Summary of ssbd-repos-000166

SSBD:database
URL

Name
ssbd-repos-000166 (166-Takubo-ECsTrajectory)
URL
DOI
-

Title
Time-lapse images and BDML file for quantiative information about tracking of Vascular endothelial cells (ECs) nuclei in branches.
Description
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Submited Date
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Release Date
2021-09-30
Updated Date
-
License
Funding information
-
File formats
Data size
5.2 GB

Organism
Mus musculus
Strain
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Cell Line
endothelial cell
Genes
-
Proteins
-

GO Molecular Function (MF)
NA
GO Biological Process (BP)
endothelial cell morphogenesis
GO Cellular Component (CC)
nucleus
Study Type
Cell Movement, Humans, Physiologic, Mice, Anisotropy, Aorta, Neovascularization, Inbred C57BL, Models, Vascular Endothelial Growth Factor A/metabolism, Animals, Theoretical, Morphogenesis, Aorta/pathology, Endothelial Cells/cytology, Endothelial Cells, Vascular Endothelial Growth Factor A
Imaging Methods
time lapse microscopy

Method Summary
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Related paper(s)

Naoko Takubo, Fumitaka Yura, Kazuaki Naemura, Ryo Yoshida, Terumasa Tokunaga, Tetsuji Tokihiro, Hiroki Kurihara (2019) Cohesive and anisotropic vascular endothelial cell motility driving angiogenic morphogenesis., Scientific reports, Volume 9, Number 1, pp. 9304

Published in 2019 Jun 26 (Electronic publication in June 26, 2019, midnight )

(Abstract) Vascular endothelial cells (ECs) in angiogenesis exhibit inhomogeneous collective migration called "cell mixing", in which cells change their relative positions by overtaking each other. However, how such complex EC dynamics lead to the formation of highly ordered branching structures remains largely unknown. To uncover hidden laws of integration driving angiogenic morphogenesis, we analyzed EC behaviors in an in vitro angiogenic sprouting assay using mouse aortic explants in combination with mathematical modeling. Time-lapse imaging of sprouts extended from EC sheets around tissue explants showed directional cohesive EC movements with frequent U-turns, which often coupled with tip cell overtaking. Imaging of isolated branches deprived of basal cell sheets revealed a requirement of a constant supply of immigrating cells for ECs to branch forward. Anisotropic attractive forces between neighboring cells passing each other were likely to underlie these EC motility patterns, as evidenced by an experimentally validated mathematical model. These results suggest that cohesive movements with anisotropic cell-to-cell interactions characterize the EC motility, which may drive branch elongation depending on a constant cell supply. The present findings provide novel insights into a cell motility-based understanding of angiogenic morphogenesis.
(MeSH Terms)

Contact(s)
Naoko Takubo, Hiroki Kurihara
Organization(s)
The University of Tokyo, The University of Tokyo , Present address: Isotope Science Center, Department of Molecular Cell Biology, Graduate School of Medicine
Image Data Contributors
Quantitative Data Contributors

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