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Published on: March 29, 2017
STING Signaling and Sterile Inflammation
Isabelle Couillin1, Nicolas Riteau1
1Experimental and Molecular Immunology and Neurogenetics Laboratory (INEM), Centre National de la Recherche Scientifique (CNRS), UMR7355 and University of Orleans, Orleans, France.
The cyclic GMP-AMP synthase (cGAS)/stimulator of interferon genes (STING) pathway detects self-DNA, impacting immunity, inflammation, and diseases like cancer. This review details STING
Area of Science:
- Immunology
- Molecular Biology
- Cell Biology
Background:
- Innate immunity relies on receptors to monitor the environment and maintain host integrity.
- Receptors detect pathogens and aberrant self-molecules, signaling disturbed homeostasis.
- The cyclic GMP-AMP synthase (cGAS)/stimulator of interferon genes (STING) pathway senses self-nucleic acids, indicating cytoplasmic DNA presence.
Purpose of the Study:
- To review recent literature on the role of self-nucleic acid detection via the STING pathway.
- To explore STING's involvement in cell physiology, sterile injury, autoimmunity, and cancer.
- To discuss mechanisms of cytoplasmic DNA sensing.
Main Methods:
- Literature review of recent scientific publications.
- Analysis of studies investigating the cGAS/STING pathway.
- Synthesis of findings on STING's role in various diseases and cellular processes.
Main Results:
- Self-nucleic acid detection through the STING pathway is crucial for numerous biological processes.
- STING plays a significant role in autoimmune diseases, inflammatory conditions, neurodegeneration, and cancer.
- The pathway is linked to autophagy and cell death, with various proposed sources for cytoplasmic DNA.
Conclusions:
- The cGAS/STING pathway is a critical regulator of host defense and homeostasis.
- Dysfunctional STING signaling contributes to various pathologies, including autoimmune and inflammatory diseases.
- Understanding cytoplasmic DNA sources and STING activation is key to developing new therapeutic strategies.
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