Kakutani T, Ebara Y, Kanja K, Hidaka M, Matsumoto Y, Nagano A, Wataya Y
Faculty of Pharmaceutical Sciences, Okayama University, Japan.
Biochem Biophys Res Commun. 1998 Jun 29;247(3):773-9. doi: 10.1006/bbrc.1998.8797.
The mode of cell death induced by 1 microM 5-fluoro-2'-deoxyuridine (FdUrd) changed in a wild-type F28-7 clone of mouse mammary tumor FM3A cells after a six-month culture. In the original stocked F28-7 clone, FdUrd-induced cell death was accompanied by necrosis-like cell swelling and DNA fragmentation to 100-200 kbp. In subclone F28-7-A isolated from F28-7 cells, which had been cultured for six months, apoptotic bodies and nucleosomal DNA-ladder fragments were observed with the treatment. Furthermore, we investigated the differences in FdUrd-induced intracellular signals between these clones. In F28-7 cells, FdUrd induced increases in caspase-3-like activity, and the mRNA levels of the c-jun, c-fos and c-myc genes, which were greater and earlier than those in F28-7-A cells. Moreover, intracellular acidification occurred in F28-7-A cells treated with FdUrd, though it was not observed in F28-7 cells. These findings suggest that FdUrd-induced cell death occurred through the death program to cell lysis (necrosis) without apoptosis when the induction of these intracellular signals was very high and when intracellular acidification was deficient. Investigation of the differences in the mode of FdUrd-induced cell death between these clones would be important for elucidating the molecular mechanism of pivotal events guiding cells toward either apoptosis or necrosis.
在对小鼠乳腺肿瘤FM3A细胞的野生型F28 - 7克隆进行6个月培养后,1 microM 5 - 氟 - 2'-脱氧尿苷(FdUrd)诱导的细胞死亡模式发生了变化。在最初保存的F28 - 7克隆中,FdUrd诱导的细胞死亡伴随着坏死样细胞肿胀以及DNA断裂成100 - 200 kbp的片段。在从F28 - 7细胞分离出并培养了6个月的亚克隆F28 - 7 - A中,处理后观察到了凋亡小体和核小体DNA梯状片段。此外,我们研究了这些克隆之间FdUrd诱导的细胞内信号差异。在F28 - 7细胞中,FdUrd诱导caspase - 3样活性增加,以及c - jun、c - fos和c - myc基因的mRNA水平升高,且比F28 - 7 - A细胞中的升高幅度更大、更早。此外,用FdUrd处理的F28 - 7 - A细胞中发生了细胞内酸化,而在F28 - 7细胞中未观察到。这些发现表明,当这些细胞内信号的诱导非常高且细胞内酸化不足时,FdUrd诱导的细胞死亡通过细胞裂解(坏死)的死亡程序发生,而无凋亡。研究这些克隆之间FdUrd诱导的细胞死亡模式差异对于阐明引导细胞走向凋亡或坏死的关键事件的分子机制具有重要意义。