University of Colorado Denver, Department of Physics, Denver, Colorado, United StatesbUniversity of Colorado Anschutz Medical Campus, Pediatric Heart Lung Center, Department of Pediatrics, Aurora, Colorado, United States.
University of Colorado Anschutz Medical Campus, Pediatric Heart Lung Center, Department of Pediatrics, Aurora, Colorado, United States.
J Biomed Opt. 2017 Jul 1;22(7):76011. doi: 10.1117/1.JBO.22.7.076011.
Retinal vasculature develops in a highly orchestrated three-dimensional (3-D) sequence. The stages of retinal vascularization are highly susceptible to oxygen perturbations. We demonstrate that optical tissue clearing of intact rat retinas and light-sheet microscopy provides rapid 3-D characterization of vascular complexity during retinal development. Compared with flat mount preparations that dissect the retina and primarily image the outermost vascular layers, intact cleared retinas imaged using light-sheet fluorescence microscopy display changes in the 3-D retinal vasculature rapidly without the need for point scanning techniques. Using a severe model of retinal vascular disruption, we demonstrate that a simple metric based on Sholl analysis captures the vascular changes observed during retinal development in 3-D. Taken together, these results provide a methodology for rapidly quantifying the 3-D development of the entire rodent retinal vasculature.
视网膜血管系统在高度协调的三维(3-D)序列中发育。视网膜血管生成的阶段对氧的干扰非常敏感。我们证明,完整大鼠视网膜的光学组织透明化和光片显微镜提供了在视网膜发育过程中快速 3-D 描述血管复杂性的方法。与解剖视网膜并主要对最外层血管层成像的平面安装相比,使用光片荧光显微镜对完整透明化的视网膜进行成像,无需点扫描技术即可快速显示 3-D 视网膜血管的变化。使用严重的视网膜血管破坏模型,我们证明了基于 Sholl 分析的简单度量可以捕获在 3-D 中观察到的视网膜发育过程中的血管变化。总之,这些结果为快速量化整个啮齿动物视网膜血管的 3-D 发育提供了一种方法。