Detail of FigS1B_2color_1p_ex_HeLa_failed_images

(Too many images for preview; see images in SSBD:OMERO Dataset)


Project
Title
Time-lapse images of 2-color labeled human HeLa cell divisions of failed chromosome segregation during mitosis.
Description
Time-lapse images of 2-color labeled human HeLa cell divisions of failed chromosome segregation during mitosis.
Release, Updated
2022-11-23
License
CC BY
Kind
Image data
File Formats
.tif
Data size
493.0 MB

Organism
Homo sapiens ( NCBI:txid9606 )
Strain(s)
-
Cell Line
HeLa cell ( CLO_0003684 )

Datatype
-
Molecular Function (MF)
Biological Process (BP)
cell division ( GO:0051301 ) mitotic cell cycle ( GO:0000278 )
Cellular Component (CC)
nucleus ( GO:0005634 )
Biological Imaging Method
time lapse microscopy ( Fbbi:00000249 )
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

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

Summary of Methods
See details in Kamada, T, et. al. (2022) Sci Rep 12, 809
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

OMERO Dataset
OMERO Project
Source