| Literature DB >> 35477991 |
Suyavaran Arumugam1, Yanqin Qin1, Ziwen Liang2, Sheng-Na Han1, S L Tejaswi Boodapati1, Junzi Li1, Qiuxia Lu1, Richard A Flavell3,4, Wajahat Z Mehal5,6, Xinshou Ouyang7.
Abstract
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.Entities:
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Year: 2022 PMID: 35477991 PMCID: PMC9525599 DOI: 10.1038/s41418-022-00997-y
Source DB: PubMed Journal: Cell Death Differ ISSN: 1350-9047 Impact factor: 12.067