Li Pengdong, Liu Feilin, Wu Chunling, Jiang Wenyue, Zhao Guifang, Liu Li, Bai Tingting, Wang Li, Jiang Yixu, Guo Lili, Qi Xiaojuan, Kou Junna, Fan Ruirui, Hao Deshun, Lan Shaowei, Li Yulin, Liu Jin Yu
Department of Pathobiology, Key Laboratory of Ministry of Education, Norman Bethune College of Medicine, Jilin University, Changchun, Jilin, 130021, People's Republic of China.
Department of Toxicology, School of Preventive Medicine, Jilin University, Changchun, Jilin, 130021, People's Republic of China.
Cell Tissue Res. 2015 Oct;362(1):69-86. doi: 10.1007/s00441-015-2182-z. Epub 2015 May 7.
The use of human mesenchymal stem cells (hMSCs) in cell therapies has increased the demand for strategies that allow efficient cell scale-up. Preliminary data on the three-dimensional (3D) spinner culture describing the potential use of microcarriers for hMSCs culture scale-up have been reported. We exploited a rich source of autologous stem cells (human hair follicle) and demonstrated the robust in vitro long-term expansion of human hair follicle-derived mesenchymal stem cells (hHF-MSCs) by using CultiSpher(®)-G microcarriers. We analyzed the feasibility of 3D culture by using hHF-MSCs/CultiSpher(®)-G microcarrier constructs for its potential applicability in regenerative medicine by comparatively analyzing the performance of hHF-MSCs adhered to the CultiSpher(®)-G microspheres in 3D spinner culture and those grown on the gelatin-coated plastic dishes (2D culture), using various assays. We showed that the hHF-MSCs seeded at various densities quickly adhered to and proliferated well on the microspheres, thus generating at least hundreds of millions of hHF-MSCs on 1 g of CultiSpher(®)-G within 12 days. This resulted in a cumulative cell expansion of greater than 26-fold. Notably, the maximum and average proliferation rates in 3D culture were significantly greater than that of the 2D culture. However, the hHF-MSCs from both the cultures retained surface marker and nestin expression, proliferation capacity and differentiation potentials toward adipocytes, osteoblasts and smooth muscle cells and showed no significant differences as evidenced by Edu incorporation, cell cycle, colony formation, apoptosis, biochemical quantification and qPCR assays.
人间充质干细胞(hMSCs)在细胞治疗中的应用增加了对高效细胞扩增策略的需求。关于三维(3D)旋转培养用于hMSCs培养扩增的微载体潜在用途的初步数据已有报道。我们利用了丰富的自体干细胞来源(人类毛囊),并通过使用CultiSpher(®)-G微载体证明了人毛囊来源的间充质干细胞(hHF-MSCs)在体外的强劲长期扩增。我们通过比较分析hHF-MSCs在3D旋转培养中附着于CultiSpher(®)-G微球上的性能与在明胶包被的塑料培养皿上生长的hHF-MSCs(二维培养)的性能,利用各种检测方法分析了使用hHF-MSCs/CultiSpher(®)-G微载体构建体进行3D培养在再生医学中的潜在适用性。我们表明,以不同密度接种的hHF-MSCs能迅速附着在微球上并良好增殖,因此在12天内1克CultiSpher(®)-G上能产生至少数亿个hHF-MSCs。这导致细胞累积扩增超过26倍。值得注意的是,3D培养中的最大增殖率和平均增殖率显著高于二维培养。然而,两种培养中的hHF-MSCs均保留了表面标志物和巢蛋白表达、增殖能力以及向脂肪细胞、成骨细胞和平滑肌细胞的分化潜能,并且通过Edu掺入、细胞周期、集落形成、凋亡、生化定量和qPCR检测未显示出显著差异。