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Dynamic heterogeneous endothelial Tie2 expression and capillary blood flow during microvascular remodeling

机译:动态异质内皮Tie2表达和微血管重塑期间的毛细血管血流

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摘要

Microvascular endothelial cell heterogeneity and its relationship to hemodynamics remains poorly understood due to a lack of sufficient methods to examine these parameters in vivo at high resolution throughout an angiogenic network. The availability of surrogate markers for functional vascular proteins, such as green fluorescent protein, enables expression in individual cells to be followed over time using confocal microscopy, while photoacoustic microscopy enables dynamic measurement of blood flow across the network with capillary-level resolution. We combined these two non-invasive imaging modalities in order to spatially and temporally analyze biochemical and biomechanical drivers of angiogenesis in murine corneal neovessels. By stimulating corneal angiogenesis with an alkali burn in Tie2-GFP fluorescent-reporter mice, we evaluated how onset of blood flow and surgically-altered blood flow affects Tie2-GFP expression. Our study establishes a novel platform for analyzing heterogeneous blood flow and fluorescent reporter protein expression across a dynamic microvascular network in an adult mammal.
机译:由于缺乏足够的方法在整个血管生成网络中以高分辨率检查体内这些参数,微血管内皮细胞异质性及其与血液动力学的关系仍然知之甚少。功能性血管蛋白(例如绿色荧光蛋白)的替代标志物的可用性使得能够使用共聚焦显微镜随着时间的推移跟踪单个细胞中的表达,而光声显微镜能够以毛细管水平的分辨率动态测量整个网络的血流。我们结合这两种非侵入性成像方式,以便在空间和时间上分析鼠角膜新生血管新生的生化和生物力学驱动力。通过在Tie2-GFP荧光报告基因小鼠中通过碱烧伤刺激角膜血管生成,我们评估了血流的发生和外科手术改变的血流如何影响Tie2-GFP的表达。我们的研究建立了一个新的平台,用于分析成年哺乳动物中跨动态微血管网络的异质血流和荧光报告蛋白表达。

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