Graduate School of Science, Nagoya City University, Nagoya, Japan
Takuya Miura
Department of Biological Sciences, Graduate School of Science, Osaka University, Toyonaka, Japan
Venkatakaushik Voleti
Departments of Biomedical Engineering and Radiology and the Zuckerman Mind Brain Behavior Institute, Columbia University, New York, United States
Kazushi Yamaguchi
Graduate School of Information Science and Technology, Hokkaido University, Sapporo, Japan; National Institute for Physiological Sciences, Okazaki, Japan
National Institute for Physiological Sciences, Okazaki, Japan; Exploratory Research Center on Life and Living Systems, Okazaki, Japan; The Graduate School for Advanced Study, Hayama, Japan
Yukako Fujie
Department of Biological Sciences, Graduate School of Science, Osaka University, Toyonaka, Japan
Exploratory Research Center on Life and Living Systems, Okazaki, Japan; National Institute for Basic Biology, National Institutes of Natural Sciences, Okazaki, Japan; The Graduate School for Advanced Study, Hayama, Japan
National Institute for Physiological Sciences, Okazaki, Japan; Exploratory Research Center on Life and Living Systems, Okazaki, Japan; The Graduate School for Advanced Study, Hayama, Japan
Graduate School of Science, Nagoya City University, Nagoya, Japan; Department of Biological Sciences, Graduate School of Science, Osaka University, Toyonaka, Japan; RIKEN center for Advanced Intelligence Project, Tokyo, Japan
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.