Ball E D, Howell A L, Shen L
Exp Hematol. 1986 Dec;14(11):998-1005.
The physiological agents gamma interferon and 1,25 dihydroxyvitamin D3 (calcitriol) are both potent inducers of monocytoid differentiation in the HL-60 promyelocytic leukemia cell line. However, the populations resulting from treatment with either inducer have differing properties, suggesting that these agents do not have identical modes of action. In this study we have compared the effects of gamma interferon (IFN gamma) and calcitriol and examined the effect of exposing HL-60 cells to both compounds simultaneously. In addition, we have examined the effects of inhibitors of protein and RNA synthesis on induction of cell surface antigens in order to gain insight into the mechanisms of action of these compounds. We found that combining IFN gamma and calcitriol resulted in greater monocytic differentiation of HL-60 cells than did either compound alone. In addition, a monocyte-associated cell surface antigen, My23, and class-I HLA antigen were induced by both agents in at least an additive manner. In contrast, combined treatment with both compounds did not augment antibody-dependent cellular cytotoxicity (ADCC) any better than did IFN gamma alone, but it did cause a decrease in the density of receptors for the Fc portion of immunoglobulin. In studies examining the effects of IFN gamma and calcitriol on the cloning potential of HL-60 cells, we found that incubation of cells with either compound alone significantly reduced the number of HL-60 colonies, and both compounds added together caused an almost total elimination of colony-forming cells. Inhibition of RNA synthesis with alpha amanitin had no effect on the action of IFN gamma on cell surface HLA, but did block the induction of My23 antigen, suggesting that the mechanism of HLA induction may involve posttranscriptional phenomena. RNA-synthesis blockade inhibited the ability of calcitriol to induce My23. These studies demonstrate that multiple and separable events accompany the monocytoid differentiation of HL-60 cells induced by different chemical mediators and that different intracellular pathways may be involved.
生理因子γ干扰素和1,25-二羟基维生素D3(骨化三醇)都是HL-60早幼粒细胞白血病细胞系中单核细胞样分化的有效诱导剂。然而,用任一诱导剂处理所产生的细胞群体具有不同的特性,这表明这些因子的作用方式并不相同。在本研究中,我们比较了γ干扰素(IFNγ)和骨化三醇的作用,并研究了同时将HL-60细胞暴露于这两种化合物的效果。此外,我们还研究了蛋白质和RNA合成抑制剂对细胞表面抗原诱导的影响,以便深入了解这些化合物的作用机制。我们发现,与单独使用任一化合物相比,联合使用IFNγ和骨化三醇可使HL-60细胞产生更大程度的单核细胞分化。此外,两种因子至少以相加的方式诱导了一种与单核细胞相关的细胞表面抗原My23和I类HLA抗原。相比之下,联合使用这两种化合物在增强抗体依赖性细胞毒性(ADCC)方面并不比单独使用IFNγ更好,但确实导致免疫球蛋白Fc部分受体的密度降低。在研究IFNγ和骨化三醇对HL-60细胞克隆潜力的影响时,我们发现单独用任一化合物孵育细胞都会显著减少HL-60集落的数量,而将两种化合物一起添加几乎会完全消除集落形成细胞。用α-鹅膏蕈碱抑制RNA合成对IFNγ诱导细胞表面HLA的作用没有影响,但确实阻断了My23抗原的诱导,这表明HLA诱导机制可能涉及转录后现象。RNA合成阻断抑制了骨化三醇诱导My23的能力。这些研究表明,不同化学介质诱导HL-60细胞单核细胞样分化伴随着多个可分离的事件,并且可能涉及不同的细胞内途径。