Argraves W Scott, Larue Amanda C, Fleming Paul A, Drake Christopher J
Cardiovascular Developmental Biology Center, Department of Cell Biology, Medical University of South Carolina, and Vasculogenix, Inc, Charleston, South Carolina 29425, USA.
Dev Dyn. 2002 Nov;225(3):298-304. doi: 10.1002/dvdy.10162.
Here we investigated the importance of vascular endothelial growth factor (VEGF) signaling to the de novo formation of embryonic blood vessels, vasculogenesis, as opposed to the maintenance of blood vessels. We found that antagonizing the activity of the VEGF signaling pathway by using soluble VEGF receptor 1 (sFlt1) or VEGF antibodies inhibited vasculogenesis that occurs in embryos and in cultures of 7.5 days postcoitus prevascular mesoderm. Antagonist treatment resulted in the formation of clusters of endothelial cells not normally observed during vasculogenesis. In contrast, when embryos with established vasculatures or cultures of vascularized mesoderm were treated with sFlt1 or VEGF antibodies, no discernible alterations to the preexisting blood vessels were observed. These observations indicate that, although VEGF signaling is required to promote the mesenchymal to epithelial transition by which angioblasts assemble into nascent endothelial tubes, it is not required by endothelial cells to maintain their organization as an endothelium.
在此,我们研究了血管内皮生长因子(VEGF)信号传导对于胚胎血管从头形成(即血管生成)的重要性,而非血管维持的重要性。我们发现,通过使用可溶性VEGF受体1(sFlt1)或VEGF抗体拮抗VEGF信号通路的活性,可抑制胚胎以及交配后7.5天前血管中胚层培养物中发生的血管生成。拮抗剂处理导致形成了血管生成过程中通常不会观察到的内皮细胞簇。相比之下,当用sFlt1或VEGF抗体处理已建立脉管系统的胚胎或血管化中胚层培养物时,未观察到对先前存在的血管有明显改变。这些观察结果表明,尽管VEGF信号传导是促进间充质向上皮转变(成血管细胞通过该转变组装成新生内皮管)所必需的,但内皮细胞维持其作为内皮的组织结构并不需要VEGF信号传导。