Inhibitory effects of carbocisteine on type A seasonal influenza virus infection in human airway epithelial cells

被引:24
|
作者
Yamaya, Mutsuo [1 ]
Nishimura, Hidekazu [2 ]
Shinya, Kyoko [3 ]
Hatachi, Yukimasa [4 ]
Sasaki, Takahiko [5 ]
Yasuda, Hiroyasu [6 ]
Yoshida, Motoki [7 ]
Asada, Masanori [7 ]
Fujino, Naoya
Suzuki, Takaya
Deng, Xue [6 ]
Kubo, Hiroshi
Nagatomi, Ryoichi
机构
[1] Tohoku Univ, Dept Adv Prevent Med Infect Dis, Sch Med, Aoba Ku, Sendai, Miyagi 9808575, Japan
[2] Sendai Natl Hosp, Virus Res Ctr, Div Clin Res, Sendai, Miyagi, Japan
[3] Kobe Univ, Div Zoonosis, Dept Microbiol & Infect Dis, Grad Sch Med, Kobe, Hyogo 657, Japan
[4] Kyoto Univ, Dept Resp Med, Grad Sch Med, Kyoto, Japan
[5] Tohoku Univ, Dept Resp Med, Sch Med, New Biomed Engn Ctr, Sendai, Miyagi 9808575, Japan
[6] Tohoku Univ, Dept Innovat, Sch Med, New Biomed Engn Ctr, Sendai, Miyagi 9808575, Japan
[7] Tohoku Univ Hosp, Dept Geriatr & Gerontol, Sendai, Miyagi, Japan
关键词
SA alpha 2,6Gal; bronchial asthma; chronic obstructive pulmonary disease; RHINOVIRUS INFECTION; S-CARBOXYMETHYLCYSTEINE; EXACERBATIONS; EXPRESSION; CULTURES; INFLAMMATION; SERUM;
D O I
10.1152/ajplung.00376.2009
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Yamaya M, Nishimura H, Shinya K, Hatachi Y, Sasaki T, Yasuda H, Yoshida M, Asada M, Fujino N, Suzuki T, Deng X, Kubo H, Nagatomi R. Inhibitory effects of carbocisteine on type A seasonal influenza virus infection in human airway epithelial cells. Am J Physiol Lung Cell Mol Physiol 299: L160-L168, 2010. First published June 11, 2010; doi: 10.1152/ajplung.00376.2009.-Type A human seasonal influenza (FluA) virus infection causes exacerbations of bronchial asthma and chronic obstructive pulmonary disease (COPD). L-carbocisteine, a mucolytic agent, reduces the frequency of common colds and exacerbations in COPD. However, the inhibitory effects of L-carbocisteine on FluA virus infection are uncertain. We studied the effects of L-carbocisteine on FluA virus infection in airway epithelial cells. Human tracheal epithelial cells were pretreated with L-carbocisteine and infected with FluA virus (H3N2). Viral titers in supernatant fluids, RNA of FluA virus in the cells, and concentrations of proinflammatory cytokines in supernatant fluids, including IL-6, increased with time after infection. L-carbocisteine reduced viral titers in supernatant fluids, RNA of FluA virus in the cells, the susceptibility to FluA virus infection, and concentrations of cytokines induced by virus infection. The epithelial cells expressed sialic acid with an alpha 2,6-linkage (SA alpha 2,6Gal), a receptor for human influenza virus on the cells, and L-carbocisteine reduced the expression of SA alpha 2,6Gal. L-carbocisteine reduced the number of acidic endosomes from which FluA viral RNA enters into the cytoplasm and reduced the fluorescence intensity from acidic endosomes. Furthermore, L-carbocisteine reduced NF-kappa B proteins including p50 and p65 in the nuclear extracts of the cells. These findings suggest that L-carbocisteine may inhibit FluA virus infection, partly through the reduced expression of the receptor for human influenza virus in the human airway epithelial cells via the inhibition of NF-kappa B and through increasing pH in endosomes. L-carbocisteine may reduce airway inflammation in influenza virus infection.
引用
收藏
页码:L160 / L168
页数:9
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