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首页> 外文期刊>Stem Cell Research & Therapy >Discrete adipose-derived stem cell subpopulations may display differential functionality after in vitro expansion despite convergence to a common phenotype distribution
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Discrete adipose-derived stem cell subpopulations may display differential functionality after in vitro expansion despite convergence to a common phenotype distribution

机译:尽管收敛到常见的表型分布,离散的脂肪来源的干细胞亚群在体外扩增后可能显示出不同的功能

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Background Complex immunophenotypic repertoires defining discrete adipose-derived stem cell (ASC) subpopulations may hold a key toward identifying predictors of clinical utility. To this end, we sorted out of the freshly established ASCs four subpopulations (SPs) according to a specific pattern of co-expression of six surface markers, the CD34, CD73, CD90, CD105, CD146, and CD271, using polychromatic flow cytometry. Method Using flow cytometry-associated cell sorting and analysis, gating parameters were set to select for a CD73+CD90+CD105+ phenotype plus one of the four following combinations, CD34?CD146?CD271? (SP1), CD34?CD146+CD271? (SP2), CD34+CD146+CD271? (SP3), and CD34?CD146+CD271+ (SP4). The SPs were expanded 700- to 1000-fold, and their surface repertoire, trilineage differentiation, and clonogenic potential, and the capacity to support wound healing were assayed. Results Upon culturing, the co-expression of major epitopes, the CD73, CD90, and CD105 was maintained, while regarding the minor markers, all SPs reverted to resemble the pre-sorted population with CD34?CD146?CD271? and CD34?CD146+CD271? representing the most prevalent combinations, followed by less frequent CD34+CD146?CD271? and CD34+CD146+CD271? variants. There was no difference in the efficiency of adipo-, osteo-, or chondrogenesis by cytochemistry and real-time RT-PCR or the CFU capacity between the individual SPs, however, the SP2CD73+90+105+34-146+271- outperformed others in terms of wound healing. Conclusions Our study shows that ASCs upon culturing inherently maintain a stable distribution of immunophenotype variants, which may potentially disguise specific functional properties of particular downstream lines. Furthermore, the outlined approach suggests a paradigm whereby discrete subpopulations could be identified to provide for a therapeutically most relevant cell product.
机译:背景技术定义离散的脂肪干细胞(ASC)亚群的复杂免疫表型库可能对确定临床效用的预测因子具有关键作用。为此,我们使用多色流式细胞术根据六个表面标志物CD34,CD73,CD90,CD105,CD146和CD271的共表达的特定模式,从刚建立的ASC中筛选出四个亚群(SP)。方法使用流式细胞仪相关细胞分选和分析,设置门控参数以选择CD73 + CD90 + CD105 + 表型加以下四个组合CD34 ? CD146 ? CD271 ?(SP1),CD34 ? CD146 + CD271 ?(SP2),CD34 + CD146 + CD271 ?(SP3)和CD34 ? CD146 + CD271 + (SP4)。将SP扩展至700到1000倍,并分析其表面库,三系分化和克隆形成潜力以及支持伤口愈合的能力。结果培养后,维持了主要表位,CD73,CD90和CD105的共表达,而对于次要标记,所有SP均恢复为与CD34 ? CD146 < sup>? CD271 ?和CD34 ? CD146 + CD271 ?代表最普遍的组合,其次是频率较低的CD34 + CD146 ? CD271 ?和CD34 + CD146 + CD271 ?变体。通过细胞化学和实时RT-PCR进行的脂肪形成,骨生成或软骨形成的效率或各个SP之间的CFU能力没有差异,但是SP2 CD73 + 90 + 105 + 34-146 +271-在伤口愈合方面胜过其他人。结论我们的研究表明,培养的ASC固有地保持了免疫表型变异体的稳定分布,这可能掩盖了特定下游细胞系的特定功能特性。此外,概述的方法提出了一种范例,通过该范例可以识别离散的亚群以提供治疗上最相关的细胞产物。

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