| Literature DB >> 33781383 |
Chentao Wen1, Takuya Miura2, Venkatakaushik Voleti3, Kazushi Yamaguchi4,5, Motosuke Tsutsumi5,6, Kei Yamamoto7,8, Kohei Otomo5,6,8, Yukako Fujie2, Takayuki Teramoto9, Takeshi Ishihara9, Kazuhiro Aoki6,7,8, Tomomi Nemoto5,6,8, Elizabeth Mc Hillman3, Koutarou D Kimura1,2,10.
Abstract
Despite recent improvements in microscope technologies, segmenting and tracking cells in three-dimensional time-lapse images (3D + T images) to extract their dynamic positions and activities remains a considerable bottleneck in the field. We developed a deep learning-based software pipeline, 3DeeCellTracker, by integrating multiple existing and new techniques including deep learning for tracking. With only one volume of training data, one initial correction, and a few parameter changes, 3DeeCellTracker successfully segmented and tracked ~100 cells in both semi-immobilized and 'straightened' freely moving worm's brain, in a naturally beating zebrafish heart, and ~1000 cells in a 3D cultured tumor spheroid. While these datasets were imaged with highly divergent optical systems, our method tracked 90-100% of the cells in most cases, which is comparable or superior to previous results. These results suggest that 3DeeCellTracker could pave the way for revealing dynamic cell activities in image datasets that have been difficult to analyze.Entities:
Keywords: C. elegans; bioimaging; cell tracking; computational biology; deep learning; neuroscience; quantitative biology; systems biology; zebrafish
Year: 2021 PMID: 33781383 PMCID: PMC8009680 DOI: 10.7554/eLife.59187
Source DB: PubMed Journal: Elife ISSN: 2050-084X Impact factor: 8.140