Activation of TGF-β/Smad2 signaling is associated with airway remodeling in asthma

被引:122
作者
Sagara, H
Okada, T
Okumura, K
Ogawa, H
Ra, C
Fukuda, T
Nakao, A
机构
[1] Juntendo Univ, Sch Med, Atopy Allergy Res Ctr, Bunkyo Ku, Tokyo 1138421, Japan
[2] Dokkyo Univ, Sch Med, Dept Pulm Med & Clin Immunol, Mibu, Tochigi, Japan
关键词
transforming growth factor beta; Smad; asthma; airway remodeling; subepithelial thickness;
D O I
10.1067/mai.2002.126078
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background: Transforming growth factor beta (TGF-beta) has been suggested to play an important role in the development of airway remodeling in asthma; this suggestion is based on evidence that expression levels of TGF-beta are correlated with unique parameters of airway remodeling, such as thickness of basement membrane. However, the relevant studies were inconclusive because they were unable to demonstrate active signaling mediated by the cytokine in the airways of asthmatic individuals. Objective: We sought to determine whether TGF-beta signaling was active in the airways of asthmatic subjects and, if so, whether it was correlated with clinicopathologic features associated with the development of airway remodeling in asthma. Methods: We examined the phosphorylation status of Smad2 in bronchial biopsy samples obtained from 40 asthmatic subjects as a marker of active TGF-beta signaling, and we studied its correlation with basement membrane thickness. Results: Expression levels of phosphorylated Smad2 in bronchial biopsy specimens from asthmatic subjects were higher than those in specimens from normal subjects, and they were correlated with basement membrane thickness in asthma. Conclusion: The findings provide evidence that TGF-beta signaling was active in asthmatic airways and that the activity was associated with the development of airway remodeling in asthma.
引用
收藏
页码:249 / 254
页数:6
相关论文
共 18 条
[1]  
Brodin G, 1999, CANCER RES, V59, P2731
[2]   Airways remodeling is a distinctive feature of asthma and is related to severity of disease [J].
Chetta, A ;
Foresi, A ;
DelDonno, M ;
Bertorelli, G ;
Pesci, A ;
Olivieri, D .
CHEST, 1997, 111 (04) :852-857
[3]   Airway remodeling in asthma [J].
Elias, JA ;
Zhu, Z ;
Chupp, G ;
Homer, RJ .
JOURNAL OF CLINICAL INVESTIGATION, 1999, 104 (08) :1001-1006
[4]   TGF-β/Smad signaling defects in inflammatory bowel disease:: mechanisms and possible novel therapies for chronic inflammation [J].
Fiocchi, C .
JOURNAL OF CLINICAL INVESTIGATION, 2001, 108 (04) :523-526
[5]  
Holgate S. T., 2001, Clinical and Experimental Allergy Reviews, V1, P59, DOI 10.1046/j.1472-9725.2001.00006.x
[6]   Bronchial subepithelial fibrosis and expression of matrix metalloproteinase-9 in asthmatic airway inflammation [J].
Hoshino, M ;
Nakamura, Y ;
Sim, JJ ;
Shimojo, J ;
Isogai, S .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1998, 102 (05) :783-788
[7]  
Makino S, 2000, INT ARCH ALLERGY IMM, V121, P1
[8]  
MAKINO S, 1984, JPN J ALLERGOL, V33, P167
[9]   THE TRANSFORMING GROWTH-FACTOR-BETA FAMILY [J].
MASSAGUE, J .
ANNUAL REVIEW OF CELL BIOLOGY, 1990, 6 :597-641
[10]   Eosinophil-associated TGF-beta(1) mRNA expression and airways fibrosis in bronchial asthma [J].
Minshall, EM ;
Leung, DYM ;
Martin, RJ ;
Song, YL ;
Cameron, L ;
Ernst, P ;
Hamid, Q .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1997, 17 (03) :326-333