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Mechanism of cigarette smoke in promoting small airway remodeling in mice via STAT 3 / PINK 1-Parkin / EMT.
- Source :
-
Free radical biology & medicine [Free Radic Biol Med] 2024 Nov 01; Vol. 224, pp. 447-456. Date of Electronic Publication: 2024 Aug 29. - Publication Year :
- 2024
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Abstract
- 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.<br />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).<br />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.<br />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.<br />Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.<br /> (Copyright © 2024 Elsevier Inc. All rights reserved.)
- Subjects :
- Animals
Mice
Male
Humans
Smoke adverse effects
Signal Transduction
Mice, Inbred C57BL
Lung pathology
Lung metabolism
Mitochondria metabolism
Mitochondria pathology
Mitophagy
Transforming Growth Factor beta1 metabolism
Transforming Growth Factor beta1 genetics
Cigarette Smoking adverse effects
Airway Remodeling
STAT3 Transcription Factor metabolism
STAT3 Transcription Factor genetics
Epithelial-Mesenchymal Transition
Ubiquitin-Protein Ligases metabolism
Ubiquitin-Protein Ligases genetics
Protein Kinases metabolism
Protein Kinases genetics
Pulmonary Disease, Chronic Obstructive pathology
Pulmonary Disease, Chronic Obstructive metabolism
Pulmonary Disease, Chronic Obstructive chemically induced
Pulmonary Disease, Chronic Obstructive etiology
Subjects
Details
- Language :
- English
- ISSN :
- 1873-4596
- Volume :
- 224
- Database :
- MEDLINE
- Journal :
- Free radical biology & medicine
- Publication Type :
- Academic Journal
- Accession number :
- 39214258
- Full Text :
- https://doi.org/10.1016/j.freeradbiomed.2024.08.036