Sasaki H, Hirabayashi Y, Ishibashi T, Inoue T, Matsuda M, Kai S, Ikuta K, Yokoyama K, Yokota T, Maruyama Y
Department of Pediatrics, Yokohama City University, School of Medicine, Japan.
Leuk Res. 1995 Feb;19(2):95-102. doi: 10.1016/0145-2126(94)00121-p.
We examined the effects of recombinant human erythropoietin (rhEPO), recombinant murine interleukin 3 (rmIL-3), recombinant human interleukin 6 (rhIL-6), recombinant human interleukin 11 (rhIL-11), recombinant murine leukemia inhibitory factor (rmLIF) and recombinant murine granulocyte-macrophage colony-stimulating factor (rmGM-CSF) on the growth of murine megakaryocytic cell lines. In serum-free methylcellulose culture supplemented with bovine serum albumin (BSA), the addition of rhEPO (0.1-10 U/ml), rmIL-3 (10-500 U/ml), rhIL-6 (100-10,000 U/ml), rmLIF (100-10,000 U/ml), or rmGM-CSF (10-1000 U/ml) enhanced colony growth in L8057Y5 cells, which had been maintained in protein-free culture, mostly in a dose-dependent fashion; rhIL-11 did not have any stimulatory effect at the tested doses (10-1000 U/ml). In addition, colony growth of L8057 cells, which had been maintained in serum-containing culture, was enhanced, but to a lesser extent, by the addition of these cytokines except rhEPO (the cultures were supplemented with 1% fetal bovine serum. Among the cytokines that showed growth-enhancing effects on L8057 cells, the expression of mRNAs encoding receptors for EPO, IL-6 and IL-3 was examined by northern blot analysis or reverse transcription polymerase chain reaction (RT-PCR). In both cell lines, mRNAs for EPO-R, IL-6R, gp130, IL-3R alpha and beta chains were constitutively expressed. The results suggest that L8057 and L8057Y5 cell lines have characteristics of megakaryoblastic cells in their biological responses to cytokines, as well as in the expression of cytokine receptor mRNAs, and that the growth-enhancing effects of these cytokines on the cell lines may be achieved through specific receptors. Our findings show the value of these cell lines for investigating the mechanisms of growth signal transduction in megakaryopoiesis.
我们研究了重组人促红细胞生成素(rhEPO)、重组小鼠白细胞介素3(rmIL-3)、重组人白细胞介素6(rhIL-6)、重组人白细胞介素11(rhIL-11)、重组小鼠白血病抑制因子(rmLIF)和重组小鼠粒细胞-巨噬细胞集落刺激因子(rmGM-CSF)对小鼠巨核细胞系生长的影响。在补充有牛血清白蛋白(BSA)的无血清甲基纤维素培养物中,添加rhEPO(0.1 - 10 U/ml)、rmIL-3(10 - 500 U/ml)、rhIL-6(100 - 10,000 U/ml)、rmLIF(100 - 10,000 U/ml)或rmGM-CSF(10 - 1000 U/ml)可增强L8057Y5细胞的集落生长,该细胞系一直维持在无蛋白培养条件下,大多呈剂量依赖性;rhIL-11在测试剂量(10 - 1000 U/ml)下没有任何刺激作用。此外,添加这些细胞因子可增强一直维持在含血清培养条件下的L8057细胞的集落生长,但程度较小,rhEPO除外(培养物补充有1%胎牛血清)。在对L8057细胞显示出生长增强作用的细胞因子中,通过Northern印迹分析或逆转录聚合酶链反应(RT-PCR)检测了编码EPO、IL-6和IL-3受体的mRNA的表达。在这两种细胞系中,EPO-R、IL-6R、gp130、IL-3Rα和β链的mRNA均组成性表达。结果表明,L8057和L8057Y5细胞系在对细胞因子的生物学反应以及细胞因子受体mRNA的表达方面具有巨核母细胞的特征,并且这些细胞因子对细胞系的生长增强作用可能是通过特定受体实现的。我们的研究结果显示了这些细胞系在研究巨核细胞生成中生长信号转导机制方面的价值。