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Flk1-GFP BAC Tg Mice: An Animal Model for the Study of Blood Vessel Development

机译:Flk1-GFP BAC Tg小鼠:血管发育研究的动物模型。

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The mouse Flk1 (also called Kdr or Vegf-r2 ) gene encodes a receptor for VEGF-A. Flk1 is expressed in endothelial cells of the developing embryo. Recent studies have shown that Flk1 is expressed by multi-potent mesodermal progenitors, which give rise to various hematopoietic and cardiovascular cell lineages during development, and in differentiating ES cells, which may be used for cell transplantation therapy to treat cardiovascular diseases. Given its developmental and clinical importance in cardiovascular tissues, an animal model of Flk1 activity would be very useful. Here, we report the generation of Flk1-GFP BAC transgenic mice for monitoring Flk1 gene expression during development. We show that GFP expression in these mice serves as a surrogate marker for developing endothelial cells. Immunohistochemical analysis showed that the regions of expression of GFP and endogenous FLK1 largely overlap. Uniform GFP expression was observed in most endothelial cells at 8.5 dpc and thereafter. Flk1-GFP BAC transgenic mice should be useful for the study of both vascular development and pathological angiogenesis.
机译:小鼠Flk1(也称为Kdr或Vegf-r2)基因编码VEGF-A的受体。 Flk1在发育中的胚胎的内皮细胞中表达。最近的研究表明,Flk1由多能中胚层祖细胞表达,在发育过程中以及分化的ES细胞中会产生多种造血和心血管细胞谱系,可用于细胞移植治疗心血管疾病。鉴于其在心血管组织中的发展和临床重要性,Flk1活性的动物模型将非常有用。在这里,我们报告Flk1-GFP BAC转基因小鼠的生成,以监测发育过程中Flk1基因的表达。我们显示在这些小鼠中的GFP表达充当发展内皮细胞的替代标记。免疫组织化学分析显示GFP和内源性FLK1的表达区域大部分重叠。在大多数内皮细胞中,在8.5 dpc及以后的时间观察到GFP的均匀表达。 Flk1-GFP BAC转基因小鼠应可用于研究血管发育和病理性血管生成。

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