Kadono Y, Shibahara K, Namiki M, Watanabe Y, Seiki M, Sato H
Department of Molecular Virology and Oncology, Cancer Research Institute, Department of Urology, Department of Surgery (1), School of Medicine, Kanazawa University, 13-1 Takara-machi, Kanazawa, 920-0934, Japan.
Biochem Biophys Res Commun. 1998 Oct 29;251(3):681-7. doi: 10.1006/bbrc.1998.9531.
Matrix metalloproteinases (MMPs) are believed to be involved in morphogenesis. Association of MMPs in a model of kidney tubulogenesis was studied using Madin-Darby canine kidney (MDCK) epithelial cells in an in vitro morphogenetic system. MDCK cells form branching tubules in three-dimensional collagen gel matrix in the presence of hepatocyte growth factor (HGF). The addition of specific MMP inhibitor BB-94 and tissue inhibitor MMP (TIMP)-2 but not TIMP-1 to such collagen gel cultures reduced the formation of branching tubules induced by HGF. The induction of membrane-type 1-matrix metalloproteinase (MT1-MMP) mRNA expression was observed in MDCK cells cultured in the collagen gel. Stable expression of MT1-MMP antisense RNA interfered with the tubule formation of MDCK cells induced by HGF-collagen gel culture. These observations implicate MT1-MMP in kidney tubulogenesis and TIMP-2-specific inhibition suggests a direct role of MT1-MMP rather than a gelatinase A-mediated effect.
基质金属蛋白酶(MMPs)被认为参与形态发生。在体外形态发生系统中,使用Madin-Darby犬肾(MDCK)上皮细胞研究了MMPs在肾小管形成模型中的关联。在肝细胞生长因子(HGF)存在的情况下,MDCK细胞在三维胶原凝胶基质中形成分支小管。向这种胶原凝胶培养物中添加特异性MMP抑制剂BB-94和组织抑制剂MMP(TIMP)-2而非TIMP-1,可减少HGF诱导的分支小管形成。在胶原凝胶中培养的MDCK细胞中观察到膜型1-基质金属蛋白酶(MT1-MMP)mRNA表达的诱导。MT1-MMP反义RNA的稳定表达干扰了HGF-胶原凝胶培养诱导的MDCK细胞的小管形成。这些观察结果表明MT1-MMP参与肾小管形成,而TIMP-2特异性抑制表明MT1-MMP具有直接作用,而非明胶酶A介导的效应。