Hammerling U, Bjelfman C, Påhlman S
Department of Pathology, University of Uppsala, Sweden.
Oncogene. 1987;2(1):73-7.
The mRNA expression of c-myc and N-myc in the human neuroblastoma cell line SH-SY5Y was found not to change appreciably during the cell cycle and was also unaffected by proliferative inhibition induced by serum starvation or polyamine depletion. However, an early (0.5-8.0 h post-induction) transient reduction of c- and N-myc transcripts were observed in these cells upon induction to differentiation with the phorbol ester 12-O-tetradecanoylphorbol-13-acetate (TPA). Treatment of these neuroblastoma cells with TPA for longer periods (1-8 days), which induces morphological and functional differentiation and growth arrest, was followed by decreased expression of both myc genes. However, the rate of disappearance differed considerably. The N-myc mRNA level was slightly decreased after 4 days and was still detectable 8 days after induction, whereas the c-myc transcript was down-regulated much faster. In contrast, when the cells were exposed to retinoic acid, which results in a maturation along an alternative pathway, the inhibition of N-myc and c-myc expression was similar. The c-fos mRNA expression increased in TPA-treated SH-SY5Y cells and remained high during extended exposure to the drug. The highest c-fos transcript level in induced cells coincided in time with the transient reduction of N-myc and c-myc. Thus, the TPA-induced neuronal differentiation of SH-SY5Y cells was compatible with high c-fos and a substantial N-myc mRNA expression.
在人神经母细胞瘤细胞系SH-SY5Y中,c-myc和N-myc的mRNA表达在细胞周期中未发现明显变化,并且不受血清饥饿或多胺耗竭诱导的增殖抑制影响。然而,在用佛波酯12-O-十四酰佛波醇-13-乙酸酯(TPA)诱导这些细胞分化后,观察到c-myc和N-myc转录本在早期(诱导后0.5 - 8.0小时)出现短暂减少。用TPA处理这些神经母细胞瘤细胞较长时间(1 - 8天),可诱导形态和功能分化以及生长停滞,随后两种myc基因的表达均降低。然而,消失速率有很大差异。N-myc mRNA水平在4天后略有下降,诱导8天后仍可检测到,而c-myc转录本下调得更快。相反,当细胞暴露于视黄酸时,会沿着另一条途径成熟,此时N-myc和c-myc表达的抑制情况相似。在TPA处理的SH-SY5Y细胞中,c-fos mRNA表达增加,并且在长时间暴露于该药物期间保持高水平。诱导细胞中c-fos转录本的最高水平与N-myc和c-myc的短暂减少在时间上一致。因此,TPA诱导的SH-SY5Y细胞神经元分化与高c-fos和大量N-myc mRNA表达相一致。