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3D visualization and quantification of microvessels in the whole ischemic mouse brain using solvent-based clearing and light sheet microscopy

机译:使用溶剂基清除和光片显微镜对整个缺血小鼠大脑中的微血管进行3D可视化和定量

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摘要

The visualization of cerebral microvessels is essential for understanding brain remodeling after stroke. Injection of dyes allows for the evaluation of perfused vessels, but has limitations related either to incomplete microvascular filling or leakage. In conventional histochemistry, the analysis of microvessels is limited to 2D structures, with apparent limitations regarding the interpretation of vascular circuits. Herein, we developed a straight-forward technique to visualize microvessels in the whole ischemic mouse brain, combining the injection of a fluorescent-labeled low viscosity hydrogel conjugate with 3D solvent clearing followed by automated light sheet microscopy. We performed transient middle cerebral artery occlusion in C57Bl/6j mice and acquired detailed 3D vasculature images from whole brains. Subsequent image processing, rendering and fitting of blood vessels to a filament model was employed to calculate vessel length density, resulting in 0.922 ± 0.176 m/mm3 in healthy tissue and 0.329 ± 0.131 m/mm3 in ischemic tissue. This analysis showed a marked loss of capillaries with a diameter ≤ 10 µm and a more moderate loss of microvessels in the range > 10 and ≤ 20 µm, whereas vessels > 20 µm were unaffected by focal cerebral ischemia. We propose that this protocol is highly suitable for studying microvascular injury and remodeling post-stroke.
机译:脑微血管的可视化对于理解脑卒中后的大脑重塑至关重要。染料的注射允许评估灌注的血管,但存在与不完全的微血管充盈或渗漏有关的局限性。在常规组织化学中,微血管的分析仅限于2D结构,对血管回路的解释有明显的局限性。在这里,我们开发了一种简单的技术来可视化整个缺血小鼠脑中的微血管,将荧光标记的低粘度水凝胶偶联物的注射与3D溶剂清除结合起来,然后进行自动光片显微镜检查。我们在C57Bl / 6j小鼠中进行了短暂的大脑中动脉闭塞,并从整个大脑中获取了详细的3D脉管系统图像。随后的图像处理,渲染和将血管拟合到细丝模型中以计算血管长度密度,从而在健康组织中产生0.922±0.176 m / mm 3 ,在0.329±0.131 m / mm 3 在缺血组织中。该分析显示直径≤10μm的毛细血管明显丢失,而> 10和≤20μm范围内的微血管损失更为适度,而whereas>20μμm的血管不受局灶性脑缺血的影响。我们建议该协议非常适合研究微血管损伤和中风后重塑。

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