Magtanong L, Ko P J, Dixon S J
Department of Biology, Stanford University, 337 Campus Drive, Stanford, CA, USA.
Cell Death Differ. 2016 Jul;23(7):1099-109. doi: 10.1038/cdd.2016.25. Epub 2016 Mar 11.
Non-apoptotic regulated cell death (RCD) is essential to maintain organismal homeostasis and may be aberrantly activated during certain pathological states. Lipids are emerging as key components of several non-apoptotic RCD pathways. For example, a direct interaction between membrane phospholipids and the pore-forming protein mixed lineage kinase domain-like (MLKL) is needed for the execution of necroptosis, while the oxidative destruction of membrane polyunsaturated fatty acids (PUFAs), following the inactivation of glutathione peroxidase 4 (GPX4), is a requisite gateway to ferroptosis. Here, we review the roles of lipids in the initiation and execution of these and other forms of non-apoptotic cell death. We also consider new technologies that are allowing for the roles of lipids and lipid metabolism in RCD to be probed in increasingly sophisticated ways. In certain cases, this new knowledge may enable the development of therapies that target lipids and lipid metabolic processes to enhance or suppress specific non-apoptotic RCD pathways.
非凋亡性调节性细胞死亡(RCD)对于维持机体稳态至关重要,并且在某些病理状态下可能会异常激活。脂质正成为几种非凋亡性RCD途径的关键组成部分。例如,坏死性凋亡的执行需要膜磷脂与成孔蛋白混合谱系激酶结构域样蛋白(MLKL)之间的直接相互作用,而在谷胱甘肽过氧化物酶4(GPX4)失活后,膜多不饱和脂肪酸(PUFA)的氧化破坏是铁死亡的必要途径。在这里,我们综述了脂质在这些以及其他形式的非凋亡性细胞死亡的起始和执行中的作用。我们还考虑了一些新技术,这些技术使得脂质和脂质代谢在RCD中的作用能够以越来越复杂的方式被探究。在某些情况下,这些新知识可能会促成开发针对脂质和脂质代谢过程的疗法,以增强或抑制特定的非凋亡性RCD途径。