Ikebuchi K, Wong G G, Clark S C, Ihle J N, Hirai Y, Ogawa M
Medical University of South Carolina, Charleston.
Proc Natl Acad Sci U S A. 1987 Dec;84(24):9035-9. doi: 10.1073/pnas.84.24.9035.
Interleukin-6 (IL-6, also known as B-cell stimulatory factor 2/interferon beta 2) was previously shown to support the proliferation of granulocyte/macrophage progenitors and indirectly support the formation of multilineage and blast cell colonies in cultures of spleen cells from normal mice. We report here that IL-3 and IL-6 act synergistically in support of the proliferation of murine multipotential progenitors in culture. The time course of total colony formation by spleen cells isolated from mice 4 days after injection of 5-fluorouracil (150 mg/kg) was significantly shortened in cultures containing both lymphokines relative to cultures supported by either of the two factors. Serial observations (mapping) of individual blast cell colonies in culture revealed that blast cell colonies emerged after random time intervals in the presence of IL-3. The average time of appearance in IL-6 alone was somewhat delayed, and in cultures containing both factors the appearance of multilineage blast cell colonies was significantly hastened relative to cultures grown in the presence of the individual lymphokines. In cultures of day-2 post-5-fluorouracil bone marrow cells, IL-6 failed to support colony formation; IL-3 alone supported the formation of a few granulocyte/macrophage colonies, but the combination of factors acted synergistically to yield multilineage and a variety of other types of colonies. In this system, IL-1 alpha also acted synergistically with IL-3, but the effect was smaller, and no multilineage colonies were seen. Together these results indicate that IL-3 and IL-6 act synergistically to support the proliferation of hemopoietic progenitors and that at least part of the effect results from a decrease in the G0 period of the individual stem cells.
白细胞介素-6(IL-6,也称为B细胞刺激因子2/干扰素β2)先前已被证明可支持粒细胞/巨噬细胞祖细胞的增殖,并间接支持正常小鼠脾细胞培养物中多谱系和原始细胞集落的形成。我们在此报告,IL-3和IL-6在支持培养的小鼠多能祖细胞增殖方面具有协同作用。相对于由这两种因子中的任何一种支持的培养物,在含有两种淋巴因子的培养物中,从注射5-氟尿嘧啶(150 mg/kg)4天后的小鼠分离的脾细胞形成总集落的时间进程显著缩短。对培养物中单个原始细胞集落的连续观察(绘图)显示,在存在IL-3的情况下,原始细胞集落在随机时间间隔后出现。单独使用IL-6时平均出现时间有所延迟,而在含有两种因子的培养物中,多谱系原始细胞集落的出现相对于在单个淋巴因子存在下生长的培养物显著加快。在5-氟尿嘧啶处理后第2天的骨髓细胞培养物中,IL-6不能支持集落形成;单独的IL-3支持形成少数粒细胞/巨噬细胞集落,但因子组合协同作用产生多谱系和多种其他类型的集落。在该系统中,IL-1α也与IL-3协同作用,但效果较小,未观察到多谱系集落。这些结果共同表明,IL-3和IL-6协同作用以支持造血祖细胞的增殖,并且至少部分作用是由于单个干细胞G0期的缩短。