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Somatosensory innervation of the oral mucosa of adult and aging mice

Oral mechanoreception is implicated in fundamental functions including speech, food intake and swallowing; yet, the neuroanatomical substrates that encode mechanical stimuli are not well understood. Tactile perception is initiated by intricate mechanosensitive machinery involving dedicated cells and...

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Autores principales: Moayedi, Yalda, Duenas-Bianchi, Lucia F., Lumpkin, Ellen A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6028454/
https://www.ncbi.nlm.nih.gov/pubmed/29967482
http://dx.doi.org/10.1038/s41598-018-28195-2
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author Moayedi, Yalda
Duenas-Bianchi, Lucia F.
Lumpkin, Ellen A.
author_facet Moayedi, Yalda
Duenas-Bianchi, Lucia F.
Lumpkin, Ellen A.
author_sort Moayedi, Yalda
collection PubMed
description Oral mechanoreception is implicated in fundamental functions including speech, food intake and swallowing; yet, the neuroanatomical substrates that encode mechanical stimuli are not well understood. Tactile perception is initiated by intricate mechanosensitive machinery involving dedicated cells and neurons. This signal transduction setup is coupled with the topology and mechanical properties of surrounding epithelium, thereby providing a sensitive and accurate system to detect stress fluctuations from the external environment. We mapped the distribution of anatomically distinct neuronal endings in mouse oral cavity using transgenic reporters, molecular markers and quantitative histomorphometry. We found that the tongue is equipped with an array of putative mechanoreceptors that express the principal mechanosensory channel Piezo2, including end bulbs of Krause innervating individual filiform papillae and a novel class of neuronal fibers innervating the epithelium surrounding taste buds. The hard palate and gums are densely populated with three classes of sensory afferents organized in discrete patterns including Merkel cell-neurite complexes, Meissner’s corpuscles and glomerular corpuscles. In aged mice, we find that palatal Merkel cells reduce in number at key time-points that correlate with impaired oral abilities, such as swallowing and mastication. Collectively, this work identifies the mechanosensory architecture of oral tissues involved in feeding.
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spelling pubmed-60284542018-07-09 Somatosensory innervation of the oral mucosa of adult and aging mice Moayedi, Yalda Duenas-Bianchi, Lucia F. Lumpkin, Ellen A. Sci Rep Article Oral mechanoreception is implicated in fundamental functions including speech, food intake and swallowing; yet, the neuroanatomical substrates that encode mechanical stimuli are not well understood. Tactile perception is initiated by intricate mechanosensitive machinery involving dedicated cells and neurons. This signal transduction setup is coupled with the topology and mechanical properties of surrounding epithelium, thereby providing a sensitive and accurate system to detect stress fluctuations from the external environment. We mapped the distribution of anatomically distinct neuronal endings in mouse oral cavity using transgenic reporters, molecular markers and quantitative histomorphometry. We found that the tongue is equipped with an array of putative mechanoreceptors that express the principal mechanosensory channel Piezo2, including end bulbs of Krause innervating individual filiform papillae and a novel class of neuronal fibers innervating the epithelium surrounding taste buds. The hard palate and gums are densely populated with three classes of sensory afferents organized in discrete patterns including Merkel cell-neurite complexes, Meissner’s corpuscles and glomerular corpuscles. In aged mice, we find that palatal Merkel cells reduce in number at key time-points that correlate with impaired oral abilities, such as swallowing and mastication. Collectively, this work identifies the mechanosensory architecture of oral tissues involved in feeding. Nature Publishing Group UK 2018-07-02 /pmc/articles/PMC6028454/ /pubmed/29967482 http://dx.doi.org/10.1038/s41598-018-28195-2 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Moayedi, Yalda
Duenas-Bianchi, Lucia F.
Lumpkin, Ellen A.
Somatosensory innervation of the oral mucosa of adult and aging mice
title Somatosensory innervation of the oral mucosa of adult and aging mice
title_full Somatosensory innervation of the oral mucosa of adult and aging mice
title_fullStr Somatosensory innervation of the oral mucosa of adult and aging mice
title_full_unstemmed Somatosensory innervation of the oral mucosa of adult and aging mice
title_short Somatosensory innervation of the oral mucosa of adult and aging mice
title_sort somatosensory innervation of the oral mucosa of adult and aging mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6028454/
https://www.ncbi.nlm.nih.gov/pubmed/29967482
http://dx.doi.org/10.1038/s41598-018-28195-2
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