ReViMS: Software Tool for Estimating the Volumes of 3-D Multicellular Spheroids Imaged Using a Light Sheet Fluorescence Microscope
Author(s) -
Filippo Piccinini,
Anna Tesei,
Michele Zai,
Alessandro Bevilacqua
Publication year - 2017
Publication title -
biotechniques
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.617
H-Index - 131
eISSN - 1940-9818
pISSN - 0736-6205
DOI - 10.2144/000114609
Subject(s) - spheroid , microscope , fluorescence microscope , microscopy , optics , volume (thermodynamics) , fluorescence , software , visualization , range (aeronautics) , biomedical engineering , materials science , computer science , chemistry , physics , artificial intelligence , medicine , composite material , biochemistry , quantum mechanics , in vitro , programming language
Cancer 3-D spheroids are widely used to test drugs and radiotherapy treatments. These 3-D cell clusters range from tens to hundreds of micrometers in size, with shapes that typically differ from a perfect sphere. Change in spheroid volume is one of the most important parameters for evaluating treatment efficacy, and using light sheet fluorescence microscopes (LSFM), optical sections of samples in that size range can be obtained. However, there remains a lack of validated methods for quantifying the volumes of 3-D multicellular aggregates. Here, we present Reconstruction and Visualization from Multiple Sections (ReViMS), an open-source, user-friendly software for automatically segmenting z-stacks of fluorescence images and estimating the volumes of 3-D multicellular spheroids. To assess the precision and accuracy of the volume estimates obtained with ReViMS, we used several cancer spheroids imaged with LSFM. Both the precision and accuracy were >95%, demonstrating the effectiveness of ReViMS.
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