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Foxp2 inhibits Th9 cell differentiation and attenuates allergic airway inflammation in a mouse model of ovalbumin-induced asthma
被引:4
|作者:
Zhang, Xinxing
[1
]
Ma, Yu
[1
]
He, Yanyu
[1
]
Gu, Wenjing
[1
]
Yan, Yongdong
[1
]
Ji, Wei
[1
]
Huang, Li
[1
]
Wang, Yuqing
[1
]
Hao, Chuangli
[1
]
Li, Gang
[2
]
Chen, Zhengrong
[1
]
机构:
[1] Childrens Hosp Soochow Univ, Dept Resp Med, Suzhou 215003, Peoples R China
[2] Childrens Hosp Soochow Univ, Inst Pediat Res, Suzhou 215025, Peoples R China
基金:
中国国家自然科学基金;
关键词:
Asthma;
Airway inflammation;
Th9 cell differentiation;
Foxp2;
T-CELLS;
INTERLEUKIN-9;
BETA;
D O I:
10.1016/j.intimp.2022.109060
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
This study aimed to explore the effects of forkhead box P2 gene (Foxp2) on T-helper 9 (Th9) differentiation in asthmatic mice. An in vivo asthmatic mouse model was induced with ovalbumin (OVA). An in vitro model was established by culturing CD4+ T cells with TGF-beta, IL-4, and anti-IFN-gamma. ELISA, flow cytometry, qRT-PCR and Western blot were performed to examine IL-9 secretion, Th9 cell number, and Th9 cell transcription factor expression, respectively. Pathological changes in lung tissues and airway mucus secretion were assessed with HE and PAS glycogen staining. Anti-IL-9 mAb reversed the elevation in Th9 cells and IL-9 expression in lung tissues and bronchoalveolar lavage fluid (BALF) of asthmatic mice. Foxp2 was downregulated in BALF and lung tissue of asthmatic mice and Th9 cells. Overexpression of Foxp2 inhibited Th9 cell differentiation in vitro and improved airway inflammation in vivo. Our study suggests that overexpression of Foxp2 attenuates allergic asthma by inhibiting Th9 cell differentiation.
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页数:8
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