Khedoe P P S J, van Schadewijk W A A M, Schwiening M, Ng-Blichfeldt J P, Marciniak S J, Stolk J, Gosens R, Hiemstra P S
Department of Pulmonology, Leiden University Medical Centre, Leiden, Netherlands.
Department of Medicine, Cambridge Institute for Medical Research, University of Cambridge, Cambridge, United Kingdom.
Front Cell Dev Biol. 2023 Sep 19;11:1165581. doi: 10.3389/fcell.2023.1165581. eCollection 2023.
Adequate lung epithelial repair relies on supportive interactions within the epithelial niche, including interactions with WNT-responsive fibroblasts. In fibroblasts from patients with chronic obstructive pulmonary disease (COPD) or upon cigarette smoke exposure, Wnt/β-catenin signalling is distorted, which may affect interactions between epithelial cells and fibroblasts resulting in inadequate lung repair. We hypothesized that cigarette smoke (CS), the main risk factor for COPD, interferes with Wnt/β-catenin signalling in fibroblasts through induction of cellular stress responses, including oxidative- and endoplasmic reticulum (ER) stress, and thereby alters epithelial repair support potential. Therefore, we assessed the effect of CS-exposure and the ER stress inducer Thapsigargin (Tg) on Wnt/β-catenin signalling activation in MRC-5 fibroblasts, and on their ability to support lung epithelial organoid formation. Exposure of MRC-5 cells for 15 min with 5 AU/mL CS extract (CSE), and subsequent 6 h incubation induced oxidative stress (). Whereas stimulation with 100 nM Tg increased markers of both the integrated stress response (ISR - /, ) and the unfolded protein response (UPR - , , and ), CSE only induced / expression. Strikingly, although treatment of MRC-5 cells with the Wnt activator CHIR99021 upregulated the Wnt/β-catenin target gene this response was diminished upon CSE or Tg pre-exposure, which was confirmed using a Wnt-reporter. Furthermore, pre-exposure of MRC-5 cells to CSE or Tg, restricted their ability to support organoid formation upon co-culture with murine pulmonary EpCam cells in Matrigel at day 14. This restriction was alleviated by pre-treatment with CHIR99021. We conclude that exposure of MRC-5 cells to CSE increases oxidative stress, expression and impairs their ability to support organoid formation. This inhibitory effect may be restored by activating the Wnt/β-catenin signalling pathway.
充足的肺上皮修复依赖于上皮生态位内的支持性相互作用,包括与WNT反应性成纤维细胞的相互作用。在慢性阻塞性肺疾病(COPD)患者的成纤维细胞中或暴露于香烟烟雾后,Wnt/β-连环蛋白信号传导会发生扭曲,这可能会影响上皮细胞与成纤维细胞之间的相互作用,导致肺修复不足。我们假设,COPD的主要危险因素香烟烟雾(CS)通过诱导细胞应激反应,包括氧化应激和内质网(ER)应激,干扰成纤维细胞中的Wnt/β-连环蛋白信号传导,从而改变上皮修复支持潜能。因此,我们评估了CS暴露和ER应激诱导剂毒胡萝卜素(Tg)对MRC-5成纤维细胞中Wnt/β-连环蛋白信号传导激活的影响,以及它们支持肺上皮类器官形成的能力。用5 AU/mL CS提取物(CSE)处理MRC-5细胞15分钟,随后孵育6小时可诱导氧化应激()。而用100 nM Tg刺激会增加整合应激反应(ISR - /, )和未折叠蛋白反应(UPR -,, 和 )的标志物,CSE仅诱导 / 表达。引人注目的是,尽管用Wnt激活剂CHIR99021处理MRC-5细胞会上调Wnt/β-连环蛋白靶基因 ,但在CSE或Tg预暴露后这种反应会减弱,这通过Wnt报告基因得到证实。此外,MRC-5细胞预先暴露于CSE或Tg后,在第14天与基质胶中的小鼠肺EpCam细胞共培养时,它们支持类器官形成的能力受到限制。用CHIR99021预处理可减轻这种限制。我们得出结论,MRC-5细胞暴露于CSE会增加氧化应激、 表达并损害其支持类器官形成的能力。这种抑制作用可通过激活Wnt/β-连环蛋白信号通路来恢复。