Respiratory Medicine, Allergology and Palliative Medicine, Department of Clinical Sciences, Lund, Lund University, 221 84 Lund, Sweden.
Respiratory Cell Biology, Department of Experimental Medical Science, Lund University, 221 84 Lund, Sweden.
Int J Mol Sci. 2024 Jun 15;25(12):6600. doi: 10.3390/ijms25126600.
Chronic obstructive pulmonary disease (COPD) is commonly caused from smoking cigarettes that induce biological stress responses. Previously we found disorganized endoplasmic reticulum (ER) in fibroblasts from COPD with different responses to chemical stressors compared to healthy subjects. Here, we aimed to investigate differences in stress-related gene expressions within lung cells from COPD and healthy subjects. Bronchoalveolar lavage (BAL) cells were collected from seven COPD and 35 healthy subjects. Lung fibroblasts were derived from 19 COPD and 24 healthy subjects and exposed to cigarette smoke extract (CSE). Gene and protein expression and cell proliferation were investigated. Compared to healthy subjects, we found lower gene expression of CHOP in lung fibroblasts from COPD subjects. Exposure to CSE caused inhibition of lung fibroblast proliferation in both groups, though the changes in ER stress-related gene expressions (ATF6, IRE1, PERK, ATF4, CHOP, BCL2L1) and genes relating to proteasomal subunits mostly occurred in healthy lung fibroblasts. No differences were found in BAL cells. In this study, we have found that lung fibroblasts from COPD subjects have an atypical ER stress gene response to CSE, particularly in genes related to apoptosis. This difference in response to CSE may be a contributing factor to COPD progression.
慢性阻塞性肺疾病(COPD)通常由吸烟引起,吸烟会引起生物应激反应。先前我们发现,COPD 患者的成纤维细胞内质网(ER)紊乱,对化学应激因子的反应与健康受试者不同。在这里,我们旨在研究 COPD 患者和健康受试者肺细胞中与应激相关的基因表达差异。从 7 名 COPD 患者和 35 名健康受试者中收集支气管肺泡灌洗液(BAL)细胞。从 19 名 COPD 患者和 24 名健康受试者中分离出肺成纤维细胞,并暴露于香烟烟雾提取物(CSE)中。研究了基因和蛋白质表达以及细胞增殖。与健康受试者相比,我们发现 COPD 患者肺成纤维细胞中 CHOP 的基因表达较低。CSE 暴露导致两组肺成纤维细胞增殖受到抑制,但 ER 应激相关基因表达(ATF6、IRE1、PERK、ATF4、CHOP、BCL2L1)和与蛋白酶体亚基相关的基因的变化主要发生在健康肺成纤维细胞中。BAL 细胞中未发现差异。在这项研究中,我们发现 COPD 患者的肺成纤维细胞对 CSE 的 ER 应激基因反应异常,特别是与细胞凋亡相关的基因。对 CSE 的这种不同反应可能是 COPD 进展的一个促成因素。