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ERnet: a tool for the semantic segmentation and quantitative analysis of endoplasmic reticulum topology.

Accepted version
Peer-reviewed

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Abstract

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.

Description

Journal Title

Nat Methods

Conference Name

Journal ISSN

1548-7091
1548-7105

Volume Title

Publisher

Springer Nature

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Except where otherwised noted, this item's license is described as All Rights Reserved
Sponsorship
Wellcome Trust (085314/Z/08/Z)
Medical Research Council (MR/K02292X/1)
This research was funded by Infinitus (China) Company Ltd (supporting M.L., C.F.K. and G.S.K.S.); a Swiss National Science Foundation Career Grant (P2EZP2_199843, to N.F.L.); a research fellowship from the Deutsche Forschungsgemeinschaft (DFG; SCHE 1672/2-1, to K.S.) and pump-prime funding from the Integrated Biological Imaging Network (IBIN; G106925, to K.S.); the UK Dementia Research Institute which receives its funding from UK DRI Ltd, funded by the UK Medical Research Council, Alzheimer's Society and Alzheimer's Research UK (supporting T.K., E.A. and C.F.K) and Alzheimer's Society 525 (AS-PhD-19a-015) supporting E.A. J.M.W.’s PhD scholarship was funded by the Department of Chemical Engineering and Biotechnology, University of Cambridge.