Non-canonical STING–PERK pathway dependent epigenetic regulation of vascular endothelial dysfunction via integrating IRF3 and NF-κB in inflammatory response

Xuesong Li(Nanjing Medical University), Xiang Chen(Nanjing Medical University), Longbin Zheng(Nanjing Medical University), Minghong Chen(Nanjing Medical University), Yunjia Zhang(Nanjing Medical University), Ruigong Zhu(Nanjing Medical University), Jiajing Chen(Fudan University), Jiaming Gu(Nanjing Medical University), Quanwen Yin(Nanjing Medical University), Hong Jiang(Nanjing Medical University), Xuan Wu(Nanjing Medical University), Xian Ji(Nanjing Medical University), Xin Tang(Nanjing Medical University), Mengdie Dong(Nanjing Medical University), Qingguo Li(Second Affiliated Hospital of Nanjing Medical University), Yuanqing Gao(Nanjing Medical University), Hongshan Chen(Huaian First People’s Hospital)
Acta Pharmaceutica Sinica B
August 17, 2023
Cited by 62Open Access
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Abstract

Inflammation-driven endothelial dysfunction is the major initiating factor in atherosclerosis, while the underlying mechanism remains elusive. Here, we report that the non-canonical stimulator of interferon genes (STING)–PKR-like ER kinase (PERK) pathway was significantly activated in both human and mice atherosclerotic arteries. Typically, STING activation leads to the activation of interferon regulatory factor 3 (IRF3) and NF-κB, thereby facilitating IFN signals and inflammation. In contrast, our study reveals the activated non-canonical STING–PERK pathway increases scaffold protein bromodomain protein 4 (BRD4) expression, which encourages the formation of super-enhancers on the promoters of proinflammatory cytokines, thereby enabling the transactivation of these cytokines by integrating activated IRF3 and NF-κB via a condensation process. Endothelium-specific STING and BRD4 deficiency significantly decreased the plaque area and inflammation. Mechanistically, this pathway is triggered by leaked mitochondria DNA (mtDNA) via mitochondrial permeability transition pore (mPTP), formed by voltage-dependent anion channel 1 (VDAC1) oligomer interaction with oxidized mtDNA upon cholesterol oxidation stimulation. Especially, compared to macrophages, endothelial STING activation plays a more pronounced role in atherosclerosis. We propose a non-canonical STING–PERK pathway-dependent epigenetic paradigm in atherosclerosis that integrates IRF3, NF-κB and BRD4 in inflammatory responses, which provides emerging therapeutic modalities for vascular endothelial dysfunction.


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