Matrix metalloproteinase-2 (MMP-2) and MMP-9 in pulmonary pathology

被引:247
作者
Chakrabarti, S
Patel, KD
机构
[1] Univ Calgary, Dept Physiol & Biophys, Calgary, AB, Canada
[2] Univ Calgary, Dept Biochem & Mol Biol, Immunol Res Grp, Calgary, AB, Canada
关键词
asthma; COPD; gelatinase; lung; neutrophil; remodeling;
D O I
10.1080/019021490944232
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
The lung is affected by a variety of disease processes that can lead to considerable morbidity and mortality. As the lung is the only organ for respiration and gas exchange, the structural and functional integrity of the lung is of primary importance. Various pathological processes affect the extracellular matrix (ECM) of the lung in an adverse manner, causing destruction of tissue integrity followed by tissue remodeling, which together impair normal pulmonary function. Matrix metalloproteinases (MMPs) are neutral proteinases that are involved in the breakdown and remodeling of the ECM under a variety of physiological and pathological conditions. MMP-2 and MMP-9, collectively known as the gelatinases, are particularly important in the pathogenesis of inflammatory, infectious, and neoplastic diseases in many organs including the lung. This review examines the expression of MMP-2 and MMP-9 in disease of the lung and discusses the role these gelatinases may play in disease progression.
引用
收藏
页码:599 / 621
页数:23
相关论文
共 127 条
[1]  
Allport JR, 2002, J LEUKOCYTE BIOL, V71, P821
[2]   Interaction of matrix metalloproteinases-2 and -9 with pregnancy zone protein and alpha(2)-macroglobulin [J].
Arbelaez, LF ;
Bergmann, U ;
Tuuttila, A ;
Shanbhag, VP ;
Stigbrand, T .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1997, 347 (01) :62-68
[3]   Matrix metalloproteinase-9 in lung remodeling [J].
Atkinson, JJ ;
Senior, RM .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 2003, 28 (01) :12-24
[4]   New concepts in chronic obstructive pulmonary disease [J].
Barnes, PJ .
ANNUAL REVIEW OF MEDICINE, 2003, 54 :113-129
[5]   Altered matrix metalloproteinase expression associated with oncogene-mediated cellular transformation and metastasis formation [J].
Baruch, RR ;
Melinscak, H ;
Lo, J ;
Liu, Y ;
Yeung, O ;
Hurta, RAR .
CELL BIOLOGY INTERNATIONAL, 2001, 25 (05) :411-420
[6]  
BEATTY K, 1980, J BIOL CHEM, V255, P3931
[7]   The role of matrix metalloproteinases (MMPs) in the pathophysiology of chronic obstructive pulmonary disease (COPD): a therapeutic role for inhibitors of MMPs? [J].
Belvisi, MG ;
Bottomley, KM .
INFLAMMATION RESEARCH, 2003, 52 (03) :95-100
[8]   Matrix metalloproteinase-9 triggers the angiogenic switch during carcinogenesis [J].
Bergers, G ;
Brekken, R ;
McMahon, G ;
Vu, TH ;
Itoh, T ;
Tamaki, K ;
Tanzawa, K ;
Thorpe, P ;
Itohara, S ;
Werb, Z ;
Hanahan, D .
NATURE CELL BIOLOGY, 2000, 2 (10) :737-744
[9]   Gelatinase B is required for alveolar bronchiolization after intratracheal bleomycin [J].
Betsuyaku, T ;
Fukuda, Y ;
Parks, WC ;
Shipley, JM ;
Senior, RM .
AMERICAN JOURNAL OF PATHOLOGY, 2000, 157 (02) :525-535
[10]   Neutrophil granule proteins in bronchoalveolar lavage fluid from subjects with subclinical emphysema [J].
Betsuyaku, T ;
Nishimura, M ;
Takeyabu, K ;
Tanino, M ;
Venge, P ;
Xu, SY ;
Kawakami, Y .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1999, 159 (06) :1985-1991