Department of Physiology, Universiti Kebangsaan Malaysia, Kuala Lumpur.
Biotechnol Appl Biochem. 2011 Jul-Aug;58(4):261-70. doi: 10.1002/bab.38. Epub 2011 Aug 9.
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 stemness 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 stemness 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 stemness genes, CD markers expression, and differentiation capability.
人脂肪来源干细胞(ASCs)在再生医学中的一个优势是可以大量采集。然而,符合良好生产规范指南的 ASCs 的干性生物标志物尚未得到很好的建立。本研究旨在通过定量实时聚合酶链反应和流式细胞术研究长期培养对 ASCs 干性特性的影响。结果表明,当 ASCs 达到 P10(倍增数;PD=26)时,其增长率达到峰值,但当扩增至 P15(PD=36)和 P20(PD=46)时,增长率开始下降。ASCs 可以在培养过程中进行扩增,其干性基因和分化群(CD)标志物的表达变化很小,直至 P10。Sox2、Nestin 和 Nanog3 的表达水平在后期传代时显著降低。CD31、CD45、CD117 和人类白细胞抗原 DR、DQ 和 DP 在 P5 和 P10 时低表达,但在 P15 或 P20 时表达显著增加。ASCs 的分化能力(成脂、成骨和成神经)也随长期培养而降低。我们的研究结果表明,P10(PD=26)应该是临床应用的“截止点”,因为传代 15 代后的 ASCs 在干性基因、CD 标志物表达和分化能力方面都发生了显著变化。