Matrix metalloproteinases and tissue inhibitor of metalloproteinase-2 in fetal rabbit lung

被引:58
作者
Fukuda, Y
Ishizaki, M
Okada, Y
Seiki, M
Yamanaka, N
机构
[1] Nippon Med Sch, Dept Pathol, Bunkyo Ku, Tokyo 1130022, Japan
[2] Keio Univ, Sch Med, Dept Pathol, Tokyo 1600016, Japan
[3] Univ Tokyo, Inst Med Sci, Dept Canc Cell Res, Tokyo 1080071, Japan
关键词
formation of alveoli; type IV collagen; membrane type 1 matrix metalloproteinase; gelatin zymography;
D O I
10.1152/ajplung.2000.279.3.L555
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
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.
引用
收藏
页码:L555 / L561
页数:7
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