Immunophenotype characterization of rat mesenchyrnal stromal cells

被引:89
作者
Harting, M. T. [1 ,2 ]
Jimenez, F. [1 ,2 ]
Pati, S. [3 ,4 ,5 ]
Baumgartner, J. [1 ]
Cox, C. S. [1 ,2 ]
机构
[1] Univ Texas Houston, Sch Med, Dept Pediat Surg, Houston, TX 77030 USA
[2] Univ Texas Houston, Sch Med, Trauma Res Ctr, Houston, TX 77030 USA
[3] Univ Texas Houston, Sch Med, Dept Neurobiol & Anat, Houston, TX 77030 USA
[4] Baylor Coll Med, Vivian L Smith Ctr Neurol Res, Houston, TX 77030 USA
[5] Baylor Coll Med, Dept Phys Med & Rehabil, Houston, TX 77030 USA
关键词
cell therapy; immunocharacterization; marker expression; mesenchymal stromal cell; rodent; stem cell;
D O I
10.1080/14653240801950000
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Background Mesenchymal stromal cells (MSC) have shown diverse therapeutic potential. While characterization of human and mouse MSC has seen significant advances, rat bone marrow-derived MSC (rBM-MSC) remain under-characterized. We detail the isolation, expansion, differentiation, and detailed immunocharacterization of rBM-MSC. Methods Rat MSC were isolated and expanded in multipotent adult progenitor cell (MAPC) media, and cell-surface marker expression through 10 passages was used to characterize the population and multipotency was confirmed via diffierentation. Results By passage 3, rBM-MSC were found to be CD11b(-), CD45(-), CD29(+), CD49e(+), CD73(+), CD90(+), CD105(+) and Stro-1(+), without the use of cell sorting. Media selection vas responsible for the isolation of a nearly homogeneous population of rBM-MSC. The rBM-MSC immunophenotype changed by passage 10, showing decreases in CD73, CD105 and Stro-1 expression, Discussion Detailed characterization of cell populations facilitates accurate and reproducible cell therapy investigation. Given the expanding body of research involving rBM-MSC, these results advance our ability to compare rBM-MSC populations.
引用
收藏
页码:243 / 253
页数:11
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