Summary of ssbd-repos-000130

SSBD:database
URL

Name
ssbd-repos-000130 (130-Sano-CellMigrationDyn)
URL
DOI
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Title
Timelapse FRET images data and BDML file for quantitative data about the cell migration in epidermis or urothelial of transgenic mice
Description
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Submited Date
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Release Date
2021-09-30
Updated Date
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License
Funding information
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File formats
Data size
4.5 GB

Organism
Mus musculus
Strain
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Cell Line
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Genes
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Proteins
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GO Molecular Function (MF)
NA
GO Biological Process (BP)
cell migration, activation of MAPERK kinase
GO Cellular Component (CC)
nucleus
Study Type
Urothelium, Wound Healing/physiology, MAP Kinase Signaling System/physiology, Epidermis/physiology, Female, Time-Lapse Imaging, Transgenic, MAP Kinase Signaling System, Wound Healing, Mice, Cell Proliferation, Cell Movement, Urothelium/cytology, Epidermis, Cultured, Animals, Cell Movement/physiology, Urothelium/physiology, Intravital Microscopy, Extracellular Signal-Regulated MAP Kinases/metabolism, Extracellular Signal-Regulated MAP Kinases, Cells
Imaging Methods
time lapse microscopy

Method Summary
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Related paper(s)

Takeshi Sano, Takashi Kobayashi, Osamu Ogawa, Michiyuki Matsuda (2018) Gliding Basal Cell Migration of the Urothelium during Wound Healing., The American journal of pathology, Volume 188, Number 11, pp. 2564-2573

Published in 2018 Nov (Electronic publication in Aug. 16, 2018, midnight )

(Abstract) Collective cell migration during wound healing has been extensively studied in the epidermis. However, it remains unknown whether the urothelium repairs wounds in a manner similar to the epidermis. By in vivo two-photon excitation microscopy of transgenic mice that express fluorescent biosensors, we studied the collective cell migration of the urothelium in comparison with that of the epidermis. In vivo time-lapse imaging revealed that, even in the absence of a wound, urothelial cells continuously moved and sometimes glided as a sheet over the underlying lamina propria. On abrasion of the epithelium, the migration speed of each epidermal cell was inversely correlated with the distance to the wound edge. Repetitive activation waves of extracellular signal-regulated kinase (ERK) were generated at and propagated away from the wound edge. In contrast, urothelial cells glided as a sheet over the lamina propria without any ERK activation waves. Accordingly, the mitogen-activated protein kinase/ERK kinase inhibitor PD0325901 decreased the migration velocity of the epidermis but not the urothelium. Interestingly, the tyrosine kinase inhibitor dasatinib inhibited migration of the urothelium as well as the epidermis, suggesting that the gliding migration of the urothelium is an active, not a passive, migration. In conclusion, the urothelium glides over the lamina propria to fill wounds in an ERK-independent manner, whereas the epidermis crawls to cover wounds in an ERK-dependent manner.
(MeSH Terms)

Contact(s)
Michiyuki Matsuda
Organization(s)
Kyoto University , Graduate School of Biostudies , Laboratory of Bioimaging and Cell Signaling
Image Data Contributors
Quantitative Data Contributors

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