Institute for Advanced Biosciences, INSERM-UGA U1209, CNRS UMR 5309, La Tronche, France.
Institut National de la Santé et de la Recherche Médicale, Inserm U1292, Biosanté, Grenoble, France.
Methods Mol Biol. 2024;2728:131-136. doi: 10.1007/978-1-0716-3495-0_11.
Normal fetal growth and placental development depend on active angiogenesis occurring at the fetomaternal interface throughout pregnancy. Nevertheless, reliable in vivo methods to assess placental angiogenesis are still missing. Here, we describe a quantitative and noninvasive in vivo method to specifically measure placental neovascularization in the gravid mouse. This method uses a technique based on the measurement of a fluorescent molecule Angiostamp700 that targets the alpha v beta 3 (αβ) integrin, a protein that is highly expressed by endothelial cells during the neovascularization and by trophoblast cells during invasion of the maternal decidua. Due to this noninvasive method, quantification of the fetomaternal angiogenic activity and information regarding the outcome of pregnancy are now possible.
正常胎儿的生长和胎盘的发育依赖于妊娠期间在胎-母界面发生的活跃血管生成。然而,可靠的胎盘血管生成的体内评估方法仍然缺失。在此,我们描述了一种定量的、非侵入性的体内方法,用于特异性地测量妊娠小鼠的胎盘新血管生成。该方法使用了一种基于荧光分子 Angiostamp700 的测量技术,该分子靶向α v β 3(αβ)整合素,该蛋白在血管生成过程中内皮细胞高度表达,在母体蜕膜浸润过程中滋养细胞表达。由于这种非侵入性方法,现在可以定量评估胎-母血管生成活性,并提供关于妊娠结局的信息。