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作 者:董文川[1] 喻新建[1] 童春容[1] 高晖[1] 陈珊珊[1] 陆道培[1]
机构地区:[1]北京医科大学人民医院血液病研究所,100044
出 处:《北京医科大学学报》1997年第3期275-277,共3页Journal of Peking University(Health Sciences)
摘 要:目的:分离脐血CD细胞,以了解其造血增殖活性。方法:应用免疫磁珠法(Isolex50系统)分离脐血CD细胞,并对其实验方法进行了改进。结果:常规方法CD纯度较低,经过改进,脐血CD细胞由分离前的(1.39±0.76)%增加至(59.46±17.35)%,CD细胞富集倍数为(62.31±55.19)倍。分离后组分CFU-GM、BFU-E、CFU-Mix较分离前分别增加了(41.05±15.77)、(13.14±8.66)及(34.80±19.58)倍,而阴性组分所形成的集落显著减少。结论:免疫磁珠法可以有效地分离CD细胞,造血祖细胞集落大多来源于CD细胞。objective: The experiments aimed at the separation of CD cells from human cord blood and evaluation of its clonogeneic ability. Methods: Immunomagnetic bead separation (Isolex50 systere) was used to enrich CD cells. Results: By improved technique, the purity of CD cells separated from the mononuclear cells of the cord blood was (59.46±17. 35) % [starting population (1. 39±0. 76) %].With the separated CD cell fraction from cord blood, CFU-GM, BFU-E and CFU-Mix were enriched to (41.05±15. 77) fold, (13. 14±8. 66) fold, and (34. 80±19. 58) fold, respectively; while CD fraction developed only a few colonies. Conclusion: Immunomagnetic bead separation was effective in separating CD cells from cord blood, and CD cells enriched most of the clonogeneic cells.
分 类 号:R331.2[医药卫生—人体生理学]
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