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How the Innate Immune DNA Sensing cGAS-STING Pathway Is Involved in Autophagy
The cGAS-STING pathway is a key component of the innate immune system and exerts crucial roles in the detection of cytosolic DNA and invading pathogens. Accumulating evidence suggests that the intrinsic cGAS-STING pathway not only facilitates the production of type I interferons (IFN-I) and inflamma...
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Published in: | International journal of molecular sciences 2021-12, Vol.22 (24), p.13232 |
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description | The cGAS-STING pathway is a key component of the innate immune system and exerts crucial roles in the detection of cytosolic DNA and invading pathogens. Accumulating evidence suggests that the intrinsic cGAS-STING pathway not only facilitates the production of type I interferons (IFN-I) and inflammatory responses but also triggers autophagy. Autophagy is a homeostatic process that exerts multiple effects on innate immunity. However, systematic evidence linking the cGAS-STING pathway and autophagy is still lacking. Therefore, one goal of this review is to summarize the known mechanisms of autophagy induced by the cGAS-STING pathway and their consequences. The cGAS-STING pathway can trigger canonical autophagy through liquid-phase separation of the cGAS-DNA complex, interaction of cGAS and Beclin-1, and STING-triggered ER stress-mTOR signaling. Furthermore, both cGAS and STING can induce non-canonical autophagy via LC3-interacting regions and binding with LC3. Subsequently, autophagy induced by the cGAS-STING pathway plays crucial roles in balancing innate immune responses, maintaining intracellular environmental homeostasis, alleviating liver injury, and limiting tumor growth and transformation. |
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Accumulating evidence suggests that the intrinsic cGAS-STING pathway not only facilitates the production of type I interferons (IFN-I) and inflammatory responses but also triggers autophagy. Autophagy is a homeostatic process that exerts multiple effects on innate immunity. However, systematic evidence linking the cGAS-STING pathway and autophagy is still lacking. Therefore, one goal of this review is to summarize the known mechanisms of autophagy induced by the cGAS-STING pathway and their consequences. The cGAS-STING pathway can trigger canonical autophagy through liquid-phase separation of the cGAS-DNA complex, interaction of cGAS and Beclin-1, and STING-triggered ER stress-mTOR signaling. Furthermore, both cGAS and STING can induce non-canonical autophagy via LC3-interacting regions and binding with LC3. 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subjects | Animals Autophagy Beclin-1 - metabolism Binding sites Biosynthesis cGAS Chromosomes Cytokines Deoxyribonucleic acid DNA DNA - immunology DNA sensing Endoplasmic reticulum Herpes viruses Homeostasis Humans IFN Immune response Immune system Immunity, Innate Inflammation Injury prevention Innate immunity Insects Interferon Kinases Life Sciences Lipids Liquid phases Membrane Proteins - metabolism Membranes Microtubule-Associated Proteins - metabolism Mitochondrial DNA Nucleotidyltransferases - metabolism Pathogens Phagocytosis Phase separation Proteins Review Signal Transduction STING TOR protein Tumors Zika virus |
title | How the Innate Immune DNA Sensing cGAS-STING Pathway Is Involved in Autophagy |
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