Isolation of mesenchymal stem cells from G-CSF-mobilized human peripheral blood using fibrin microbeads

被引:182
作者
Kassis, I
Zangi, L
Rivkin, R
Levdansky, L
Samuel, S
Marx, G
Gorodetsky, R
机构
[1] Hebrew Univ Jerusalem, Hadassah Med Ctr, Sharett Inst Oncol, Radiobiol & Biotechnol Lab, IL-91120 Jerusalem, Israel
[2] Hebrew Univ Jerusalem, Hadassah Med Ctr, Dept Bone Marrow Transplantat, IL-91120 Jerusalem, Israel
[3] HAPTO Biotech Ltd, Jerusalem, Israel
基金
以色列科学基金会;
关键词
mesenchymal stem cells (MSC); granulocyte; colony-stimulating factor (G-CSF); mobilization; fibrin microbeads (FMB); differentiation; human peripheral blood;
D O I
10.1038/sj.bmt.1705358
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Adult mesenchymal stem cells (MSC) that are able to differentiate into various mesenchymal cell types are typically isolated from bone marrow, but their significant presence in human peripheral blood (PB) is controversial. Fibrin microbeads (FMB) that bind matrix-dependent cells were used to isolate MSC from the mononuclear fraction of mobilized PB of adult healthy human donors treated with a granulocyte colony-stimulating factor. Isolation by plastic adherence resulted in a negligible number of MSC in all samples tested, whereas FMB-based isolation yielded spindle-shaped cell samples that could further expand on plastic or on FMB in eight out of the 11 samples. The yield of these cells at days 17-18 after the harvest was similar to 0.5% of the initial cell number. The isolated cells were grown on plastic and characterized by FACS analysis and immunohistochemistry for specific markers. Following culturing and first passage, the FMB-isolated cells stained positive for mesenchymal stromal cell markers CD90 and CD105, expressed vimentin and fibronectin and were negative for hematopoietic markers CD45 and CD34. These cells could differentiate into osteoblasts, adipocytes and chondrocytes. This study indicates that FMB may have special advantage in isolating MSC from sources such as mobilized PB, where the number of such cells is scarce.
引用
收藏
页码:967 / 976
页数:10
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