Wen Wen, Yu Guoqing, Liu Wei, Gu Lei, Chu Jiahui, Zhou Xiao, Liu Yuebin, Lai Guoxiang
Department of Respiratory and Critical Care Medicine, Fuzhou General Hospital of Fujian Medical University, Dongfang Hospital of Xiamen University, 900th Hospital of the Joint Logistics Support Force, Fuzhou, P.R. China.
J Cell Biochem. 2019 Oct;120(10):17602-17615. doi: 10.1002/jcb.29028. Epub 2019 Jun 25.
Chronic obstructive pulmonary disease (COPD) is a major global epidemic with increasing incidence worldwide. The pathogenesis of COPD is involved with mitochondrial autophagy. Recently, it has been reported that FUN14 domain containing 1 (FUNDC1) is a mediator of mitochondrial autophagy. Therefore, we hypothesized that FUNDC1 was involved in cigarette smoke (CS)-induced COPD progression by regulating mitochondrial autophagy. In vitro cigarette smoke extract (CSE)-treated human bronchial epithelial cell (hBEC) Beas-2B cell line and in vivo CS-induced COPD mouse models were developed, in which FUNDC1 expression was measured. Next, whether FUNDC1 interacted with dynamin-related protein 1 (DRP1) in COPD was investigated. The functional mechanism of FUNDC1 in COPD was evaluated through gain- or loss-of-function studies. Then, pulmonary function, mitochondrial transmembrane potential (MTP) and mucociliary clearance (MCC) were examined. Levels of interleukin-6 (IL-6) and tumor necrosis factor-α (TNF-α) and expression of autophagy-specific markers (light chain 3 [LC3] II, LC3 I, and Tom20) were measured. Finally, apoptosis and mitochondrial autophagy were assessed. FUNDC1 was highly expressed in CSE-treated hBECs and COPD mice. Meanwhile, FUNDC1 was proved to interact with DRP1 in CSE-treated cells. Moreover, in CSE-treated hBECs, silencing FUNDC1 was observed to reduce levels of IL-6 and TNF-α, and MTP but increase MCC, and inhibit CSE-induced mitochondrial autophagy and Beas-2B cell apoptosis, which was consistent with the trend in COPD mouse models. In addition, pulmonary function of COPD mouse models was increased in response to FUNDC1 silencing. Finally, silencing of DRP1 also inhibited mitochondrial autophagy and Beas-2B cell apoptosis. Collectively, FUNDC1 silencing could suppress the progression of COPD by inhibiting mitochondrial autophagy and hBEC apoptosis through interaction with DRP1, highlighting a potential therapeutic target for COPD treatment.
慢性阻塞性肺疾病(COPD)是一种主要的全球性流行病,在全球范围内发病率不断上升。COPD的发病机制与线粒体自噬有关。最近,有报道称含FUN14结构域1(FUNDC1)是线粒体自噬的介导因子。因此,我们推测FUNDC1通过调节线粒体自噬参与香烟烟雾(CS)诱导的COPD进展。建立了体外香烟烟雾提取物(CSE)处理的人支气管上皮细胞(hBEC)Beas-2B细胞系和体内CS诱导的COPD小鼠模型,并检测了FUNDC1的表达。接下来,研究了COPD中FUNDC1是否与动力相关蛋白1(DRP1)相互作用。通过功能获得或功能丧失研究评估了FUNDC1在COPD中的功能机制。然后,检测了肺功能、线粒体跨膜电位(MTP)和黏液纤毛清除率(MCC)。测量了白细胞介素-6(IL-6)和肿瘤坏死因子-α(TNF-α)的水平以及自噬特异性标志物(轻链3 [LC3] II、LC3 I和Tom20)的表达。最后,评估了细胞凋亡和线粒体自噬。FUNDC1在CSE处理的hBECs和COPD小鼠中高表达。同时,在CSE处理的细胞中证明FUNDC1与DRP1相互作用。此外,在CSE处理的hBECs中,观察到沉默FUNDC1可降低IL-6和TNF-α水平以及MTP,但增加MCC,并抑制CSE诱导的线粒体自噬和Beas-2B细胞凋亡,这与COPD小鼠模型中的趋势一致。此外,COPD小鼠模型的肺功能因FUNDC1沉默而增强。最后,沉默DRP1也抑制了线粒体自噬和Beas-2B细胞凋亡。总的来说,FUNDC1沉默可通过与DRP1相互作用抑制线粒体自噬和hBEC凋亡,从而抑制COPD的进展,突出了一个潜在的COPD治疗靶点。