双光子显微镜在疾病进展过程中对脑微血管和神经血管单元进行连续成像的功能分析

IF 2.2
Kareem El-Ghazawi, William A. Mills (III), Shayn M. Peirce, Ukpong B. Eyo
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引用次数: 0

摘要

微血管损伤是许多脑部疾病的主要问题。事实上,它们通常被认为是阿尔茨海默病等神经退行性疾病中最早的病理现象,或者是中风等病理位点。然而,人们对导致这些损伤的机制和细胞水平的事件知之甚少。鉴于神经血管单元(NVU)在维持脑组织功能方面的重要性,NVU细胞类型的改变对疾病进展的研究很重要。使用双光子显微镜,微血管和细胞可以在整个疾病进展过程中成像和评估。在这里,我们的目标是提供一个全面的方案,建立和使用双光子显微镜对神经血管单位细胞类型(即周细胞、星形胶质细胞和小胶质细胞)进行系列成像。我们还描述了通过多个时间点解释基于疾病或功能测试的细胞和血管变化的结果。©2025作者。Wiley期刊有限责任公司发表的当前协议基本协议1:小鼠设置串行,实时双光子成像基本协议2:在多个时间点上的视场采集基本协议3:获取红细胞指标的行扫描采集基本协议4:血管和细胞变化的定量测量基本协议5:记录星形胶质细胞形态的变化,随后使用Rose Bengal诱导瞬时局灶性光血栓性卒中
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Two-Photon Microscopy Functional Assays for Serial Imaging of Brain Microvessels and the Neurovascular Unit Through Disease Progression

Two-Photon Microscopy Functional Assays for Serial Imaging of Brain Microvessels and the Neurovascular Unit Through Disease Progression

Two-Photon Microscopy Functional Assays for Serial Imaging of Brain Microvessels and the Neurovascular Unit Through Disease Progression

Two-Photon Microscopy Functional Assays for Serial Imaging of Brain Microvessels and the Neurovascular Unit Through Disease Progression

Two-Photon Microscopy Functional Assays for Serial Imaging of Brain Microvessels and the Neurovascular Unit Through Disease Progression

Microvascular impairments are a major issue in many diseases of the brain. In fact, they are often considered the earliest pathological phenomena in neurodegenerative diseases like Alzheimer's Disease or the locus of pathology as in stroke. Still, little is known about the mechanistic and cellular level events that contribute to these impairments. Given the importance of the neurovascular unit (NVU) in maintaining functional brain tissue, alterations to NVU cell types are important to study in the context of disease progression. With the use of two-photon microscopy, microvessels and cells can be imaged and evaluated throughout disease progression. Herein we aim to provide a comprehensive protocol for setting up and using two-photon microscopy for serial imaging of neurovascular unit cell types (i.e., pericytes, astrocytes, and microglia). We also describe interpreting results from cell and vessel changes based on disease or functional tests through multiple timepoints. © 2025 The Author(s). Current Protocols published by Wiley Periodicals LLC.

Basic Protocol 1: Mouse set up for serial, live 2-photon imaging

Basic Protocol 2: Field of view acquisitions over multiple timepoints

Basic Protocol 3: Line scan acquisitions for acquiring red blood cell metrics

Basic Protocol 4: Quantitative measurements of vessel and cell changes

Basic Protocol 5: Documenting changes in astrocyte morphology following induction of transient focal photothrombotic stroke using Rose Bengal

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