Understanding 3-Dimensional World from 2-Dimensional Immunofluorescent Adjacent Sections

S. Fujisawa, D. Yarilin, Ning Fan, M. Turkekul, Ke Xu, A. Barlas, K. Manova-Todorova
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Abstract

In many fields of biological sciences including embryology and cancer research, understanding of 3-dimensional structures is crucial to uncovering normal and pathological phenomena. While the most optimal method would be to directly observe the complete object without any destruction, staining and imaging of thick sections and whole mount samples can be challenging. For decades, researchers have serially sectioned large tissues stained each with chromogenbased immunohistologicalmethods and painstakingly reconstructed the 3-dimensional volume. The limiting factor with immunohistological staining is the difficulty in detecting multiple antigens with different chromogens on the same tissue. At our Molecular Cytology Core Facility at Memorial Sloan-Kettering Cancer Center, we successfully and routinely perform immunofluorescent staining using automated staining machines and have combined IF staining and 3D reconstruction of serial sections.This method allows simultaneous detection of up to four different antigens on the same sections in a highly reproducible and specific manner. The resulting stack can be a stunning visualization of 3D structure and be quantitatively analyzed.
从二维免疫荧光相邻切片了解三维世界
在包括胚胎学和癌症研究在内的许多生物科学领域,对三维结构的理解对于揭示正常和病理现象至关重要。虽然最理想的方法是直接观察完整的物体而不受任何破坏,但厚切片和整个样品的染色和成像可能具有挑战性。几十年来,研究人员用基于染色体的免疫组织学方法对大组织进行了连续切片,并精心重建了三维体积。免疫组织学染色的限制因素是难以在同一组织中检测到具有不同染色体的多种抗原。在纪念斯隆-凯特琳癌症中心的分子细胞学核心设施,我们成功地常规使用自动染色机进行免疫荧光染色,并结合IF染色和连续切片的3D重建。这种方法允许同时检测多达四种不同的抗原在相同的切片高度可重复性和特异性的方式。由此产生的堆栈可以是一个令人惊叹的三维结构可视化和定量分析。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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