Celletti F L, Waugh J M, Amabile P G, Brendolan A, Hilfiker P R, Dake M D
Cardiovascular and Interventional Radiology, Stanford University Medical Center, Stanford, California, USA.
Nat Med. 2001 Apr;7(4):425-9. doi: 10.1038/86490.
Vascular endothelial growth factor (VEGF) can promote angiogenesis but may also exert certain effects to alter the rate of atherosclerotic plaque development. To evaluate this potential impact on plaque progression, we treated cholesterol-fed mice doubly deficient in apolipoprotein E/apolipoprotein B100 with low doses of VEGF (2 microg/kg) or albumin. VEGF significantly increased macrophage levels in bone marrow and peripheral blood and increased plaque area 5-, 14- and 4-fold compared with controls at weeks 1, 2 and 3, respectively. Plaque macrophage and endothelial cell content also increased disproportionately over controls. In order to confirm that the VEGF-mediated plaque progression was not species-specific, the experiment was repeated in cholesterol-fed rabbits at the three-week timepoint, which showed comparable increases in plaque progression.
血管内皮生长因子(VEGF)可促进血管生成,但也可能产生某些影响,改变动脉粥样硬化斑块的发展速度。为评估其对斑块进展的潜在影响,我们用低剂量VEGF(2微克/千克)或白蛋白处理载脂蛋白E/载脂蛋白B100双缺陷的高脂喂养小鼠。与对照组相比,VEGF在第1、2和3周时分别使骨髓和外周血中的巨噬细胞水平显著增加,斑块面积分别增加了5倍、14倍和4倍。斑块中的巨噬细胞和内皮细胞含量也比对照组增加得更多。为了证实VEGF介导的斑块进展不是物种特异性的,在三周时间点对高脂喂养的兔子重复了该实验,结果显示斑块进展有类似的增加。