Johnson V L, Cooper I R, Jenkins J R, Chow S C
Centre for Mechanisms of Human Toxicity, University of Leicester, Leicester, LE1 9HN, United Kingdom.
Exp Cell Res. 1999 Aug 25;251(1):175-84. doi: 10.1006/excr.1999.4557.
The effects of Bcl-2 overexpression on several of its multifunctional characteristics, which include anti-apoptotic properties, impeding of cell proliferation, and telomerase activity, were examined in four Jurkat T cell clones overexpressing different levels of Bcl-2. When treated with anti-Fas or staurosporine, only three of the four clones showed resistance to apoptosis that correlated with the level of Bcl-2 expression. Surprisingly, the clone having no anti-apoptotic characteristic expressed the highest level of Bcl-2. When all the clones were treated with anti-Fas the processing of caspase-2, -3, and -7 but not -8 was inhibited in the resistant clones to a similar extent by the differential overexpression of Bcl-2. However, with staurosporine treatment the processing of all the caspases examined was inhibited to a similar degree by the different levels of Bcl-2 expression in the resistant clones. These results suggest that Bcl-2 blocked Fas-mediated cell death by acting downstream of caspase-8, which is in contrast to staurosporine-induced apoptosis where Bcl-2 is acting upstream of caspase-8. When the anti-proliferative effect of Bcl-2 was examined, a direct correlation between a decrease in cell proliferation and the level of Bcl-2 overexpressed in the clones was observed. The clone overexpressing the greatest amount of Bcl-2 protein, which had no resistance to apoptosis, had the slowest proliferative rate. This suggests that the anti-apoptotic effect of Bcl-2 can be separated from its anti-proliferative effect. The possible effect of overexpression of Bcl-2 on telomerase activity, which is known to control the proliferative capacity of normal cells and cellular senescence, was also determined. Our results suggest that Bcl-2 had no effect on telomerase activity or telomere length in the clones. In summary, our results further suggest that some properties of Bcl-2, such as anti-apoptotic and inhibition of cell proliferation, are individual features of a multifaceted protein.
在四个过表达不同水平Bcl-2的Jurkat T细胞克隆中,研究了Bcl-2过表达对其多种多功能特性的影响,这些特性包括抗凋亡特性、抑制细胞增殖和端粒酶活性。用抗Fas或星形孢菌素处理时,四个克隆中只有三个显示出对凋亡的抗性,且这种抗性与Bcl-2表达水平相关。令人惊讶的是,没有抗凋亡特性的克隆表达的Bcl-2水平最高。当所有克隆用抗Fas处理时,抗凋亡克隆中Bcl-2的差异过表达以相似程度抑制了caspase-2、-3和-7而非caspase-8的加工过程。然而,用星形孢菌素处理时,抗凋亡克隆中不同水平的Bcl-2表达以相似程度抑制了所有检测的半胱天冬酶的加工过程。这些结果表明,Bcl-2通过在caspase-8下游起作用来阻断Fas介导的细胞死亡,这与星形孢菌素诱导的凋亡相反,在后者中Bcl-2在caspase-8上游起作用。当检测Bcl-2的抗增殖作用时,观察到细胞增殖的降低与克隆中过表达的Bcl-2水平之间存在直接相关性。过表达量最大的Bcl-2蛋白且无凋亡抗性的克隆,其增殖速率最慢。这表明Bcl-2的抗凋亡作用可以与其抗增殖作用分开。还确定了Bcl-2过表达对端粒酶活性的可能影响,已知端粒酶活性控制正常细胞的增殖能力和细胞衰老。我们的结果表明,Bcl-2对克隆中的端粒酶活性或端粒长度没有影响。总之,我们的结果进一步表明,Bcl-2的一些特性,如抗凋亡和抑制细胞增殖,是一种多面蛋白的个体特征。