槲皮素能改善慢性阻塞性肺病患者气道基底细胞的上皮再生能力

IF 4.7 2区 医学 Q1 RESPIRATORY SYSTEM Respiratory Research Pub Date : 2024-03-11 DOI:10.1186/s12931-024-02742-0
Elizabeth S. McCluskey, Nathan Liu, Abhimaneu Pandey, Nathaniel Marchetti, Steven G. Kelsen, Umadevi S. Sajjan
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引用次数: 0

摘要

慢性阻塞性肺病(COPD)患者的气道基底细胞(BC)会再生出异常的气道上皮,这与参与上皮修复的多个基因表达量减少有关。槲皮素能减少慢性阻塞性肺病模型中的气道上皮重塑和炎症,因此我们研究了槲皮素是否能通过改变基因表达促进慢性阻塞性肺病BC的正常上皮再生。用 DMSO 或 1 µM 槲皮素处理 COPD BC 三天后,在空气/液体界面(ALI)培养长达 4 周。在 ALI 条件下培养的健康供体 BC 作为对照。在 ALI 8 天时测定细胞的极化。分化细胞培养物中的细胞类型和 IL-8 表达分别通过流式细胞仪和 ELISA 进行量化。对经 DMSO 或 1 µM 槲皮素处理 3 天的 COPD BC 进行微阵列分析,以确定差异调控基因(DEG)。为了证实槲皮素对基因表达的影响,研究人员对年龄和疾病状况相似的慢性阻塞性肺病患者进行了为期 6 个月的支气管刷检,这些患者分别接受了安慰剂(4 人)或每天 2000 毫克槲皮素(7 人)的治疗。与安慰剂相比,接受槲皮素治疗的慢性阻塞性肺疾病 BC 患者的跨上皮阻力明显增加,纤毛细胞增多,鹅口疮细胞减少,IL-8 降低。槲皮素能上调 COPD BC 中与组织和上皮发育及分化相关的基因。接受槲皮素治疗的慢性阻塞性肺病患者(而非安慰剂)的两个发育基因HOXB2和ELF3的表达量有所增加,槲皮素治疗的慢性阻塞性肺病BC中这两个基因的表达量也有所增加,FDR<0.001。活跃吸烟者的TGF-β(0.067)和IL-8(22.0)的mRNA表达增加,槲皮素治疗后这两种基因的表达分别减少了3.6倍和4.14倍。这些结果表明,槲皮素可通过增加慢性阻塞性肺病患者上皮发育/分化相关基因的表达来改善气道上皮再生。本研究于2019年6月18日在ClinicalTrials.gov注册。研究编号为 NCT03989271。
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Quercetin improves epithelial regeneration from airway basal cells of COPD patients
Airway basal cells (BC) from patients with chronic obstructive pulmonary disease (COPD) regenerate abnormal airway epithelium and this was associated with reduced expression of several genes involved in epithelial repair. Quercetin reduces airway epithelial remodeling and inflammation in COPD models, therefore we examined whether quercetin promotes normal epithelial regeneration from COPD BC by altering gene expression. COPD BC treated with DMSO or 1 µM quercetin for three days were cultured at air/liquid interface (ALI) for up to 4 weeks. BC from healthy donors cultured at ALI were used as controls. Polarization of cells was determined at 8 days of ALI. The cell types and IL-8 expression in differentiated cell cultures were quantified by flow cytometry and ELISA respectively. Microarray analysis was conducted on DMSO or 1 µM quercetin-treated COPD BC for 3 days to identify differentially regulated genes (DEG). Bronchial brushings obtained from COPD patients with similar age and disease status treated with either placebo (4 subjects) or 2000 mg/day quercetin (7 subjects) for 6 months were used to confirm the effects of quercetin on gene expression. Compared to placebo-, quercetin-treated COPD BC showed significantly increased transepithelial resistance, more ciliated cells, fewer goblet cells, and lower IL-8. Quercetin upregulated genes associated with tissue and epithelial development and differentiation in COPD BC. COPD patients treated with quercetin, but not placebo showed increased expression of two developmental genes HOXB2 and ELF3, which were also increased in quercetin-treated COPD BC with FDR < 0.001. Active smokers showed increased mRNA expression of TGF-β (0.067) and IL-8 (22.0), which was reduced by 3.6 and 4.14 fold respectively after quercetin treatment. These results indicate that quercetin may improve airway epithelial regeneration by increasing the expression of genes involved in epithelial development/differentiation in COPD. This study was registered at ClinicalTrials.gov on 6-18-2019. The study number is NCT03989271.
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来源期刊
Respiratory Research
Respiratory Research 医学-呼吸系统
自引率
1.70%
发文量
314
期刊介绍: Respiratory Research publishes high-quality clinical and basic research, review and commentary articles on all aspects of respiratory medicine and related diseases. As the leading fully open access journal in the field, Respiratory Research provides an essential resource for pulmonologists, allergists, immunologists and other physicians, researchers, healthcare workers and medical students with worldwide dissemination of articles resulting in high visibility and generating international discussion. Topics of specific interest include asthma, chronic obstructive pulmonary disease, cystic fibrosis, genetics, infectious diseases, interstitial lung diseases, lung development, lung tumors, occupational and environmental factors, pulmonary circulation, pulmonary pharmacology and therapeutics, respiratory immunology, respiratory physiology, and sleep-related respiratory problems.
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