Sui X, Tsuji K, Tanaka R, Tajima S, Muraoka K, Ebihara Y, Ikebuchi K, Yasukawa K, Taga T, Kishimoto T
Department of Clinical Oncology, University of Tokyo, Japan.
Proc Natl Acad Sci U S A. 1995 Mar 28;92(7):2859-63. doi: 10.1073/pnas.92.7.2859.
gp130, a signal-transducing receptor component of interleukin 6 (IL-6), associates with an IL-6 and IL-6 receptor (IL-6) complex and transduces signals. To examine the role of gp130 signaling in the expansion of human hemopoietic progenitor cells, we tested the effects of a recombinant soluble human IL-6 receptor (sIL-6R) and/or IL-6 in combination with other cytokines on purified human umbilical cord blood CD34+ cells, using methylcellulose clonal assay and suspension culture in the presence or absence of serum. A combination of sIL-6R and IL-6 (sIL-6R/IL-6), but not sIL-6R or IL-6 alone, was found to dramatically stimulate expansion of hemopoietic progenitor cells as well as CD34+ cells in the presence of stem cell factor. Significant generation of multipotential hemopoietic progenitors over a period of 3 weeks in suspension culture and efficient formation of colonies, especially multilineage and blast cell colonies, in methylcellulose assay supplemented with a combination of sIL-6R/IL-6 together with stem cell factor were observed in serum-containing and serum-free culture. Addition of anti-gp130 monoclonal antibodies or anti-IL-6R monoclonal antibodies to the above cultures dose-dependently inhibited the expansion of progenitor cells in suspension culture and also completely blocked the formation of multilineage colonies in methylcellulose culture. These findings demonstrated that the significant expansion of human primitive hemopoietic progenitors could be achieved with the gp130 and c-Kit signalings initiated by the sIL-6R/IL-6 complex in the presence of stem cell factor and suggested the possible application of this method for ex vivo expansion of CD34+ cells for bone marrow transplantation.
gp130是白细胞介素6(IL-6)的一种信号转导受体成分,它与IL-6和IL-6受体(IL-6R)复合物结合并转导信号。为了研究gp130信号在人类造血祖细胞扩增中的作用,我们使用甲基纤维素克隆测定法以及在有或无血清存在的情况下进行悬浮培养,测试了重组可溶性人类IL-6受体(sIL-6R)和/或IL-6与其他细胞因子联合作用于纯化的人类脐带血CD34+细胞的效果。发现在存在干细胞因子的情况下,sIL-6R和IL-6的组合(sIL-6R/IL-6)能显著刺激造血祖细胞以及CD34+细胞的扩增,而单独的sIL-6R或IL-6则无此作用。在含血清和无血清培养中均观察到,在悬浮培养3周的时间里多能造血祖细胞显著生成,并且在补充了sIL-6R/IL-6与干细胞因子组合的甲基纤维素测定中高效形成集落,尤其是多谱系和原始细胞集落。向上述培养物中添加抗gp130单克隆抗体或抗IL-6R单克隆抗体,能剂量依赖性地抑制悬浮培养中祖细胞的扩增,并且也完全阻断甲基纤维素培养中多谱系集落的形成。这些发现表明在存在干细胞因子的情况下,由sIL-6R/IL-6复合物启动的gp130和c-Kit信号能够实现人类原始造血祖细胞的显著扩增,并提示该方法可能用于体外扩增用于骨髓移植的CD34+细胞。