1. Academic Validation
  2. Synergistic inflammatory signaling by cGAS may be involved in the development of atherosclerosis

Synergistic inflammatory signaling by cGAS may be involved in the development of atherosclerosis

  • Aging (Albany NY). 2021 Feb 11;13(4):5650-5673. doi: 10.18632/aging.202491.
Guan-Feng Lu 1 Sheng-Cai Chen 1 Yuan-Peng Xia 1 Zi-Ming Ye 1 2 Fei Cao 1 Bo Hu 1
Affiliations

Affiliations

  • 1 Department of Neurology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, China.
  • 2 Department of Neurology, The First Affiliated Hospital, Guangxi Medical University, Nanning 530021, Guangxi, China.
Abstract

Inappropriate activation or overactivation of Cyclic GMP-AMP Synthase (cGAS) by double-stranded deoxyribonucleic acid (dsDNA) initiates a regulatory signaling cascade triggering a variety of inflammatory responses, which are a great threat to human health. This study focused on identifying the role of cGAS in atherosclerosis and its potential mechanisms. The relationship between cGAS and atherosclerosis was identified in an ApoE -/- mouse model. Meanwhile, RNA sequencing (RNA-seq) analysis of the underlying mechanisms of atherosclerosis in RAW264.7 macrophages treated with cGAS inhibition was conducted. Results showed that cGAS was positively correlated with atherosclerotic plaque area, and was mainly distributed in macrophages. RNA-seq analysis revealed that inflammatory response, immune response and cytokine-cytokine receptor interaction may play important roles in the development of atherosclerosis. Real-time quantitative polymerase chain reaction (RT-qPCR) results showed that the expression of the pro-inflammatory factors, signal transducer and activator of transcription (STAT), interferon regulatory factor (Irf), toll-like receptors (Tlrs), and type I interferons (Ifns) were synergistically reduced when cGAS was inhibited. Furthermore, cGAS inhibition significantly inhibited RAW264.7 macrophage M1 polarization. These results demonstrate that cGAS may contribute to the development of atherosclerosis through synergistic inflammatory signaling of TLRs, STAT/IRF as well as IFNs, leading to macrophage M1 polarization.

Keywords

M1 polarization; RNA-seq; atherosclerosis; cGAS; synergistic inflammatory signaling.

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