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Quercetin Improves Epithelial Regeneration from Airway Basal Cells of COPD Patients

Overview
Journal Respir Res
Specialty Pulmonary Medicine
Date 2024 Mar 12
PMID 38468259
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Abstract

Background: 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.

Methods: 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.

Results: 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.

Conclusions: These results indicate that quercetin may improve airway epithelial regeneration by increasing the expression of genes involved in epithelial development/differentiation in COPD.

Trial Registration: This study was registered at ClinicalTrials.gov on 6-18-2019. The study number is NCT03989271.

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References
1.
Gohy S, Hupin C, Fregimilicka C, Detry B, Bouzin C, Gaide Chevronay H . Imprinting of the COPD airway epithelium for dedifferentiation and mesenchymal transition. Eur Respir J. 2015; 45(5):1258-72. DOI: 10.1183/09031936.00135814. View

2.
Rock J, Onaitis M, Rawlins E, Lu Y, Clark C, Xue Y . Basal cells as stem cells of the mouse trachea and human airway epithelium. Proc Natl Acad Sci U S A. 2009; 106(31):12771-5. PMC: 2714281. DOI: 10.1073/pnas.0906850106. View

3.
Unger B, Ganesan S, Comstock A, Faris A, Hershenson M, Sajjan U . Nod-like receptor X-1 is required for rhinovirus-induced barrier dysfunction in airway epithelial cells. J Virol. 2014; 88(7):3705-18. PMC: 3993547. DOI: 10.1128/JVI.03039-13. View

4.
Ganesan S, Pham D, Jing Y, Farazuddin M, Hudy M, Unger B . TLR2 Activation Limits Rhinovirus-Stimulated CXCL-10 by Attenuating IRAK-1-Dependent IL-33 Receptor Signaling in Human Bronchial Epithelial Cells. J Immunol. 2016; 197(6):2409-20. PMC: 5070654. DOI: 10.4049/jimmunol.1502702. View

5.
Comstock A, Ganesan S, Chattoraj A, Faris A, Margolis B, Hershenson M . Rhinovirus-induced barrier dysfunction in polarized airway epithelial cells is mediated by NADPH oxidase 1. J Virol. 2011; 85(13):6795-808. PMC: 3126521. DOI: 10.1128/JVI.02074-10. View