Department of Internal Medicine, Osaka Dental University, Osaka, Japan.
Leuk Res. 2014 Jun;38(6):706-13. doi: 10.1016/j.leukres.2014.02.002. Epub 2014 Feb 10.
Caspase-independent programmed necrotic cell death (necroptosis) has recently been described. Previously described models of necroptosis required 16h or more of induction, which made the interpretation of findings somewhat difficult. In human monocytic leukemia cell line U937 necroptosis could be induced within 6h by combination of TNF and Z-VAD-fmk. Here we show that the reduction in intracellular ATP levels may not be the sole determinant of necroptosis, and that necroptosis is associated with the loss of mitochondrial membrane potential, but not the activation of Bak/Bax or calcineurin.
细胞程序性坏死(坏死性凋亡)最近被描述为一种不依赖于半胱天冬酶的细胞死亡方式。先前描述的坏死性凋亡模型需要 16 小时或更长时间的诱导,这使得对研究结果的解释变得有些困难。在人单核白血病细胞系 U937 中,TNF 和 Z-VAD-fmk 的联合作用可以在 6 小时内诱导坏死性凋亡。在这里,我们表明细胞内 ATP 水平的降低可能不是坏死性凋亡的唯一决定因素,并且坏死性凋亡与线粒体膜电位的丧失有关,但与 Bak/Bax 的激活或钙调神经磷酸酶无关。