P38 Mitogen-activated protein kinase accelerates emphysema in mouse model of chronic obstructive pulmonary disease. (August 2014)

• Record Type: Journal Article
• Authors: Amano, Hiroyuki; Murata, Kazuya; Matsunaga, Hirofumi; Tanaka, Kensuke; Yoshioka, Kento; Kobayashi, Takeshi; Ishida, Junji; Fukamizu, Akiyoshi; Sugiyama, Fumihiro; Sudo, Tatsuhiko; Kimura, Sadao; Tatsumi, Koichiro; Kasuya, Yoshitoshi
• Is Part Of: Journal of receptor and signal transduction research. Volume 34:Number 4(2014)
• Page Start: 299
• Page End: 306
• Publication Date: 2014-08
• Subjects: Cell receptors -- Periodicals; Cellular signal transduction -- Periodicals; 571.6
• DOI: 10.3109/10799893.2014.896380
• Languages: English
• ISSNs: 1079-9893

Abstract

<abstract> <title>Abstract</title> <p> <italic>Context</italic>: There are few short-term mouse models of chronic obstructive pulmonary disease (COPD) mimicking the human disease. In addition, p38 is recently recognized as a target for the treatment of COPD. However, the precise mechanism how p38 contributes to the pathogenesis of COPD is still unknown. <italic>Objective</italic>: We attempted to create a new mouse model for COPD by intra-tracheal administration of a mixture of lipopolysaccharide (LPS) and cigarette smoke solution (CSS), and investigated the importance of the p38 mitogen-activated protein kinase (p38) pathway in the pathogenesis of COPD. <italic>Methods</italic>: Mice were administered LPS + CSS once a day on days 0–4 and 7–11. Thereafter, CSS alone was administered to mice once a day on days 14–18. On day 28, histopathological changes of the lung were evaluated, and bronchoalveolar lavage fluid (BALF) was subjected to western blot array for cytokines. Transgenic (TG) mice expressing a constitutive-active form of MKK6, a p38-specific activator in the lung, were subjected to our experimental protocol of COPD model. <italic>Results</italic>: LPS + CSS administration induced enlargement of alveolar air spaces and destruction of lung parenchyma. BALF analyses of the LPS + CSS group revealed an increase in expression levels of several cytokines involved in the pathogenesis of human COPD. These results suggest that our experimental protocol can induce COPD in mice. Likewise, histopathological findings of the lung and induction of cytokines in BALF from MKK6 c.a.-TG mice were more marked than those in WT mice. <italic>Conclusion</italic>: In a new experimental COPD mouse model, p38 accelerates the development of emphysema.</p> </abstract>