Gibbs D F, Shanley T P, Warner R L, Murphy H S, Varani J, Johnson K J
Department of Pathology, University of Michigan Medical School, Ann Arbor, Michigan 48109-0602, USA.
Am J Respir Cell Mol Biol. 1999 Jun;20(6):1145-54. doi: 10.1165/ajrcmb.20.6.3482.
Matrix metalloproteinases (MMPs) have been implicated in the tissue injury seen in neutrophil-dependent models of acute lung injury. However, the role of MMPs in macrophage-dependent models of lung injury is unknown. To address this issue, the macrophage-dependent immunoglobulin A immune complex-induced lung injury model and the macrophage-dependent portion of the lipopolysaccharide-induced acute lung injury model in the rat were assessed for MMP involvement and for the source of these activities. In both models, injury was inhibited by the recombinant human tissue inhibitor of metalloproteinases-2. Bronchoalveolar lavage fluids (BALFs) from injured animals in both models showed increased levels of MMPs. Characterization of MMP production by isolated lung fibroblasts, endothelial cells, type II epithelial cells, and alveolar macrophages revealed that only the macrophage had the same spectrum of MMP activity as seen in the BALF. Further, isolated alveolar macrophages from injured lungs showed evidence of in vivo activation with the release of the same spectrum of MMP activities. Together these studies show that MMPs are produced during macrophage-dependent lung injury, that these MMPs play a role in the development of the lung injury, and that the alveolar macrophage is the likely source of these MMPs.
基质金属蛋白酶(MMPs)与急性肺损伤中性粒细胞依赖性模型中所见的组织损伤有关。然而,MMPs在巨噬细胞依赖性肺损伤模型中的作用尚不清楚。为解决这一问题,对大鼠巨噬细胞依赖性免疫球蛋白A免疫复合物诱导的肺损伤模型和脂多糖诱导的急性肺损伤模型中巨噬细胞依赖性部分进行了评估,以确定MMPs的参与情况及其活性来源。在这两种模型中,损伤均被重组人金属蛋白酶组织抑制剂-2抑制。两种模型中受伤动物的支气管肺泡灌洗液(BALFs)中MMPs水平均升高。对分离的肺成纤维细胞、内皮细胞、II型上皮细胞和肺泡巨噬细胞产生MMPs的特性分析表明,只有巨噬细胞具有与BALF中所见相同的MMP活性谱。此外,从受伤肺中分离的肺泡巨噬细胞显示出体内激活的证据,释放出相同谱的MMP活性。这些研究共同表明,MMPs在巨噬细胞依赖性肺损伤过程中产生,这些MMPs在肺损伤的发展中起作用,并且肺泡巨噬细胞可能是这些MMPs的来源。