Respiratory Research Division, Department of Medicine, Royal College of Surgeons in Ireland, Education and Research Centre, Beaumont Hospital, Dublin, Ireland.
Br J Pharmacol. 2009 Oct;158(4):1048-58. doi: 10.1111/j.1476-5381.2009.00448.x.
Chronic inflammatory lung diseases such as cystic fibrosis and emphysema are characterized by higher-than-normal levels of pulmonary proteases. While these enzymes play important roles such as bacterial killing, their dysregulated expression or activity can adversely impact on the inflammatory process. The existence of efficient endogenous control mechanisms that can dampen or halt this overexuberant protease activity in vivo is essential for the effective resolution of inflammatory lung disease. The function of pulmonary antiproteases is to fulfil this role. Interestingly, in addition to their antiprotease activity, protease inhibitors in the lung also often possess other intrinsic properties that contribute to microbial killing or termination of the inflammatory process. This review will outline important features of chronic inflammation that are regulated by pulmonary proteases and will describe the various mechanisms by which antiproteases attempt to counterbalance exaggerated protease-mediated inflammatory events. These proteases, antiproteases and their modifiers represent interesting targets for therapeutic intervention.
慢性炎症性肺部疾病,如囊性纤维化和肺气肿,其特点是肺部蛋白酶水平高于正常水平。虽然这些酶在细菌杀伤等方面发挥着重要作用,但它们的表达或活性失调可能会对炎症过程产生不利影响。有效的内源性调控机制的存在,可以在体内抑制或阻止这种过度活跃的蛋白酶活性,这对于炎症性肺部疾病的有效治疗至关重要。肺部抗蛋白酶的作用就是实现这一目标。有趣的是,除了抗蛋白酶活性外,肺部的蛋白酶抑制剂通常还具有其他内在特性,有助于杀灭微生物或终止炎症过程。这篇综述将概述慢性炎症受肺部蛋白酶调控的重要特征,并描述抗蛋白酶试图平衡过度蛋白酶介导的炎症事件的各种机制。这些蛋白酶、抗蛋白酶及其修饰物是治疗干预的有趣靶点。