RETRACTED: Curcumin Inhibits Heat-Induced Apoptosis by Suppressing NADPH Oxidase 2 and Activating the Akt/mTOR Signaling Pathway in Bronchial Epithelial Cells (Retracted article. See vol. 56, pg. 609, 2022)

被引:13
|
作者
Peng, Yuan [1 ]
Pu, Junliang [2 ]
Tang, Chengyong [3 ]
Wu, Zhongjun [2 ]
机构
[1] Chongqing Med Univ, Clin Coll 1, Chongqing, Peoples R China
[2] Chongqing Med Univ, Dept Hepatobiliary Surg, Affiliated Hosp 1, Chongqing 400016, Peoples R China
[3] Chongqing Med Univ, Dept Clin Pharmacol, Affiliated Hosp 1, Chongqing, Peoples R China
关键词
Curcumin; Heat; Apoptosis; NADPH Oxidase 2; Akt/mTOR; Thermal Inhalation Injury; OXIDATIVE STRESS; CIGARETTE-SMOKE; INHALATION; EXPRESSION; INFLAMMATION; AIRWAY;
D O I
10.1159/000475444
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Background: Heat causes bronchial epithelial cell apoptosis, which is a known factor contributing to airway damage during inhalation injury. Accumulating evidence has shown the effect of curcumin on inhibiting apoptosis. In this study, we investigated whether curcumin suppresses heat-induced apoptosis in bronchial epithelial cells and the underlying mechanism. Methods: Bronchial epithelial cell line 16HBE140 cells were incubated at either 42 degrees C, 47 degrees C, 52 degrees C, or 57 degrees C for 5 min in a cell incubator and then returned back to normal culture conditions (37 degrees C). An in vivo thermal inhalation injury rat model was established with a heat gun blowing hot air into the airway of rats. 16HBE140 cells and lung tissue were obtained for further study with or without curcumin treatment. Cell viability was determined by measuring the absorbance of 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT). 2',7'-dichlorofluorescein diacetate fluorescence was used as a measure of reactive oxygen species (ROS) production. Levels of Bcl2, Bax, alpha-ATP, cleaved Poly (ADP-ribose) polymerase (PARP), cleaved caspase-3, gp91(phox), p47(phox), p67(phox), p22(phox), p40(phox), and Rac were determined by Western blotting. TUNEL staining was used to determine apoptosis. Results: Heat treatment triggered the apoptosis of 16HBE140 cells as shown by the increase in apoptosis molecular markers, including Bcl-2, Bax, cleaved PARP, and cleaved caspase-3. Administration of curcumin significantly inhibited apoptosis of 16HBE140 cells and suppressed the membrane translocation of NADPH oxidase 2 cytosolic components, as well as ROS production. Downregulation of Akt and mTOR phosphorylation induced by heat was also reversed by curcumin. Furthermore, we demonstrated that NADPH oxidase 2 is upstream of Akt/mTOR in heat-induced apoptosis. The protective role of curcumin on bronchial epithelia apoptosis was also confirmed in vivo by a rat inhalation injury model. Conclusion: This study demonstrates that one of the critical mechanisms underlying curcumin inhibiting heat-induced apoptosis is through suppressing NADPH Oxidase 2 and activating the Akt/mTOR signaling pathway in bronchial epithelial cells. (C) 2017 The Author(s) Published by S. Karger AG, Basel.
引用
收藏
页码:2091 / 2103
页数:13
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