Yamada Hiroyuki, Makino Shin-Ichi, Okunaga Issei, Miyake Takafumi, Yamamoto-Nonaka Kanae, Oliva Trejo Juan Alejandro, Tominaga Takahiro, Empitu Maulana A, Kadariswantiningsih Ika N, Kerever Aurelien, Komiya Akira, Ichikawa Tomohiko, Arikawa-Hirasawa Eri, Yanagita Motoko, Asanuma Katsuhiko
Department of Nephrology, Graduate School of Medicine, Chiba University, Chiba 260-8677, Japan.
The Laboratory for Kidney Research (TMK Project), Medical Innovation Center, Graduate School of Medicine, Kyoto University, Kyoto 606-8397, Japan.
PNAS Nexus. 2024 Jan 8;3(1):pgad433. doi: 10.1093/pnasnexus/pgad433. eCollection 2024 Jan.
The spatial organization of various cell populations is critical for the major physiological and pathological processes in the kidneys. Most evaluation of these processes typically comes from a conventional 2D tissue cross-section, visualizing a limited amount of cell organization. Therefore, the 2D analysis of kidney biopsy introduces selection bias. The 2D analysis potentially omits key pathological findings outside a 1- to 10-μm thin-sectioned area and lacks information on tissue organization, especially in a particular irregular structure such as crescentic glomeruli. In this study, we introduce an easy-to-use and scalable method for obtaining high-quality images of molecules of interest in a large tissue volume, enabling a comprehensive evaluation of the 3D organization and cellular composition of kidney tissue, especially the glomerular structure. We show that CUBIC and ScaleS clearing protocols could allow a 3D analysis of the kidney tissues in human and animal models of kidney disease. We also demonstrate that the paraffin-embedded human biopsy specimens previously examined via 2D evaluation could be applicable to 3D analysis, showing a potential utilization of this method in kidney biopsy tissue collected in the past. In summary, the 3D analysis of kidney biopsy provides a more comprehensive analysis and a minimized selection bias than 2D tissue analysis. Additionally, this method enables a quantitative evaluation of particular kidney structures and their surrounding tissues, with the potential utilization from basic science investigation to applied diagnostics in nephrology.
各种细胞群体的空间组织对于肾脏的主要生理和病理过程至关重要。对这些过程的大多数评估通常来自传统的二维组织横截面,只能观察到有限的细胞组织。因此,肾活检的二维分析会引入选择偏倚。二维分析可能会遗漏1至10微米薄切片区域之外的关键病理发现,并且缺乏关于组织组织的信息,尤其是在特定的不规则结构(如新月体性肾小球)中。在本研究中,我们介绍了一种易于使用且可扩展的方法,用于在大组织体积中获取感兴趣分子的高质量图像,从而能够全面评估肾组织的三维组织和细胞组成,尤其是肾小球结构。我们表明,CUBIC和ScaleS清除方案可以对人类和动物肾脏疾病模型中的肾组织进行三维分析。我们还证明,先前通过二维评估检查的石蜡包埋人类活检标本可用于三维分析,显示出该方法在过去收集的肾活检组织中的潜在应用价值。总之,肾活检的三维分析比二维组织分析提供了更全面的分析和最小化的选择偏倚。此外,该方法能够对特定的肾脏结构及其周围组织进行定量评估,具有从基础科学研究到肾脏病应用诊断的潜在应用价值。