Targeting HDAC6 attenuates nicotine-induced macrophage pyroptosis via NF-κB/NLRP3 pathway

Background and aims: During the development of atherosclerosis, nicotine activates macrophage inflammation. However, whether nicotine induces macrophage pyroptosis and the underlying mechanisms remain unclear. This study aimed to investigate the role of histone deacetylase 6 (HDAC6) in nicotine-induced macrophage pyroptosis. Methods: For the in vivo study, nicotine was administered to 8-week-old ApoE-/mice fed a high-fat diet (HFD) for 12 weeks. TUNEL/CD68 and Caspase-1/CD68 staining was used to assess macrophage pyroptosis in plaque. For the in vitro study, Western blotting, lactic dehydrogenase activity (LDH), coimmunoprecipitation, chromatin immunoprecipitation and immunofluorescence were used to evaluate pyroptosis and related signaling pathway in RAW264.7 cells. Results: A high-fat diet and nicotine upregulated macrophage pyroptosis in atherosclerotic lesions. Nicotine promoted pyroptosis in RAW264.7 cells, as evidenced by increased expression of cleaved Caspase1, NLRP3, IL1 beta, IL-18, and elevated LDH release. Inhibition of HDAC6 suppressed nicotine-induced pyroptosis, which is partly mediated by p65 acetylation and NLRP3 transcription. Silencing p65 or NLRP3 resulted in decreased pyroptosis in RAW264.7 cells. Conclusions: Nicotine induces macrophage pyroptosis in atherosclerosis through HDAC6/NF-kappa B/NLRP3 signaling pathway.

Automated summary

This study found that nicotine induces macrophage pyroptosis in atherosclerosis through the HDAC6/NF-kappa B/NLRP3 signaling pathway. These results suggest that nicotine promotes macrophage pyroptosis via this signaling pathway, which may contribute to a better understanding of the mechanisms of nicotine in atherosclerosis.