Summary of 26-Kinoshita-iPSCellDyn

SSBD:database
SSBD:database URL
Title
-
Description
-
Relase date
2017-10-03
Updated date
2018-11-15
License
CC BY
Kind
Image data based on Experiment
Number of Datasets
2 ( Image datasets: 2, Quantitative data datasets: 0 )
Size of Datasets
105.3 MB ( Image datasets: 105.3 MB, Quantitative data datasets: 0 bytes )

Organism(s)
M. musculus
Strain(s)
iPS
Protein name(s)
Nrlp
Protein tag(s)
eGFP

Datatype
cell dynamics
Molecular Function (MF)
Biological Process (BP)
-
Cellular Component (CC)
cell
Biological Imaging Method
-
XYZ Scale
XY: 0.6251697 micrometer/pixel, Z: 18.73 micrometer/slice, XY: 0.6251697 micrometer/pixel, Z: 3.6530612 micrometer/slice
T scale
66.7 second for each time interval, 67.2 second for each time interval

Image Acquisition
Experiment type
TimeLapse
Microscope type
ConfocalMicroscope
Acquisition mode
LaserScanningConfocalMicroscopy
Contrast method
Fluorescence
Microscope model
LSM700
Detector model
-
Objective model
-
Filter set
-

Related paper(s)

Hirofumi Kinoshita, Kiyoshi Suzuma, Jun Kaneko, Michiko Mandai, Takashi Kitaoka, Masayo Takahashi (2016) Induction of Functional 3D Ciliary Epithelium-Like Structure From Mouse Induced Pluripotent Stem Cells., Investigative ophthalmology & visual science, Volume 57, Number 1, pp. 153-61

Published in 2016 Jan 1

(Abstract) PURPOSE: To generate ciliary epithelium (CE) from mouse induced pluripotent stem (iPS) cells. METHODS: Recently, a protocol for self-organizing optic cup morphogenesis in three-dimensional culture was reported, and it was suggested that ocular tissue derived from neural ectoderm could be differentiated. We demonstrated that a CE-like double-layered structure could be induced in simple culture by using a modified Eiraku differentiation protocol. RESULTS: Differentiation of a CE-like double-layered structure could be promoted by glycogen synthase kinase 3beta (GSK-3beta) inhibitor. Connexin43 and aquaporin1 were expressed in both thin layers, and induced CE-like cells expressed ciliary marker genes, such as cyclinD2, zic1, tgfb2, aldh1a3, wfdc1, otx1, BMP4, and BMP7. Increases in cytoplasmic and nuclear beta-catenin in aggregates of the CE-like double-layered structure were confirmed by Western blot analysis. In addition, tankyrase inhibitor prevented the induction of the CE-like double-layered structure by GSK-3beta inhibitor. Dye movement from pigmented cells to nonpigmented cells in the mouse iPS cell-derived CE-like structure was observed in a fluid movement experiment, consistent with the physiological function of CE in vivo. CONCLUSIONS: We could differentiate CE from mouse iPS cells in the present study. In the future, we hope that this CE-like complex will become useful as a graft for transplantation therapy in pathologic ocular hypotension due to CE dysfunction, and as a screening tool for the development of drugs for diseases associated with CE function.
(MeSH Terms)

Contact
Kiyoshi Suzuma , Nagasaki University , Department of Ophthalmology and Visual Sciences, Graduate School of Biomedical Sciences
Contributors
Hirofumi Kinoshita, Kiyoshi Suzuma, Jun Kaneko, Michiko Mandai, Takashi Kitaoka, Masayo Takahashi


Dataset List of 26-Kinoshita-iPSCellDyn

#
Dataset ID
Kind
Size
4D View
SSBD:OMERO
Download BDML
Download Images
# 885
Datast ID Fig4A_CE
Dataset Kind Image data
Dataset Size 52.6 MB
4D view
SSBD:OMERO
Download BDML
Download Image data

# 886
Datast ID Fig4B_NR
Dataset Kind Image data
Dataset Size 52.6 MB
4D view
SSBD:OMERO
Download BDML
Download Image data