Mondragón Laura, Galluzzi Lorenzo, Mouhamad Shahul, Orzáez Mar, Vicencio José-Miguel, Vitale Ilio, Moure Alejandra, Messeguer Angel, Perez-Paya Enrique, Kroemer Guido
U848, INSERM, 94805 Villejuif, France.
Apoptosis. 2009 Feb;14(2):182-90. doi: 10.1007/s10495-008-0310-x.
QM31 represents a new class of cytoprotective agents that inhibit the formation of the apoptosome, the caspase activation complex composed by Apaf-1, cytochrome c, dATP and caspase-9. Here, we analyzed the cellular effects of QM31, as compared to the prototypic caspase inhibitor Z-VAD-fmk. QM31 was as efficient as Z-VAD-fmk in suppressing caspase-3 activation, and conferred a similar cytoprotective effect. In contrast to Z-VAD-fmk, QM31 inhibited the release of cytochrome c from mitochondria, an unforeseen property that may contribute to its pronounced cytoprotective activity. Moreover, QM31 suppressed the Apaf-1-dependent intra-S-phase DNA damage checkpoint. These results suggest that QM31 can interfere with the two known functions of Apaf-1, namely apoptosome assembly/activation and intra-S-phase cell cycle arrest. Moreover, QM31 can inhibit mitochondrial outer membrane permeabilization, an effect that is independent from its action on Apaf-1.
QM31代表了一类新型的细胞保护剂,它能抑制凋亡小体的形成,凋亡小体是由凋亡蛋白酶激活因子-1(Apaf-1)、细胞色素c、三磷酸脱氧腺苷(dATP)和半胱天冬酶-9组成的半胱天冬酶激活复合物。在此,我们分析了QM31的细胞效应,并与典型的半胱天冬酶抑制剂Z-VAD-fmk进行了比较。QM31在抑制半胱天冬酶-3激活方面与Z-VAD-fmk一样有效,并具有类似的细胞保护作用。与Z-VAD-fmk不同的是,QM31抑制了细胞色素c从线粒体的释放,这一意外特性可能有助于其显著的细胞保护活性。此外,QM31抑制了依赖Apaf-1的S期内DNA损伤检查点。这些结果表明,QM31可以干扰Apaf-1的两个已知功能,即凋亡小体组装/激活和S期内细胞周期停滞。此外,QM31可以抑制线粒体外膜通透性,这一效应独立于其对Apaf-1的作用。