Puelles Victor G, Moeller Marcus J, Bertram John F
aCardiovascular Program, Monash Biomedicine Discovery Institute and Department of Anatomy and Developmental Biology, School of Biomedical Sciences, Monash University, Melbourne, Victoria, Australia bDivision of Nephrology and Clinical Immunology, Medical Faculty, RWTH Aachen University, Aachen, Germany.
Curr Opin Nephrol Hypertens. 2017 May;26(3):179-186. doi: 10.1097/MNH.0000000000000314.
For more than a century, kidney microscopic imaging was driven by the need for greater and greater resolution. This was in part provided by the analysis of thinner tissue sections. As a result, most kidney morphometry was performed in 'two' dimensions, largely ignoring the three-dimensionality of kidney tissue and cells. Although stereological techniques address this issue, they have generally been considered laborious and expensive and thereby unattractive for routine use.
The past 2 decades have witnessed the development of optical clearing techniques, which enables visualization of thick slices of kidney tissue and even whole kidneys. This review describes the three main optical clearing strategies (solvent-based, aqueous-based and hydrogel embedding) with their respective advantages and disadvantages. We also describe how optical clearing provides new approaches to kidney morphometrics, including general kidney morphology (i.e. identification and quantitation of atubular glomeruli), glomerular numbers and volumes, numbers of specific glomerular cells (i.e. podocytes) and cell-specific stress-related changes (i.e. foot process effacement).
The new clearing and morphometric approaches described in this review provide a new toolbox for imaging and quantification of kidney microanatomy. These approaches will make it easier to visualize the three-dimensional microanatomy of the kidney and decrease our reliance on biased two-dimensional morphometric techniques and time-consuming stereological approaches. They will also accelerate our research of structure-function relations in the healthy and diseased kidney.
一个多世纪以来,肾脏显微成像一直受追求更高分辨率的需求驱动。部分通过对更薄组织切片的分析得以实现。结果,大多数肾脏形态测量是在“二维”层面进行的,很大程度上忽略了肾脏组织和细胞的三维特性。尽管体视学技术解决了这个问题,但它们通常被认为费力且昂贵,因此对于常规使用缺乏吸引力。
过去20年见证了光学透明技术的发展,该技术能够实现对肾脏组织厚切片甚至整个肾脏的可视化。本综述描述了三种主要的光学透明策略(基于溶剂的、基于水的和水凝胶包埋)及其各自的优缺点。我们还描述了光学透明如何为肾脏形态测量提供新方法,包括一般肾脏形态(即识别和定量无肾小管肾小球)、肾小球数量和体积、特定肾小球细胞(即足细胞)数量以及细胞特异性应激相关变化(即足突消失)。
本综述中描述的新的透明和形态测量方法为肾脏微观解剖学的成像和定量提供了一个新的工具箱。这些方法将使肾脏三维微观解剖学的可视化更容易,并减少我们对有偏差的二维形态测量技术和耗时的体视学方法的依赖。它们还将加速我们对健康和患病肾脏结构 - 功能关系的研究。