髓系白血病
上睑下垂
炎症体
生物
白血病
细胞生物学
癌症研究
细胞培养
程序性细胞死亡
细胞凋亡
免疫学
炎症
生物化学
遗传学
作者
Darren C. Johnson,Cornelius Y. Taabazuing,Marian C. Okondo,Ashley J. Chui,Sahana D. Rao,Fiona C. Brown,Casie Reed,Elizabeth Peguero,Elisa de Stanchina,Alex Kentsis,Daniel A. Bachovchin
出处
期刊:Nature Medicine
[Nature Portfolio]
日期:2018-06-29
卷期号:24 (8): 1151-1156
被引量:309
标识
DOI:10.1038/s41591-018-0082-y
摘要
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 macrophages1,2. In mouse myeloid cells, Dpp8/9 inhibition activates the inflammasome sensor Nlrp1b, which in turn activates pro-caspase-1 to mediate cell death3, 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.
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