Miyamoto Yoshitaka, Ikeuchi Masashi, Noguchi Hirofumi, Yagi Tohru, Hayashi Shuji
Department of Advanced Medicine in Biotechnology and Robotics, Nagoya University Graduate School of Medicine, Showa-ku, Nagoya, Japan; †Research Center for Advanced Science and Technology, The University of Tokyo, Tokyo, Japan.
†Research Center for Advanced Science and Technology, The University of Tokyo, Tokyo, Japan; ‡PRESTO, Japan Science and Technology (JST), Saitama, Japan.
Cell Med. 2016 Sep 14;9(1-2):35-44. doi: 10.3727/215517916X693096. eCollection 2017 Jan 8.
The application of stem cells for cell therapy has been extensively studied in recent years. Among the various types of stem cells, human adipose tissue-derived stem cells (ASCs) can be obtained in large quantities with relatively few passages, and they possess a stable quality. ASCs can differentiate into a number of cell types, such as adipose cells and ectodermal cells. We therefore focused on the in vitro microenvironment required for such differentiation and attempted to induce the differentiation of human stem cells into microtissues using a microelectromechanical system. We first evaluated the adipogenic differentiation of human ASC spheroids in a three-dimensional (3D) culture. We then created the in vitro microenvironment using a 3D combinatorial TASCL device and attempted to induce the adipogenic differentiation of human ASCs. The differentiation of human ASC spheroids cultured in maintenance medium and those cultured in adipocyte differentiation medium was evaluated via Oil red O staining using lipid droplets based on the quantity of accumulated triglycerides. The differentiation was confirmed in both media, but the human ASCs in the 3D cultures contained higher amounts of triglycerides than those in the 2D cultures. In the short culture period, greater adipogenic differentiation was observed in the 3D cultures than in the 2D cultures. The 3D culture using the TASCL device with adipogenic differentiation medium promoted greater differentiation of human ASCs into adipogenic lineages than either a 2D culture or a culture using a maintenance medium. In summary, the TASCL device created a hospitable in vitro microenvironment and may therefore be a useful tool for the induction of differentiation in 3D culture. The resultant human ASC spheroids were "adipose-like microtissues" that formed spherical aggregation perfectly and are expected to be applicable in regenerative medicine as well as cell transplantation.
近年来,干细胞在细胞治疗中的应用得到了广泛研究。在各种类型的干细胞中,人脂肪组织来源的干细胞(ASCs)可以大量获取,传代次数相对较少,且质量稳定。ASCs 可以分化为多种细胞类型,如脂肪细胞和外胚层细胞。因此,我们专注于这种分化所需的体外微环境,并尝试使用微机电系统诱导人干细胞分化为微组织。我们首先评估了人 ASC 球体在三维(3D)培养中的成脂分化。然后,我们使用 3D 组合 TASCL 装置创建了体外微环境,并尝试诱导人 ASCs 的成脂分化。基于甘油三酯的积累量,通过使用脂滴的油红 O 染色来评估在维持培养基中培养的人 ASC 球体和在脂肪细胞分化培养基中培养的人 ASC 球体的分化情况。在两种培养基中均证实了分化,但 3D 培养中的人 ASCs 比 2D 培养中的含有更多的甘油三酯。在短培养期内,3D 培养中观察到的成脂分化比 2D 培养中更明显。使用 TASCL 装置和脂肪生成分化培养基的 3D 培养比 2D 培养或使用维持培养基的培养更能促进人 ASCs 向脂肪生成谱系的分化。总之,TASCL 装置创建了一个适宜的体外微环境,因此可能是 3D 培养中诱导分化的有用工具。所得的人 ASC 球体是完美形成球形聚集的“脂肪样微组织”,有望应用于再生医学以及细胞移植。