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Published in: BMC Pulmonary Medicine 1/2018

Open Access 01-12-2018 | Research article

Regional heterogeneity in response of airway epithelial cells to cigarette smoke

Authors: Hario Baskoro, Tadashi Sato, Keiko Karasutani, Yohei Suzuki, Aki Mitsui, Naoko Arano, Fariz Nurwidya, Motoyasu Kato, Fumiyuki Takahashi, Yuzo Kodama, Kuniaki Seyama, Kazuhisa Takahashi

Published in: BMC Pulmonary Medicine | Issue 1/2018

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Abstract

Background

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.

Methods

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.

Results

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.

Conclusions

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.
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Metadata
Title
Regional heterogeneity in response of airway epithelial cells to cigarette smoke
Authors
Hario Baskoro
Tadashi Sato
Keiko Karasutani
Yohei Suzuki
Aki Mitsui
Naoko Arano
Fariz Nurwidya
Motoyasu Kato
Fumiyuki Takahashi
Yuzo Kodama
Kuniaki Seyama
Kazuhisa Takahashi
Publication date
01-12-2018
Publisher
BioMed Central
Published in
BMC Pulmonary Medicine / Issue 1/2018
Electronic ISSN: 1471-2466
DOI
https://doi.org/10.1186/s12890-018-0715-4

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