Mohan R, Sivak J, Ashton P, Russo L A, Pham B Q, Kasahara N, Raizman M B, Fini M E
Vision Research Laboratories of New England Eye Center and the Department of Ophthalmology, Tufts University School of Medicine, Boston, Massachusetts 02111, USA.
J Biol Chem. 2000 Apr 7;275(14):10405-12. doi: 10.1074/jbc.275.14.10405.
We have studied mechanisms controlling activation of the gelatinase B gene (matrix metalloproteinase-9) by fibroblast growth factor-2 (FGF-2) during angiogenesis, and the effects of the natural product curcuminoids on this process. Using a transgenic mouse (line 3445) harboring a gelatinase B promoter/lacZ fusion gene, we demonstrate FGF-2 stimulation of reporter gene expression in endothelial cells of invading neocapillaries in the corneal micropocket assay. Using cultured corneal cells, we show that FGF-2 stimulates DNA binding activity of transcription factor AP-1 but not NF-kappaB and that AP-1 stimulation is inhibited by curcuminoids. We further show that induction of gelatinase B transcriptional promoter activity in response to FGF-2 is dependent on AP-1 but not NF-kappaB response elements and that promoter activity is also inhibited by curcuminoids. In rabbit corneas, the angiogenic response induced by implantation of an FGF-2 pellet is inhibited by the co-implantation of a curcuminoid pellet, and this correlates with inhibition of endogenous gelatinase B expression induced by FGF-2. Angiostatic efficacy in the cornea is also observed when curcuminoids are provided to mice in the diet. Our findings provide evidence that curcuminoids target the FGF-2 angiogenic signaling pathway and inhibit expression of gelatinase B in the angiogenic process.
我们研究了血管生成过程中,成纤维细胞生长因子-2(FGF-2)控制明胶酶B基因(基质金属蛋白酶-9)激活的机制,以及天然产物姜黄素对此过程的影响。利用携带明胶酶B启动子/lacZ融合基因的转基因小鼠(3445品系),我们在角膜微袋试验中证明了FGF-2对侵入性新毛细血管内皮细胞中报告基因表达的刺激作用。利用培养的角膜细胞,我们发现FGF-2刺激转录因子AP-1的DNA结合活性,但不刺激NF-κB,并且姜黄素可抑制AP-1的刺激作用。我们进一步表明,响应FGF-2的明胶酶B转录启动子活性的诱导依赖于AP-1而非NF-κB反应元件,并且启动子活性也受到姜黄素的抑制。在兔角膜中,植入FGF-2微丸诱导的血管生成反应受到同时植入姜黄素微丸的抑制,这与抑制FGF-2诱导的内源性明胶酶B表达相关。当在饮食中给小鼠提供姜黄素时,在角膜中也观察到了血管生成抑制效果。我们的研究结果证明,姜黄素靶向FGF-2血管生成信号通路,并在血管生成过程中抑制明胶酶B的表达。