Regional heterogeneity in response of airway epithelial cells to cigarette smoke

• Published in: BMC pulmonary medicine 2018-09, Vol.18 (1), p.148-148, Article 148
• Main Authors: Baskoro, Hario, Sato, Tadashi, Karasutani, Keiko, Suzuki, Yohei, Mitsui, Aki, Arano, Naoko, Nurwidya, Fariz, Kato, Motoyasu, Takahashi, Fumiyuki, Kodama, Yuzo, Seyama, Kuniaki, Takahashi, Kazuhisa
• Format: Article
• Language: English
• Subjects: Airway epithelial cells; Airway management; Animals; Blotting, Western; Bronchi - metabolism; Cell growth; Cells, Cultured; Chronic obstructive pulmonary disease; Cigarette smoke; Cigarettes; Cyclooxygenase-2; DNA microarrays; Emphysema; Epithelial cells; Epithelial Cells - metabolism; Fibroblasts; Gene expression; Health aspects; Humans; Immunohistochemistry; Inflammation; Lung - metabolism; Lung diseases; Lung diseases, Obstructive; Lungs; Mice; Microarray Analysis; Mortality; mRNA; Obstructive lung disease; Protein expression; Proteins; Pulmonology; Real-Time Polymerase Chain Reaction; Respiratory diseases; Respiratory Mucosa - metabolism; Respiratory tract; Risk factors; Signal Transduction; Small airway; Smoking; Smoking - adverse effects; Smoking cessation; Transcriptome
• ISSN: 1471-2466; 1471-2466
• DOI: 10.1186/s12890-018-0715-4

Cigarette smoke (CS) exposure causes an abnormal inflammatory response, which can result in chronic obstructive pulmonary disease (COPD). Previous studies show that this disorder predominantly occurs in peripheral or small-airway areas, whereas the same condition has not been identified in the larger airways during the course of COPD. However, the different biochemical and genetic alterations occurring in response to CS exposure among airway epithelial cells from different sites in the lungs have not been fully investigated. Human small airway epithelial cells (SAECs) and normal human bronchial epithelial cells (NHBEs) were exposed to CS extract (CSE), and microarray analysis was used to determine gene- and protein-expression profiles and identify alterations following CSE exposure in both cell types. An in vivo smoking experiment was also performed to confirm differential responses to CS between sites in the lung. Microarray analysis of SAECs and NHBEs following 24 h of CSE exposure showed that inflammatory related pathways and terms, including the tumor necrosis factor-signaling pathway, were overrepresented, especially in SAECs. Clustering analysis highlighted prostaglandin-endoperoxide synthase-2 [also known as cyclooxygenase (COX)-2] as a gene specifically upregulated in SAECs, with COX-2 mRNA and protein expression significantly elevated by CSE exposure in SAECs (3.1- and 3.1-fold, respectively), but not in NHBEs. Furthermore, time-course analysis of COX-2 expression revealed earlier increases in SAECs compared with NHBEs following CS exposure. Short-term exposure of mouse lungs to CS was found to predominantly induce COX-2 expression in the small airway. The small airway is more susceptible to CSE than the large airway and could be the initial site of development of CS-related respiratory diseases, such as COPD.