诱导多能干细胞
SOX2
生物
重编程
同源盒蛋白纳米
干细胞
间充质干细胞
细胞生物学
KLF4公司
再生医学
脂肪生成
成体干细胞
骨髓
细胞分化
干细胞移植修复关节软骨
免疫学
胚胎干细胞
细胞
遗传学
基因
作者
Lina Tang,Yupeng Yin,Zhou Haole,Guangqi Song,Anran Fan,Bo Tang,Wei Shi,Ziyi Li
出处
期刊:Cellular Reprogramming
[Mary Ann Liebert, Inc.]
日期:2012-08-01
卷期号:14 (4): 342-352
被引量:25
标识
DOI:10.1089/cell.2011.0098
摘要
Direct reprogramming of somatic cells to induced pluripotent stem cells (iPSCs) provides an invaluable resource for regenerative medicine. Because of some ethical and logistical barriers, human iPSCs cannot be used to generate a chimera, which is one of markers representing pluripotency. As the most attractive model for preclinical studies, pigs offer another path to improve clinical medicine. In this study, porcine adult stem cells (pASCs), including adipose mesenchymal stem cells (AMSCs) and bone marrow mesenchymal stem cells (BMSCs), were collected and cultured under the same conditions in vitro. Real-time PCR, immunocytochemical staining, apoptosis analysis, and induced differentiation and reprogramming techniques were used to investigate the proliferative capacity and pluripotent characteristics of pASCs. Our results showed that both AMSCs and BMSCs displayed a similar immunophenotype, and their proliferative capacity appeared as a downward trend as the cell passage number increased. The cell proliferative capacity of AMSCs was significantly lower than that of BMSCs (p<0.05). Moreover, each type of pASCs went through 20 passages without undergoing alterations in the expression of reprogramming transcriptional factors (Oct4, Sox2, c-Myc, and Nanog). All pASCs had adipogenic and osteogenic differentiation potential. In addition, they also could be reprogrammed to pig induced pluripotent stem cells (piPSCs) with similar time and efficiency. In conclusion, porcine BMSCs had a higher proliferative capacity than AMSCs, and the pluripotency of pASCs was stable in long-term culture.
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