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首页> 外文期刊>Developmental biology >VASCULAR ENDOTHELIAL GROWTH FACTOR (VEGF) AND VEGF RECEPTOR 2 (FLK-1) ARE EXPRESSED DURING VASCULOGENESIS AND VASCULAR DIFFERENTIATION IN THE QUAIL EMBRYO
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VASCULAR ENDOTHELIAL GROWTH FACTOR (VEGF) AND VEGF RECEPTOR 2 (FLK-1) ARE EXPRESSED DURING VASCULOGENESIS AND VASCULAR DIFFERENTIATION IN THE QUAIL EMBRYO

机译:鹌鹑胚胎血管增生和血管分化过程中表达血管内皮生长因子(VEGF)和VEGF受体2(FLK-1)。

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Vasculogenesis, the de novo formation of embryonic blood vessels from their angioblastic precursors in situ, is supposed to be under the control of polypeptide growth factors and their receptors. The receptor tyrosine kinase flk-1 and its high-affinity ligand vascular endothelial growth factor (VEGF) represent an endothelial specific signal transduction system expressed during embryonic vascular growth in the mouse. We have cloned the quail homologs of VEGF and flk-1 using PCR and have investigated their expression pattern in vivo. As shown by Northern analysis and reverse transcription PCR, VEGF and flk-1 mRNA (3.9 and 5.8 kb, respectively) were already present in the unincubated blastodisc at low levels and were largely upregulated during gastrulation at Embryonic Day 1. As detected by in situ hybridization, flk-1 mRNA was initially present in the entire mesoderm of Day 1 embryos but from Day 2 on was restricted to endothelial cells. At Day 2 VEGF was ubiquitously expressed in the embryo proper and was mainly restricted to the vascularized part (area vasculosa) in the yolk sac. Later On VEGF expression was detected in all organs. In the kidney VEGF mRNA was mainly localized to the glomeruli. This pattern of expression is consistent with the pattern found during mouse embryogenesis. We have recently established an in vitro model of vasculogenesis in which hemangioblastic precursors are induced in cell cultures from the unincubated quail blastodisc by basic fibroblast growth factor (bFGF) and give rise to blood vessels in vitro. Taking advantage of this in vitro model we examined whether FGF and VEGF act in concert during vasculogenesis. We found that the flk-1 receptor mRNA is dramatically upregulated within 24 hr upon the addition of FGF to quail blastodisc cell cultures. This inducibility in response to FGF is confined to the first 24 hr of culture. The early expression of the flk-1 mRNA may characterize the differentiation of hemangioblastic precursors from pluripotent epiblast cells which in vivo is initiated during gastrulation. Thus, the time course and the pattern of expression during embryogenesis in different species suggest a major role for the VEGF/flk-1 signal transduction system in vasculogenesis and angiogenesis. (C) 1995 Academic Press, Inc. [References: 39]
机译:血管生成,即从它们的原位成血管细胞前体从头开始形成的新生血管,应在多肽生长因子及其受体的控制下进行。受体酪氨酸激酶flk-1及其高亲和力配体血管内皮生长因子(VEGF)代表在小鼠胚胎血管生长过程中表达的内皮特异性信号转导系统。我们已使用PCR克隆了VEGF和flk-1的鹌鹑同源物,并研究了它们在体内的表达模式。如Northern分析和逆转录PCR所示,未孵育的胚盘中已经存在低水平的VEGF和flk-1 mRNA(分别为3.9和5.8 kb),并在胚胎第1天的胃形成过程中被大大上调。杂交后,flk-1 mRNA最初存在于第1天胚胎的整个中胚层中,但从第2天开始仅限于内皮细胞。在第2天,VEGF在胚胎中适当地表达,并且主要限于卵黄囊中的血管化部分(血管区域)。稍后,在所有器官中检测到VEGF表达。在肾脏中,VEGF mRNA主要定位于肾小球。这种表达模式与小鼠胚胎发生过程中发现的模式一致。我们最近建立了一种血管生成的体外模型,其中成纤维细胞前体是由碱性成纤维细胞生长因子(bFGF)在未培养的鹌鹑胚盘细胞中从细胞培养物中诱导出来的,并在体外产生血管。利用该体外模型,我们检查了FGF和VEGF在血管生成过程中是否协同作用。我们发现flk-1受体mRNA在将FGF添加到鹌鹑胚盘细胞培养物中后24小时内显着上调。这种对FGF的诱导能力仅限于培养的最初24小时。 flk-1 mRNA的早期表达可能表征成血管成纤维细胞前体与多能上皮细胞的分化,而这种分化是在胃造胃过程中开始的。因此,在不同物种的胚胎发生过程中的时间进程和表达方式表明,VEGF / flk-1信号转导系统在血管生成和血管生成中起着重要作用。 (C)1995 Academic Press,Inc. [参考:39]

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