Isolation and Imaging of Microvessels From Brain Tissue.

IF 1.1 Q3 BIOLOGY
Josephine K Buff, Carolyn R Bertozzi, Tony Wyss-Coray, Sophia M Shi
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引用次数: 0

Abstract

Proper brain function depends on the integrity of the blood-brain barrier (BBB), which is formed by a specialized network of microvessels in the brain. Reliable isolation of these microvessels is crucial for studying BBB composition and function in both health and disease. Here, we describe a protocol for the mechanical dissociation and density-based separation of microvessels from fresh or frozen human and murine brain tissue. The isolated microvessels retain their molecular integrity and are compatible with downstream applications, including fluorescence imaging and biochemical analyses. This method enables direct comparisons across species and disease states using the same workflow, facilitating translational research on BBB biology. Key features • The protocol employs mechanical dissociation and density-based separation to isolate microvessels from brain tissues. • The protocol was used to study molecular changes in brain microvessels in neurodegeneration and aging. • Validated downstream applications of this method include fluorescence imaging, RNA sequencing, proteomics, western blotting, and ELISA. • The protocol can be applied to fresh and frozen human and murine brain samples.

Abstract Image

Abstract Image

Abstract Image

脑组织微血管的分离与成像。
正常的脑功能依赖于血脑屏障(BBB)的完整性,而血脑屏障是由大脑中一个专门的微血管网络形成的。可靠地分离这些微血管对于研究血脑屏障的组成和在健康和疾病中的功能至关重要。在这里,我们描述了一种从新鲜或冷冻的人类和小鼠脑组织中机械分离和基于密度的微血管分离的方案。分离的微血管保持其分子完整性,并与下游应用兼容,包括荧光成像和生化分析。这种方法可以使用相同的工作流程直接比较物种和疾病状态,促进血脑屏障生物学的转化研究。•该方案采用机械解离和基于密度的分离,从脑组织中分离微血管。•该方案用于研究神经变性和衰老时脑微血管的分子变化。•该方法的下游应用包括荧光成像、RNA测序、蛋白质组学、western blotting和ELISA。•该方案可适用于新鲜和冷冻的人类和小鼠脑样本。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
1.50
自引率
0.00%
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