Engels I H, Stepczynska A, Stroh C, Lauber K, Berg C, Schwenzer R, Wajant H, Jänicke R U, Porter A G, Belka C, Gregor M, Schulze-Osthoff K, Wesselborg S
Department of Immunology and Cell Biology, University of Münster, Germany.
Oncogene. 2000 Sep 21;19(40):4563-73. doi: 10.1038/sj.onc.1203824.
Caspase-8 plays an essential role in apoptosis triggered by death receptors. Through the cleavage of Bid, a proapoptotic Bcl-2 member, it further activates the mitochondrial cytochrome c/Apaf-1 pathway. Because caspase-8 can be processed also by anticancer drugs independently of death receptors, we investigated its exact role and order in the caspase cascade. We show that in Jurkat cells either deficient for caspase-8 or overexpressing its inhibitor c-FLIP apoptosis mediated by CD95, but not by anticancer drugs was inhibited. In the absence of active caspase-8, anticancer drugs still induced the processing of caspase-9, -3 and Bid, indicating that Bid cleavage does not require caspase-8. Overexpression of Bcl-x(L) prevented the processing of caspase-8 as well as caspase-9, -6 and Bid in response to drugs, but was less effective in CD95-induced apoptosis. Similar responses were observed by overexpression of a dominant-negative caspase-9 mutant. To further determine the order of caspase-8 activation, we employed MCF7 cells lacking caspase-3. In contrast to caspase-9 that was cleaved in these cells, anticancer drugs induced caspase-8 activation only in caspase-3 transfected MCF7 cells. Thus, our data indicate that, unlike its proximal role in receptor signaling, in the mitochondrial pathway caspase-8 rather functions as an amplifying executioner caspase.
半胱天冬酶 -8在死亡受体触发的细胞凋亡中起关键作用。通过切割促凋亡的Bcl-2家族成员Bid,它进一步激活线粒体细胞色素c/Apaf-1途径。由于半胱天冬酶 -8也可被抗癌药物独立于死亡受体进行加工处理,我们研究了其在半胱天冬酶级联反应中的具体作用和顺序。我们发现,在缺乏半胱天冬酶 -8或过表达其抑制剂c-FLIP的Jurkat细胞中,由CD95介导的细胞凋亡受到抑制,但由抗癌药物介导的细胞凋亡不受影响。在没有活性半胱天冬酶 -8的情况下,抗癌药物仍能诱导半胱天冬酶 -9、-3和Bid的加工处理,这表明Bid的切割不需要半胱天冬酶 -8。Bcl-x(L)的过表达可阻止药物诱导的半胱天冬酶 -8以及半胱天冬酶 -9、-6和Bid的加工处理,但在CD95诱导的细胞凋亡中效果较差。过表达显性负性半胱天冬酶 -9突变体也观察到类似的反应。为了进一步确定半胱天冬酶 -8激活的顺序,我们使用了缺乏半胱天冬酶 -3的MCF7细胞。与在这些细胞中被切割的半胱天冬酶 -9不同,抗癌药物仅在转染了半胱天冬酶 -3的MCF7细胞中诱导半胱天冬酶 -8的激活。因此,我们的数据表明,与它在受体信号传导中的近端作用不同,在线粒体途径中半胱天冬酶 -8更像是一个放大的执行性半胱天冬酶。