Summary of 224-Kamada-MitosisDyn

SSBD:database
SSBD:database URL
Title
Time-lapse confocal images of visulization of mitotic progression in HeLa cells or BY-2 cells.
Description
-
Relase date
2022-11-23
Updated date
-
License
CC BY
Kind
Image data based on Experiment
Number of Datasets
8 ( Image datasets: 8, Quantitative data datasets: 0 )
Size of Datasets
7.4 GB ( Image datasets: 7.4 GB, Quantitative data datasets: 0 bytes )

Organism(s)
Nicotiana tabacum, Homo sapiens
Strain(s)
BY-2
Cell lines(s)
HeLa cell

Datatype
-
Molecular Function (MF)
Biological Process (BP)
cell division, mitotic cell cycle
Cellular Component (CC)
nucleus
Biological Imaging Method
time lapse microscopy
X scale
0.23 micrometer/pixel
Y scale
0.23 micrometer/pixel
Z scale
0.5 micrometer/slice
T scale
90 seconds per time interval, 60 seconds per time interval

Image Acquisition
Experiment type
-
Microscope type
-
Acquisition mode
-
Contrast method
-
Microscope model
-
Detector model
-
Objective model
-
Filter set
-

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
Kohei Otomo, Tomomi Nemoto , Juntendo University, National Institutes of Natural Sciences , Graduate School of Medicine, Exploratory Research Center on Life and Living Systems
Contributors


Dataset List of 224-Kamada-MitosisDyn

#
Dataset ID
Kind
Size
4D View
SSBD:OMERO
Download BDML
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# 7785
Dataset Kind Image data
Dataset Size 1.0 GB
4D view
SSBD:OMERO
Download BDML
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# 7786
Dataset Kind Image data
Dataset Size 584.4 MB
4D view
SSBD:OMERO
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# 7787
Dataset Kind Image data
Dataset Size 1.5 GB
4D view
SSBD:OMERO
Download BDML
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# 7788
Dataset Kind Image data
Dataset Size 905.3 MB
4D view
SSBD:OMERO
Download BDML
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# 7789
Dataset Kind Image data
Dataset Size 1.3 GB
4D view
SSBD:OMERO
Download BDML
Download Image data

# 7790
Dataset Kind Image data
Dataset Size 1.2 GB
4D view
SSBD:OMERO
Download BDML
Download Image data

# 7791
Dataset Kind Image data
Dataset Size 419.4 MB
4D view
SSBD:OMERO
Download BDML
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# 7792
Dataset Kind Image data
Dataset Size 493.0 MB
4D view
SSBD:OMERO
Download BDML
Download Image data