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通过透明化、免疫染色、共聚焦和光片荧光显微镜对感染 HIV 的组织中的免疫细胞群体进行 3D 可视化。

3D Visualization of Immune Cell Populations in HIV-Infected Tissues via Clearing, Immunostaining, Confocal, and Light Sheet Fluorescence Microscopy.

机构信息

Department of Microbiology, University of Illinois at Urbana-Champaign.

Department of Medicine, University of California San Diego.

出版信息

J Vis Exp. 2021 May 6(171). doi: 10.3791/62441.

Abstract

Human Immunodeficiency Virus (HIV), the causative agent of Acquired Immune Deficiency Syndrome (AIDS), is a major global health concern with nearly 40 million individuals infected worldwide and no widely accessible cure. Despite intensive efforts, a detailed understanding of virus and host cell interactions in tissues during infection and in response to therapy remains incomplete. To address these limitations, water-based tissue clearing techniques CUBIC (Clear, Unobstructed Brain/Body Imaging Cocktails and Computational analysis) and CLARITY (Clear Lipid-exchanged Acrylamide-hybridized Rigid Imaging/Immunostaining/in situ-hybridization-compatible Tissue hYdrogel) are applied to visualize complex virus host-cell interactions in HIV-infected tissues from animal models and humans using confocal and light sheet fluorescence microscopy. Optical sectioning of intact tissues and image analysis allows rapid reconstruction of spatial information contained within whole tissues and quantification of immune cell populations during infection. These methods are applicable to most tissue sources and diverse biological questions, including infectious disease and cancer.

摘要

人类免疫缺陷病毒(HIV),即获得性免疫缺陷综合征(AIDS)的病原体,是一个全球性的主要健康关注点,全球近 4000 万人感染,且尚无广泛适用的治愈方法。尽管付出了巨大努力,但对于感染期间和治疗反应中病毒和宿主细胞在组织中的相互作用,我们仍未完全了解。为了解决这些局限性,水基组织透明化技术 CUBIC(透明、无阻碍的脑/体成像鸡尾酒和计算分析)和 CLARITY(透明脂质交换丙烯酰胺杂交刚性成像/免疫荧光原位杂交兼容组织水凝胶)被应用于使用共聚焦和光片荧光显微镜观察动物模型和人类的 HIV 感染组织中复杂的病毒-宿主细胞相互作用。完整组织的光学切片和图像分析允许快速重建整个组织中包含的空间信息,并在感染期间定量免疫细胞群体。这些方法适用于大多数组织来源和各种生物学问题,包括传染病和癌症。

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本文引用的文献

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Curr Protoc Cytom. 2018 Oct;86(1):e38. doi: 10.1002/cpcy.38. Epub 2018 Jul 13.
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J Histochem Cytochem. 2017 Jan;65(1):5-20. doi: 10.1369/0022155416673995. Epub 2016 Oct 23.

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