Cargando…

Increased susceptibility to otitis media in a Splunc1-deficient mouse model

Otitis media (inflammation of the middle ear) is one of the most common diseases of early childhood. Susceptibility to otitis is influenced by a number of factors, including the actions of innate immune molecules secreted by the epithelia lining the nasopharynx, middle ear and Eustachian tube. The S...

Descripción completa

Detalles Bibliográficos
Autores principales: Bartlett, Jennifer A., Meyerholz, David K., Wohlford-Lenane, Christine L., Naumann, Paul W., Salzman, Nita H., McCray, Paul B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4415896/
https://www.ncbi.nlm.nih.gov/pubmed/25765466
http://dx.doi.org/10.1242/dmm.019646
_version_ 1782369145335054336
author Bartlett, Jennifer A.
Meyerholz, David K.
Wohlford-Lenane, Christine L.
Naumann, Paul W.
Salzman, Nita H.
McCray, Paul B.
author_facet Bartlett, Jennifer A.
Meyerholz, David K.
Wohlford-Lenane, Christine L.
Naumann, Paul W.
Salzman, Nita H.
McCray, Paul B.
author_sort Bartlett, Jennifer A.
collection PubMed
description Otitis media (inflammation of the middle ear) is one of the most common diseases of early childhood. Susceptibility to otitis is influenced by a number of factors, including the actions of innate immune molecules secreted by the epithelia lining the nasopharynx, middle ear and Eustachian tube. The SPLUNC1 (short palate, lung, nasal epithelial clone 1) protein is a highly abundant secretory product of the mammalian nasal, oral and respiratory mucosa that is thought to play a multifunctional role in host defense. In this study we investigated Splunc1 expression in the ear of the mouse, and examined whether this protein contributes to overall host defense in the middle ear and/or Eustachian tube. We found that Splunc1 is highly expressed in both the surface epithelium and in submucosal glands in these regions in wild-type mice. In mice lacking Splunc1, we noted histologically an increased frequency of otitis media, characterized by the accumulation of leukocytes (neutrophils with scattered macrophages), proteinaceous fluid and mucus in the middle ear lumens. Furthermore, many of these mice had extensive remodeling of the middle ear wall, suggesting a chronic course of disease. From these observations, we conclude that loss of Splunc1 predisposes mice to the development of otitis media. The Splunc1(−/−) mouse model should help investigators to better understand both the biological role of Splunc1 as well as host defense mechanisms in the middle ear.
format Online
Article
Text
id pubmed-4415896
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher The Company of Biologists
record_format MEDLINE/PubMed
spelling pubmed-44158962015-05-27 Increased susceptibility to otitis media in a Splunc1-deficient mouse model Bartlett, Jennifer A. Meyerholz, David K. Wohlford-Lenane, Christine L. Naumann, Paul W. Salzman, Nita H. McCray, Paul B. Dis Model Mech Research Article Otitis media (inflammation of the middle ear) is one of the most common diseases of early childhood. Susceptibility to otitis is influenced by a number of factors, including the actions of innate immune molecules secreted by the epithelia lining the nasopharynx, middle ear and Eustachian tube. The SPLUNC1 (short palate, lung, nasal epithelial clone 1) protein is a highly abundant secretory product of the mammalian nasal, oral and respiratory mucosa that is thought to play a multifunctional role in host defense. In this study we investigated Splunc1 expression in the ear of the mouse, and examined whether this protein contributes to overall host defense in the middle ear and/or Eustachian tube. We found that Splunc1 is highly expressed in both the surface epithelium and in submucosal glands in these regions in wild-type mice. In mice lacking Splunc1, we noted histologically an increased frequency of otitis media, characterized by the accumulation of leukocytes (neutrophils with scattered macrophages), proteinaceous fluid and mucus in the middle ear lumens. Furthermore, many of these mice had extensive remodeling of the middle ear wall, suggesting a chronic course of disease. From these observations, we conclude that loss of Splunc1 predisposes mice to the development of otitis media. The Splunc1(−/−) mouse model should help investigators to better understand both the biological role of Splunc1 as well as host defense mechanisms in the middle ear. The Company of Biologists 2015-05-01 /pmc/articles/PMC4415896/ /pubmed/25765466 http://dx.doi.org/10.1242/dmm.019646 Text en © 2015. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Research Article
Bartlett, Jennifer A.
Meyerholz, David K.
Wohlford-Lenane, Christine L.
Naumann, Paul W.
Salzman, Nita H.
McCray, Paul B.
Increased susceptibility to otitis media in a Splunc1-deficient mouse model
title Increased susceptibility to otitis media in a Splunc1-deficient mouse model
title_full Increased susceptibility to otitis media in a Splunc1-deficient mouse model
title_fullStr Increased susceptibility to otitis media in a Splunc1-deficient mouse model
title_full_unstemmed Increased susceptibility to otitis media in a Splunc1-deficient mouse model
title_short Increased susceptibility to otitis media in a Splunc1-deficient mouse model
title_sort increased susceptibility to otitis media in a splunc1-deficient mouse model
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4415896/
https://www.ncbi.nlm.nih.gov/pubmed/25765466
http://dx.doi.org/10.1242/dmm.019646
work_keys_str_mv AT bartlettjennifera increasedsusceptibilitytootitismediainasplunc1deficientmousemodel
AT meyerholzdavidk increasedsusceptibilitytootitismediainasplunc1deficientmousemodel
AT wohlfordlenanechristinel increasedsusceptibilitytootitismediainasplunc1deficientmousemodel
AT naumannpaulw increasedsusceptibilitytootitismediainasplunc1deficientmousemodel
AT salzmannitah increasedsusceptibilitytootitismediainasplunc1deficientmousemodel
AT mccraypaulb increasedsusceptibilitytootitismediainasplunc1deficientmousemodel