapting type I mechanoreception. Although MCs are known to express voltage-gated Ca2+ channels and hypotonic-induced membrane deformation is known to lead to Ca2+ transients, whether MCs...

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Main Authors: Nicholas Boulais, Jean-Pierre Pennec, Nicolas Lebonvallet, Ulysse Pereira, Nathalie Rougier, Germaine Dorange, Christophe Chesné, Laurent Misery
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2009-11-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC2770322?pdf=render
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spelling doaj-0642792c751f4f158b491ad1cfdf41342020-11-25T01:41:43ZengPublic Library of Science (PLoS)PLoS ONE1932-62032009-11-01411e775910.1371/journal.pone.0007759Rat Merkel cells are mechanoreceptors and osmoreceptors.Nicholas BoulaisJean-Pierre PennecNicolas LebonvalletUlysse PereiraNathalie RougierGermaine DorangeChristophe ChesnéLaurent MiseryMerkel cells (MCs) associated with nerve terminals constitute MC-neurite complexes, which are involved in slowly-adapting type I mechanoreception. Although MCs are known to express voltage-gated Ca2+ channels and hypotonic-induced membrane deformation is known to lead to Ca2+ transients, whether MCs initiate mechanotransduction is currently unknown. To answer to this question, rat MCs were transfected with a reporter vector, which enabled their identification.Their properties were investigated through electrophysiological studies. Voltage-gated K+, Ca2+ and Ca2+-activated K+ (KCa)channels were identified, as previously described. Here, we also report the activation of Ca2+ channels by histamine and their inhibition by acetylcholine. As a major finding, we demonstrated that direct mechanical stimulations induced strong inward Ca2+ currents in MCs. Depolarizations were dependent on the strength and the length of the stimulation. Moreover, touch-evoked currents were inhibited by the stretch channel antagonist gadolinium. These data confirm the mechanotransduction capabilities of MCs. Furthermore, we found that activation of the osmoreceptor TRPV4 in FM1-43-labeled MCs provoked neurosecretory granule exocytosis. Since FM1-43 blocks mechanosensory channels, this suggests that hypo-osmolarity activates MCs in the absence of mechanotransduction. Thus, mechanotransduction and osmoreception are likely distinct pathways.http://europepmc.org/articles/PMC2770322?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Nicholas Boulais
Jean-Pierre Pennec
Nicolas Lebonvallet
Ulysse Pereira
Nathalie Rougier
Germaine Dorange
Christophe Chesné
Laurent Misery
spellingShingle Nicholas Boulais
Jean-Pierre Pennec
Nicolas Lebonvallet
Ulysse Pereira
Nathalie Rougier
Germaine Dorange
Christophe Chesné
Laurent Misery
Rat Merkel cells are mechanoreceptors and osmoreceptors.
PLoS ONE
author_facet Nicholas Boulais
Jean-Pierre Pennec
Nicolas Lebonvallet
Ulysse Pereira
Nathalie Rougier
Germaine Dorange
Christophe Chesné
Laurent Misery
author_sort Nicholas Boulais
title Rat Merkel cells are mechanoreceptors and osmoreceptors.
title_short Rat Merkel cells are mechanoreceptors and osmoreceptors.
title_full Rat Merkel cells are mechanoreceptors and osmoreceptors.
title_fullStr Rat Merkel cells are mechanoreceptors and osmoreceptors.
title_full_unstemmed Rat Merkel cells are mechanoreceptors and osmoreceptors.
title_sort rat merkel cells are mechanoreceptors and osmoreceptors.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2009-11-01
description Merkel cells (MCs) associated with nerve terminals constitute MC-neurite complexes, which are involved in slowly-adapting type I mechanoreception. Although MCs are known to express voltage-gated Ca2+ channels and hypotonic-induced membrane deformation is known to lead to Ca2+ transients, whether MCs initiate mechanotransduction is currently unknown. To answer to this question, rat MCs were transfected with a reporter vector, which enabled their identification.Their properties were investigated through electrophysiological studies. Voltage-gated K+, Ca2+ and Ca2+-activated K+ (KCa)channels were identified, as previously described. Here, we also report the activation of Ca2+ channels by histamine and their inhibition by acetylcholine. As a major finding, we demonstrated that direct mechanical stimulations induced strong inward Ca2+ currents in MCs. Depolarizations were dependent on the strength and the length of the stimulation. Moreover, touch-evoked currents were inhibited by the stretch channel antagonist gadolinium. These data confirm the mechanotransduction capabilities of MCs. Furthermore, we found that activation of the osmoreceptor TRPV4 in FM1-43-labeled MCs provoked neurosecretory granule exocytosis. Since FM1-43 blocks mechanosensory channels, this suggests that hypo-osmolarity activates MCs in the absence of mechanotransduction. Thus, mechanotransduction and osmoreception are likely distinct pathways.
url http://europepmc.org/articles/PMC2770322?pdf=render
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