Chen Gecai, Yue Aihuan, Ruan Zhongbao, Yin Yigang, Wang Ruzhu, Ren Yin, Zhu Li
Department of Cardiology, Taizhou Renmin Hospital, Taizhou, 225300, Jiangsu Province, China.
Cell Tissue Bank. 2014 Dec;15(4):513-21. doi: 10.1007/s10561-014-9420-6. Epub 2014 Jan 10.
Mesenchymal stem cells (MSCs) are multipotent adult stem cells that have an immunosuppressive effect. The biological stability of MSCs in serum-free medium during long-term culture in vitro has not been elucidated clearly. The morphology, immunophenotype and multi-lineage potential were analyzed at passages 3, 5, 10, 15, 20, and 25 (P3, P5, P10, P15, P20, and P25, respectively). The cell cycle distribution, apoptosis, and karyotype of human umbilical cord-derived (hUC)-MSCs were analyzed at P3, P5, P10, P15, P20, and P25. From P3 to P25, the three defining biological properties of hUC-MSCs [adherence to plastic, specific surface antigen expression, multipotent differentiation potential] met the standards proposed by the International Society for Cellular Therapy for definition of MSCs. The cell cycle distribution analysis at the P25 showed that the percentage of cells at G0/G1 was increased, compared with the cells at P3 (P < 0.05). Cells at P25 displayed an increase in the apoptosis rate (to 183 %), compared to those at P3 (P < 0.01). Within subculture generations 3-20 (P3-P20), the differences between the cell apoptotic rates were not statistically significant (P > 0.05). There were no detectable chromosome eliminations, displacements, or chromosomal imbalances, as assessed by the karyotyping guidelines of the International System for Human Cytogenetic Nomenclature (ISCN, 2009). Long-term culture affects the biological stability of MSCs in serum-free MesenCult-XF medium. MSCs can be expanded up to the 25th passage without chromosomal changes by G-band. The best biological activity period and stability appeared between the third to 20th generations.
间充质干细胞(MSCs)是具有免疫抑制作用的多能成体干细胞。体外长期无血清培养期间MSCs的生物学稳定性尚未明确阐明。在第3、5、10、15、20和25代(分别为P3、P5、P10、P15、P20和P25)分析其形态、免疫表型和多向分化潜能。在P3、P5、P10、P15、P20和P25分析人脐带源(hUC)-MSCs的细胞周期分布、凋亡和核型。从P3到P25,hUC-MSCs的三个定义生物学特性[贴壁于塑料、特异性表面抗原表达、多能分化潜能]符合国际细胞治疗协会提出的MSCs定义标准。P25时的细胞周期分布分析表明,与P3时的细胞相比,G0/G1期细胞百分比增加(P<0.05)。与P3时的细胞相比,P25时的细胞凋亡率增加(至183%)(P<0.01)。在传代3-20代(P3-P20)内,细胞凋亡率之间的差异无统计学意义(P>0.05)。根据国际人类细胞遗传学命名系统(ISCN,2009)的核型分析指南,未检测到染色体消除、移位或染色体失衡。长期培养影响无血清MesenCult-XF培养基中MSCs的生物学稳定性。通过G带分析,MSCs可扩增至第25代而无染色体变化。最佳生物学活性期和稳定性出现在第3至20代之间。