University of Massachusetts Medical School Faculty Publications
Title
Metabolic danger signals, uric acid and ATP, mediate inflammatory cross-talk between hepatocytes and immune cells in alcoholic liver disease
UMMS Affiliation
Department of Medicine, Division of Gastroenterology; Department of Medicine, Division of Infectious Diseases and Immunology
Publication Date
2015-08-01
Document Type
Article
Subjects
Adenosine Triphosphate; Adult; Animals; Carrier Proteins; Cell Communication; Culture Media, Conditioned; Female; Gene Deletion; Gene Expression; Hepatocytes; Humans; Inflammasomes; Interleukin-1beta; Leukocytes, Mononuclear; Lipopolysaccharides; Liver; Liver Diseases, Alcoholic; Male; Mice; Mice, Inbred C57BL; Middle Aged; Primary Cell Culture; Signal Transduction; Tumor Necrosis Factor-alpha; Uric Acid
Disciplines
Digestive System Diseases | Gastroenterology | Hepatology | Immunity | Immunopathology
Abstract
Inflammation defines the progression of ALD from reversible to advanced stages. Translocation of bacterial LPS to the liver from the gut is necessary for alcohol-induced liver inflammation. However, it is not known whether endogenous, metabolic danger signals are required for inflammation in ALD. Uric acid and ATP, 2 major proinflammatory danger signals, were evaluated in the serum of human volunteers exposed to a single dose of ethanol or in supernatants of primary human hepatocytes exposed to ethanol. In vitro studies were used to evaluate the role of uric acid and ATP in inflammatory cross-talk between hepatocytes and immune cells. The significance of signaling downstream of uric acid and ATP in the liver was evaluated in NLRP3-deficient mice fed a Lieber-DeCarli ethanol diet. Exposure of healthy human volunteers to a single dose of ethanol resulted in increased serum levels of uric acid and ATP. In vitro, we identified hepatocytes as a significant source of these endogenous inflammatory signals. Uric acid and ATP mediated a paracrine inflammatory cross-talk between damaged hepatocytes and immune cells and significantly increased the expression of LPS-inducible cytokines, IL-1beta and TNF-alpha, by immune cells. Deficiency of NLRP3, a ligand-sensing component of the inflammasome recognizing uric acid and ATP, prevented the development of alcohol-induced liver inflammation in mice and significantly ameliorated liver damage and steatosis. Endogenous metabolic danger signals, uric acid, and ATP are involved in inflammatory cross-talk between hepatocytes and immune cells and play a crucial role in alcohol-induced liver inflammation.
Keywords
DAMPs, NLRP3, inflammasome, liver inflammation, sterile inflammatory response
DOI of Published Version
10.1189/jlb.3AB1214-590R
Source
J Leukoc Biol. 2015 Aug;98(2):249-56. doi: 10.1189/jlb.3AB1214-590R. Epub 2015 May 1. Link to article on publisher's site
Related Resources
Journal/Book/Conference Title
Journal of leukocyte biology
PubMed ID
25934928
Repository Citation
Petrasek, Jan; Iracheta-Vellve, Arvin; Saha, Banishree; Satishchandran, Abhishek; Kodys, Karen; Fitzgerald, Katherine A.; Kurt-Jones, Evelyn A.; and Szabo, Gyongyi, "Metabolic danger signals, uric acid and ATP, mediate inflammatory cross-talk between hepatocytes and immune cells in alcoholic liver disease" (2015). University of Massachusetts Medical School Faculty Publications. 954.
https://escholarship.umassmed.edu/faculty_pubs/954