Summary of ssbd-repos-000224

SSBD:database
URL

Name
ssbd-repos-000224 (224-Kamada-MitosisDyn)
URL
DOI
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Title
Time-lapse confocal images of visulization of mitotic progression in HeLa cells or BY-2 cells.
Description
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Submited Date
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Release Date
2022-11-23
Updated Date
-
License
Funding information
-
File formats
Data size
7.4 GB

Organism
Nicotiana tabacum, Homo sapiens
Strain
BY-2
Cell Line
HeLa cell
Genes
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Proteins
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GO Molecular Function (MF)
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GO Biological Process (BP)
cell division, mitotic cell cycle
GO Cellular Component (CC)
nucleus
Study Type
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Imaging Methods
time lapse microscopy

Method Summary
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Related paper(s)

Takafumi Kamada, Kohei Otomo, Takashi Murata, Kaito Nakata, Shota Hiruma, Ryota Uehara, Mitsuyasu Hasebe, Tomomi Nemoto (2022) Low-invasive 5D visualization of mitotic progression by two-photon excitation spinning-disk confocal microscopy., Scientific reports, Volume 12, Number 1, pp. 809

Published in 2022 Jan 17 (Electronic publication in Jan. 17, 2022, midnight )

(Abstract) Non-linear microscopy, such as multi-photon excitation microscopy, offers spatial localities of excitations, thereby achieving 3D cross-sectional imaging with low phototoxicity even in thick biological specimens. We had developed a multi-point scanning two-photon excitation microscopy system using a spinning-disk confocal scanning unit. However, its severe color cross-talk has precluded multi-color simultaneous imaging. Therefore, in this study, we introduced a mechanical switching system to select either of two NIR laser light pulses and an image-splitting detection system for 3- or 4-color imaging. As a proof of concept, we performed multi-color fluorescent imaging of actively dividing human HeLa cells and tobacco BY-2 cells. We found that the proposed microscopy system enabled time-lapse multi-color 3D imaging of cell divisions while avoiding photodamage. Moreover, the application of a linear unmixing method to the 5D dataset enabled the precise separation of individual intracellular components in multi-color images. We thus demonstrated the versatility of our new microscopy system in capturing the dynamic processes of cellular components that could have multitudes of application.
(MeSH Terms)

Contact(s)
Kohei Otomo, Tomomi Nemoto
Organization(s)
Juntendo University, National Institutes of Natural Sciences , Graduate School of Medicine, Exploratory Research Center on Life and Living Systems
Image Data Contributors
Quantitative Data Contributors

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