Detail of harderian_natural_D1

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


Project
Title
Phase-contrast image of the development of natural harderian gland germ in organ culture for day1
Description
NA
Release, Updated
2019-11-20
License
CC BY
Kind
Image data based on Experiment
File Formats
Data size
912.9 KB

Organism
M. musculus ( NCBI:txid10090 )
Strain(s)
-
Cell Line
-

Datatype
gland regeneration
Molecular Function (MF)
Biological Process (BP)
lacrimal gland development ( GO:0032808 ) harderian gland development ( GO:0070384 )
Cellular Component (CC)
-
Biological Imaging Method
XYZ Scale
XY: 1.290 micrometer/pixel, Z: NA
T scale
1 day for each time interval

Image Acquisition
Experiment type
Other
Microscope type
Other
Acquisition mode
BrightField
Contrast method
Phase
Microscope model
Carl Zeiss Axioimager A1
Detector model
-
Objective model
-
Filter set
-

Summary of Methods
See details in Hirayama et al. (2013) Nat Commun, 4: 2497.
Related paper(s)

Masatoshi Hirayama, Miho Ogawa, Masamitsu Oshima, Yurie Sekine, Kentaro Ishida, Kentaro Yamashita, Kazutaka Ikeda, Shigeto Shimmura, Tetsuya Kawakita, Kazuo Tsubota, Takashi Tsuji (2013) Functional lacrimal gland regeneration by transplantation of a bioengineered organ germ., Nature communications, Volume 4, pp. 2497

Published in 2013

(Abstract) The lacrimal gland has a multifaceted role in maintaining a homeostatic microenvironment for a healthy ocular surface via tear secretion. Dry-eye disease, which is caused by lacrimal gland dysfunction, is one of the most prevalent eye diseases that cause corneal epithelial damage and results in significant loss of vision and a reduction in the quality of life. Here we demonstrate orthotopic transplantation of bioengineered lacrimal gland germs into adult mice with an extra-orbital lacrimal gland defect, a mouse model that mimics the corneal epithelial damage caused by lacrimal gland dysfunction. The bioengineered lacrimal gland germs and harderian gland germs both develop in vivo and achieve sufficient physiological functionality, including tear production in response to nervous stimulation and ocular surface protection. This study demonstrates the potential for bioengineered organ replacement to functionally restore the lacrimal gland.
(MeSH Terms)

Contact
Takashi Tsuji , Tokyo University of Science, , Research Institute for Science and Technology
Contributors
Masatoshi Hirayama, Miho Ogawa, Masamitsu Oshima, Yurie Sekine, Kentaro Ishida, Kentaro Yamashita, Kazutaka Ikeda, Shigeto Shimmura, Tetsuya Kawakita, Kazuo Tsubota, Takashi Tsuji

OMERO Dataset
OMERO Project
Source