Bae Yoo-Jin, Kwon Yong-Rim, Kim Hye Joung, Lee Seok, Kim Yoo-Jin
Laboratory of Hematological Disease and Immunology, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea.
Leukemia Research Institute, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea.; Department of Hematology, Catholic Blood and Marrow Transplantation Center, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea.
Blood Res. 2017 Mar;52(1):18-24. doi: 10.5045/br.2017.52.1.18. Epub 2017 Mar 27.
Mesenchymal stromal cells (MSCs) are useful for cell therapy because of their potential for multilineage differentiation. However, MSCs that are expanded in traditional two-dimensional (2D) culture systems eventually lose their differentiation abilities. Therefore, we investigated whether azacitidine (AZA) supplementation and three-dimensional culture (3D) could improve the differentiation properties of MSCs.
2D- or 3D-cultured MSCs which were prepared according to the conventional or hanging-drop culture method respectively, were treated with or without AZA (1 µM for 72 h), and their osteogenic and adipogenic differentiation potential were determined and compared.
AZA treatment did not affect the cell apoptosis or viability in both 2D- and 3D-cultured MSCs. However, compared to conventionally cultured 2D-MSCs, AZA-treated 2D-MSCs showed marginally increased differentiation abilities. In contrast, 3D-MSCs showed significantly increased osteogenic and adipogenic differentiation ability. When 3D culture was performed in the presence of AZA, the osteogenic differentiation ability was further increased, whereas adipogenic differentiation was not affected.
3D culture efficiently promoted the multilineage differentiation of MSCs, and in combination with AZA, it could help MSCs to acquire greater osteogenic differentiation ability. This optimized culture method can enhance the therapeutic potential of MSCs.
间充质基质细胞(MSCs)因其多向分化潜能而对细胞治疗有用。然而,在传统二维(2D)培养系统中扩增的MSCs最终会失去其分化能力。因此,我们研究了补充阿扎胞苷(AZA)和三维培养(3D)是否能改善MSCs的分化特性。
分别根据常规培养法或悬滴培养法制备的2D或3D培养的MSCs,用或不用AZA(1 μM,处理72小时)处理,测定并比较它们的成骨和成脂分化潜能。
AZA处理不影响2D和3D培养的MSCs中的细胞凋亡或活力。然而,与常规培养的2D-MSCs相比,经AZA处理的2D-MSCs的分化能力略有增加。相比之下,3D-MSCs的成骨和成脂分化能力显著增加。当在AZA存在下进行3D培养时,成骨分化能力进一步提高,而成脂分化不受影响。
3D培养有效地促进了MSCs的多向分化,并且与AZA联合使用时,它可以帮助MSCs获得更强的成骨分化能力。这种优化的培养方法可以增强MSCs的治疗潜力。