A Protein Complex of Liver Origin Activates a Pro-inflammatory Program That Drives Hepatic and Intestinal Injury in Alcohol-Associated Liver Disease

Cell Mol Gastroenterol Hepatol. 2024;18(3):101362. doi: 10.1016/j.jcmgh.2024.05.010. Epub 2024 May 23.

Abstract

Background & aims: There is limited information on how the liver-to-gut axis contributes to alcohol-associated liver disease (AALD). We previously identified that high-mobility group box-1 (HMGB1) undergoes oxidation in hepatocytes and demonstrated elevated serum levels of oxidized HMGB1 ([O] HMGB1) in alcoholic patients. Since interleukin-1 beta (IL-1B) increases in AALD, we hypothesized hepatocyte-derived [O] HMGB1 could interact with IL-1B to activate a pro-inflammatory program that, besides being detrimental to the liver, drives intestinal barrier dysfunction.

Results: Alcohol-fed RageΔMye mice exhibited decreased nuclear factor kappa B signaling, a pro-inflammatory signature, and reduced total intestinal permeability, resulting in protection from AALD. In addition, [O] HMGB1 bound and signaled through the receptor for advanced-glycation end-products (RAGE) in myeloid cells, driving hepatic inflammation, intestinal permeability, and increased portal blood lipopolysaccharide in AALD. We identified that [O] HMGB1 formed a complex with IL-1B, which was found in the livers of patients with acute alcoholic hepatitis and mice with AALD. This complex originated from the liver, because it was absent in the intestine when hepatocytes did not produce [O] HMGB1. Mechanistically, the complex bound RAGE in Kupffer cells and macrophages induced a pro-inflammatory program. Moreover, it bound RAGE in intestinal macrophages and epithelial cells, leading to intestinal inflammation, altered intestinal epithelial cell tight junction protein expression, increased intestinal permeability, and elevated portal blood lipopolysaccharide, enhancing AALD pathogenesis.

Conclusions: We identified a protein complex of liver origin that amplifies the pro-inflammatory feedback loop in AALD; therefore, targeting this complex could have significant therapeutic potential.

Keywords: Disulfide High-Mobility Group Box-1; Interleukin-1 Beta; Intestinal Epithelial Cells; Macrophages; Receptor for Advanced-Glycation End-Products.

MeSH terms

  • Animals
  • Disease Models, Animal
  • HMGB1 Protein* / metabolism
  • Hepatocytes / metabolism
  • Hepatocytes / pathology
  • Humans
  • Inflammation / metabolism
  • Inflammation / pathology
  • Interleukin-1beta* / metabolism
  • Intestinal Mucosa / metabolism
  • Intestinal Mucosa / pathology
  • Intestines / pathology
  • Liver Diseases, Alcoholic* / metabolism
  • Liver Diseases, Alcoholic* / pathology
  • Liver* / metabolism
  • Liver* / pathology
  • Male
  • Mice
  • Mice, Inbred C57BL
  • NF-kappa B / metabolism
  • Permeability
  • Receptor for Advanced Glycation End Products* / metabolism
  • Signal Transduction

Substances

  • HMGB1 Protein
  • Receptor for Advanced Glycation End Products
  • Interleukin-1beta
  • HMGB1 protein, mouse
  • Ager protein, mouse
  • NF-kappa B