Cargando…

Mycobacterium vaccae Nebulization Can Protect against Asthma in Balb/c Mice by Regulating Th9 Expression

Asthma is a heterogeneous disease characterized by chronic airway inflammation. CD4(+) T-helper 9 (Th9) cells are closely linked to asthma, helping to regulate inflammation and immunity. Epidemiological studies showed that mycobacteria infections are negatively associated with asthma. Our previous r...

Descripción completa

Detalles Bibliográficos
Autores principales: Li, Chaoqian, Jiang, Xiaohong, Luo, Mingjie, Feng, Guangyi, Sun, Qixiang, Chen, Yiping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4982628/
https://www.ncbi.nlm.nih.gov/pubmed/27518187
http://dx.doi.org/10.1371/journal.pone.0161164
_version_ 1782447808243040256
author Li, Chaoqian
Jiang, Xiaohong
Luo, Mingjie
Feng, Guangyi
Sun, Qixiang
Chen, Yiping
author_facet Li, Chaoqian
Jiang, Xiaohong
Luo, Mingjie
Feng, Guangyi
Sun, Qixiang
Chen, Yiping
author_sort Li, Chaoqian
collection PubMed
description Asthma is a heterogeneous disease characterized by chronic airway inflammation. CD4(+) T-helper 9 (Th9) cells are closely linked to asthma, helping to regulate inflammation and immunity. Epidemiological studies showed that mycobacteria infections are negatively associated with asthma. Our previous research showed that inactivated Mycobacterium phlei nebulization alleviated the airway hyperresponsiveness and inflammation of asthma. However, the relationship between Th9 cells and mycobacteria remains unknown. Here, we evaluated the relationship between Mycobacterium vaccae nebulization and Th9 cells in asthmatic mice. Eighteen Balb/c mice were randomized into 3 groups of 6 mice each (normal control group, asthma control group, and nebulization asthma group [Neb. group]). The Neb. group was nebulized with M. vaccae one month before establishment of the asthmatic model with ovalbumin (OVA) sensitization, and the normal and asthma control groups were nebulized with phosphate-buffered saline. The hyperresponsiveness of the mouse airways was assessed using a non-invasive lung function machine. Lung airway inflammation was evaluated by hematoxylin and eosin and periodic acid-Schiff staining. Cytokine interlukin-9 (IL-9) concentration and OVA-specific IgE in the bronchoalveolar lavage fluid were measured by enzyme-linked immunosorbent assays. The percentages of γδTCR(+) CD3(+), IL-9(+)CD3(+), IL-10(+)CD3(+) lymphocytes, and IL9(+)γδT and IL-10(+)γδT cells were detected by flow cytometry. The airway inflammation and concentration of IL-9 and OVA-specific IgE were significantly reduced in the Neb. group compared to the asthma control group. The Neb. group had lower airway hyperresponsiveness, percentages of γδTCR(+)CD3(+) and IL-9(+)CD3(+) lymphocytes, and IL9(+)γδT cells, and higher percentages of IL-10(+)CD3(+) lymphocytes and IL-10(+)γδT cells compared to the asthma control group. Thus, mouse bronchial asthma could be prevented by M. vaccae nebulization. The mechanism could involve M. vaccae-mediated effects on induction of IL-9 secretion and suppression of IL-10 secretion from γδT cells. γδT cells showed prominent IL-10 expression, indicating that they possibly belong to the Th9 family.
format Online
Article
Text
id pubmed-4982628
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-49826282016-08-29 Mycobacterium vaccae Nebulization Can Protect against Asthma in Balb/c Mice by Regulating Th9 Expression Li, Chaoqian Jiang, Xiaohong Luo, Mingjie Feng, Guangyi Sun, Qixiang Chen, Yiping PLoS One Research Article Asthma is a heterogeneous disease characterized by chronic airway inflammation. CD4(+) T-helper 9 (Th9) cells are closely linked to asthma, helping to regulate inflammation and immunity. Epidemiological studies showed that mycobacteria infections are negatively associated with asthma. Our previous research showed that inactivated Mycobacterium phlei nebulization alleviated the airway hyperresponsiveness and inflammation of asthma. However, the relationship between Th9 cells and mycobacteria remains unknown. Here, we evaluated the relationship between Mycobacterium vaccae nebulization and Th9 cells in asthmatic mice. Eighteen Balb/c mice were randomized into 3 groups of 6 mice each (normal control group, asthma control group, and nebulization asthma group [Neb. group]). The Neb. group was nebulized with M. vaccae one month before establishment of the asthmatic model with ovalbumin (OVA) sensitization, and the normal and asthma control groups were nebulized with phosphate-buffered saline. The hyperresponsiveness of the mouse airways was assessed using a non-invasive lung function machine. Lung airway inflammation was evaluated by hematoxylin and eosin and periodic acid-Schiff staining. Cytokine interlukin-9 (IL-9) concentration and OVA-specific IgE in the bronchoalveolar lavage fluid were measured by enzyme-linked immunosorbent assays. The percentages of γδTCR(+) CD3(+), IL-9(+)CD3(+), IL-10(+)CD3(+) lymphocytes, and IL9(+)γδT and IL-10(+)γδT cells were detected by flow cytometry. The airway inflammation and concentration of IL-9 and OVA-specific IgE were significantly reduced in the Neb. group compared to the asthma control group. The Neb. group had lower airway hyperresponsiveness, percentages of γδTCR(+)CD3(+) and IL-9(+)CD3(+) lymphocytes, and IL9(+)γδT cells, and higher percentages of IL-10(+)CD3(+) lymphocytes and IL-10(+)γδT cells compared to the asthma control group. Thus, mouse bronchial asthma could be prevented by M. vaccae nebulization. The mechanism could involve M. vaccae-mediated effects on induction of IL-9 secretion and suppression of IL-10 secretion from γδT cells. γδT cells showed prominent IL-10 expression, indicating that they possibly belong to the Th9 family. Public Library of Science 2016-08-12 /pmc/articles/PMC4982628/ /pubmed/27518187 http://dx.doi.org/10.1371/journal.pone.0161164 Text en © 2016 Li et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Li, Chaoqian
Jiang, Xiaohong
Luo, Mingjie
Feng, Guangyi
Sun, Qixiang
Chen, Yiping
Mycobacterium vaccae Nebulization Can Protect against Asthma in Balb/c Mice by Regulating Th9 Expression
title Mycobacterium vaccae Nebulization Can Protect against Asthma in Balb/c Mice by Regulating Th9 Expression
title_full Mycobacterium vaccae Nebulization Can Protect against Asthma in Balb/c Mice by Regulating Th9 Expression
title_fullStr Mycobacterium vaccae Nebulization Can Protect against Asthma in Balb/c Mice by Regulating Th9 Expression
title_full_unstemmed Mycobacterium vaccae Nebulization Can Protect against Asthma in Balb/c Mice by Regulating Th9 Expression
title_short Mycobacterium vaccae Nebulization Can Protect against Asthma in Balb/c Mice by Regulating Th9 Expression
title_sort mycobacterium vaccae nebulization can protect against asthma in balb/c mice by regulating th9 expression
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4982628/
https://www.ncbi.nlm.nih.gov/pubmed/27518187
http://dx.doi.org/10.1371/journal.pone.0161164
work_keys_str_mv AT lichaoqian mycobacteriumvaccaenebulizationcanprotectagainstasthmainbalbcmicebyregulatingth9expression
AT jiangxiaohong mycobacteriumvaccaenebulizationcanprotectagainstasthmainbalbcmicebyregulatingth9expression
AT luomingjie mycobacteriumvaccaenebulizationcanprotectagainstasthmainbalbcmicebyregulatingth9expression
AT fengguangyi mycobacteriumvaccaenebulizationcanprotectagainstasthmainbalbcmicebyregulatingth9expression
AT sunqixiang mycobacteriumvaccaenebulizationcanprotectagainstasthmainbalbcmicebyregulatingth9expression
AT chenyiping mycobacteriumvaccaenebulizationcanprotectagainstasthmainbalbcmicebyregulatingth9expression