Funovics Philip, Brostjan Christine, Nigisch Anneliese, Fila Anna, Grochot Anna, Mleczko Katarzyna, Was Halina, Weigel Guenter, Dulak Jozef, Jozkowicz Alicja
Medical Faculty, University of Vienna, Austria.
Prostaglandins Other Lipid Mediat. 2006 May;79(3-4):230-44. doi: 10.1016/j.prostaglandins.2006.02.002. Epub 2006 Mar 31.
15-Deoxy-Delta(12,14)-prostaglandin-J(2) (15d-PGJ(2)) upregulates expression of vascular endothelial growth factor (VEGF), but may inhibit angiogenesis. We found that 15d-PGJ(2) (1-10muM) attenuated all VEGF-induced angiogenic activities in human umbilical vein endothelial cells (HUVEC). It blocked almost completely cell proliferation, potently reduced migration, assembly into tube-like network on matrigel, and growth of capillaries into collagen gel. 15d-PGJ(2) inhibited expression of VEGFR-1 and VEGFR-2 receptors both at mRNA and protein levels. This inhibition, however, was transient (observed after 6-12h, but not after 24h) and weak (20-30%), and could not fully explain inhibition of response to VEGF. Accordingly, proliferation was inhibited when 15d-PGJ(2) was added 24h after VEGF or in cells stimulated with basic fibroblast growth factor. Interestingly, 15d-PGJ(2) decreased activities of c-jun and c-myc in HUVEC and overexpression of c-myc attenuated its antiproliferative effects. This suggests that inhibition of this transcription factor by 15d-PGJ(2) contributes to decrease in angiogenic response.
15-脱氧-Δ(12,14)-前列腺素-J2(15d-PGJ2)可上调血管内皮生长因子(VEGF)的表达,但可能抑制血管生成。我们发现,15d-PGJ2(1-10μM)可减弱人脐静脉内皮细胞(HUVEC)中所有VEGF诱导的血管生成活性。它几乎完全阻断细胞增殖,显著降低迁移能力,抑制细胞在基质胶上组装成管状网络以及毛细血管在胶原凝胶中的生长。15d-PGJ2在mRNA和蛋白质水平均抑制VEGFR-1和VEGFR-2受体的表达。然而,这种抑制是短暂的(在6-12小时后观察到,但24小时后未观察到)且较弱(20-30%),无法完全解释对VEGF反应的抑制。因此,在VEGF作用24小时后添加15d-PGJ2或在碱性成纤维细胞生长因子刺激的细胞中添加15d-PGJ2时,细胞增殖受到抑制。有趣的是,15d-PGJ2降低了HUVEC中c-jun和c-myc的活性,而c-myc的过表达减弱了其抗增殖作用。这表明15d-PGJ2对该转录因子的抑制作用有助于降低血管生成反应。