Ke Hui, Wang Peng, Yu Weihua, Liu Xiaoming, Liu Chang, Yang Fan, Mao Frank Fuxiang, Zhang Liangming, Zhang Xiuming, Lahn Bruce T, Xiang Andy Peng
Center for Stem Cell Biology and Tissue Engineering, The Key Laboratory for Stem Cells and Tissue Engineering, Sun Yat-Sen University, Ministry of Education, Guangzhou 510080, China.
Differentiation. 2009 Mar;77(3):256-62. doi: 10.1016/j.diff.2008.09.021. Epub 2008 Dec 2.
Mesenchymal stem cells (MSCs) have received considerable attention in recent years. Particularly exciting is the prospect that MSCs could be differentiated into specialized cells of interest, which could then be used for cell therapy and tissue engineering. MSCs derived from nonhuman primates could be a powerful tool for investigating the differentiation potential in vitro and in vivo for preclinical research. The purpose of this study was to isolate cynomolgus mesenchymal stem cells (cMSCs) from adult bone marrow and characterize their growth properties and multipotency. Mononuclear cells were isolated from cynomolgus monkey bone marrow by density-gradient centrifugation, and adherent fibroblast-like cells grew well in the complete growth medium with 10 microM Tenofovir. cMSCs expressed mesenchymal markers, such as CD29, CD105, CD166 and were negative for hematopoietic markers such as CD34, CD45. Furthermore, the cells were capable of differentiating into osteogenic, chondrogenic, and adipogenic lineages under certain conditions, maintaining normal karyotype throughout extended culture. We also compared different methods (lipofection, nucleofection and lentivirus) for genetic modification of cMSCs and found lentivirus proved to be the most effective method with transduction efficiency of up to 44.6% and lowest level of cell death. The cells after transduction stably expressed green fluorescence protein (GFP) and maintained the abilities to differentiate down osteogenic and adipogenic lineages. In conclusion, these data showed that cMSCs isolated from cynomolgus bone marrow shared similar characteristics with human MSCs and might provide an attractive cell type for cell-based therapy in higher-order mammalian species disorder models.
近年来,间充质干细胞(MSCs)受到了广泛关注。特别令人兴奋的是,MSCs有望分化为感兴趣的特定细胞,进而用于细胞治疗和组织工程。源自非人灵长类动物的MSCs可能是一种强大的工具,可用于临床前研究中体外和体内分化潜能的研究。本研究的目的是从成年骨髓中分离食蟹猴间充质干细胞(cMSCs),并表征其生长特性和多能性。通过密度梯度离心从食蟹猴骨髓中分离单核细胞,贴壁的成纤维细胞样细胞在含有10 microM替诺福韦的完全生长培养基中生长良好。cMSCs表达间充质标志物,如CD29、CD105、CD166,而造血标志物如CD34、CD45呈阴性。此外,这些细胞在特定条件下能够分化为成骨、成软骨和成脂谱系,在长期培养过程中保持正常核型。我们还比较了cMSCs基因修饰的不同方法(脂质转染、核转染和慢病毒),发现慢病毒被证明是最有效的方法,转导效率高达44.6%,细胞死亡率最低。转导后的细胞稳定表达绿色荧光蛋白(GFP),并保持向下分化为成骨和成脂谱系的能力。总之,这些数据表明,从食蟹猴骨髓中分离的cMSCs与人类MSCs具有相似的特征,可能为高阶哺乳动物疾病模型的细胞治疗提供一种有吸引力的细胞类型。