NLRP3 regulates platelet integrin αIIbβ3 outside-in signaling, hemostasis and arterial thrombosis.

Abstract

In addition to their hemostatic function, platelets play an important role in regulating the inflammatory response. The platelet NLRP3 inflammasome not only promotes interleukin-1β secretion, but was also found to be upregulated during platelet activation and thrombus formation in vitro However, the role of NLRP3 in platelet function and thrombus formation in vivo remains unclear. In this study, we aimed to investigate the role of NLRP3 in platelet integrin αIIbβ3 signaling transduction. Using NLRP3-/- mice, we showed that NLRP3-deficient platelets do not have significant differences in expression of the platelet-specific adhesive receptors αIIbβ3 integrin, GPIba or GPVI; however, NLRP3-/- platelets transfused into wild-type mice resulted in prolonged tail-bleeding time and delayed arterial thrombus formation, as well as exhibiting impaired spreading on immobilized fibrinogen and defective clot retraction, concomitant with decreased phosphorylation of c-Src, Syk and PLCγ2 in response to thrombin stimulation. Interestingly, addition of exogenous recombinant interleukin-1β reversed the defect in NLRP3-/- platelet spreading and clot retraction, and restored thrombin-induced phosphorylation of c-Src/Syk/PLCγ2, whereas an anti-interleukin-1β antibody blocked spreading and clot retraction mediated by wild-type platelets. Using the direct NLRP3 inhibitor, CY-09, we demonstrated significantly reduced human platelet aggregation in response to threshold concentrations of collagen and ADP, as well as impaired clot retraction in CY-09-treated human platelets, supporting a role for NLRP3 also in regulating human platelet αIIbβ3 outside-in signaling. This study identifies a novel role for NLRP3 and interleukin-1β in platelet function, and provides a new potential link between thrombosis and inflammation, suggesting that therapies targeting NLRP3 or interleukin-1β might be beneficial for treating inflammation-associated thrombosis.

• Authors: Jianlin Qiao, Xiaoqing Wu, Qi Luo, Guangyu Wei, Mengdi Xu, Yulu Wu, Yun Liu, Xiaoqian Li, Jie Zi, Wen Ju, Lin Fu, Chong Chen, Qingyun Wu, Shengyun Zhu, Kunming Qi, Depeng Li, Zhenyu Li, Robert K Andrews, Lingyu Zeng, Elizabeth E Gardiner, Kailin Xu
• Journal: Haematologica (Haematologica) Vol. 103 Issue 9 Pg. 1568-1576 (09 2018) ISSN: 1592-8721 [Electronic] Italy
• PMID: 29794149 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
• Copyright: Copyright© 2018 Ferrata Storti Foundation.

Chemical References

• Biomarkers
• NLR Family, Pyrin Domain-Containing 3 Protein
• NLRP3 protein, human
• Platelet Glycoprotein GPIIb-IIIa Complex

Topics

• Animals
• Biomarkers
• Blood Coagulation (genetics)
• Blood Platelets (metabolism)
• Cell Degranulation
• Clot Retraction
• Disease Models, Animal
• Gene Expression
• Hemostasis
• Humans
• Mice
• Mice, Knockout
• NLR Family, Pyrin Domain-Containing 3 Protein (genetics, metabolism)
• Platelet Activation
• Platelet Aggregation (genetics)
• Platelet Function Tests
• Platelet Glycoprotein GPIIb-IIIa Complex (metabolism)
• Signal Transduction
• Thrombosis (etiology, metabolism, pathology)