Wei Ba, Yue Pang, Qingwei Li
College of Life Science, Liaoning Normal University, Dalian 116029, China; Lamprey Research Center, Liaoning Normal University, Dalian 116029, China.
Yi Chuan. 2014 Jun;36(6):519-24. doi: 10.3724/SP.J.1005.2014.0519.
Programmed necrosis called necroptosis, is different from traditional necrosis and apoptosis, it has attracted considerable attention over the last few years. Necroptosis can be initiated through many factors such as tumor necrosis factor receptor (TNFR) or pattern recognition receptor (PRR), and receptor-interacting protein (RIP) 1 and 3 are two key proteins during the process. A lot of molecules have been characterized as modulators and effectors of necroptosis, including poly(ADP-ribose) polymerase (PARP-1), reactive oxygen species (ROS), Ca(2+), which can destruct mitochondria or other organelles and induce cell dead through caspase-independent pathway. Then, damage-associated molecular pattern (DAMP) molecules were released from necroptosis cells, recognized and internalized by phagocytes. Here, we briefly discuss the initiation and execution of necroptosis and the clearance of death cells.
程序性坏死即坏死性凋亡,不同于传统的坏死和凋亡,在过去几年中受到了相当多的关注。坏死性凋亡可通过多种因素引发,如肿瘤坏死因子受体(TNFR)或模式识别受体(PRR),而受体相互作用蛋白(RIP)1和3是这一过程中的两个关键蛋白。许多分子已被鉴定为坏死性凋亡的调节因子和效应因子,包括聚(ADP-核糖)聚合酶(PARP-1)、活性氧(ROS)、Ca(2+),它们可破坏线粒体或其他细胞器,并通过不依赖半胱天冬酶的途径诱导细胞死亡。然后,损伤相关分子模式(DAMP)分子从坏死性凋亡细胞中释放出来,被吞噬细胞识别并内化。在此,我们简要讨论坏死性凋亡的起始和执行以及死亡细胞的清除。