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Quantitative assessment of angiogenesis, perfused blood vessels and endothelial tip cells in the postnatal mouse brain

机译:出生后小鼠大脑中血管生成,灌注血管和内皮尖细胞的定量评估

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摘要

During development and in various diseases of the CNS, new blood vessel formation starts with endothelial tip cell selection and vascular sprout migration, followed by the establishment of functional, perfused blood vessels. Here we describe a method that allows the assessment of these distinct angiogenic steps together with antibody-based protein detection in the postnatal mouse brain. Intravascular and perivascular markers such as Evans blue (EB), isolectin B4 (IB4) or laminin (LN) are used alongside simultaneous immunofluorescence on the same sections. By using confocal laser-scanning microscopy and stereological methods for analysis, detailed quantification of the 3D postnatal brain vasculature for perfused and nonperfused vessels (e. g., vascular volume fraction, vessel length and number, number of branch points and perfusion status of the newly formed vessels) and characterization of sprouting activity (e.g., endothelial tip cell density, filopodia number) can be obtained. The entire protocol, from mouse perfusion to vessel analysis, takes similar to 10 d.
机译:在中枢神经系统的发展和各种疾病中,新血管的形成始于内皮尖细胞的选择和血管新芽的迁移,然后是功能性灌注血管的建立。在这里,我们描述了一种方法,该方法可以评估这些不同的血管生成步骤以及产后小鼠大脑中基于抗体的蛋白质检测。血管内和血管周标记物,如伊文思蓝(EB),异凝集素B4(IB4)或层粘连蛋白(LN),与同一部分的同时免疫荧光法同时使用。通过使用共聚焦激光扫描显微镜和体视学方法进行分析,对灌注和非灌注血管的3D产后脑血管进行了详细量化(例如,血管体积分数,血管长度和数量,分支点数以及新形成血管的灌注状态) )和发芽活性的表征(例如,内皮尖端细胞密度,丝状伪足数)。从小鼠灌注到血管分析的整个过程大约需要10天。

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