Intestinal and lung inflammatory group 2 innate lymphoid cells (iILC2s) and their related cytokines in chronic obstructive pulmonary disease.
- Author:
Qian XU
1
;
Xi TAN
1
;
Tingting HU
1
;
Min JIANG
2
Author Information
1. Traditional Chinese Medicine Hospital Affiliated to Xinjiang Medical University & National Clinical Research Base of Traditional Chinese Medicine, Xinjiang Laboratory Of Respiratory Disease Research, Urumqi 830000, China.
2. Traditional Chinese Medicine Hospital Affiliated to Xinjiang Medical University & National Clinical Research Base of Traditional Chinese Medicine, Xinjiang Laboratory Of Respiratory Disease Research, Urumqi 830000, China. *Corresponding author, E-mail: 250579087@qq.com.
- Publication Type:Journal Article
- MeSH:
Mice;
Animals;
Cytokines;
Immunity, Innate;
Interleukin-13;
Interleukin-4;
Lymphocytes;
Lung/pathology*;
Pulmonary Disease, Chronic Obstructive;
Bronchoalveolar Lavage Fluid;
Disease Models, Animal;
Intestines
- From:
Chinese Journal of Cellular and Molecular Immunology
2023;39(7):599-603
- CountryChina
- Language:Chinese
-
Abstract:
Objective To investigate the relationship between intestinal inflammatory group 2 innate lymphoid cells (iILC2s) and lung ILC2s and its inflammatory response in chronic obstructive pulmonary disease (COPD). Methods Mouse COPD model was established by smoking method. The mice were randomly divided into normal group and COPD group. HE staining was used to detect the pathological changes in lung and intestine tissues of mice in normal group and COPD group, and the contents of natural ILC2s(nILC2s) and iILC2s cells were measured by flow cytometry. Wright-Giemsa staining was used to measure the number of immune cells in the bronchoalveolar lavage fluid (BALF) of mice in normal group and COPD group, and the concentration of IL-13 and IL-4 was detected by ELISA. Results In COPD mice, epithelial cells of the lung and intestinal tissues exhibited pathological hyperplasia, partial atrophy or deletion, inflammatory cell infiltration, increased pathological score and significantly increased neutrophils, monocytes, and lymphocytes in BALF. Lung iILC2s, intestinal nILC2s and iILC2s were increased significantly in the COPD group. The contents of IL-13 and IL-4 in BALF were significantly increased. Conclusion The increase of iILC2s and their related cytokines in COPD lung may be related to intestinal inflammatory ILC2s.
