Dumont D J, Jussila L, Taipale J, Lymboussaki A, Mustonen T, Pajusola K, Breitman M, Alitalo K
Ontario Cancer Institute and Amgen Institute, Department of Medical Biophysics, University of Toronto, Toronto, Ontario, Canada M5G 2C1.
Science. 1998 Oct 30;282(5390):946-9. doi: 10.1126/science.282.5390.946.
Vascular endothelial growth factor (VEGF) is a key regulator of blood vessel development in embryos and angiogenesis in adult tissues. Unlike VEGF, the related VEGF-C stimulates the growth of lymphatic vessels through its specific lymphatic endothelial receptor VEGFR-3. Here it is shown that targeted inactivation of the gene encoding VEGFR-3 resulted in defective blood vessel development in early mouse embryos. Vasculogenesis and angiogenesis occurred, but large vessels became abnormally organized with defective lumens, leading to fluid accumulation in the pericardial cavity and cardiovascular failure at embryonic day 9.5. Thus, VEGFR-3 has an essential role in the development of the embryonic cardiovascular system before the emergence of the lymphatic vessels.
血管内皮生长因子(VEGF)是胚胎血管发育和成人组织血管生成的关键调节因子。与VEGF不同,相关的VEGF-C通过其特异性淋巴管内皮受体VEGFR-3刺激淋巴管生长。本文表明,编码VEGFR-3的基因靶向失活导致早期小鼠胚胎血管发育缺陷。血管发生和血管生成过程发生,但大血管变得异常组织化,管腔有缺陷,导致心包腔积液和胚胎第9.5天出现心血管衰竭。因此,VEGFR-3在淋巴管出现之前的胚胎心血管系统发育中具有重要作用。