香烟烟雾通过 STAT 3 / PINK 1-Parkin / EMT 促进小鼠小气道重塑的机制

IF 7.1 2区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Free Radical Biology and Medicine Pub Date : 2024-08-29 DOI:10.1016/j.freeradbiomed.2024.08.036
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引用次数: 0

摘要

背景气道重塑是慢性阻塞性肺疾病(COPD)气流受限的重要病理机制,但其机制仍有待进一步明确:动物:将4-6周龄的健康雄性C57BL/6小鼠随机分为对照组和烟雾(CS)组。CS组小鼠被置于自制的玻璃熏蒸器中,5支/次,40分钟/次,4次/天,5天/周,共24周。细胞:BEAS-2B细胞用0.1%香烟烟雾提取物(CSE)刺激,HE染色、免疫组化染色和Masson染色观察肺组织的病理变化,透射电镜观察支气管上皮细胞线粒体的结构。Western印迹法检测STAT3、转化生长因子-β1(TGF-β1)、微管相关蛋白1A/1B-轻链3(LC3)、PINK1、Parkin、E-adherin、Zonula occludens1(ZO-1)、波形蛋白和蜗牛家族转录抑制因子1(Snail1)的表达,MitoSOX Red法检测线粒体活性氧(mtROS)的表达:与对照组相比,CS组小鼠全肺匀浆中p-STAT3、TGF-β1和EMT的表达增加;CS组小鼠支气管上皮细胞线粒体结构破坏,PINK1-Parkin依赖的有丝分裂功能受损。体外实验表明,CSE 暴露导致 STAT3 激活、TGF-β1 增加、EMT 和 PINK1-Parkin 介导的有丝分裂增强。抑制有丝分裂可减少 STAT3 诱导的 EMT:CS激活STAT3,激活的STAT3通过增强PINK1-Parkin介导的有丝分裂和TGF-β1信号传导,促进支气管上皮细胞的EMT。
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Mechanism of cigarette smoke in promoting small airway remodeling in mice via STAT 3 / PINK 1-Parkin / EMT

Background

Airway remodeling is an important pathological of airflow limitation in chronic obstructive pulmonary disease (COPD).However,its mechanism still needs to be further clarify.

Methods

Animals:Healthy male C57BL/6 mice aged 4–6 weeks were randomly divided into control group and cigarette smoke(CS)group. Mice in the CS group were placed in a homemade glass fumigator, 5 cigarettes/time, 40 min/time, 4 times/day, 5 days/week, for 24 weeks. Mice in the control group were placed in a normal air environment.Cells:BEAS-2B cells were stimulated with 0.1%cigarette smoke extract(CSE).HE staining, immunohistochemical staining and Masson staining were used to observe the pathological of lung tissues, transmission electron microscopy was used to observe the structural of mitochondria in bronchial epithelial cells.Western blotting was used to detect the expression of STAT3,transforming growth factor-β1(TGF-β1),microtubule-associated protein 1A/1B-light chain3(LC3),PINK1,Parkin,E-cadherin,zonula occludens1(ZO-1),vimentin and snail family transcriptional inhibitor1 (Snail1),and MitoSOX Red was used to detect mitochondrial reactive oxygen species(mtROS).

Results

CS exposure causes lung parenchymal destruction and airway remodeling in mice.Compared to the control group,the expression of p-STAT3,TGF-β1 and EMT in the whole lung homogenate of the CS group was increased.Mitochondrial architecture disruption in bronchial epithelial cells of CS mice, with impaired PINK1-Parkin-dependent mitophagy.In vitro experiments showed that CSE exposure led to STAT3 activation, increased TGF-β1,EMT and enhanced PINK1-Parkin-mediated mitophagy.STAT3 inhibition reversed TGF-β1 upregulation induced by CSE and improved CSE-induced EMT and mitophagy.Inhibition of mitophagy improves EMT induced by CSE. Inhibition of mitophagy reduces STAT3-induced EMT.

Conclusion

CS activates the STAT3,and activated STAT3 promotes EMT in bronchial epithelial cells by enhancing PINK1-Parkin-mediated mitophagy and TGF-β1 signaling.Moreover, activated STAT3 can promote EMT directly.This may be one of the mechanisms by which CS causes small airway remodeling in COPD.

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来源期刊
Free Radical Biology and Medicine
Free Radical Biology and Medicine 医学-内分泌学与代谢
CiteScore
14.00
自引率
4.10%
发文量
850
审稿时长
22 days
期刊介绍: Free Radical Biology and Medicine is a leading journal in the field of redox biology, which is the study of the role of reactive oxygen species (ROS) and other oxidizing agents in biological systems. The journal serves as a premier forum for publishing innovative and groundbreaking research that explores the redox biology of health and disease, covering a wide range of topics and disciplines. Free Radical Biology and Medicine also commissions Special Issues that highlight recent advances in both basic and clinical research, with a particular emphasis on the mechanisms underlying altered metabolism and redox signaling. These Special Issues aim to provide a focused platform for the latest research in the field, fostering collaboration and knowledge exchange among researchers and clinicians.
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