STEM Biomethod Corporation
STEM Biomethod Corporation
Yasuda T.,Kyushu Institute of Technology |
Takase G.,Kyushu Institute of Technology |
Jung K.Y.,Kyushu Institute of Technology |
Yamanaka M.,Kyushu Institute of Technology |
And 2 more authors.
Proceedings of the 16th International Conference on Miniaturized Systems for Chemistry and Life Sciences, MicroTAS 2012 | Year: 2012
We developed a microdevice for chemical stimulation of neurospheres. The device consists of 8 × 8 microwells for cell culture and 8 microchannels for transportation of stimulating solutions. The bottom of each well is made of a SiN membrane of 1 μm in thickness, and has 24 × 24 microholes of 2 μm in diameter which are used for diffusive release of stimulant molecules from the microchannel to the microwell. We succeeded in formation of a single neurosphere having average diameter of 160 μm in each well. Also, it was found that the stimulation using 20 % FBS (fetal bovine serum) highly enhanced the differentiation from NSCs (neural stem cells) to neurons.
Sakai Y.,University of Kitakyushu |
Yoshida S.,University of Kitakyushu |
Yoshiura Y.,University of Kitakyushu |
Mori R.,University of Kitakyushu |
And 8 more authors.
Journal of Bioscience and Bioengineering | Year: 2010
The formation of three-dimensional cell microspheres such as spheroids, embryoid bodies, and neurospheres has attracted attention as a useful culture technique. In this study, we investigated a technique for effective cell microsphere production by using specially prepared microchip. The basic chip design was a multimicrowell structure in triangular arrangement within a 100-mm 2 region in the center of a polymethylmethacrylate (PMMA) plate (24×24 mm 2), the surface of which was modified with polyethylene glycol (PEG) to render it nonadhesive to cells. We also designed six similar chips with microwell diameters of 200, 300, 400, 600, 800, and 1000 μm to investigate the effect of the microwell diameter on the cell microsphere diameter. Rat hepatocytes, HepG2 cells, mouse embryonic stem (ES) cells, and mouse neural progenitor/stem (NPS) cells formed hepatocyte spheroids, HepG2 spheroids, embryoid bodies, and neurospheres, respectively, in the microwells within 5 days of culture. For all the cells, a single microsphere was formed in each microwell under all the chip conditions, and such microsphere configurations remained throughout the culture period. Furthermore, the microsphere diameters of each type of cell were strongly positively correlated with the microwell diameters of the chips, suggesting that microsphere diameter can be factitiously controlled by using different chip conditions. Thus, this chip technique is a promising cellular platform for tissue engineering or regenerative medicine research, pharmacological and toxicological studies, and fundamental studies in cell biology. © 2010 The Society for Biotechnology, Japan.
Yamauchi K.,Kyushu University |
Yamauchi N.,Kyushu University |
Yamagami K.,Kyushu University |
Nakamura N.,Kyushu University |
And 7 more authors.
Animal Science Journal | Year: 2015
This study aimed to develop an in vitro model for the analysis of the bovine endometrium. Immunofluorescent staining revealed that the hetero-spheroids and the cultured explants showed almost similar structure in the localization of bovine endometrial epithelial cells and endometrial stromal cells, except the glandular-like structure of the epithelial cells inside the explants. Gelatin zymography revealed that the hetero-spheroids did not express matrix metalloproteinases (MMPs) after 4 days of culture, but strong MMP expressions were observed in the cultured explants until 7 days of culture. Additionally, expression of progesterone receptor (PR), estrogen receptor alpha (ERα), type I interferon receptor 1 (IFNAR1) and 2 (IFNAR2) messenger RNA was observed both in the homo- and hetero-spheroids. The expression of oxytocin receptor (OTR) mRNA in E2 and E2+P4 (1,3,5(10)-Estratrien-3, 17β-diol + 4-Pregnen-3, 20-dinone) treated groups were significantly (P<0.05) higher than that of the control group of spheroids. In case of cultured explants, the expression of PR and OTR mRNA were significantly (P<0.05) higher in E2 treated groups compared to the control groups. Hepatocyte growth factor (HGF) mRNA expression was also higher in P4 treated groups at 10 days in culture (P<0.05). In a nutshell, the in vitro model developed in this study for the analysis of the endometrium may provide a new platform for extensive research on bovine endometrial function. © 2014 Japanese Society of Animal Science.