Casie Chetty Satish, Rost Megan S, Enriquez Jacob Ryan, Schumacher Jennifer A, Baltrunaite Kristina, Rossi Andrea, Stainier Didier Y R, Sumanas Saulius
Division of Developmental Biology, Cincinnati Children's Hospital Medical Center, 3333 Burnet Ave, Cincinnati, OH 45229, USA; Molecular and Developmental Biology Graduate Program, University of Cincinnati College of Medicine, 3230 Eden Ave, Cincinnati, OH 45267, USA.
Division of Developmental Biology, Cincinnati Children's Hospital Medical Center, 3333 Burnet Ave, Cincinnati, OH 45229, USA.
Dev Biol. 2017 Apr 15;424(2):147-161. doi: 10.1016/j.ydbio.2017.03.005. Epub 2017 Mar 7.
Vasculogenesis involves the differentiation of vascular endothelial progenitors de novo from undifferentiated mesoderm, their migration and coalescence to form the major embryonic vessels and the acquisition of arterial or venous identity. Vascular Endothelial Growth Factor (Vegf) signaling plays multiple roles during vascular development. However, its function during embryonic vasculogenesis has been controversial. Previous studies have implicated Vegf signaling in either regulating arteriovenous specification or overall vascular endothelial differentiation. To clarify the role of Vegf in embryonic vasculogenesis and identify its downstream targets, we used chemical inhibitors of Vegf receptor (Vegfr) signaling in zebrafish embryos as well as zebrafish genetic mutants. A high level of chemical inhibition of Vegfr signaling resulted in the reduction of overall vascular endothelial marker gene expression, including downregulation of both arterial and venous markers, ultimately leading to the apoptosis of vascular endothelial cells. In contrast, a low level of Vegfr inhibition specifically blocked arterial specification while the expression of venous markers appeared largely unaffected or increased. Inhibition of Vegfr signaling prior to the initiation of vasculogenesis reduced overall vascular endothelial differentiation, while inhibition of Vegfr signaling starting at mid-somitogenesis stages largely inhibited arterial specification. Conversely, Vegf overexpression resulted in the expansion of both arterial and pan-endothelial markers, while the expression of several venous-specific markers was downregulated. We further show that Vegf signaling affects overall endothelial differentiation by modulating the expression of the ETS transcription factor etv2/ etsrp. etv2 expression was downregulated in Vegfr- inhibited embryos, and expanded in Vegfaa-overexpressing embryos. Furthermore, vascular-specific overexpression of etv2 in Vegfr-inhibited embryos rescued defects in vascular endothelial differentiation. Similarly, vegfaa genetic mutants displayed a combination of the two phenotypes observed with chemical Vegfr inhibition: the expression of arterial and pan-endothelial markers including etv2 was downregulated while the expression of most venous markers was either expanded or unchanged. Based on these results we propose a revised model which explains the different phenotypes observed upon inhibition of Vegf signaling: low levels of Vegf signaling promote overall vascular endothelial differentiation and cell survival by upregulating etv2 expression, while high levels of Vegf signaling promote arterial and inhibit venous specification.
血管生成涉及未分化的中胚层中血管内皮祖细胞从头分化,它们迁移并融合形成主要的胚胎血管,并获得动脉或静脉特性。血管内皮生长因子(Vegf)信号通路在血管发育过程中发挥多种作用。然而,其在胚胎血管生成过程中的功能一直存在争议。先前的研究表明Vegf信号通路参与调节动静脉分化或整体血管内皮分化。为了阐明Vegf在胚胎血管生成中的作用并确定其下游靶点,我们在斑马鱼胚胎中使用了Vegf受体(Vegfr)信号通路的化学抑制剂以及斑马鱼基因敲除模型。高水平的Vegfr信号通路化学抑制导致整体血管内皮标记基因表达减少,包括动脉和静脉标记物的下调,最终导致血管内皮细胞凋亡。相反,低水平的Vegfr抑制特异性地阻断动脉分化,而静脉标记物的表达在很大程度上不受影响或增加。在血管生成开始前抑制Vegfr信号通路会降低整体血管内皮分化,而在体节形成中期开始抑制Vegfr信号通路则主要抑制动脉分化。相反,Vegf过表达导致动脉和泛内皮标记物的扩增,而几种静脉特异性标记物的表达下调。我们进一步表明,Vegf信号通路通过调节ETS转录因子etv2/etsrp的表达来影响整体内皮分化。在Vegfr抑制的胚胎中,etv2表达下调,而在Vegfaa过表达的胚胎中则扩增。此外,在Vegfr抑制的胚胎中血管特异性过表达etv2挽救了血管内皮分化的缺陷。同样,vegfaa基因敲除模型表现出与化学抑制Vegfr所观察到的两种表型的组合:包括etv2在内的动脉和泛内皮标记物的表达下调,而大多数静脉标记物的表达要么扩增要么不变。基于这些结果,我们提出了一个修订模型,该模型解释了抑制Vegf信号通路时观察到的不同表型:低水平的Vegf信号通路通过上调etv2表达促进整体血管内皮分化和细胞存活,而高水平的Vegf信号通路促进动脉分化并抑制静脉分化。