Kim Byung Ju, Kim Mi-Suk, Kim Ki-Bae, Kim Ki-Woo, Hong Yeon-Mi, Kim In-Ki, Lee Han-Woong, Jung Yong-Keun
Department of Life Science, Kwangju Institute of Science and Technology, 1 Oryong-dong Puk-gu, Kwangju 500-712, Korea.
Carcinogenesis. 2002 Sep;23(9):1411-7. doi: 10.1093/carcin/23.9.1411.
Tumor necrosis factor (TNF)-alpha and TNF-related apoptosis inducing ligand (TRAIL) share a common signaling pathway. Here we show a novel potentiating effect of cadmium on TNF-alpha- or TRAIL-mediated cell death via distinct signaling. TNF-alpha or TRAIL sensitized otherwise resistant NIH3T3 embryo fibroblast cells to death, when exposed to cadmium. The potentiating effects elicited by TNF-alpha or TRAIL on cell death were NF-kappaB- and SAPK/JNK-independent and were not diminished by the expression of Bcl-2. TNF-alpha potentiated the cadmium-induced accumulation of p53 but did not affect expression levels of Bax, Mdm2 and p21(WAF/CIP). A similar pattern of p53 accumulation was also observed in Balbc/3T3 fibroblasts but not in human tumor cell lines, MCF7 and HeLa cells. The synergistic cell death evoked by TNF-alpha and cadmium was attenuated by transient expression of a dominant negative p53(Val135) mutant in NIH3T3 cells and was not observed in p53(-/-) mouse embryo fibroblasts, indicating that p53 accumulation appears to contribute to cell death. In contrast, TRAIL did not further increase the cadmium-induced accumulation of p53 despite its potentiation effects on the cadmium-induced cell death. Expression of p53(Val135) mutant did not reduce TRAIL- and cadmium-mediated cell death. Taken together, these results suggest that TNF-alpha and TRAIL potentiate the cadmium-mediated cell death via distinct p53 expression patterns.
肿瘤坏死因子(TNF)-α与肿瘤坏死因子相关凋亡诱导配体(TRAIL)共享一条共同的信号通路。在此我们展示了镉通过不同信号对TNF-α或TRAIL介导的细胞死亡具有一种新的增强作用。当暴露于镉时,TNF-α或TRAIL使原本具有抗性的NIH3T3胚胎成纤维细胞对死亡敏感。TNF-α或TRAIL对细胞死亡产生的增强作用不依赖于核因子κB(NF-κB)和应激激活蛋白激酶/应激活化蛋白激酶(SAPK/JNK),并且不受Bcl-2表达的影响。TNF-α增强了镉诱导的p53蓄积,但不影响Bax、Mdm2和p21(WAF/CIP)的表达水平。在Balbc/3T3成纤维细胞中也观察到了类似的p53蓄积模式,但在人肿瘤细胞系MCF7和HeLa细胞中未观察到。TNF-α与镉引发的协同细胞死亡在NIH3T3细胞中通过显性阴性p53(Val135)突变体的瞬时表达而减弱,并且在p53基因敲除(p53(-/-))的小鼠胚胎成纤维细胞中未观察到,这表明p53蓄积似乎促成了细胞死亡。相比之下,尽管TRAIL对镉诱导的细胞死亡具有增强作用,但它并未进一步增加镉诱导的p53蓄积。p53(Val135)突变体的表达并未降低TRAIL和镉介导的细胞死亡。综上所述,这些结果表明TNF-α和TRAIL通过不同的p53表达模式增强了镉介导的细胞死亡。