Department of Stem Cells and Human Disease Models, Research Center for Animal Life Science, Shiga University of Medical Science, Otsu, Shiga, Japan.
Animal Resource Center, University of Tsukuba, Tsukuba, Ibaraki, Japan.
PLoS One. 2019 Jan 2;14(1):e0210060. doi: 10.1371/journal.pone.0210060. eCollection 2019.
Vascular endothelial growth factor receptor 3 (Vegfr3) has been widely used as a marker for lymphatic and vascular endothelial cells during mouse embryonic development and in adult mouse, making it valuable for studying angiogenesis and lymphangiogenesis under normal and pathological conditions. Here, we report the generation of a novel transgenic (Tg) mouse that expresses a membrane-localized fluorescent reporter protein, Gap43-Venus, under the control of the Vegfr3 regulatory sequence. Vegfr3-Gap43-Venus BAC Tg recapitulated endogenous Vegfr3 expression in vascular and lymphatic endothelial cells during embryonic development and tumor development. Thus, this Tg mouse line contributes a valuable model to study angiogenesis and lymphangiogenesis in physiological and pathological contexts.
血管内皮生长因子受体 3(Vegfr3)在小鼠胚胎发育和成年小鼠中被广泛用作淋巴管和血管内皮细胞的标志物,使其成为研究正常和病理条件下血管生成和淋巴管生成的有价值工具。在这里,我们报告了一种新型转基因(Tg)小鼠的产生,该小鼠在 Vegfr3 调节序列的控制下表达膜定位的荧光报告蛋白 Gap43-Venus。Vegfr3-Gap43-Venus BAC Tg 在胚胎发育和肿瘤发育过程中重现了内源性 Vegfr3 在血管和淋巴管内皮细胞中的表达。因此,这条 Tg 小鼠品系为研究生理和病理环境中的血管生成和淋巴管生成提供了一个有价值的模型。