Kozanoglu Ilknur, Boga Can, Ozdogu Hakan, Sozer Oktay, Maytalman Erkan, Yazici Ayse Canan, Sahin Feride Iffet
Department of Physiology, Baskent University Faculty of Medicine, Ankara, Turkey.
Cytotherapy. 2009;11(5):527-33. doi: 10.1080/14653240902923153.
Mesenchymal stromal cells (MSC) exhibit non-specific hematopoietic cell and/or stromal cell markers (e.g. CD73, CD105 and CD166) that have been used to identify MSC by flow cytometry. Because a neural glial antigen, NG2 (a progenitor cell marker in the central nervous system), is expressed by several tissue cells originating in the mesenchyme but not hematopoietic cells, it might be useful for isolating and identifying MSC. We investigated NG2 expression on culture-expanded MSC by flow cytometry.
Human bone marrow (BM) samples taken from 12 donors were cultured for MSC to be used in up to nine serial passages. Using flow cytometry, the neural glial antigen NG2 and commonly used MSC markers CD73, CD105 and CD166, were analyzed on the surface of culture-expanded MSC. The multipotential differentiation of the MSC was examined by adipogenic and osteogenic induction.
The percentage of cells positive for NG2 was similar to the percentages of cells positive for CD73, CD105 and CD166 in all passages of BM samples. The mean fluorescent intensities of NG2 did not change with culture passage. The MSC was successfully differentiated into adipogenic and osteogenic lines. The cells showed no karyotypic abnormalities.
NG2 seems to be a promising marker for investigating the biology of MSC.
间充质基质细胞(MSC)表达非特异性造血细胞和/或基质细胞标志物(如CD73、CD105和CD166),这些标志物已被用于通过流式细胞术鉴定MSC。由于一种神经胶质抗原NG2(中枢神经系统中的祖细胞标志物)在起源于间充质的几种组织细胞中表达,但在造血细胞中不表达,它可能有助于分离和鉴定MSC。我们通过流式细胞术研究了培养扩增的MSC上NG2的表达情况。
从12名供体采集的人骨髓(BM)样本用于培养MSC,传代次数最多为9次。使用流式细胞术分析培养扩增的MSC表面的神经胶质抗原NG2以及常用的MSC标志物CD73、CD105和CD166。通过成脂和成骨诱导检测MSC的多能分化情况。
在BM样本的所有传代中,NG2阳性细胞的百分比与CD73、CD105和CD166阳性细胞的百分比相似。NG2的平均荧光强度不随培养传代而变化。MSC成功分化为成脂和成骨细胞系。细胞未显示核型异常。
NG2似乎是研究MSC生物学特性的一个有前景的标志物。