基础医学与临床 ›› 2024, Vol. 44 ›› Issue (12): 1670-1677.doi: 10.16352/j.issn.1001-6325.2024.12.1670

• 研究论文 • 上一篇    下一篇

抑制miR-34a减轻慢性阻塞性肺疾病急性加重期炎性反应

杜敬宇1, 应站专1, 侯宾2, 多杰2, 赵振1*   

  1. 1.南通大学杏林学院附属惠山医院 无锡市惠山区人民医院 呼吸内科,江苏 无锡 214187;
    2.青海省人民医院 呼吸内科,青海 西宁 810007
  • 收稿日期:2024-03-05 修回日期:2024-07-10 出版日期:2024-12-05 发布日期:2024-11-26
  • 通讯作者: *eting@126.com
  • 基金资助:
    无锡市卫生健康委资助科研项目(Q202047); 无锡市第二届“双百”中青年医疗卫生拔尖人才项目(HB2023120)

Inhibition of miR-34a reduces inflammatory response in acute exacerbation of chronic obstructive pulmonary disease

DU Jingyu1, YING Zhanzhuan1, HOU Bin2, DUO Jie2, ZHAO Zhen1*   

  1. 1. Department of Respiratory, Affiliated Hushan Hospital of Nantong University Xingling College, Wuxi Huishan District People's Hospital, Wuxi 214187;
    2. Department of Respiratory, Qinghai Provincial People's Hospital, Xining 810007, China
  • Received:2024-03-05 Revised:2024-07-10 Online:2024-12-05 Published:2024-11-26
  • Contact: *eting@126.com

摘要: 目的 观察慢性阻塞性肺疾病急性加重期(AECOPD)患者肺泡灌洗液中miR-34a及其炎性相关因子的表达水平及其相关机制。方法 分别纳入 COPD 急性加重期患者20例为研究对象组,同期COPD 稳定期患者20例为对照组,采集肺泡灌洗液,同时培养鉴定A549细胞,构建AECOPD模型,分别对细胞进行过表达、抑制 miR-34a及沉默HIF-1α,采集上清液及肺泡上皮细胞。ELISA法检测肺泡灌洗液及细胞上清液中炎性因子IL-6、IL-8、TNF-α、TGF-β的水平,RT-qPCR检测miR-34a和HIF-1α表达,Western blot检测HIF-1α表达。结果 相比于对照组,AECOPD组炎性因子、miR-34a及HIF-1α表达水平明显升高(P<0.05),过表达miR-34a可致HIF-1α和炎性因子表达水平进一步升高(P<0.05),阻断miR-34a可使HIF-1α和炎性因子表达水平明显下降(P<0.05)。AECOPD组HIF-1α表达明显升高(P<0.05),沉默HIF-1α可明显降低炎性因子表达水平(P<0.05),而miR-34a表达水平无明显变化。结论 miR-34a在COPD急性加重期患者中通过调控HIF-1α参与炎性反应损伤,干扰miR-34a/HIF-1α通路可减轻炎性反应程度,为COPD急性加重的靶向干预提供了新的可能性。

关键词: 慢性阻塞性肺疾病急性加重期(AECOPD), 炎性反应, miR-34a, 缺氧诱导因子-1α (HIF-1α)

Abstract: Objective To observe the expression levels and related mechanisms of miR-34a and its inflammatory-related factors in broncho-alveolar lavage fluid of patients with acute exacerbation of chronic obstructive pulmonary disease (AECOPD). Methods Totally 20 patients with acute exacerbation of COPD were recruited as the study group and 20 patients in stable period of COPD were recruited as control group. Bronchoalveolar lavage fluid was collected, A549 cell was cultured and AECOPD cell model was built for evaluating the effects of over-expression of miR-34a, inhibition of miR-34a, and silencing of HIF-1α in cells. ELISA assay was applied to detect the expression of inflammatory factors IL-6, IL-8, TNF-αand TGF-β in bronchoalveolar lavage fluid and cell supernatant. The expression of miR-34a and HIF-1 αwere measured by RT-qPCR, and Western blot was used to detect the expression of HIF-1α. Results Compared with the control group, the expression of inflammatory factors, miR-34a, and HIF-1α in the AECOPD group were significantly elevated (P<0.05). Over-expression of miR-34a led to further elevation of HIF-1α and inflammatory factor expression (P<0.05). Inhibition of miR-34a resulted in a significant decrease of HIF-1α and inflammatory factors (P<0.05). The expression of HIF-1α in the AECOPD group was significantly elevated (P<0.05), and silencing HIF-1α significantly reduced the expression of inflammatory factors(P<0.05). The expression of miR-34a had no significant change. Conclusions miR-34a is involved in the inflammatory damage in patients with acute exacerbation of COPD by regulating HIF-1α. Interfering with the miR-34a/HIF-1α pathway alleviates inflammatory response, so it is a potential target in the treatment of acute exacerbation of COPD.

Key words: acute exacerbation of chronic obstructive pulmonary disease (AECOPD), inflammatory response, miR-34a, hypoxia inducible factor-1α (HIF-1α)

中图分类号: