Pourzand C, Rossier G, Reelfs O, Borner C, Tyrrell R M
School of Pharmacy and Pharmacology, University of Bath, United Kingdo
Cancer Res. 1997 Apr 15;57(8):1405-11.
We examined the effect of broad spectrum UVA (320-380 nm) and UVB (290-320 nm) radiation on the induction of apoptosis in the rat 6 fibroblast cell line (R6). UVA, but not UVB, induces apoptosis in this cell line. The morphological changes and DNA ladders associated with apoptosis occurred within the first 4 h after UVA irradiation, a phenomenon referred to as "immediate" apoptosis. From previous studies, it is known that Bcl-2 inhibits most types of apoptotic cell death. Overexpression of mouse Bcl-2 in the R6 fibroblasts inhibited the UVA-induced immediate apoptosis. The induction of the heme oxygenase 1 (HO-1) gene by UVA is a general response to oxidative stress. As a marker of oxidative stress, we monitored the effect of Bcl-2 overexpression on the level of HO-1 mRNA accumulation after UVA irradiation. The results showed that the overexpression of Bcl-2 in the R6 fibroblasts strongly reduces the level of HO-1 induction from 12.5- to 4.9-fold. We propose that Bcl-2 expression inhibits UVA-induced immediate apoptosis via an antioxidant pathway, suppressing either the generation or effects of specific UVA-mediated reactive oxygen species.
我们研究了广谱紫外线A(320 - 380纳米)和紫外线B(290 - 320纳米)辐射对大鼠6成纤维细胞系(R6)凋亡诱导的影响。紫外线A而非紫外线B能诱导该细胞系发生凋亡。与凋亡相关的形态学变化和DNA梯状条带在紫外线A照射后的最初4小时内出现,这种现象被称为“即时”凋亡。从先前的研究可知,Bcl - 2可抑制大多数类型的凋亡性细胞死亡。在R6成纤维细胞中过表达小鼠Bcl - 2可抑制紫外线A诱导的即时凋亡。紫外线A诱导血红素加氧酶1(HO - 1)基因表达是对氧化应激的一种普遍反应。作为氧化应激的标志物,我们监测了Bcl - 2过表达对紫外线A照射后HO - 1 mRNA积累水平的影响。结果显示,在R6成纤维细胞中过表达Bcl - 2可使HO - 1的诱导水平从12.5倍大幅降至4.9倍。我们推测,Bcl - 2的表达通过抗氧化途径抑制紫外线A诱导的即时凋亡,抑制特定紫外线A介导的活性氧的产生或作用。