Silica Nanoparticles Elicit Pulmonary Inflammation via STING-Dependent Activation of NF-κB p65 Signaling Pathway.

Silica nanoparticles (SiNPs) are common nanoparticles that are widely used in industrial and medical applications. Inhalation exposure to SiNPs is frequently unavoidable in occupational and everyday settings. While the adverse effects of SiNPs on lung injury have been extensively documented, the intrinsic mechanisms underlying SiNPs-induced pulmonary inflammation remain incompletely understood. This study demonstrates that the stimulator of interferon genes (STING) plays an essential role in SiNPs-triggered lung inflammation. In vitro, SiNPs induced death of bone marrow-derived macrophages (BMDMs) and activated the STING pathway. Knockout of STING expression alleviated SiNPs-induced inflammatory responses and subsequent cell death. Further mechanistic investigations revealed that STING activation promotes nuclear translocation of NF-κB p65 and subsequent activation of the NF-κB pathway, ultimately driving the secretion of inflammatory cytokines. In vivo, SiNPs-induced NF-κB activation and inflammatory cell infiltration were significantly attenuated in STING-deficient (STING