Saarela Ulla, Akram Saad Ullah, Desgrange Audrey, Rak-Raszewska Aleksandra, Shan Jingdong, Cereghini Silvia, Ronkainen Veli-Pekka, Heikkilä Janne, Skovorodkin Ilya, Vainio Seppo J
Faculty of Biochemistry and Molecular Medicine, University of Oulu, 90220 Oulu, Finland.
Laboratory of Developmental Biology, Biocenter Oulu and InfoTech, 90220 Oulu, Finland.
Development. 2017 Mar 15;144(6):1113-1117. doi: 10.1242/dev.142950. Epub 2017 Feb 20.
Tissue, organ and organoid cultures provide suitable models for developmental studies, but our understanding of how the organs are assembled at the single-cell level still remains unclear. We describe here a novel fixed -direction (FiZD) culture setup that permits high-resolution confocal imaging of organoids and embryonic tissues. In a FiZD culture a permeable membrane compresses the tissues onto a glass coverslip and the spacers adjust the thickness, enabling the tissue to grow for up to 12 days. Thus, the kidney rudiment and the organoids can adjust to the limited -directional space and yet advance the process of kidney morphogenesis, enabling long-term time-lapse and high-resolution confocal imaging. As the data quality achieved was sufficient for computer-assisted cell segmentation and analysis, the method can be used for studying morphogenesis at the level of the single constituent cells of a complex mammalian organogenesis model system.
组织、器官和类器官培养为发育研究提供了合适的模型,但我们对器官在单细胞水平上如何组装的理解仍不清楚。我们在此描述一种新型的固定方向(FiZD)培养装置,它允许对类器官和胚胎组织进行高分辨率共聚焦成像。在FiZD培养中,一个可渗透的膜将组织压缩到一个玻璃盖玻片上,间隔物调节厚度,使组织能够生长长达12天。因此,肾原基和类器官可以适应有限的定向空间,同时推进肾脏形态发生过程,实现长期延时和高分辨率共聚焦成像。由于所获得的数据质量足以进行计算机辅助细胞分割和分析,该方法可用于在复杂的哺乳动物器官发生模型系统的单个组成细胞水平上研究形态发生。