Novel fixed Z-dimension (FiZD) kidney primordia and an organoid culture system for time-lapse confocal imaging
Author(s) -
Ulla Saarela,
Saad Ullah Akram,
Audrey Desgrange,
Aleksandra RakRaszewska,
Jingdong Shan,
Silvia Cereghini,
VeliPekka Ronkainen,
Janne Heikkilä,
Ilya Skovorodkin,
Seppo Vainio
Publication year - 2017
Publication title -
development
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.754
H-Index - 325
eISSN - 1477-9129
pISSN - 0950-1991
DOI - 10.1242/dev.142950
Subject(s) - organoid , biology , morphogenesis , live cell imaging , confocal , microbiology and biotechnology , confocal microscopy , process (computing) , organ culture , primordium , anatomy , cell , computer science , in vitro , biochemistry , genetics , geometry , mathematics , gene , operating system
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 z -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 z -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 ex vivo at the level of the single constituent cells of a complex mammalian organogenesis model system.
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