脐带血
川地34
促红细胞生成素
间充质干细胞
干细胞
白细胞介素3
干细胞因子
免疫学
细胞生物学
骨髓
生物
CD40
细胞因子
体外
造血
男科
医学
内分泌学
抗原提呈细胞
T细胞
免疫系统
细胞毒性T细胞
生物化学
作者
Jia Yanjun,Jiang Liu,Keying Zhang,Xiaoyan Shan,Wei Li,Xiaomei He,Lijun Wang,Na Liu,Lin Wang,Shuang Cui,Lei Ni,Botao Zhao,Zhi-Yin Gong,Dongmei Wang,Song-Ming Gao,Zhixin Zhang
出处
期刊:PubMed
日期:2009-06-01
卷期号:17 (3): 787-92
摘要
This study was aimed to investigate a beneficial approach for resolving the deficiency of blood source, preventing the infection resulting from blood transfusion and overcoming the knotty match of patients with rare blood group by using massive expansion of erythroid cells from cord blood CD34(+) cells in vitro. The CD34(+) cells from human cord blood were cultured in serum-free medium supplemented with stem cell factor (SCF), interleukin-3 (IL-3) and erythropoietin (EPO) for 1 week, then expansion and differentiation of CD34(+) cells into erythroid cells were supported by co-culture with human mesenchymal stem cells (MSCs) derived from bone marrow for 2 weeks. The results indicated that after culture for 23 days, the expansion multiple of total cell number reached 2.52 x 10(5), and over 95% of these cells were erythroid cells as compared with less than 1% of myelomonocytic (CD14(+) or CD15(+)) cells and megakaryocytic (CD41(+)) cells. However, the culture system without MSC support was significantly disadvantaged both in expansion ability and ratio of erythroid cells when compared with MSC supporting system. It is concluded that the erythroid cells can be produced from CD34(+) cells in large scale by culturing in the system comprised of cytokine sets and MSC feeders, in which MSCs can support the proliferation and differentiation of erythroid cells.
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