Pipili-Synetos E, Papadimitriou E, Maragoudakis M E
Department of Pharmacology, Medical School, University of Patras, Greece.
Br J Pharmacol. 1998 Nov;125(6):1252-7. doi: 10.1038/sj.bjp.0702191.
The involvement of platelets in neovascularization was investigated in the matrigel tube formation assay, an in vitro model of angiogenesis. Platelets promoted the formation of capillary-like structures (expressed as relative tube area) number- and time-dependently. Relative tube area increased from 0.98+/-0.02 (n = 8) in the presence of 6.25 x 10(4), to 3.21+/-0.12 (n=8) in the presence of 10(6) platelets/well compared to 0.54+/-0.04 (n=8) in their absence. This increase was unaffected by acetyl salicylic acid (ASA), apyrase, and hirudin. Photographs from representative experiments, showed that platelets adhered along the differentiating endothelium. Addition of alpha-thrombin (0.1-1 i.u. ml(-1)), the nitric oxide (NO) donor sodium nitroprusside (SNP; 1-100 microM) or the NO synthase inhibitor, L-NG-arginine-methylester (L-NAME, 30-300 microM) to the assay, had no effect on tube formation compared to that seen with platelets alone. Neuraminidase (0.01 i.u./10(7) platelets), which strips sialic acid residues from membrane glycoproteins, abolished the promoting effect of platelets on tube formation. The relative tube area in the presence of neuraminidase-treated platelets was 0.81+/-0.03 (n = 8), in the presence of untreated platelets 1.69+/-0.09, P<0.001 (n=8) and in the absence of platelets, 0.80+/-0.04 (n=8). The tetrapeptide Arg-Gly-Asp-Ser (RGDS; 20-200 microM) which inhibits von Willebrand factor, fibrinogen and fibronectin-mediated adhesion, had no effect on the promoting effect of platelets on tube formation. These results indicate that platelets promote angiogenesis in vitro. This effect is largely independent from activation by alpha-thrombin, is not modified by manipulating NO and prostaglandin metabolism and proceeds possibly through adhesion of the platelets to the differentiating endothelium.
在基质胶管形成试验(一种血管生成的体外模型)中研究了血小板在新生血管形成中的作用。血小板以数量和时间依赖性方式促进毛细血管样结构的形成(以相对管面积表示)。与不存在血小板时的0.54±0.04(n = 8)相比,在每孔存在6.25×10⁴个血小板时,相对管面积从0.98±0.02(n = 8)增加到每孔存在10⁶个血小板时的3.21±0.12(n = 8)。这种增加不受乙酰水杨酸(ASA)、腺苷三磷酸双磷酸酶和水蛭素的影响。代表性实验的照片显示,血小板沿分化的内皮细胞黏附。向试验中添加α-凝血酶(0.1 - 1国际单位/毫升)、一氧化氮(NO)供体硝普钠(SNP;1 - 100微摩尔)或NO合酶抑制剂L - NG - 精氨酸甲酯(L - NAME,30 - 300微摩尔),与单独使用血小板相比,对管形成没有影响。神经氨酸酶(0.01国际单位 / 10⁷个血小板)可去除膜糖蛋白上的唾液酸残基,消除了血小板对管形成的促进作用。在存在经神经氨酸酶处理的血小板时,相对管面积为0.81±0.03(n = 8),在存在未处理的血小板时为1.69±0.09,P<0.001(n = 8),在不存在血小板时为0.80±0.04(n = 8)。抑制血管性血友病因子、纤维蛋白原和纤连蛋白介导的黏附的四肽Arg - Gly - Asp - Ser(RGDS;20 - 200微摩尔)对血小板对管形成的促进作用没有影响。这些结果表明血小板在体外促进血管生成。这种作用在很大程度上独立于α-凝血酶的激活,不受一氧化氮和前列腺素代谢调节的影响,可能通过血小板与分化的内皮细胞黏附来实现。