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首页> 外文期刊>Microcirculation: The official journal of the Microcirculatory Society >The synergistic action of a VEGF-receptor tyrosine-kinase inhibitor and a sensitizing PDGF-receptor blocker depends upon the stage of vascular maturation.
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The synergistic action of a VEGF-receptor tyrosine-kinase inhibitor and a sensitizing PDGF-receptor blocker depends upon the stage of vascular maturation.

机译:VEGF受体酪氨酸激酶抑制剂和致敏PDGF受体阻滞剂的协同作用取决于血管成熟的阶段。

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摘要

OBJECTIVE: To investigate the effects of tyrosine-kinase inhibitors of vascular endothelial growth factor (VECF) and platelet-derived growth factor (PDCF)-receptors on non-malignant tissue and whether they depend upon the stage of vascular maturation. MATERIALS AND METHODS: PTK787/ZK222584 and CGP53716 (VEGF- and PDGF-receptor inhibitor respectively), both alone and combined, were applied on chicken chorioallantoic membrane (CAM). RESULTS: On embryonic day of CAM development (E)8, only immature microvessels, which lack coverage of pericytes, are present: whereas the microvessels on E12 have pericytic coverage. This development was reflected in the expression levels of pericytic markers (alpha-smooth muscle actin, PDGF-receptor beta and desmin), which were found by immunoblotting to progressively increase between E8 and E12. Monotherapy with 2 microg of PTK787/ZK222584 induced significant vasodegeneration on E8, but not on E12. Monotherapy with CGP53716 affected only pericytes. When CGP53716 was appliedprior to treatment with 2 microg of PTK787/ZK222584, vasodegeneration occurred also on E12. The combined treatment increased the apoptotic rate. as evidenced by the cDNA levels of caspase-9 and the TUNEL-assay. CONCLUSION: Anti-angiogenic treatment strategies for non-neoplastic disorders should aim to interfere with the maturation stage of the target vessels: monotherapy with VEGF-receptor inhibitor for immature vessels, and combined anti-angiogenic treatment for well developed mature vasculature.
机译:目的:探讨血管内皮生长因子(VECF)和血小板源性生长因子(PDCF)受体酪氨酸激酶抑制剂对非恶性组织的影响以及它们是否取决于血管成熟阶段。材料与方法:将PTK787 / ZK222584和CGP53716(分别为VEGF和PDGF受体抑制剂)单独和组合应用在鸡绒膜尿囊膜(CAM)上。结果:在CAM发育(E)8的胚胎天,仅存在缺乏周细胞覆盖的未成熟微血管:而E12上的微血管具有周细胞覆盖。这种发展反映在周细胞标志物(α平滑肌肌动蛋白,PDGF受体β和结蛋白)的表达水平上,这些水平通过免疫印迹发现在E8和E12之间逐渐增加。用2微克PTK787 / ZK222584进行的单药治疗在E8上诱导了显着的血管生成,但在E12上却没有。 CGP53716的单药治疗仅影响周细胞。在用2微克PTK787 / ZK222584治疗之前应用CGP53716时,E12上也发生了血管生成。联合治疗可增加细胞凋亡率。如caspase-9的cDNA水平和TUNEL分析所证明的。结论:针对非肿瘤性疾病的抗血管生成治疗策略应旨在干扰目标血管的成熟阶段:针对未成熟血管的VEGF受体抑制剂单药治疗,以及针对成熟发达的脉管系统的联合抗血管生成治疗。

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