Graduate School of Science, Nagoya City University, Nagoya, Japan.
Department of Biological Sciences, Graduate School of Science, Osaka University, Toyonaka, Japan.
Elife. 2021 Mar 30;10:e59187. doi: 10.7554/eLife.59187.
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.
尽管显微镜技术最近有所改进,但在三维时移图像(3D + T 图像)中分割和跟踪细胞以提取其动态位置和活动仍然是该领域的一个相当大的瓶颈。我们通过整合多个现有和新技术,包括用于跟踪的深度学习,开发了一个基于深度学习的软件管道 3DeeCellTracker。仅使用一个训练数据集、一个初始校正和几个参数更改,3DeeCellTracker 就成功地分割和跟踪了半固定和“拉直”的自由移动蠕虫大脑中的约 100 个细胞、自然跳动的斑马鱼心脏中的约 100 个细胞和 3D 培养的肿瘤球体中的约 1000 个细胞。虽然这些数据集是用高度不同的光学系统成像的,但我们的方法在大多数情况下跟踪了 90-100%的细胞,这与以前的结果相当或更优。这些结果表明,3DeeCellTracker 可以为揭示以前难以分析的图像数据集的动态细胞活动铺平道路。