内质网
分割
计算机科学
表型
人工智能
计算生物学
拓扑(电路)
机器学习
生物
细胞生物学
基因
遗传学
数学
组合数学
作者
Meng Lü,Charles N. Christensen,Jana M. Weber,Tasuku Konno,Nino F. Läubli,Katharina M. Scherer,Edward Avezov,Píetro Lió,Alexei A. Lapkin,Gabriele S. Kaminski Schierle,Clemens F. Kaminski
出处
期刊:Nature Methods
[Nature Portfolio]
日期:2023-03-30
卷期号:20 (4): 569-579
被引量:17
标识
DOI:10.1038/s41592-023-01815-0
摘要
The ability to quantify structural changes of the endoplasmic reticulum (ER) is crucial for understanding the structure and function of this organelle. However, the rapid movement and complex topology of ER networks make this challenging. Here, we construct a state-of-the-art semantic segmentation method that we call ERnet for the automatic classification of sheet and tubular ER domains inside individual cells. Data are skeletonized and represented by connectivity graphs, enabling precise and efficient quantification of network connectivity. ERnet generates metrics on topology and integrity of ER structures and quantifies structural change in response to genetic or metabolic manipulation. We validate ERnet using data obtained by various ER-imaging methods from different cell types as well as ground truth images of synthetic ER structures. ERnet can be deployed in an automatic high-throughput and unbiased fashion and identifies subtle changes in ER phenotypes that may inform on disease progression and response to therapy. ERnet is a deep learning-based software tool for automatic segmentation and classification of structures in the endoplasmic reticulum. ERnet is compatible with many fluorescence imaging modalities and can uncover subtle phenotypic changes.
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