Genes Nutr. 2010 Sep;5(3):263-74. doi: 10.1007/s12263-010-0166-x. Epub 2010 Feb 2.
A single high-fat challenge induces plasmatic pro-inflammatory and pro-oxidative responses in the postprandial state, even in healthy men. This period is also associated with vascular endothelial dysfunction, which is an early event in the development of cardiovascular diseases. However, knowledge about the mechanisms involved in postprandial hyperlipaemia-induced endothelial dysfunction is sparse. An objective of our study was to characterize the behaviour and gene expression of vascular endothelial cells exposed to postprandial hyperlipaemic sera. Human umbilical vein endothelial cells (HUVECs) were cultured in media containing 10% serum from healthy men withdrawn either before or 4 h after a high-fat challenge. Endothelial cell proliferation, adhesion and migration were then assessed. The transcriptomic profiles of endothelial cells exposed to pre and postprandial sera were also compared. Exposure to postprandial hyperlipaemic sera significantly decreased HUVEC proliferation when compared to preprandial serum (P < 0.0001), while no changes in migration or endothelial/monocyte interactions were observed. The transcriptomic analysis revealed changes in the expression of 675 genes, of which 431 have a known function. Among them, a set of differentially expressed genes was linked to cell cycle regulation and apoptosis and are regulated in favour of cell cycle arrest or death. This result was confirmed by measuring the induction of apoptosis after postprandial sera exposure (P = 0.011). Taken together, the transcriptomic results and pathway analysis showed that postprandial serum promotes apoptosis in HUVECs, potentially through the activation of the p53 network. We conclude that upon postprandial serum exposure, vascular endothelial cells transcriptionally regulate genes involved in the control of cell cycle and death to favour growth arrest and apoptosis. These findings support the hypothesis that postprandial hyperlipaemia is associated with vascular dysfunction and offer new insights into the mechanisms involved.
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研究餐后高脂血症血清诱导的血管内皮细胞功能障碍的分子机制。
将人脐静脉内皮细胞(HUVEC)培养于正常男性高脂肪餐后 4 小时或餐前血清中,观察内皮细胞增殖、黏附和迁移能力的变化,并进行转录组分析。
与餐前血清相比,餐后高脂血症血清显著降低 HUVEC 的增殖能力(P<0.0001),而对迁移或内皮细胞/单核细胞黏附无影响。转录组分析显示,675 个基因的表达发生变化,其中 431 个基因具有已知功能。其中,一组差异表达的基因与细胞周期调控和细胞凋亡有关,有利于细胞周期阻滞或凋亡。这一结果通过检测餐后血清诱导的细胞凋亡得到了进一步证实(P=0.011)。
餐后高脂血症血清可促进 HUVEC 凋亡,可能通过激活 p53 网络发挥作用。这些发现支持了餐后高脂血症与血管功能障碍相关的假说,并为相关机制提供了新的见解。