Dept of Pathology, University of British Columbia, 2211 Wesbrook Mall, Vancouver, BC V6T 2B5, Canada.
Eur Respir J. 2012 Jan;39(1):197-209. doi: 10.1183/09031936.00121611. Epub 2011 Sep 15.
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.
有大量证据表明,基质金属蛋白酶(MMPs)在慢性阻塞性肺疾病(COPD)中上调和/或下调,特别是在肺气肿中,它们可能参与对肺泡壁基质的蛋白水解攻击。最近的数据表明,MMPs 还在驱动炎症或使其平息,以及调节成纤维生长因子的释放方面发挥重要作用,这些过程在 COPD 的各种病变的发生中很重要。在香烟烟雾诱导的肺气肿动物模型中,MMP-12 似乎起着一致而重要的作用,而其他 MMP 的数据则难以解释。在人肺中,MMPs 作用的证据更加薄弱,文献中存在许多矛盾。关于 MMPs 在小气道重塑、香烟烟雾引起的肺动脉高压和慢性支气管炎中的作用知之甚少,但 MMP-12 参与了实验性小气道建模。迄今为止,累积的数据表明,选择性抑制 MMP-12 可能是治疗肺气肿和小气道重塑的可行方法,但 MMP-12 在动物和人类中的功能存在细微差异,需要谨慎使用这种方法。抑制其他 MMP 是否有用尚不清楚。