Kane D J, Sarafian T A, Anton R, Hahn H, Gralla E B, Valentine J S, Ord T, Bredesen D E
Department of Neurology, University of California, Los Angeles 90024.
Science. 1993 Nov 19;262(5137):1274-7. doi: 10.1126/science.8235659.
The proto-oncogene bcl-2 inhibits apoptotic and necrotic neural cell death. Expression of Bcl-2 in the GT1-7 neural cell line prevented death as a result of glutathione depletion. Intracellular reactive oxygen species and lipid peroxides rose rapidly in control cells depleted of glutathione, whereas cells expressing Bcl-2 displayed a blunted increase and complete survival. Modulation of the increase in reactive oxygen species influenced the degree of cell death. Yeast mutants null for superoxide dismutase were partially rescued by expression of Bcl-2. Thus, Bcl-2 prevents cell death by decreasing the net cellular generation of reactive oxygen species.
原癌基因bcl - 2可抑制神经细胞的凋亡和坏死性死亡。GT1 - 7神经细胞系中Bcl - 2的表达可防止因谷胱甘肽耗竭导致的细胞死亡。在谷胱甘肽耗竭的对照细胞中,细胞内活性氧和脂质过氧化物迅速增加,而表达Bcl - 2的细胞其增加则较为平缓且细胞完全存活。活性氧增加的调节影响细胞死亡程度。超氧化物歧化酶缺失的酵母突变体通过表达Bcl - 2得到部分挽救。因此,Bcl - 2通过减少细胞内活性氧的净生成来防止细胞死亡。