Cigarette smoke extract mediates cell premature senescence in chronic obstructive pulmonary disease patients by up-regulating USP7 to activate p300-p53/p21 pathway. (15th April 2022)

• Record Type: Journal Article
• Authors: Zeng, Menghao; Zhang, Xuefeng; Xing, Wei; Wang, Qianlu; Liang, Guibin; He, Zhihui
• Is Part Of: Toxicology letters. Volume 359(2022)
• Page Start: 31
• Page End: 45
• Publication Date: 2022-04-15
• Subjects: COPD -- EPCs -- USP7 -- p300 -- p53 - p21 pathway; Toxicology -- Periodicals; 363.179
• DOI: 10.1016/j.toxlet.2022.01.017
• Languages: English
• ISSNs: 0378-4274

Abstract

Highlights: In this study, we tried to explore the interaction and regulation mechanism of USP7 and p300 in EPCs of COPD patients and COPD mouse model. CSE was also used to test the p300 - p53 / p21 pathway activity, so as to propose valuable ideas for inhibiting EPC cell aging, and provide new therapeutic targets and methods for the treatment of smoking caused COPD. In addition, this study showed that targeting p53 / p21 pathway had potential clinical application prospects in the treatment of COPD. Abstract: Objectives: Tobacco hazard is one of the most severe public health issues in the world. It is believed that smoking is the most important factor leading to chronic obstructive pulmonary disease (COPD). Endothelial progenitor cells (EPCs) originate from the bone marrow and can effectively repair vascular endothelial damage and improve vascular endothelial function. Current studies suggest that EPCs senescence and EPCs depletion exist in smoking-related COPD, but the molecular mechanism remains unclear. Methods: Co-immunoprecipitation was used to detect the interaction between USP7 and p300. EPCs from smoking COPD patients were isolated, and the expressions of USP7 and p300 were detected by RT-PCR and Western Blot. Different concentrations of cigarette smoke extract (CSE) and USP7 or p300 inhibitors were used to treat EPCs, then the expression of p53, p53 target genes and aging-related genes were detected. Cell Counting Kit - 8 (CCK8) was used to detect cell proliferation, flow cytometry was used to detect cell cycle distribution, β-galactosidase (β-gal) staining and Lamp1 immunofluorescence was used to detect the proportion of aging cells. COPD mouse models were used to confirm the molecular mechanism. Results: USP7 and p300 interacted with each other, and USP7 affected the protein stability of p300 by regulating the ubiquitination of p300. There existed high expressions of USP7 and p300 proteins in EPCs of smoking COPD patients and COPD mouse model. CSE promoted the high expressions of USP7 and p300 in EPCs. Further studies showed that CSE mediated the USP7/p300-dependent high expression of p53 and activated the expression of p53 target genes especially p21. Activation of p53 - p21 pathway finally inhibited cell activity, led to cell cycle arrest and premature senescence of EPCs. Conclusion: CSE mediated up-regulation of USP7 and p300 activated p53 - p21 pathway was a molecular mechanism that might lead to COPD.