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Enhanced Adipogenic Differentiation of Human Adipose-Derived Stem Cells in an in vitro Microenvironment: The Preparation of Adipose-Like Microtissues Using a Three-Dimensional Culture

机译:在体外微环境中增强人类脂肪干细胞的成脂分化:使用三维培养制备类似脂肪的微组织

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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.
机译:近年来,干细胞在细胞治疗中的应用已得到广泛研究。在各种类型的干细胞中,可以以相对较少的传代次数大量获得人脂肪组织来源的干细胞(ASC),并且它们具有稳定的质量。 ASC可以分化为多种细胞类型,例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类干细胞分化为微组织。我们首先在三维(3D)文化中评估了人类ASC球状体的成脂分化。然后,我们使用3D组合TASCL设备创建了体外微环境,并试图诱导人ASC的成脂分化。基于脂质甘油三酯的量,使用脂质液滴通过油红O染色,评价了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。在两种培养基中都证实了这种分化,但是3D培养物中的人ASC中甘油三酯的含量高于2D培养物中的甘油三酯。在较短的培养期内,与2D培养相比,在3D培养中观察到更大的成脂分化。使用TASCL装置和成脂分化培养基的3D培养比2D培养或使用维持培养基的培养促进了人类ASCs向成脂谱系的分化。总而言之,TASCL设备创造了一个好客的体外微环境,因此可能是诱导3D培养中分化的有用工具。所得的人类ASC球状体是“脂肪样微组织”,可以完美地形成球形聚集体,并有望应用于再生医学和细胞移植中。

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