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作 者:隋星卫[1] 王红美[1] 侯怀水[1] 曾凤华[2] 张丽萍[1] 沈柏均[2]
机构地区:[1]山东医科大学附属医院低温医学研究室,济南250012 [2]山东医科大学附属医院儿科,济南250012
出 处:《中国实验血液学杂志》1999年第4期302-304,共3页Journal of Experimental Hematology
基 金:国家自然科学基金 编号39670369
摘 要:1995年,我们发现由于细胞因子(SCF)和白细胞介素6(IL-6)/可溶性白细胞介素6受体(sIL-6R)复合物同时激活c-kit和gp130信号系统,有利于CD34^+细胞的扩增。在此基础上,我们进一步研究了同时激活这两个信号系统对更原始的脐血长期培养启动细胞(long-term culture-initiating cell,LTC-IC)和混合造血细胞集落形成单位(CFU-Mix)的扩增作用。The object of this study was to elucidate the effect of coactivating signals through gpl30 and c-kit on the expansion of cord blood hematopoietic stem/progenitor cells. CD34+ cells were isolated from human umbilical cord blood by Dynal beads M-450 CD34 im-munoselection system and expanded with different cytokines or cytokine combinations including SCF, IL-6, sIL-6R and IL-3 in a 21-day suspension culture system. The expansion efficiency of CFU-Mix and LTC-IC by methylcellulose culture and limiting dilution assay was studied, respectively. A combination of SCF, IL-6 and sIL-6R, but not SCF, IL-6 or sIL-6R alone, produced dramatic increase in the population of various cell lineages. The highest expansion efficiency in the combination of SCF, IL-6 and sIL-6R was found during 7 - 14 days after culture, and CFU-Mix and LTC-IC increased 22.5 - and 3.5- fold, respectively, while CD34 + cells treated with combination of SCF, IL-6 and IL-3 after two weeks CFU-Mix only increased 13. 0 - fold and LTC-IC 1.9- fold. These results suggested that gp130 signaling in association with c-kit activation may provide a novel approach for ex vivo expansion of human primitive hematopoietic progenitors.
关 键 词:IL-6 SIL-6R SCF GP130 c-kit 脐血 CD34^+细胞
分 类 号:R331.1[医药卫生—人体生理学] R973[医药卫生—基础医学]
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