Department of Immunology, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
DNA Cell Biol. 2020 Jul;39(7):1091-1095. doi: 10.1089/dna.2020.5616. Epub 2020 May 12.
The crosstalk between cellular stress responses and innate immune signaling pathways remains poorly understood. Cells can respond to stressors by assembling stress granules that store 40S ribosomes, translation initiation factors, and mRNAs, and allow the cell to survive. Some stressors can activate the NLRP3 inflammasome, which leads to pyroptotic cell death. Stress granules and the NLRP3 inflammasome provide distinct cell fate choices to the cell. These complexes also involve distinct types of phase transitions-liquid-liquid phase separation for stress granules and prionoid phase transition for the NLRP3 inflammasome. We recently reported that DDX3X modulates this crosstalk by acting as a common essential factor for NLRP3 inflammasome activation and stress granule assembly. Here, we discuss the role of DDX3X in modulating the liquid-liquid phase separation and prionoid phase transition required for making cell fate decisions under stress conditions.
细胞应激反应和先天免疫信号通路之间的串扰仍然知之甚少。细胞可以通过组装应激颗粒来应对应激,应激颗粒储存 40S 核糖体、翻译起始因子和 mRNAs,使细胞能够存活。一些应激源可以激活 NLRP3 炎性体,导致细胞发生细胞焦亡。应激颗粒和 NLRP3 炎性体为细胞提供不同的命运选择。这些复合物还涉及不同类型的相转变——应激颗粒的液-液相分离和 NLRP3 炎性体的朊病毒样相变。我们最近报道称,DDX3X 通过充当 NLRP3 炎性体激活和应激颗粒组装的共同必需因子来调节这种串扰。在这里,我们讨论了 DDX3X 在调节液-液相分离和朊病毒样相变中的作用,这是在应激条件下做出细胞命运决定所必需的。