Peng Qiuyue, Alipour Hiva, Porsborg Simone, Fink Trine, Zachar Vladimir
Department of Health Science and Technology, Regenerative Medicine Group, Aalborg University, Fredrik Bajers Vej 3B, 9220 Aalborg, Denmark.
Int J Mol Sci. 2020 Feb 19;21(4):1408. doi: 10.3390/ijms21041408.
Adipose-derived stromal/stem cells (ASCs) are currently being considered for clinical use for a number of indications. In order to develop standardized clinical protocols, it is paramount to have a full characterization of the stem cell preparations. The surface marker expression of ASCs has previously been characterized in multiple studies. However, most of these studies have provided a cross-sectional description of ASCs in either earlier or later passages. In this study, we evaluate the dynamic changes of 15 different surface molecules during culture. Using multichromatic flow cytometry, ASCs from three different donors each in passages 1, 2, 4, 6, and 8 were analyzed for their co-expression of markers associated with mesenchymal stem cells, wound healing, immune regulation, ASC markers, and differentiation capacity, respectively. We confirmed that at an early stage, ASC displayed a high heterogeneity with a plethora of subpopulations, which by culturing became more homogeneous. After a few passages, virtually all ASCs expressed CD29, CD166 and CD201, in addition to canonical markers CD73, CD90, and CD105. However, even at passage 8, there were several predominant lineages that differed with respect to the expression of CD34, CD200 and CD271. Although the significance of remaining subpopulations still needs to be elucidated, our results underscore the necessity to fully characterize ASCs prior to clinical use.
脂肪来源的基质/干细胞(ASC)目前正被考虑用于多种适应症的临床应用。为了制定标准化的临床方案,全面表征干细胞制剂至关重要。此前已有多项研究对ASC的表面标志物表达进行了表征。然而,这些研究大多对早期或晚期传代的ASC进行了横断面描述。在本研究中,我们评估了培养过程中15种不同表面分子的动态变化。使用多色流式细胞术,分别分析了来自三个不同供体的第1、2、4、6和8代ASC与间充质干细胞、伤口愈合、免疫调节、ASC标志物和分化能力相关标志物的共表达情况。我们证实,在早期阶段,ASC表现出高度异质性,存在大量亚群,通过培养变得更加均一。经过几代培养后,除了经典标志物CD73、CD90和CD105外,几乎所有ASC都表达CD29、CD166和CD201。然而,即使在第8代,仍有几个主要谱系在CD34、CD200和CD271的表达上存在差异。尽管剩余亚群的意义仍有待阐明,但我们的结果强调了在临床应用前对ASC进行全面表征的必要性。