Laboratory of Angiogenesis and Neurovascular Link, Vesalius Research Center, Vlaams Instituut voor Biotechnologie (VIB), Department of Oncology, Katholieke Universiteit Leuven (KU Leuven), Herestraat 49, 3000 Leuven, Belgium.
Trends Endocrinol Metab. 2013 Dec;24(12):589-96. doi: 10.1016/j.tem.2013.08.006. Epub 2013 Sep 27.
Vessel sprouting by endothelial cells (ECs) during angiogenesis relies on a navigating tip cell and on proliferating stalk cells that elongate the shaft. To date, only genetic signals have been shown to regulate vessel sprouting. However, emerging evidence indicates that the angiogenic switch also requires a metabolic switch. Indeed, angiogenic signals not only induce a change in EC metabolism but this metabolic adaptation also co-determines vessel sprouting. The glycolytic activator PFKFB3 regulates stalk cell proliferation and renders ECs more competitive to reach the tip. We discuss the emerging link between angiogenesis and EC metabolism during the various stages of vessel sprouting, focusing only on genetic signals for which an effect on EC metabolism has been documented.
血管生成过程中内皮细胞(ECs)的血管发芽依赖于一个导航尖端细胞和增殖的茎细胞,这些细胞延长了轴。迄今为止,只有遗传信号被证明可以调节血管发芽。然而,新出现的证据表明,血管生成开关还需要代谢开关。事实上,血管生成信号不仅诱导 EC 代谢的变化,而且这种代谢适应也共同决定了血管发芽。糖酵解激活剂 PFKFB3 调节茎细胞的增殖,并使 EC 更具竞争力以到达尖端。我们讨论了血管生成和 EC 代谢在血管发芽的各个阶段之间的新联系,仅关注已记录对 EC 代谢有影响的遗传信号。