Modulating oxidative stress counteracts specific antigen-induced regulatory T-cell apoptosis in mice

被引:5
|
作者
Zhang, Yuan-Yi [1 ,2 ,3 ]
Feng, Bai-Sui [4 ]
Zhang, Huanping [5 ]
Yang, Gui [6 ]
Jin, Qiao-Ruo [3 ]
Luo, Xiang-Qian [7 ]
Ma, Na [4 ]
Huang, Qin-Miao [1 ]
Yang, Li-Teng [1 ]
Zhang, Guo-Hao [3 ]
Liu, Da-Bo [7 ]
Yu, Yong [8 ]
Liu, Zhi-Gang [3 ]
Zheng, Peng-Yuan [8 ]
Yang, Ping-Chang [2 ,3 ]
机构
[1] Shenzhen Univ, Affiliated Hosp 3, Dept Respirol, Shenzhen, Peoples R China
[2] Shenzhen Univ, Sch Med, Guangdong Prov Key Lab Reg Immun & Dis, Shenzhen, Peoples R China
[3] Shenzhen Univ, Sch Med, Res Ctr Allergy & Immunol, Shenzhen, Peoples R China
[4] Zhengzhou Univ, Affiliated Hosp 2, Dept Gastroenterol, Zhengzhou, Peoples R China
[5] Shanxi Med Univ, Bethune Hosp, Dept Allergy Med, Taiyuan, Peoples R China
[6] Longgang Cent Hosp, Dept Otolaryngol, Shenzhen, Peoples R China
[7] Southern Med Univ, Shenzhen Hosp, Dept Pediat Otolaryngol, Shenzhen, Peoples R China
[8] Zhengzhou Univ, Affiliated Hosp 5, Dept Gastroenterol, Zhengzhou, Peoples R China
关键词
apoptosis; oxidative stress; Regulatory T cell; superoxide dismutase; TGF‐ β SUPEROXIDE-DISMUTASE; TGF-BETA; ORAL TOLERANCE; EXPRESSION; ACTIVATION; DYSFUNCTION; RESPONSES; DISEASE; ALLERGY; LATENT;
D O I
10.1002/eji.202049112
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Treg are known to have a central role in orchestrating immune responses, but less is known about the destiny of Treg after being activated by specific Ags. This study aimed to investigate the role of superoxide dismutase, an active molecule in the regulation of oxidative stress in the body, in the prevention of Treg apoptosis induced by specific Ags. Ag-specific Tregs were isolated from the DO11.10 mouse intestine. A food allergy mouse model was developed with ovalbumin as the specific Ag and here, we observed that exposure to specific Ag induced Treg apoptosis through converting the precursor of TGF-beta to its mature form inside the Tregs. Oxidative stress was induced in Tregs upon exposure to specific Ags, in which Smad3 bound the latency-associated peptide to induce its degradation, converting the TGF-beta precursor to its mature form, TGF-beta. Suppressing oxidative stress in Tregs alleviated the specific Ag-induced Treg apoptosis in in vitro experiments and suppressed experimental food allergy by preventing the specific Ag-induced Treg apoptosis in the intestine. In conclusion, exposure to specific Ags induces Treg apoptosis and it can be prevented by upregulating superoxide dismutase or suppressing reactive oxidative species in Tregs.
引用
收藏
页码:1748 / 1761
页数:14
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