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利用CT和光学成像技术对大鼠细胞外囊泡进行追踪和定量分析

Extracellular Vesicles Tracking and Quantification Using CT and Optical Imaging in Rats.

作者信息

Guo Shaowei, Betzer Oshra, Perets Nisim, Landau Shira, Offen Daniel, Popovtzer Rachela, Levenberg Shulamit

机构信息

Faculty of Biomedical Engineering, Technion-Israel Institute of Technology, Haifa, Israel.

The First Affiliated Hospital, Shantou University Medical College, Shantou, China.

出版信息

Bio Protoc. 2020 Jun 5;10(11):e3635. doi: 10.21769/BioProtoc.3635.

Abstract

Exosomes, a subtype of extracellular vesicles, are nanovesicles of endocytic origin. Exosomes contain a plethora of proteins, lipids, and genetic materials of parent cells to facilitate intercellular communications. Tracking exosomes is fundamentally important to understand their biodistribution pattern and the mechanism of biological actions in experimental models. Until now, a number of tracking protocols have been developed, including fluorescence labeling, bioluminescence imaging, magnetic resonance imaging, and computed tomography (CT) tracking of exosomes. Recently, we have shown the tracking and quantification of exosomes in a spinal cord injury model, by using two tracking approaches. More specifically, following intranasal administration of gold nanoparticle-encapsulated exosomes to rats bearing complete spinal cord injury, exosomes in the whole central nervous system were tracked by using microCT, and quantified by using inductively coupled plasma and flame atomic absorption spectroscopy. In addition, optical imaging of fluorescently labeled exosomes was performed to understand the abundance of migrating exosomes in the spinal cord lesion, as compared to the healthy controls, and to further examine their affinity to different cell types in the lesion. Thus, the protocol presented here aids in the study of exosome biodistribution at both cellular and organ levels, in the context of spinal cord injury. This protocol will also enable researchers to better elucidate the fate of administered exosomes in other models of interest.

摘要

外泌体是细胞外囊泡的一种亚型,是内吞起源的纳米囊泡。外泌体包含大量母细胞的蛋白质、脂质和遗传物质,以促进细胞间通讯。追踪外泌体对于了解其在实验模型中的生物分布模式和生物学作用机制至关重要。到目前为止,已经开发了许多追踪方案,包括外泌体的荧光标记、生物发光成像、磁共振成像和计算机断层扫描(CT)追踪。最近,我们通过两种追踪方法展示了在脊髓损伤模型中外泌体的追踪和定量。更具体地说,在将金纳米颗粒包裹的外泌体经鼻给予完全性脊髓损伤大鼠后,使用微型CT追踪整个中枢神经系统中的外泌体,并使用电感耦合等离子体和火焰原子吸收光谱法进行定量。此外,与健康对照相比,对荧光标记的外泌体进行光学成像,以了解脊髓损伤部位迁移外泌体的丰度,并进一步检查它们对损伤部位不同细胞类型的亲和力。因此,本文介绍的方案有助于在脊髓损伤的背景下,在细胞和器官水平上研究外泌体的生物分布。该方案还将使研究人员能够更好地阐明在其他感兴趣的模型中给予的外泌体的命运。

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本文引用的文献

1
Advances in imaging strategies for in vivo tracking of exosomes.用于外泌体体内追踪的成像策略的进展。
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In Vivo Neuroimaging of Exosomes Using Gold Nanoparticles.利用金纳米颗粒进行外泌体的体内神经影像学研究。
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