Omerzu Manja, Fenderico Nicola, de Barbanson Buys, Sprangers Joep, de Ridder Jeroen, Maurice Madelon M
Oncode Institute and Department of Cell Biology, Centre for Molecular Medicine, University Medical Centre Utrecht, 3584 CX Utrecht, The Netherlands.
Oncode Institute and Department of Genetics, Center for Molecular Medicine, University Medical Center Utrecht, 3584 CG, Utrecht, The Netherlands.
Biol Open. 2019 Aug 9;8(8):bio042812. doi: 10.1242/bio.042812.
The culturing of mini-organs (organoids) in three-dimensions (3D) presents a simple and powerful tool to investigate the principles underlying human organ development and tissue self-organization in both healthy and diseased states. Applications of single molecule analysis are highly informative for a comprehensive understanding of the complexity underlying tissue and organ physiology. To fully exploit the potential of single molecule technologies, the adjustment of protocols and tools to 3D tissue culture is required. Single molecule RNA fluorescence hybridization (smFISH) is a robust technique for visualizing and quantifying individual transcripts. In addition, smFISH can be employed to study splice variants, fusion transcripts as well as transcripts of multiple genes at the same time. Here, we develop a 3-day protocol and validation method to perform smFISH in 3D in whole human organoids. We provide a number of applications to exemplify the diverse possibilities for the simultaneous detection of distinct mRNA transcripts, evaluation of their spatial distribution and the identification of divergent cell lineages in 3D in organoids.
三维(3D)培养微型器官(类器官)为研究健康和患病状态下人类器官发育及组织自组织的潜在原理提供了一种简单而强大的工具。单分子分析的应用对于全面理解组织和器官生理学的复杂性具有高度的信息量。为了充分发挥单分子技术的潜力,需要将实验方案和工具调整到3D组织培养。单分子RNA荧光杂交(smFISH)是一种用于可视化和定量单个转录本的强大技术。此外,smFISH可用于同时研究剪接变体、融合转录本以及多个基因的转录本。在此,我们开发了一种为期3天的实验方案和验证方法,用于在全人类类器官中进行3D smFISH。我们提供了一些应用实例,以说明在类器官中3D同时检测不同mRNA转录本、评估其空间分布以及识别不同细胞谱系的多种可能性。