Airway smooth muscle - its relationship to the extracellular matrix

被引:49
作者
Black, JL [1 ]
Burgess, JK [1 ]
Johnson, PRA [1 ]
机构
[1] Univ Sydney, Woolcock Inst Med Res, Dept Pharmacol, Sydney, NSW 2006, Australia
关键词
airways; smooth muscle; disease; asthma; airway smooth muscle remodeling; enzymes; metalloproteases; mammals; humans; mediators; connective tissue growth factor; CTGF; TGF beta; muscle; smooth; airway; proteins; extracellular matrix;
D O I
10.1016/S1569-9048(03)00157-5
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
The airway smooth muscle cell has a variety of properties, which confer on it the ability to participate actively in the inflammatory process and the remodeling events, which accompany severe, persistent asthma. Among these properties is its relationship to the extracellular matrix (ECM) with which it interacts by releasing matrix proteins, matrix metalloproteinases (MMPs) and their tissue inhibitors (TIMPs). Muscle cells derived from asthmatic subjects proliferate faster, release a different profile of matrix proteins, produce more connective tissue growth factor (CTGF) in response to TGFbeta stimulation and these changes may impact on airway smooth muscle contraction and proliferation. Integrins on the surface of the airway smooth muscle transduce signals between the muscle cell and the ECM, but whether the expression and/or function of these is altered in asthma is not known. It is unlikely that current therapy is effective in preventing or reversing remodeling, and therefore, understanding the pathophysiological events, which underlie its mechanism is critical. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:339 / 346
页数:8
相关论文
共 39 条
[1]   Local overexpression of TIMP-1 prevents aortic aneurysm degeneration and rupture in a rat model [J].
Allaire, E ;
Forough, R ;
Clowes, W ;
Starcher, B ;
Clowes, AW .
JOURNAL OF CLINICAL INVESTIGATION, 1998, 102 (07) :1413-1420
[2]   Structure and biological activity of the extracellular matrix [J].
Aumailley, M ;
Gayraud, B .
JOURNAL OF MOLECULAR MEDICINE-JMM, 1998, 76 (3-4) :253-265
[3]   The effect of age and duration of disease on airway structure in fatal asthma [J].
Bai, TR ;
Cooper, J ;
Koelmeyer, T ;
Paré, PD ;
Weir, TD .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2000, 162 (02) :663-669
[4]   Divergent effects of tissue inhibitor of metalloproteinase-1, -2, or -3 overexpression on rat vascular smooth muscle cell invasion, proliferation, and death in vitro - TIMP-3 promotes apoptosis [J].
Baker, AH ;
Zaltsman, AB ;
George, SJ ;
Newby, AC .
JOURNAL OF CLINICAL INVESTIGATION, 1998, 101 (06) :1478-1487
[5]   Expression of βig-h3 by human bronchial smooth muscle cells localization to the extracellular matrix and nucleus [J].
Billings, PC ;
Herrick, DJ ;
Howard, PS ;
Kucich, U ;
Engelsberg, BN ;
Rosenbloom, J .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 2000, 22 (03) :352-359
[6]   ASTHMA - A DISEASE REMODELING THE AIRWAYS [J].
BOUSQUET, J ;
CHANEZ, P ;
LACOSTE, JY ;
WHITE, R ;
VIC, P ;
GODARD, P ;
MICHEL, FB .
ALLERGY, 1992, 47 (01) :3-11
[7]   AIRWAYS REMODELING IN ASTHMA - NO DOUBT, NO MORE [J].
BOUSQUET, J ;
VIGNOLA, AM ;
CHANEZ, P ;
CAMPBELL, AM ;
BONSIGNORE, G ;
MICHEL, FB .
INTERNATIONAL ARCHIVES OF ALLERGY AND IMMUNOLOGY, 1995, 107 (1-3) :211-214
[8]   COLLAGENASE INCREASES SHORTENING OF HUMAN BRONCHIAL SMOOTH-MUSCLE IN-VITRO [J].
BRAMLEY, AM ;
ROBERTS, CR ;
SCHELLENBERG, RR .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1995, 152 (05) :1513-1517
[9]   Localization of matrix metalloproteinase MMP-2 to the surface of invasive cells by interaction with integrin alpha v beta 3 [J].
Brooks, PC ;
Stromblad, S ;
Sanders, LC ;
vonSchalscha, TL ;
Aimes, RT ;
StetlerStevenson, WG ;
Quigley, JP ;
Cheresh, DA .
CELL, 1996, 85 (05) :683-693
[10]  
BURGESS JK, 2003, AM J RESP CRIT CARE, V167