Cargando…
Regulation of γδT17 cells by Mycobacterium vaccae through interference with Notch/Jagged1 signaling pathway
The objective of this study was to investigate the effect of Mycobacterium vaccae on Jagged 1 and gamma delta T17 (γδT17) cells in asthmatic mice. An asthma mouse model was established through immunization with ovalbumin (OVA). Gamma-secretase inhibitor (DAPT) was used to block the Notch signaling p...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Associação Brasileira de Divulgação Científica
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7552905/ https://www.ncbi.nlm.nih.gov/pubmed/33053115 http://dx.doi.org/10.1590/1414-431X20209551 |
_version_ | 1783593497889079296 |
---|---|
author | Yao, Yi En Zhang, Jing Hong Chen, Xiao Ju Huang, Jian Lin Sun, Qi Xiang Liu, Wei Wei Zeng, Huan Li, Chao Qian |
author_facet | Yao, Yi En Zhang, Jing Hong Chen, Xiao Ju Huang, Jian Lin Sun, Qi Xiang Liu, Wei Wei Zeng, Huan Li, Chao Qian |
author_sort | Yao, Yi En |
collection | PubMed |
description | The objective of this study was to investigate the effect of Mycobacterium vaccae on Jagged 1 and gamma delta T17 (γδT17) cells in asthmatic mice. An asthma mouse model was established through immunization with ovalbumin (OVA). Gamma-secretase inhibitor (DAPT) was used to block the Notch signaling pathway. M. vaccae was used to treat asthma, and related indicators were measured. Blocking Notch signaling inhibited the production of γδT17 cells and secretion of cytokine interleukin (IL)-17, which was accompanied by a decrease in Jagged1 mRNA and protein expression in the treated asthma group compared with the untreated asthma group. Similarly, treatment with M. vaccae inhibited Jagged1 expression and γδT17 cell production, which was associated with decreased airway inflammation and reactivity. The Notch signaling pathway may play a role in the pathogenesis of asthma through the induction of Jagged1 receptor. On the other hand, the inhibitory effect of M. vaccae on Jagged1 receptor in γδT17 cells could be used for the prevention and treatment of asthma. |
format | Online Article Text |
id | pubmed-7552905 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Associação Brasileira de Divulgação Científica |
record_format | MEDLINE/PubMed |
spelling | pubmed-75529052020-10-23 Regulation of γδT17 cells by Mycobacterium vaccae through interference with Notch/Jagged1 signaling pathway Yao, Yi En Zhang, Jing Hong Chen, Xiao Ju Huang, Jian Lin Sun, Qi Xiang Liu, Wei Wei Zeng, Huan Li, Chao Qian Braz J Med Biol Res Research Article The objective of this study was to investigate the effect of Mycobacterium vaccae on Jagged 1 and gamma delta T17 (γδT17) cells in asthmatic mice. An asthma mouse model was established through immunization with ovalbumin (OVA). Gamma-secretase inhibitor (DAPT) was used to block the Notch signaling pathway. M. vaccae was used to treat asthma, and related indicators were measured. Blocking Notch signaling inhibited the production of γδT17 cells and secretion of cytokine interleukin (IL)-17, which was accompanied by a decrease in Jagged1 mRNA and protein expression in the treated asthma group compared with the untreated asthma group. Similarly, treatment with M. vaccae inhibited Jagged1 expression and γδT17 cell production, which was associated with decreased airway inflammation and reactivity. The Notch signaling pathway may play a role in the pathogenesis of asthma through the induction of Jagged1 receptor. On the other hand, the inhibitory effect of M. vaccae on Jagged1 receptor in γδT17 cells could be used for the prevention and treatment of asthma. Associação Brasileira de Divulgação Científica 2020-10-07 /pmc/articles/PMC7552905/ /pubmed/33053115 http://dx.doi.org/10.1590/1414-431X20209551 Text en https://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Yao, Yi En Zhang, Jing Hong Chen, Xiao Ju Huang, Jian Lin Sun, Qi Xiang Liu, Wei Wei Zeng, Huan Li, Chao Qian Regulation of γδT17 cells by Mycobacterium vaccae through interference with Notch/Jagged1 signaling pathway |
title | Regulation of γδT17 cells by Mycobacterium vaccae through interference with Notch/Jagged1 signaling pathway |
title_full | Regulation of γδT17 cells by Mycobacterium vaccae through interference with Notch/Jagged1 signaling pathway |
title_fullStr | Regulation of γδT17 cells by Mycobacterium vaccae through interference with Notch/Jagged1 signaling pathway |
title_full_unstemmed | Regulation of γδT17 cells by Mycobacterium vaccae through interference with Notch/Jagged1 signaling pathway |
title_short | Regulation of γδT17 cells by Mycobacterium vaccae through interference with Notch/Jagged1 signaling pathway |
title_sort | regulation of γδt17 cells by mycobacterium vaccae through interference with notch/jagged1 signaling pathway |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7552905/ https://www.ncbi.nlm.nih.gov/pubmed/33053115 http://dx.doi.org/10.1590/1414-431X20209551 |
work_keys_str_mv | AT yaoyien regulationofgdt17cellsbymycobacteriumvaccaethroughinterferencewithnotchjagged1signalingpathway AT zhangjinghong regulationofgdt17cellsbymycobacteriumvaccaethroughinterferencewithnotchjagged1signalingpathway AT chenxiaoju regulationofgdt17cellsbymycobacteriumvaccaethroughinterferencewithnotchjagged1signalingpathway AT huangjianlin regulationofgdt17cellsbymycobacteriumvaccaethroughinterferencewithnotchjagged1signalingpathway AT sunqixiang regulationofgdt17cellsbymycobacteriumvaccaethroughinterferencewithnotchjagged1signalingpathway AT liuweiwei regulationofgdt17cellsbymycobacteriumvaccaethroughinterferencewithnotchjagged1signalingpathway AT zenghuan regulationofgdt17cellsbymycobacteriumvaccaethroughinterferencewithnotchjagged1signalingpathway AT lichaoqian regulationofgdt17cellsbymycobacteriumvaccaethroughinterferencewithnotchjagged1signalingpathway |