Tri-institutional PhD Program in Chemical Biology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Chemical Biology Program, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Nat Med. 2018 Aug;24(8):1151-1156. doi: 10.1038/s41591-018-0082-y. Epub 2018 Jul 2.
Small-molecule inhibitors of the serine dipeptidases DPP8 and DPP9 (DPP8/9) induce a lytic form of cell death called pyroptosis in mouse and human monocytes and macrophages. In mouse myeloid cells, Dpp8/9 inhibition activates the inflammasome sensor Nlrp1b, which in turn activates pro-caspase-1 to mediate cell death, but the mechanism of DPP8/9 inhibitor-induced pyroptosis in human myeloid cells is not yet known. Here we show that the CARD-containing protein CARD8 mediates DPP8/9 inhibitor-induced pro-caspase-1-dependent pyroptosis in human myeloid cells. We further show that DPP8/9 inhibitors induce pyroptosis in the majority of human acute myeloid leukemia (AML) cell lines and primary AML samples, but not in cells from many other lineages, and that these inhibitors inhibit human AML progression in mouse models. Overall, this work identifies an activator of CARD8 in human cells and indicates that its activation by small-molecule DPP8/9 inhibitors represents a new potential therapeutic strategy for AML.
丝氨酸二肽酶 DPP8 和 DPP9(DPP8/9)的小分子抑制剂在小鼠和人单核细胞和巨噬细胞中诱导一种称为细胞焦亡的裂解形式的细胞死亡。在小鼠髓系细胞中,Dpp8/9 抑制激活了炎症小体传感器 Nlrp1b,后者反过来激活了 pro-caspase-1 以介导细胞死亡,但 DPP8/9 抑制剂诱导人髓系细胞发生细胞焦亡的机制尚不清楚。在这里,我们证明含有 CARD 的蛋白 CARD8 介导了 DPP8/9 抑制剂诱导的人髓系细胞中 pro-caspase-1 依赖性细胞焦亡。我们进一步表明,DPP8/9 抑制剂在大多数人类急性髓细胞白血病(AML)细胞系和原发性 AML 样本中诱导细胞焦亡,但在许多其他谱系的细胞中不诱导,并且这些抑制剂在小鼠模型中抑制了人类 AML 的进展。总的来说,这项工作鉴定了人类细胞中 CARD8 的激活剂,并表明其被小分子 DPP8/9 抑制剂激活代表了 AML 的一种新的潜在治疗策略。