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The role of cGAS-STING signalling in liver diseases

Authors :
Jiamin Du
Ruihan Chen
Qi Ling
Hong Zhu
Source :
JHEP Reports
Publication Year :
2021

Abstract

Summary The recently identified novel cytosolic DNA sensor cyclic GMP-AMP synthase (cGAS) activates the downstream adaptor protein stimulator of interferon genes (STING) by catalysing the synthesis of cyclic GMP-AMP. This in turn initiates an innate immune response through the release of various cytokines, including type I interferon. Foreign DNA (microbial infection) or endogenous DNA (nuclear or mitochondrial leakage) can serve as cGAS ligands and lead to the activation of cGAS-STING signalling. Therefore, the cGAS-STING pathway plays essential roles in infectious diseases, sterile inflammation, tumours, and autoimmune diseases. In addition, cGAS-STING signalling affects the progression of liver inflammation through other mechanisms, such as autophagy and metabolism. In this review, we summarise recent advances in our understanding of the role of cGAS-STING signalling in the innate immune modulation of different liver diseases. Furthermore, we discuss the therapeutic potential of targeting the cGAS-STING pathway in the treatment of liver diseases.

Subjects

Subjects :
nonalcoholic fatty liver disease
cGAS-STING signalling
ssRNA, single-stranded RNA
Review
SAVI, STING-associated vasculopathy with onset in infancy
PD-L1, programmed cell death protein ligand-1
GVHD, graft-versus-host disease
IFN-I, type I interferon
TNF, tumour necrosis factor
chemistry.chemical_compound
NK cells, natural killer cells
Immunology and Allergy
ALD, alcohol-related liver disease
dsDNA, double-strand DNA
Toll-like receptor
PD-1, programmed cell death protein-1
XRCC, X-ray repair cross complementing
Gastroenterology
Pattern recognition receptor
hepatocellular carcinoma
Cell biology
TGF-β1, transforming growth factor-β1
Stimulator of interferon genes
IRI, ischaemia refusion injury
APCs, antigen-presenting cells
DCs, dendritic cells
HSCs, hepatic stellate cells
liver injury
TLR, Toll-like receptor
AIM2, absent in melanoma 2
NAFLD, non-alcoholic fatty liver disease
aHSCT, allogeneic haematopoietic stem cell transplantation
viral hepatitis
mTOR, mammalian target of rapamycin
STING, stimulator of interferon genes
Biology
CDNs, cyclic dinucleotides
ER, endoplasmic reticulum
AIM2
Cyclic guanosine monophosphate–adenosine monophosphate
PAMPs, pathogen-associated molecular patterns
Internal Medicine
MHC, major histocompatibility complex
NPCs, non-parenchymal cells
Innate immune system
Hepatology
IRF3, interferon regulatory factor 3
Pathogen-associated molecular pattern
LSECs, liver sinusoidal endothelial cells
PPRs, pattern recognition receptors
eye diseases
IL, interleukin
mtDNA, mitochondrial DNA
chemistry
siRNA, small interfering RNA
DAMPs, damage-associated molecular patterns
TBK1, TANK-binding kinase 1
innate immune response
KCs, Kupffer cells
cGAMP, cyclic guanosine monophosphate-adenosine monophosphate
cGAS, cyclic guanosine monophosphate-adenosine monophosphate synthase
HCC, hepatocellular carcinoma
IRF3

Details

ISSN :
25895559
Volume :
3
Issue :
5
Database :
OpenAIRE
Journal :
JHEP reports : innovation in hepatology
Accession number :
edsair.doi.dedup.....35ff00e7f3f8684bd27542de7a9f4e94