Peng Yuan, Pu Junliang, Tang Chengyong, Wu Zhongjun
The first clinical college of Chongqing Medical University, Chongqing, China.
Department of Hepatobiliary Surgery, the First Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Cell Physiol Biochem. 2017;41(5):2091-2103. doi: 10.1159/000475444. Epub 2017 Apr 17.
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.
Bronchial epithelial cell line 16HBE140 cells were incubated at either 42 °C, 47 °C, 52 °C, or 57 °C for 5 min in a cell incubator and then returned back to normal culture conditions (37 °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, α-ATP, cleaved Poly (ADP-ribose) polymerase (PARP), cleaved caspase-3, gp91phox, p47phox, p67phox, p22phox, p40phox, and Rac were determined by Western blotting. TUNEL staining was used to determine apoptosis.
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.
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.
热会导致支气管上皮细胞凋亡,这是吸入性损伤期间气道损伤的一个已知因素。越来越多的证据表明姜黄素具有抑制细胞凋亡的作用。在本研究中,我们调查了姜黄素是否能抑制支气管上皮细胞中热诱导的细胞凋亡及其潜在机制。
将支气管上皮细胞系16HBE140细胞在细胞培养箱中分别于42℃、47℃、52℃或57℃孵育5分钟,然后恢复到正常培养条件(37℃)。用热枪向大鼠气道吹入热空气建立体内热吸入损伤大鼠模型。在有或没有姜黄素处理的情况下,获取16HBE140细胞和肺组织用于进一步研究。通过测量3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐(MTT)的吸光度来测定细胞活力。用2',7'-二氯荧光素二乙酸酯荧光来衡量活性氧(ROS)的产生。通过蛋白质印迹法测定Bcl2、Bax、α-ATP、裂解的聚(ADP-核糖)聚合酶(PARP)、裂解的半胱天冬酶-3、gp91phox、p47phox、p67phox、p22phox、p40phox和Rac的水平。用TUNEL染色来测定细胞凋亡。
热处理引发了16HBE140细胞的凋亡,凋亡分子标志物包括Bcl-2、Bax、裂解的PARP和裂解的半胱天冬酶-3的增加表明了这一点。给予姜黄素显著抑制了16HBE140细胞的凋亡,并抑制了NADPH氧化酶2胞质成分的膜转位以及ROS的产生。姜黄素还逆转了热诱导的Akt和mTOR磷酸化的下调。此外,我们证明了在热诱导的细胞凋亡中,NADPH氧化酶2在Akt/mTOR的上游。大鼠吸入损伤模型在体内也证实了姜黄素对支气管上皮细胞凋亡的保护作用。
本研究表明,姜黄素抑制热诱导细胞凋亡的关键机制之一是通过抑制NADPH氧化酶2并激活支气管上皮细胞中的Akt/mTOR信号通路。