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The human olfactory cleft mucus proteome and its age-related changes

Age-related decreases in olfactory sensitivity are often accompanied by a decrease in the quality of life. However, the molecular mechanisms underlying these changes are not well described. Inhaled substances including odorants are detected by sensory neurons in the olfactory cleft covered with a la...

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Autores principales: Yoshikawa, Keiichi, Wang, Hong, Jaen, Cristina, Haneoka, Mai, Saito, Naoko, Nakamura, Junji, Adappa, Nithin D., Cohen, Noam A., Dalton, Pamela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6249231/
https://www.ncbi.nlm.nih.gov/pubmed/30464187
http://dx.doi.org/10.1038/s41598-018-35102-2
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author Yoshikawa, Keiichi
Wang, Hong
Jaen, Cristina
Haneoka, Mai
Saito, Naoko
Nakamura, Junji
Adappa, Nithin D.
Cohen, Noam A.
Dalton, Pamela
author_facet Yoshikawa, Keiichi
Wang, Hong
Jaen, Cristina
Haneoka, Mai
Saito, Naoko
Nakamura, Junji
Adappa, Nithin D.
Cohen, Noam A.
Dalton, Pamela
author_sort Yoshikawa, Keiichi
collection PubMed
description Age-related decreases in olfactory sensitivity are often accompanied by a decrease in the quality of life. However, the molecular mechanisms underlying these changes are not well described. Inhaled substances including odorants are detected by sensory neurons in the olfactory cleft covered with a layer of mucus. This olfactory mucus is the first molecular machinery responsible for tissue protection and for detection of environmental odorants. Yet, little is known about the molecular identities of the actors because of the lack of information on the mucus proteome and its age-related changes. Here, we sampled human mucus from different nasal locations and from young and elderly subjects. The composition of the mucus was extensively analyzed by shotgun proteomic analysis for a vast array of proteins. We also explored correlations between the levels of each mucus proteins with the olfactory sensitivity of subjects. This analysis revealed previously unrecognized proteins with potentially important functions in olfaction. Taken together, this report describes the most comprehensive catalogue of the nasal mucus proteins to date, their positional and age-related differences, and candidate proteins associated with olfaction. This catalogue will provide fundamental information useful for future studies, such as identification of olfactory auxiliary proteins, causes of age-related declines in olfaction, and biomarkers for neurodegenerative disorders.
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spelling pubmed-62492312018-11-28 The human olfactory cleft mucus proteome and its age-related changes Yoshikawa, Keiichi Wang, Hong Jaen, Cristina Haneoka, Mai Saito, Naoko Nakamura, Junji Adappa, Nithin D. Cohen, Noam A. Dalton, Pamela Sci Rep Article Age-related decreases in olfactory sensitivity are often accompanied by a decrease in the quality of life. However, the molecular mechanisms underlying these changes are not well described. Inhaled substances including odorants are detected by sensory neurons in the olfactory cleft covered with a layer of mucus. This olfactory mucus is the first molecular machinery responsible for tissue protection and for detection of environmental odorants. Yet, little is known about the molecular identities of the actors because of the lack of information on the mucus proteome and its age-related changes. Here, we sampled human mucus from different nasal locations and from young and elderly subjects. The composition of the mucus was extensively analyzed by shotgun proteomic analysis for a vast array of proteins. We also explored correlations between the levels of each mucus proteins with the olfactory sensitivity of subjects. This analysis revealed previously unrecognized proteins with potentially important functions in olfaction. Taken together, this report describes the most comprehensive catalogue of the nasal mucus proteins to date, their positional and age-related differences, and candidate proteins associated with olfaction. This catalogue will provide fundamental information useful for future studies, such as identification of olfactory auxiliary proteins, causes of age-related declines in olfaction, and biomarkers for neurodegenerative disorders. Nature Publishing Group UK 2018-11-21 /pmc/articles/PMC6249231/ /pubmed/30464187 http://dx.doi.org/10.1038/s41598-018-35102-2 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
Yoshikawa, Keiichi
Wang, Hong
Jaen, Cristina
Haneoka, Mai
Saito, Naoko
Nakamura, Junji
Adappa, Nithin D.
Cohen, Noam A.
Dalton, Pamela
The human olfactory cleft mucus proteome and its age-related changes
title The human olfactory cleft mucus proteome and its age-related changes
title_full The human olfactory cleft mucus proteome and its age-related changes
title_fullStr The human olfactory cleft mucus proteome and its age-related changes
title_full_unstemmed The human olfactory cleft mucus proteome and its age-related changes
title_short The human olfactory cleft mucus proteome and its age-related changes
title_sort human olfactory cleft mucus proteome and its age-related changes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6249231/
https://www.ncbi.nlm.nih.gov/pubmed/30464187
http://dx.doi.org/10.1038/s41598-018-35102-2
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