期刊
BIOTECHNOLOGY AND APPLIED BIOCHEMISTRY
卷 58, 期 4, 页码 261-270出版社
WILEY
DOI: 10.1002/bab.38
关键词
human; adipose-derived stem cells; stemness; gene expression; culture expansion; flow cytometry; biomarker
资金
- Ministry of Science, Technology & Innovation of Malaysia [02-01-02 SF0290]
One of the advantages of human adipose-derived stem cells (ASCs) in regenerative medicine is that they can be harvested in abundance. However, the stemness biomarkers, which marked the safety and efficacy of ASCs in accordance with the good manufacturing practice guidelines, is not yet well established. This study was designed to investigate the effect of long-term culture on the sternness properties of ASCs using quantitative real-time polymerase chain reaction and flow cytometry. Results showed the growth rate of ASCs was at its peak when they reached P10 (population doubling; PD = 26) but started to decrease when they were expanded to P15 (PD = 36) and P20 (PD = 46). The ASCs can be culture expanded with minimal alteration in the sternness genes and cluster of differentiation (CD) markers expression up to P10. Expression level of Sox2, Nestin, and Nanog3 was significantly decreased at later passage. CD31, CD45, CD117, and human leukocyte antigen DR, DQ, and DP were lowly expressed at P5 and P10 but their expressions increased significantly at P15 or P20. The differentiation ability of ASCs (adipogenesis, osteogenesis, and neurogenesis) also decreased in long-term culture. Our findings suggested that P10 (PD = 26) should be the cutoff point for clinical usage because ASCs at passage 15 onward showed significant changes in the sternness genes, CD markers expression, and differentiation capability.
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