Cigarette smoke augments the expression and responses of toll-like receptor 3 in human macrophages

Akira Koarai, Satoru Yanagisawa, Hisatoshi Sugiura, Tomohiro Ichikawa, Keiichiro Akamatsu, Tsunahiko Hirano, Masanori Nakanishi, Kazuto Matsunaga, Yoshiaki Minakata, Masakazu Ichinose

Research output: Contribution to journalArticlepeer-review

17 Citations (Scopus)

Abstract

Background and objective: Cigarette smoking is the main risk factor for the development of chronic obstructive pulmonary disease (COPD). Recently, toll-like receptor 3 (TLR3) was shown to recognize pathogen-associated molecular patterns, especially viral-derived double-stranded RNA, and to be involved in immune responses. However, the effects of cigarette smoke on TLR3 remain unclear. In this study, it was examined whether cigarette smoke affects the expression and responses of TLR3 in human macrophages. Methods: The expression of TLR3 in alveolar macrophages from human lung tissues was analysed by immunohistochemistry, and the correlation of TLR3 expression with smoking history and lung function was evaluated. In addition, the effect of cigarette smoke on the expression and responses of TLR3 in macrophage lineage cells was investigated. Results: TLR3-positive alveolar macrophage numbers were significantly increased in smokers and COPD patients compared with non-smoking control subjects, but there was no difference between smokers and COPD patients. TLR3-positive macrophage numbers were positively correlated with smoking history and inversely correlated with corrected carbon monoxide diffusing capacity, but were not correlated with % predicted forced expiratory volume in 1 s. Furthermore, cigarette smoke extract potentiated the expression of TLR3 in monocyte-derived macrophages and significantly augmented the release of interleukin-8, as well as total matrix metalloproteinase-9 activity, in cells treated with TLR3 ligand. Conclusions: These data suggest that cigarette smoke augments the expression and responses of TLR3 in human macrophages, and this may contribute to neutrophilic airway inflammation and parenchymal destruction in the lungs of smokers and patients with COPD. The expression of TLR3 was increased in macrophages from smokers and COPD patients, and cigarette smoke potentiated the expression and responses of TLR3 in macrophage lineage cells. This may contribute to neutrophilic airway inflammation and parenchymal destruction in the lungs of smokers and COPD patients.

Original languageEnglish
Pages (from-to)1018-1025
Number of pages8
JournalRespirology
Volume17
Issue number6
DOIs
Publication statusPublished - 2012 Aug

Keywords

  • chronic obstructive pulmonary disease
  • innate immunity
  • metalloproteinase
  • pulmonary diffusing capacity
  • smoking

ASJC Scopus subject areas

  • Pulmonary and Respiratory Medicine

Fingerprint Dive into the research topics of 'Cigarette smoke augments the expression and responses of toll-like receptor 3 in human macrophages'. Together they form a unique fingerprint.

Cite this