Tajima Shuhei, Tabata Yasuhiko
Department of Biomaterials, Institute for Life and Frontier Medical Sciences, Kyoto University, 53 Kawara-cho Shogoin, Sakyo-ku, Kyoto 606-8507, Japan.
Regen Ther. 2017 Aug 4;7:34-44. doi: 10.1016/j.reth.2017.07.001. eCollection 2017 Dec.
The objective of this study is to investigate the effect of matrigel microspheres (MM), gelatin hydrogel microspheres (GM), and matrigel-coated GM on the proliferated and biological functions of epithelial cells in cell aggregates incorporating the microspheres. The MM were prepared by a coacelvation method. When mammary epithelial EpH4 cells were cultured with the MM, GM, and matrigel-coated GM in round U-bottom wells of 96-multiwell culture plates which had been coated with poly (vinyl alcohol) (PVA) to suppress the cell adhesion, EpH4 cell aggregates with each microspheres homogeneously incorporated were formed. Higher EpH4 cells proliferation was observed for cell aggregates incorporating MM, GM, and matrigel-coated GM compared with the conventional 3-dimensional (3D) culture method. When examined to evaluate the epithelial differentiation of EpH4 cells, the β-casein expression was significantly higher for the cell aggregates incorporating MM than that of aggregates incorporating GM and matrigel-coated GM or the conventional 3D culture method. It is concluded that the proliferation and differentiation of mammary epithelial EpH4 cells were promoted by the incorporation of MM.
本研究的目的是探讨基质胶微球(MM)、明胶水凝胶微球(GM)以及基质胶包被的GM对包含微球的细胞聚集体中上皮细胞增殖和生物学功能的影响。MM通过凝聚法制备。当在已用聚乙烯醇(PVA)包被以抑制细胞黏附的96孔培养板的圆形U型底孔中,将乳腺上皮EpH4细胞与MM、GM以及基质胶包被的GM一起培养时,形成了均匀掺入每种微球的EpH4细胞聚集体。与传统的三维(3D)培养方法相比,观察到掺入MM、GM以及基质胶包被的GM的细胞聚集体中EpH4细胞增殖更高。当检测以评估EpH4细胞的上皮分化时,掺入MM的细胞聚集体中β-酪蛋白表达显著高于掺入GM和基质胶包被的GM的聚集体或传统3D培养方法。得出结论,掺入MM可促进乳腺上皮EpH4细胞的增殖和分化。