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免疫标记肾脏组织的光学清除与成像

Optical Clearing and Imaging of Immunolabeled Kidney Tissue.

作者信息

Saritas Turgay, Puelles Victor G, Su Xiao-Tong, Ellison David H, Kramann Rafael

机构信息

Division of Nephrology and Clinical Immunology, University Hospital RWTH Aachen;

Division of Nephrology and Clinical Immunology, University Hospital RWTH Aachen; III. Department of Medicine, University Medical Center, Hamburg-Eppendorf; Department of Nephrology, Monash Health.

出版信息

J Vis Exp. 2019 Jul 22(149). doi: 10.3791/60002.

Abstract

Optical clearing techniques render tissue transparent by equilibrating the refractive index throughout a sample for subsequent three-dimensional (3-D) imaging. They have received great attention in all research areas for the potential to analyze microscopic multicellular structures that extend over macroscopic distances. Given that kidney tubules, vasculature, nerves, and glomeruli extend in many directions, which have been only partially captured by traditional two-dimensional techniques so far, tissue clearing also opened up many new areas of kidney research. The list of optical clearing methods is rapidly growing, but it remains difficult for beginners in this field to choose the best method for a given research question. Provided here is a simple method that combines antibody labeling of thick mouse kidney slices; optical clearing with cheap, non-toxic and ready-to-use chemical ethyl cinnamate; and confocal imaging. This protocol describes how to perfuse kidneys and use an antigen-retrieval step to increase antibody- binding without requiring specialized equipment. Its application is presented in imaging different multicellular structures within the kidney, and how to troubleshoot poor antibody penetration into tissue is addressed. We also discuss the potential difficulties of imaging endogenous fluorophores and acquiring very large samples and how to overcome them. This simple protocol provides an easy-to-setup and comprehensive tool to study tissue in three dimensions.

摘要

光学透明技术通过使整个样本的折射率平衡,使组织变得透明,以便后续进行三维(3-D)成像。它们在所有研究领域都备受关注,因为有潜力分析跨越宏观距离的微观多细胞结构。鉴于肾小管、脉管系统、神经和肾小球向多个方向延伸,而传统二维技术到目前为止仅部分捕捉到这些结构,组织透明技术也为肾脏研究开辟了许多新领域。光学透明方法的清单正在迅速增加,但该领域的初学者仍然很难为特定的研究问题选择最佳方法。本文提供了一种简单的方法,该方法结合了对厚小鼠肾脏切片进行抗体标记;使用廉价、无毒且即用型化学物质肉桂酸乙酯进行光学透明处理;以及共聚焦成像。本方案描述了如何灌注肾脏以及如何使用抗原修复步骤来增加抗体结合,而无需专门设备。介绍了其在对肾脏内不同多细胞结构进行成像中的应用,以及如何解决抗体难以穿透组织的问题。我们还讨论了对内源性荧光团进行成像和获取非常大的样本时可能遇到的困难以及如何克服这些困难。这个简单的方案提供了一个易于设置且全面的工具,用于三维研究组织。

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