SERIES "MATRIX METALLOPROTEINASES IN LUNG HEALTH AND DISEASE" Matrix metalloproteinases in COPD

被引:234
作者
Churg, A. [1 ]
Zhou, S. [1 ]
Wright, J. L. [1 ]
机构
[1] Univ British Columbia, Dept Pathol, Vancouver, BC V6T 2B5, Canada
关键词
Cigarette smoke; chronic obstructive pulmonary disease; emphysema; matrix metalloproteinases; matrix metalloproteinase-12; small airway remodelling; OBSTRUCTIVE PULMONARY-DISEASE; SMOKE-INDUCED EMPHYSEMA; NECROSIS-FACTOR-ALPHA; SURFACTANT PROTEIN-D; CIGARETTE-SMOKE; ALVEOLAR MACROPHAGES; GUINEA-PIGS; AIRWAY INFLAMMATION; TISSUE INHIBITOR; GENE-EXPRESSION;
D O I
10.1183/09031936.00121611
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
100201 [内科学];
摘要
There is considerable evidence that matrix metalloproteinases (MMPs) are up- and/or downregulated in chronic obstructive pulmonary disease (COPD), particularly in emphysema, in which they probably participate in proteolytic attack on the alveolar wall matrix. Recent data suggest that MMPs also have major roles in driving inflammation or shutting it down, as well as modifying the release of fibrogenic growth factors, processes that are important in the genesis of the various lesions of COPD. In cigarette smoke-induced animal models of emphysema, MMP-12 appears to play a consistent and important role, whereas the data for other MMPs are difficult to interpret. In human lungs, evidence for a role for MMPs is more tenuous and there are numerous contradictions in the literature. Little is known about the effects of MMPs in small airway remodelling, smoke-induced pulmonary hypertension and chronic bronchitis, but MMP-12 participates in experimental small airway modelling. To date, the accumulated data suggest that selective inhibition of MMP-12 might be a viable therapy for emphysema and small airway remodelling, but subtle differences in the functions of MMP-12 in animals and humans mandate caution with this approach. Whether inhibition of other MMPs might be useful is unclear.
引用
收藏
页码:197 / 209
页数:13
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