Belhumeur P, Lanoix J, Blais Y, Forget D, Steyaert A, Skup D
Institut du Cancer de Montréal, Québec, Canada.
Mol Cell Biol. 1993 May;13(5):2846-57. doi: 10.1128/mcb.13.5.2846-2857.1993.
In the current study, we have addressed the role of interferons (IFNs) in controlling the differentiation of pluripotent P19 embryonal carcinoma (EC) cells. Blocking IFN activity in the culture medium of differentiating cells with antibodies leads to a strong decrease in the degree of differentiation. The antibodies are active for a relatively short time. During this time, IFN-beta mRNA can be detected in the differentiating cells, as can increases of IFN stimulation response element-binding activity and NF-KB. The timing of IFN action also coincides with the accumulation of cytoplasmic double-stranded RNA (dsRNA) and with a drop in dsRNA unwindase-modificase activity. A model for the involvement of autoinduction of IFN by intracellular dsRNA in the control of differentiation in this system is presented.
在当前的研究中,我们探讨了干扰素(IFN)在控制多能性P19胚胎癌细胞分化中的作用。用抗体阻断分化细胞培养基中的IFN活性会导致分化程度大幅降低。这些抗体的活性持续时间相对较短。在此期间,可在分化细胞中检测到IFN-β mRNA,同时IFN刺激反应元件结合活性和NF-κB也会增加。IFN作用的时间也与细胞质双链RNA(dsRNA)的积累以及dsRNA解旋酶-修饰酶活性的下降相吻合。本文提出了一个关于细胞内dsRNA自诱导IFN参与该系统分化控制的模型。