Fukuda Y, Ishizaki M, Okada Y, Seiki M, Yamanaka N
Department of Pathology, Nippon Medical School, Tokyo 113-0022, Japan.
Am J Physiol Lung Cell Mol Physiol. 2000 Sep;279(3):L555-61. doi: 10.1152/ajplung.2000.279.3.L555.
Cell-extracellular matrix interaction and extracellular matrix remodeling are known to be important in fetal lung development. We investigated the localization of matrix metalloproteinases (MMPs) in fetal rabbit lungs. Immunohistochemistry for type IV collagen, MMP-1, MMP-2, MMP-9, membrane type (MT) 1 MMP, and tissue inhibitor of metalloproteinase (TIMP)-2 and in situ hybridization for MMP-9 mRNA were performed. Gelatin zymography and Western blotting for MT1-MMP in lung tissue homogenates were also studied. MMP-1 and MT1-MMP were detected in epithelial cells, and MMP-2 and TIMP-2 were detected in epithelial cells and some mesenchymal cells in each stage. MMP-9 was found in epithelial cells mainly in the late stage. Gelatin zymography revealed that the ratio of active MMP-2 to latent MMP-2 increased dramatically during the course of development. MT1-MMP was detected in tissue homogenates, especially predominant in the late stage. These findings suggest that MMPs and their inhibitors may contribute to the formation of airways and alveoli in fetal lung development and that activated MMP-2 of alveolar epithelial cells may function to provide an extremely wide alveolar surface.
细胞与细胞外基质的相互作用以及细胞外基质重塑在胎儿肺发育中起着重要作用。我们研究了基质金属蛋白酶(MMPs)在胎兔肺中的定位。进行了IV型胶原、MMP-1、MMP-2、MMP-9、膜型(MT)1 MMP以及金属蛋白酶组织抑制剂(TIMP)-2的免疫组织化学检测,以及MMP-9 mRNA的原位杂交检测。还研究了肺组织匀浆中MT1-MMP的明胶酶谱分析和蛋白质印迹分析。在每个阶段,上皮细胞中均检测到MMP-1和MT1-MMP,上皮细胞和一些间充质细胞中检测到MMP-2和TIMP-2。MMP-9主要在晚期上皮细胞中被发现。明胶酶谱分析显示,在发育过程中,活性MMP-2与潜伏性MMP-2的比例急剧增加。在组织匀浆中检测到MT1-MMP,尤其在晚期占主导地位。这些发现表明,MMPs及其抑制剂可能在胎儿肺发育过程中对气道和肺泡的形成起作用,并且肺泡上皮细胞中活化的MMP-2可能发挥作用以提供极其广阔的肺泡表面。