International Center for Materials Nanoarchitectonics, National Institute for Materials Science , 1-1 Namiki, Tsukuba, Ibaraki 305-0044, Japan.
Institute for Materials Chemistry and Engineering, Kyushu University , 744 Motooka, Nishi-ku, Fukuoka, Fukuoka 819-0395, Japan.
Biomacromolecules. 2016 Nov 14;17(11):3808-3815. doi: 10.1021/acs.biomac.6b01340. Epub 2016 Nov 3.
Stem cell differentiation is an important issue in regenerative medicine and tissue engineering. It has been reported that cell shape is one of the factors that determine the lineage commitment of mesenchymal stem cells (MSCs). Therefore, the substrates have been developed to control their shapes. Recently, we found that poly(2-methoxyethyl acrylate) (PMEA) analogs can control tumor cell shape through the alteration of protein adsorption. Here, the adipogenesis of an adipocyte-progenitor cell, 3T3-L1 cells, was attempted; adipogenesis was to be regulated by surfaces coated with PMEA analogs through the control of their shape. The adipogenesis of 3T3-L1 cells was promoted on the surfaces coated with PMEA and its analogs, PMe3A and PMe2A. Evident focal adhesions were hardly observed on these surfaces, suggesting that integrin signal activation was suppressed. Additionally, actin assembly and cell spreading were suppressed on these surfaces. Therefore, the surfaces coated with PMEA analogs are expected to be suitable surfaces to regulate adipogenesis through the suppression of cell spreading. Additionally, we found that protein adsorption correlated with actin assembly and adipogenesis.
干细胞分化是再生医学和组织工程中的一个重要问题。据报道,细胞形状是决定间充质干细胞(MSCs)谱系分化的因素之一。因此,已经开发出了基底来控制它们的形状。最近,我们发现聚(2-甲氧基乙基丙烯酸酯)(PMEA)类似物可以通过改变蛋白质吸附来控制肿瘤细胞的形状。在这里,尝试了脂肪细胞祖细胞 3T3-L1 细胞的脂肪生成;通过控制其形状,用 PMEA 类似物涂覆的表面来调节脂肪生成。3T3-L1 细胞在涂覆有 PMEA 及其类似物 PMe3A 和 PMe2A 的表面上促进脂肪生成。在这些表面上几乎观察不到明显的焦点粘连,表明整合素信号激活受到抑制。此外,在这些表面上肌动蛋白组装和细胞铺展受到抑制。因此,预计涂覆有 PMEA 类似物的表面通过抑制细胞铺展来调节脂肪生成。此外,我们发现蛋白质吸附与肌动蛋白组装和脂肪生成相关。