Institut National de la Santé et de la Recherche Médicale (INSERM), Unité 823, Institut Albert Bonniot, Rond-point de la Chantourne, 38700 La Tronche, France ; Université Grenoble Alpes, 38041 Grenoble, France.
Commissariat à l'Énergie Atomique et aux Énergies Alternatives, Institut de Recherches en Sciences et Technologies pour le Vivant (iRTSV), Biologie du Cancer et de l'Infection, 17 rue des Martyrs, 38054 Grenoble, France.
Biomed Res Int. 2014;2014:309082. doi: 10.1155/2014/309082. Epub 2014 Jul 10.
Angiogenesis is a key process for proper placental development and for the success of pregnancy. Although numerous in vitro methods have been developed for the assessment of this process, relatively few reliable in vivo methods are available to evaluate this activity throughout gestation. Here we report an in vivo technique that specifically measures placental neovascularization. The technique is based on the measurement of a fluorescent alpha v beta 3 (αvβ3) integrin-targeting molecule called Angiolone-Alexa-Fluor 700. The αvβ3 integrin is highly expressed by endothelial cells during the neovascularization and by trophoblast cells during their invasion of the maternal decidua. Angiolone was injected to gravid mice at 6.5 and 11.5 days post coitus (dpc). The fluorescence was analyzed one day later at 7.5 and 12.5 dpc, respectively. We demonstrated that (i) Angiolone targets αvβ3 protein in the placenta with a strong specificity, (ii) this technique is quantitative as the measurement was correlated to the increase of the placental size observed with increasing gestational age, and (iii) information on the outcome is possible, as abnormal placentation could be detected early on during gestation. In conclusion, we report the validation of a new noninvasive and quantitative method to assess the placental angiogenic activity, in vivo.
血管生成是胎盘正常发育和妊娠成功的关键过程。尽管已经开发出许多用于评估该过程的体外方法,但可用于评估整个妊娠期该活性的可靠体内方法相对较少。在这里,我们报告了一种专门测量胎盘新血管生成的体内技术。该技术基于对荧光 αvβ3(αvβ3)整联蛋白靶向分子 Angiolone-Alexa-Fluor 700 的测量。αvβ3 整联蛋白在血管生成过程中高度表达内皮细胞,并在滋养细胞侵入母体蜕膜时表达。Angiolone 在交配后 6.5 天和 11.5 天分别注射到妊娠小鼠体内。在分别在 7.5 和 12.5 天妊娠时分析荧光。我们证明了 (i) Angiolone 以强烈的特异性靶向胎盘上的 αvβ3 蛋白,(ii) 该技术是定量的,因为测量结果与随着妊娠年龄的增加而观察到的胎盘大小的增加相关,以及 (iii) 可以获得关于结果的信息,因为可以在妊娠早期检测到异常胎盘形成。总之,我们报告了一种新的非侵入性和定量方法来评估胎盘血管生成活性的验证,体内。