Department of Internal Medicine, Section of Digestive Diseases, Yale University School of Medicine, New Haven, CT, 06520, USA.
Department of Endocrinology, First Affiliated Hospital of Army Medical University (Third Military Medical University), Chongqing, 400038, China.
Cell Death Differ. 2022 Oct;29(10):2060-2069. doi: 10.1038/s41418-022-00997-y. Epub 2022 Apr 27.
Subcellular machinery of NLRP3 is essential for inflammasome assembly and activation. However, the stepwise process and mechanistic basis of NLRP3 engagement with organelles remain unclear. Herein, we demonstrated glycogen synthase kinase 3β (GSK3β) as a molecular determinant for the spatiotemporal dynamics of NLRP3 inflammasome activation. Using live cell multispectral time-lapse tracking acquisition, we observed that upon stimuli NLRP3 was transiently associated with mitochondria and subsequently recruited to the Golgi network (TGN) where it was retained for inflammasome assembly. This occurred in relation to the temporal contact of mitochondria to Golgi apparatus. NLRP3 stimuli initiate GSK3β activation with subsequent binding to NLRP3, facilitating NLRP3 recruitment to mitochondria and transition to TGN. GSK3β activation also phosphorylates phosphatidylinositol 4-kinase 2 Α (PI4k2A) in TGN to promote sustained NLRP3 oligomerization. Our study has identified the interplay between GSK3β signaling and the organelles dynamics of NLRP3 required for inflammasome activation and opens new avenues for therapeutic intervention.
NLRP3 的亚细胞机制对于炎症小体的组装和激活是必不可少的。然而,NLRP3 与细胞器结合的逐步过程和机制基础仍不清楚。在此,我们证明糖原合酶激酶 3β(GSK3β)是 NLRP3 炎症小体激活时空动力学的分子决定因素。通过活细胞多光谱时间 lapse 跟踪采集,我们观察到,在刺激下,NLRP3 与线粒体短暂相关联,随后被招募到高尔基体网络(TGN),在那里它被保留用于炎症小体组装。这与线粒体与高尔基体装置的时间接触有关。NLRP3 刺激物启动 GSK3β 激活,随后与 NLRP3 结合,促进 NLRP3 向线粒体的招募和向 TGN 的转变。GSK3β 激活还会在 TGN 中磷酸化磷脂酰肌醇 4-激酶 2A(PI4k2A),以促进持续的 NLRP3 寡聚化。我们的研究确定了 GSK3β 信号通路与 NLRP3 细胞器动力学之间的相互作用,这是炎症小体激活所必需的,为治疗干预开辟了新的途径。