Resveratrol attenuates inflammation and apoptosis through alleviating endoplasmic reticulum stress via Akt/mTOR pathway in fungus-induced allergic airways inflammation

被引:16
作者
Wang, Sijiao [1 ]
Gong, Linjing [4 ]
Mo, Yuqing [1 ]
Zhang, Jun [1 ]
Jiang, Zhilong [1 ]
Tian, Zhengan [3 ]
Shao, Changzhou [1 ,2 ]
机构
[1] Fudan Univ, Zhongshan Hosp, Shanghai Resp Res Inst, Dept Pulm Med, Shanghai 200032, Peoples R China
[2] Fudan Univ, Zhongshan Hosp, Dept Pulm Med, Xiamen Branch, Xiamen 361015, Peoples R China
[3] Shanghai Int Travel Hlth Care Ctr, Shanghai 200335, Peoples R China
[4] Sichuan Univ, West China Hosp, Dept Resp & Crit Care Med, Chengdu 610041, Peoples R China
基金
中国国家自然科学基金;
关键词
Resveratrol; Allergic lung disease; Aspergillus fumigatus; Endoplasmic reticulum stress; Apoptosis; BRONCHOPULMONARY ASPERGILLOSIS; ASTHMA; MODEL; MICE;
D O I
10.1016/j.intimp.2021.108489
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Background: Resveratrol has shown pleiotropic effects against inflammation and oxidative response. The present study aimed to investigate the effects and mechanisms of resveratrol on fungus-induced allergic airway inflammation. Methods: Female BALB/c mice were injected intraperitoneally with Aspergillus fumigatus (Af) extract emulsified with aluminum on day 0 and 7 and intranasally challenged with Af extracts on day 14 and 15. Resveratrol or dexamethasone or a vehicle was injected intraperitoneally 1 h before each challenge. Mice were sacrificed for serum, bronchoalveolar lavage fluid (BALF), and lungs 24 h after the last challenge. The control group was administered with saline. BEAS-2B was used for the experiments in vitro that Af-exposed airway epithelial cells. Results: Resveratrol and dexamethasone attenuated the airway inflammation and eosinophilia, and reduced not only the production of IL-4, IL-5, and IL-13 in the BALF and lung tissues but also the mRNA levels of lung IL-6, TNF-alpha, and TGF-beta induced by Af challenge (P < 0.05). Furthermore, Af-induced lung endoplasmic reticulum (ER) stress-related proteins PERK, CHOP, and GRP78 and the apoptosis markers including cleaved caspase-3 and cleaved caspase-7 were both suppressed significantly by resveratrol (P < 0.05). In vitro, activation of ER stress and the Akt/mTOR pathway in Af-exposed BEAS-2B cells were effectively ameliorated by resveratrol. Inhibition of the Akt/mTOR pathway using LY294002 suppressed the ER stress while ER stress inhibitor 4-PBA decreased the apoptosis in Af-exposed BEAS-2B cells. Conclusions: Our findings collectively revealed that resveratrol alleviated the Af-exposed allergic inflammation and apoptosis through inhibiting ER stress via Akt/mTOR pathway, exerting therapeutic effects on the fungus induced allergic lung disorder.
引用
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页数:10
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