Department of Regenerative Medicine and Cell Biology, Medical University of South Carolina.
Department of Regenerative Medicine and Cell Biology, Medical University of South Carolina;
J Vis Exp. 2024 Jul 19(209). doi: 10.3791/66977.
The intestine is a complex organ composed of the small and the large intestines. The small intestine can be further divided into duodenum, jejunum, and ileum. Each anatomical region of the intestine has a unique function that is reflected by differences in cellular structure. Investigating changes in the intestine requires an in-depth analysis of different tissue regions and cellular alterations. To study the intestine and visualize large pieces of tissue, researchers commonly use a technique known as intestinal Swiss rolls. In this technique, the intestine is divided into each anatomical region and fixed in a flat orientation. Then, the tissue is carefully rolled and processed for paraffin embedding. Proper tissue fixation and orientation is an often-overlooked laboratory technique but is critically important for downstream analysis. Additionally, improper Swiss rolling of intestinal tissue can damage the fragile intestinal epithelium, leading to poor tissue quality for immunostaining. Ensuring well-fixed and properly oriented tissue with intact cellular structures is a crucial step that ensures optimal visualization of intestinal cells. We present a cost-effective and simple method for making Swiss rolls to include all sections of the intestine in a single paraffin-embedded block. We also describe optimized immunofluorescence staining of intestinal tissue to study various aspects of the intestinal epithelium. The following protocol provides researchers with a comprehensive guide to obtaining high-quality immunofluorescence images through intestinal tissue fixation, Swiss-roll technique, and immunostaining. Employing these refined approaches preserves the intricate morphology of the intestinal epithelium and fosters a deeper understanding of intestinal physiology and pathobiology.
肠是一个由小肠和大肠组成的复杂器官。小肠可以进一步分为十二指肠、空肠和回肠。肠道的每个解剖区域都具有独特的功能,这反映在细胞结构的差异上。研究肠道的变化需要对不同的组织区域和细胞变化进行深入分析。为了研究肠道并可视化大块组织,研究人员通常使用一种称为肠道瑞士卷的技术。在该技术中,将肠道分为每个解剖区域并以平面取向固定。然后,小心地将组织卷起并进行石蜡包埋处理。适当的组织固定和定向是一种经常被忽视的实验室技术,但对下游分析至关重要。此外,肠道组织的不当瑞士卷可能会损坏脆弱的肠上皮,从而导致免疫染色的组织质量差。确保具有完整细胞结构的固定良好且定向正确的组织是确保肠道细胞最佳可视化的关键步骤。我们提出了一种经济高效且简单的方法来制作瑞士卷,以便将肠道的所有部分包含在单个石蜡包埋块中。我们还描述了优化的肠道组织免疫荧光染色,以研究肠道上皮的各个方面。以下方案为研究人员提供了通过肠道组织固定、瑞士卷技术和免疫染色获得高质量免疫荧光图像的综合指南。采用这些改进的方法可以保留肠道上皮的复杂形态,并促进对肠道生理学和病理生理学的更深入理解。