Onguchi Tatsuya, Han Kyu Yeon, Chang Jin-Hong, Azar Dimitri T
Department of Ophthalmology and Visual Sciences, Illinois Eye and Ear Infirmary, University of Illinois at Chicago, 1855 West Taylor St., Chicago, IL 60612, USA.
Am J Pathol. 2009 Apr;174(4):1564-71. doi: 10.2353/ajpath.2009.080452. Epub 2009 Mar 5.
Corneal neovascularization is one of the leading causes of blindness. The aim of this study was to evaluate the pro-angiogenic role of corneal fibroblast-derived membrane type-1 matrix metalloproteinase (MT1-MMP) on basic fibroblast growth factor (bFGF)-induced corneal neovascularization in vivo and in vitro. Immunohistochemical studies demonstrated that MT1-MMP was expressed in keratocytes and immortalized corneal fibroblast cell lines. Vascular endothelial growth factor protein levels were increased after bFGF-stimulation of wild-type fibroblast cells compared with MT1-MMP knockout fibroblast cells. Corneal vascularization was significantly increased after a combination of bFGF pellet implantation and naked MT1-MMP DNA injection in wild-type mouse corneas compared with either bFGF pellet implantation or naked MT1-MMP DNA-injected corneas. Western blotting analysis of the phosphorylation levels of the key signaling molecules (p38, JNK, and ERK) demonstrated that phosphorylation levels of both p38 and JNK were diminished after bFGF stimulation of MT1-MMP knockout cells compared with wild-type and MT1-MMP knockin cells. These results suggest that MT1-MMP potentiates bFGF-induced corneal neovascularization, likely by modulating the bFGF signal transduction pathway.
角膜新生血管形成是导致失明的主要原因之一。本研究的目的是评估角膜成纤维细胞衍生的膜型1基质金属蛋白酶(MT1-MMP)在体内和体外对碱性成纤维细胞生长因子(bFGF)诱导的角膜新生血管形成的促血管生成作用。免疫组织化学研究表明,MT1-MMP在角膜细胞和永生化角膜成纤维细胞系中表达。与MT1-MMP基因敲除成纤维细胞相比,bFGF刺激野生型成纤维细胞后血管内皮生长因子蛋白水平升高。与单独植入bFGF微丸或注射裸MT1-MMP DNA的角膜相比,在野生型小鼠角膜中联合植入bFGF微丸和注射裸MT1-MMP DNA后角膜血管化显著增加。对关键信号分子(p38、JNK和ERK)磷酸化水平的蛋白质印迹分析表明,与野生型和MT1-MMP基因敲入细胞相比,bFGF刺激MT1-MMP基因敲除细胞后p38和JNK的磷酸化水平均降低。这些结果表明,MT1-MMP可能通过调节bFGF信号转导途径增强bFGF诱导的角膜新生血管形成。