Nzengue Yves, Steiman Régine, Guiraud Pascale
Université Joseph Fourier, Domaine de La Merci, La Tronche, France.
Free Radic Res. 2008 Feb;42(2):142-53. doi: 10.1080/10715760701837100.
Cell death resulting from cadmium (Cd) intoxication has been confirmed to induce both necrosis and apoptosis. The ratio between both types of cell death is dose- and cell-type-dependent. This study used the human keratinocytes HaCaT expressing a mutated p53 and the rat glial cells C6 expressing a wild p53 as models to characterize Cd-induced apoptosis, using sub-lethal and lethal doses. At these concentrations, features of apoptosis were observed 24 h after C6 cell treatment: apoptotic DNA fragmentation and caspase-9 activation, whereas Cd did not induce caspase-3. In HaCaT, Cd did not induce apoptotic DNA fragmentation or caspase-9 and -3 activation. The results also showed that the inhibition of p53 led to a resistance of the C6 cells to 20 microm Cd, decreased the apoptosis and increased the metallothioneins in these cells. p53 restoration increased the sensitivity of HaCaT cells to Cd but did not affect the MT expression. The results suggest that Cd induced apoptosis in C6 cells but a non-apoptotic cellular death in HaCaT cells.
镉(Cd)中毒导致的细胞死亡已被证实可诱导坏死和凋亡。这两种细胞死亡类型之间的比例取决于剂量和细胞类型。本研究以表达突变型p53的人角质形成细胞HaCaT和表达野生型p53的大鼠神经胶质细胞C6为模型,使用亚致死剂量和致死剂量来表征镉诱导的凋亡。在这些浓度下,C6细胞处理24小时后观察到凋亡特征:凋亡性DNA片段化和半胱天冬酶-9激活,而镉未诱导半胱天冬酶-3激活。在HaCaT细胞中,镉未诱导凋亡性DNA片段化或半胱天冬酶-9和-3激活。结果还表明,p53的抑制导致C6细胞对20微摩尔镉产生抗性,减少了这些细胞中的凋亡并增加了金属硫蛋白。p53的恢复增加了HaCaT细胞对镉的敏感性,但不影响金属硫蛋白的表达。结果表明,镉在C6细胞中诱导凋亡,但在HaCaT细胞中诱导非凋亡性细胞死亡。