Mechanisms of mucin production by rhinovirus infection in cultured human airway epithelial cells

被引:59
作者
Inoue, Daisuke
Yamaya, Mutsuo
Kubo, Hiroshi
Sasaki, Takahiko
Hosoda, Masayoshi
Numasaki, Muneo
Tomioka, Yoshihisa
Yasuda, Hiroyasu
Sekizawa, Kiyohisa
Nishimura, Hidekazu
Sasaki, Hidetada
机构
[1] Tohoku Univ, Sch Med, Dept Geriatr & Resp Med, Aoba Ku, Sendai, Miyagi 9808574, Japan
[2] Tohoku Univ Hosp, Dept Pharmacol Sci, Sendai, Miyagi 9808574, Japan
[3] Univ Tsukuba, Inst Clin Med, Dept Pulm Med, Tsukuba, Ibaraki 3058575, Japan
[4] Natl Hosp Org, Sendai Med Ctr, Virus Res Ctr, Div Clin Res, Sendai, Miyagi 9830045, Japan
关键词
airway epithelium; rhinovirus; mucin; NF-kappa B; MAPK/ERK;
D O I
10.1016/j.resp.2005.11.006
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Mucus hypersecretion relates to exacerbations of bronchial asthma and chronic obstructive pulmonary disease (COPD) caused by rhinovirus (RV) infection. We examined the mechanisms of RV infection-induced mucin production in human tracheal surface epithelial cells and submucosal gland cells. RV14 up-regulated the mRNA expression of MUC2, MUC3, MUC5AC, MUC5B and MUC6, and increased MUC5AC and total mucin concentration in supernatants and lysates of the surface cells. An inhibitor of the nuclear factor kappa B caffeic acid phenylethyl ester, inhibitors of selective p44/42 mitogen-activated protein kinase-kinase PD98059 and U0126, and a selective Src inhibitor PP1 attenuated MUC5AC mRNA expression, and secretion and production of MUC5AC and total mucin glycoprotein in the surface cells. In the gland cells, RV14 also increased mRNA expression of MUC2, MUC5AC, MUC5B and MUC7, and the inhibitors attenuated the secretion of total mucin glycoprotein. Src-related p44/42 mitogen-activated protein kinase pathway may be associated with RV-induced mucin hypersecretion in human airways. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:484 / 499
页数:16
相关论文
共 40 条
[1]  
ABI, 1997, ABI US B
[2]   Control of mucin transcription by diverse injury-induced signaling pathways [J].
Basbaum, C ;
Lemjabbar, H ;
Longphre, M ;
Li, DZ ;
Gensch, E ;
McNamara, N .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1999, 160 (05) :S44-S48
[3]   Developmental mucin gene expression in the human respiratory tract [J].
Buisine, MP ;
Devisme, L ;
Copin, MC ;
Durand-Réville, M ;
Gosselin, B ;
Aubert, JP ;
Porchet, N .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1999, 20 (02) :209-218
[4]   Mucinous bronchioloalveolar carcinomas display a specific pattern of mucin gene expression among primary lung adenocarcinomas [J].
Copin, MC ;
Buisine, MP ;
Leteurtre, E ;
Marquette, CH ;
Porte, H ;
Aubert, JP ;
Gosselin, B ;
Porchet, N .
HUMAN PATHOLOGY, 2001, 32 (03) :274-281
[5]  
DeSilva DR, 1998, J IMMUNOL, V160, P4175
[6]   Mucin gene (MUC 2 and MUC 5AC) upregulation by Gram-positive and Gram-negative bacteria [J].
Dohrman, A ;
Miyata, S ;
Gallup, M ;
Li, JD ;
Chapelin, C ;
Coste, A ;
Escudier, E ;
Nadel, J ;
Basbaum, C .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 1998, 1406 (03) :251-259
[7]   THE MAJOR HUMAN RHINOVIRUS RECEPTOR IS ICAM-1 [J].
GREVE, JM ;
DAVIS, G ;
MEYER, AM ;
FORTE, CP ;
YOST, SC ;
MARIOR, CW ;
KAMARCK, ME ;
MCCLELLAND, A .
CELL, 1989, 56 (05) :839-847
[8]   Quantitation of mucin RNA by PCR reveals induction of both MUC2 and MUC5AC mRNA levels by retinoids [J].
Guzman, K ;
Gray, TE ;
Yoon, JH ;
Nettesheim, P .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 1996, 271 (06) :L1023-L1028
[9]   c-Jun N-terminal kinase is required for metalloproteinase expression and joint destruction in inflammatory arthritis (vol 108, pg 73, 2001) [J].
Han, ZN ;
Boyle, DL ;
Chang, LF ;
Bennett, B ;
Karin, M ;
Yang, L ;
Manning, AM ;
Firestein, GS .
JOURNAL OF CLINICAL INVESTIGATION, 2001, 108 (12) :1883-1883
[10]  
Han ZN, 2001, J CLIN INVEST, V108, P73, DOI 10.1172/JCI12466