A chemical inhibitor of Apaf-1 exerts mitochondrioprotective functions and interferes with the intra-S-phase DNA damage checkpoint

Laura Mondragón, Lorenzo Galluzzi, Shahul Mouhamad, Mar Orzáez, José Miguel Vicencio, Ilio Vitale, Alejandra Moure, Angel Messeguer, Enrique Perez-Paya, Guido Kroemer

    Résultats de recherche: Contribution à un journalArticleRevue par des pairs

    34 Citations (Scopus)

    Résumé

    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.

    langue originaleAnglais
    Pages (de - à)182-190
    Nombre de pages9
    journalApoptosis
    Volume14
    Numéro de publication2
    Les DOIs
    étatPublié - 1 févr. 2009

    Contient cette citation