Department of Immunology, University of Washington, Seattle, WA 98109, USA; Molecular and Cellular Biology Program, University of Washington, Seattle, WA 98109, USA.
Department of Immunology, University of Washington, Seattle, WA 98109, USA.
Cell Rep. 2019 Aug 27;28(9):2275-2287.e5. doi: 10.1016/j.celrep.2019.07.077.
Necroptosis is a form of programmed cell death that is defined by activation of the kinase RIPK3 and subsequent cell membrane permeabilization by the effector MLKL. RIPK3 activation can also promote immune responses via production of cytokines and chemokines. How active cytokine production is coordinated with the terminal process of necroptosis is unclear. Here, we report that cytokine production continues within necroptotic cells even after they have lost cell membrane integrity and irreversibly committed to death. This continued cytokine production is dependent on mRNA translation and requires maintenance of endoplasmic reticulum integrity that remains after plasma membrane integrity is lost. The continued translation of cytokines by cellular corpses contributes to necroptotic cell uptake by innate immune cells and priming of adaptive immune responses to antigens associated with necroptotic corpses. These findings imply that cell death and production of inflammatory mediators are coordinated to optimize the immunogenicity of necroptotic cells.
细胞坏死是一种程序性细胞死亡形式,其特征是激酶 RIPK3 的激活以及随后效应蛋白 MLKL 导致细胞膜通透性增加。RIPK3 的激活还可以通过细胞因子和趋化因子的产生来促进免疫反应。细胞因子的产生如何与坏死的终末过程协调尚不清楚。在这里,我们报告说,即使在坏死细胞失去细胞膜完整性并不可逆地走向死亡后,细胞因子的产生仍在继续。这种持续的细胞因子产生依赖于 mRNA 翻译,并且需要在质膜完整性丧失后保持内质网的完整性。细胞尸体持续翻译细胞因子有助于先天免疫细胞摄取坏死细胞,并为与坏死细胞相关的抗原的适应性免疫反应做好准备。这些发现意味着细胞死亡和炎症介质的产生是协调一致的,以优化坏死细胞的免疫原性。