Paxillin mediates ATP-induced activation of P2X7 receptor and NLRP3 inflammasome
Wenbiao Wang,
Dingwen Hu,
Yuqian Feng,
Caifeng Wu,
Yunting Song,
Weiyong Liu,
Aixin Li,
Yingchong Wang,
Keli Chen,
Mingfu Tian,
Feng Xiao,
Qi Zhang,
Weijie Chen,
Pan Pan,
Pin Wan,
Yingle Liu,
Huiyao Lan,
Kailang Wu,
Jianguo Wu
Affiliations
Wenbiao Wang
Guangdong Provincial Key Laboratory of Virology, Institute of Medical Microbiology, Jinan University
Dingwen Hu
State Key Laboratory of Virology, College of Life Sciences, Wuhan University
Yuqian Feng
Guangdong Provincial Key Laboratory of Virology, Institute of Medical Microbiology, Jinan University
Caifeng Wu
Guangdong Provincial Key Laboratory of Virology, Institute of Medical Microbiology, Jinan University
Yunting Song
State Key Laboratory of Virology, College of Life Sciences, Wuhan University
Weiyong Liu
Department of Clinical Laboratory, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology
Aixin Li
State Key Laboratory of Virology, College of Life Sciences, Wuhan University
Yingchong Wang
State Key Laboratory of Virology, College of Life Sciences, Wuhan University
Keli Chen
State Key Laboratory of Virology, College of Life Sciences, Wuhan University
Mingfu Tian
State Key Laboratory of Virology, College of Life Sciences, Wuhan University
Feng Xiao
State Key Laboratory of Virology, College of Life Sciences, Wuhan University
Qi Zhang
State Key Laboratory of Virology, College of Life Sciences, Wuhan University
Weijie Chen
Guangdong Provincial Key Laboratory of Virology, Institute of Medical Microbiology, Jinan University
Pan Pan
Guangdong Provincial Key Laboratory of Virology, Institute of Medical Microbiology, Jinan University
Pin Wan
Guangdong Provincial Key Laboratory of Virology, Institute of Medical Microbiology, Jinan University
Yingle Liu
Guangdong Provincial Key Laboratory of Virology, Institute of Medical Microbiology, Jinan University
Huiyao Lan
Department of Medicine & Therapeutics, Li Ka Shing Institute of Health Sciences, Lui Che Woo Institute of Innovative Medicine, The Chinese University of Hong Kong
Kailang Wu
State Key Laboratory of Virology, College of Life Sciences, Wuhan University
Jianguo Wu
Guangdong Provincial Key Laboratory of Virology, Institute of Medical Microbiology, Jinan University
Abstract Background Extracellular adenosine triphosphate (ATP), a key danger-associated molecular pattern (DAMP) molecule, is released to the extracellular medium during inflammation by injured parenchymal cells, dying leukocytes, and activated platelets. ATP directly activates the plasma membrane channel P2X7 receptor (P2X7R), leading to an intracellular influx of K+, a key trigger inducing NLRP3 inflammasome activation. However, the mechanism underlying P2X7R-mediated activation of NLRP3 inflammasome is poorly understood, and additional molecular mediators have not been identified. Here, we demonstrate that Paxillin is the molecule connecting the P2X7 receptor and NLRP3 inflammasome through protein interactions. Results We show a distinct mechanism by which Paxillin promotes ATP-induced activation of the P2X7 receptor and NLRP3 inflammasome. Extracellular ATP induces Paxillin phosphorylation and then facilitates Paxillin-NLRP3 interaction. Interestingly, Paxillin enhances NLRP3 deubiquitination and activates NLRP3 inflammasome upon ATP treatment and K+ efflux. Moreover, we demonstrated that USP13 is a key enzyme for Paxillin-mediated NLRP3 deubiquitination upon ATP treatment. Notably, extracellular ATP promotes Paxillin and NLRP3 migration from the cytosol to the plasma membrane and facilitates P2X7R-Paxillin interaction and PaxillinNLRP3 association, resulting in the formation of the P2X7R-Paxillin-NLRP3 complex. Functionally, Paxillin is essential for ATP-induced NLRP3 inflammasome activation in mouse BMDMs and BMDCs as well as in human PBMCs and THP-1-differentiated macrophages. Conclusions We have identified paxillin as a mediator of NLRP3 inflammasome activation. Paxillin plays key roles in ATP-induced activation of the P2X7 receptor and NLRP3 inflammasome by facilitating the formation of the P2X7R-Paxillin-NLRP3 complex.