Author
Listed:
- Adam Cliffe
(Institute of Molecule and Cell Biology (IMCB), Computational Bioimage Analysis Unit, A*STAR)
- David P. Doupé
(Institute of Molecule and Cell Biology (IMCB), Computational Bioimage Analysis Unit, A*STAR)
- HsinHo Sung
(Institute of Molecule and Cell Biology (IMCB), Computational Bioimage Analysis Unit, A*STAR)
- Isaac Kok Hwee Lim
(Institute of Molecule and Cell Biology (IMCB), Computational Bioimage Analysis Unit, A*STAR)
- Kok Haur Ong
(Institute of Molecule and Cell Biology (IMCB), Computational Bioimage Analysis Unit, A*STAR)
- Li Cheng
(Bioinformatics Institute (BII), A*STAR)
- Weimiao Yu
(Institute of Molecule and Cell Biology (IMCB), Computational Bioimage Analysis Unit, A*STAR)
Abstract
Understanding the mechanisms of collective cell migration is crucial for cancer metastasis, wound healing and many developmental processes. Imaging a migrating cluster in vivo is feasible, but the quantification of individual cell behaviours remains challenging. We have developed an image analysis toolkit, CCMToolKit, to quantify the Drosophila border cell system. In addition to chaotic motion, previous studies reported that the migrating cells are able to migrate in a highly coordinated pattern. We quantify the rotating and running migration modes in 3D while also observing a range of intermediate behaviours. Running mode is driven by cluster external protrusions. Rotating mode is associated with cluster internal cell extensions that could not be easily characterized. Although the cluster moves slower while rotating, individual cells retain their mobility and are in fact slightly more active than in running mode. We also show that individual cells may exchange positions during migration.
Suggested Citation
Adam Cliffe & David P. Doupé & HsinHo Sung & Isaac Kok Hwee Lim & Kok Haur Ong & Li Cheng & Weimiao Yu, 2017.
"Quantitative 3D analysis of complex single border cell behaviors in coordinated collective cell migration,"
Nature Communications, Nature, vol. 8(1), pages 1-13, April.
Handle:
RePEc:nat:natcom:v:8:y:2017:i:1:d:10.1038_ncomms14905
DOI: 10.1038/ncomms14905
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