Urashima M, Hoshi Y, Akiyama M, Kamijo M, Kato Y, Akatsuka J, Maekawa K, Matsuzaki M, Ohnishi J, Kaihara C
Department of Pediatrics, Jikei University of School of Medicine, Minato-ku, Japan.
Acta Paediatr Jpn. 1995 Apr;37(2):160-5. doi: 10.1111/j.1442-200x.1995.tb03289.x.
Ex vivo expansion of hematopoietic progenitor cells in the umbilical cord blood mononuclear cells (CB-MNC) was investigated in liquid culture system with various combinations of cytokines (stem cell factor [SCF], interleukin [IL]-3, IL-6, granulocyte-colony stimulating factor [G-CSF], erythropoietin [EPO], and interferon [INF]-gamma). Non-lineage-committed hematopoietic progenitor cells and lineage committed hematopoietic progenitor cells were represented as CD34+CD38- and CD34+CD38+ subpopulations, respectively. Although absolute CD34+CD38- cell numbers decreased even in the presence of multicytokines, the combinations of SCF plus IL-6 and SCF plus IL-3 plus IL-6 plus IFN-gamma were significantly effective in maintaining CD34+CD38- cells than the other combinations (P < 0.05). After 4 weeks of culture. CD34+CD38- cells disappeared in all combinations of cytokines. Absolute CD34+CD38+ cell numbers increased in the presence of cytokines. Maximal expansion of CD34+CD38+ cells were observed in the combinations of SCF plus IL-3 plus IL-6 plus EPO (19.8 +/- 3.3-fold) and SCF plus IL-3 plus IL-6 plus G-CSF (18.3 +/- 2.6). The combination of SCF plus IL-3 plus IL-6 was also effective to expand CD34+CD38- cells (15.8 +/- 3.9). However, the expansion was transient and they decreased to zero within 3 weeks. In the combinations of SCF plus IL-6 and SCF plus IL-3 plus IL-6 plus INF-gamma, maximal expansion was inferior to the others but CD34+CD38+ cells were maintained more than 4 weeks. These results suggested that the indication of CBT can be expanded into older children by ex vivo augmentation of CB hematopoietic progenitor cells using multi-cytokines.
在液体培养系统中,使用多种细胞因子组合(干细胞因子[SCF]、白细胞介素[IL]-3、IL-6、粒细胞集落刺激因子[G-CSF]、促红细胞生成素[EPO]和干扰素[INF]-γ)研究了脐带血单个核细胞(CB-MNC)中造血祖细胞的体外扩增。未分化的造血祖细胞和已分化的造血祖细胞分别以CD34+CD38-和CD34+CD38+亚群表示。尽管即使在存在多种细胞因子的情况下,绝对CD34+CD38-细胞数量仍会减少,但SCF加IL-6以及SCF加IL-3加IL-6加IFN-γ的组合在维持CD34+CD38-细胞方面比其他组合更有效(P<0.05)。培养4周后,所有细胞因子组合中的CD34+CD38-细胞均消失。在存在细胞因子的情况下,绝对CD34+CD38+细胞数量增加。在SCF加IL-3加IL-6加EPO(19.8±3.3倍)和SCF加IL-3加IL-6加G-CSF(18.3±2.6)的组合中观察到CD34+CD38+细胞的最大扩增。SCF加IL-3加IL-6的组合也有效地扩增了CD34+CD38-细胞(15.8±3.9)。然而,这种扩增是短暂的,它们在3周内降至零。在SCF加IL-6以及SCF加IL-3加IL-6加IFN-γ的组合中,最大扩增低于其他组合,但CD34+CD38+细胞维持超过4周。这些结果表明,通过使用多种细胞因子对CB造血祖细胞进行体外扩增,CBT的适应症可以扩大到年龄较大的儿童。