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在用依托泊苷处理的人白血病细胞中,gadd153信使核糖核酸水平升高与细胞凋亡相关。

Increased gadd153 messenger RNA level is associated with apoptosis in human leukemic cells treated with etoposide.

作者信息

Eymin B, Dubrez L, Allouche M, Solary E

机构信息

Laboratory of Oncohematology and Pharmacology, CJF INSERM 94-08, UFR of Medicine/Pharmacy, Dijon, France.

出版信息

Cancer Res. 1997 Feb 15;57(4):686-95.

PMID:9044846
Abstract

Treatment of leukemic cells with topoisomerase inhibitors can lead to growth arrest and subsequent apoptotic cell death. The relationships between cell cycle regulation and apoptosis triggering remain poorly understood. The gadd153 gene encodes the nuclear protein CHOP 10 that acts as a negative modulator of CCAAT/enhancer binding protein transcriptional factors and inhibits cell cycle progression. We have investigated the relationships between gadd153 gene expression and apoptosis induction in four human leukemic cell lines with different sensitivities to apoptosis induced by etoposide (VP-16), a topoisomerase II inhibitor. The gadd153 gene was constitutively expressed in the four studied cell lines. In U937 and HL-60 cells that were very sensitive to apoptosis induction by the drug, VP-16 induced a time- and dose-dependent increase of gadd153 gene mRNA expression. Using agarose gel electrophoresis and a quantitative filter elution assay, apoptotic DNA fragmentation was observed to begin when gadd153 gene expression increased. Equitoxic doses of VP-16 (as defined using a 96-h 3-4,5-dimethylthiazol-2,5-diphenyltetrazolium bromide assay) did not increase the gadd153 mRNA level in K562 and KCL22 cell lines that were more resistant to apoptosis induction by the drug. Nuclear run-on and mRNA stability experiments demonstrated that VP-16 treatment increased gadd153 gene transcription in the sensitive U937 cells. Cycloheximide did not prevent gadd153 expression increase. Both gadd153 mRNA level increase and internucleosomal DNA fragmentation were inhibited by N-tosyl-L-phenylalanine chloromethylketone, a serine threonine protease inhibitor, N-acetyl-leucyl-leucyl-norleucinal, an inhibitor of calpain, N-acetylcysteine, an inhibitor of oxidative metabolism, and overexpression of Bcl-2. Z-VAD and Z-DEVD peptides that inhibit interleukin 1beta-converting enzyme-like proteases suppressed DNA fragmentation without preventing gadd153 mRNA increase in VP-16-treated U937 cells. These results indicate that gadd153 gene expression increase occurs downstream of events sensitive to N-tosyl-L-phenylalanine chloromethylketone, calpain inhibitor I, and Bcl-2 and upstream of interleukin 1beta-converting enzyme-related proteases activation in leukemic cells in which treatment with VP-16 induces rapid apoptosis.

摘要

用拓扑异构酶抑制剂处理白血病细胞可导致生长停滞及随后的凋亡性细胞死亡。细胞周期调控与凋亡触发之间的关系仍了解甚少。gadd153基因编码核蛋白CHOP 10,它作为CCAAT/增强子结合蛋白转录因子的负调节剂,抑制细胞周期进程。我们研究了gadd153基因表达与四种对拓扑异构酶II抑制剂依托泊苷(VP-16)诱导的凋亡敏感性不同的人白血病细胞系中凋亡诱导之间的关系。gadd153基因在四个研究的细胞系中组成性表达。在对药物诱导凋亡非常敏感的U937和HL-60细胞中,VP-16诱导gadd153基因mRNA表达呈时间和剂量依赖性增加。使用琼脂糖凝胶电泳和定量滤膜洗脱试验,当gadd153基因表达增加时,观察到凋亡性DNA片段化开始。等毒性剂量的VP-16(如使用96小时3-(4,5-二甲基噻唑-2)-2,5-二苯基四氮唑溴盐试验所定义)并未增加对药物诱导凋亡更具抗性的K562和KCL22细胞系中的gadd153 mRNA水平。核转录和mRNA稳定性实验表明,VP-16处理增加了敏感的U937细胞中gadd153基因的转录。放线菌酮并未阻止gadd153表达增加。N-对甲苯磺酰-L-苯丙氨酸氯甲基酮(一种丝氨酸苏氨酸蛋白酶抑制剂)、N-乙酰-亮氨酰-亮氨酰-正亮氨酸(一种钙蛋白酶抑制剂)、N-乙酰半胱氨酸(一种氧化代谢抑制剂)以及Bcl-2的过表达均抑制了gadd153 mRNA水平的增加和核小体间DNA片段化。抑制白细胞介素1β转换酶样蛋白酶的Z-VAD和Z-DEVD肽在VP-16处理的U937细胞中抑制了DNA片段化,但未阻止gadd153 mRNA增加。这些结果表明,在VP-16处理诱导快速凋亡的白血病细胞中,gadd153基因表达增加发生在对N-对甲苯磺酰-L-苯丙氨酸氯甲基酮、钙蛋白酶抑制剂I和Bcl-2敏感的事件下游以及白细胞介素1β转换酶相关蛋白酶激活上游。

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