Age-related sensitivity to endotoxin-induced liver inflammation: Implication of inflammasome/IL-1β for steatohepatitis

Aging Cell. 2015 Aug;14(4):524-33. doi: 10.1111/acel.12305. Epub 2015 Apr 7.

Abstract

Aging is associated with increased vulnerability to inflammatory challenge. However, the effects of altered inflammatory response on the metabolic status of tissues or organs are not well documented. In this study, we present evidence demonstrating that lipopolysaccharide (LPS)-induced upregulation of the inflammasome/IL-1β pathway is accompanied with an increased inflammatory response and abnormal lipid accumulation in livers of aged rats. To monitor the effects of aging on LPS-induced inflammation, we administered LPS (2 mg kg(-1) ) to young (6-month old) and aged (24-month old) rats and found abnormal lipid metabolism in only aged rats with increased lipid accumulation in the liver. This lipid accumulation in the liver was due to the dysregulation of PPARα and SREBP1c. We also observed severe liver inflammation in aged rats as indicated by increased ALT levels in serum and increased Kupffer cells in the liver. Importantly, among many inflammation-associated factors, the aged rat liver showed chronically increased IL-1β production. Increased levels of IL-1β were caused by the upregulation of caspase-1 activity and inflammasome activation. In vitro studies with HepG2 cells demonstrated that treatment with IL-1β significantly induced lipid accumulation in hepatocytes through the regulation of PPARα and SREBP1c. In summary, we demonstrated that LPS-induced liver inflammation and lipid accumulation were associated with a chronically overactive inflammasome/IL-1β pathway in aged rat livers. Based on the present findings, we propose a mechanism of aging-associated progression of steatohepatitis induced by endotoxin, delineating a pathogenic role of the inflammasome/IL-1β pathway involved in lipid accumulation in the liver.

Keywords: IL-1β; LPS; aging; inflammasome; inflammation; lipid accumulation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Age Factors
  • Aging / genetics*
  • Aging / immunology
  • Alanine Transaminase / blood
  • Alanine Transaminase / genetics
  • Animals
  • Caspase 1 / genetics
  • Caspase 1 / immunology
  • Fatty Liver / chemically induced
  • Fatty Liver / genetics*
  • Fatty Liver / immunology
  • Fatty Liver / pathology
  • Gene Expression Regulation
  • Hep G2 Cells
  • Humans
  • Inflammasomes / genetics*
  • Inflammasomes / immunology
  • Interleukin-1beta / genetics*
  • Interleukin-1beta / immunology
  • Kupffer Cells / immunology
  • Kupffer Cells / metabolism
  • Kupffer Cells / pathology
  • Lipid Metabolism / genetics
  • Lipid Metabolism / immunology
  • Lipopolysaccharides
  • Liver / immunology
  • Liver / metabolism*
  • Liver / pathology
  • Male
  • PPAR alpha / genetics*
  • PPAR alpha / immunology
  • Rats
  • Rats, Sprague-Dawley
  • Signal Transduction
  • Sterol Regulatory Element Binding Protein 1 / genetics*
  • Sterol Regulatory Element Binding Protein 1 / immunology

Substances

  • Inflammasomes
  • Interleukin-1beta
  • Lipopolysaccharides
  • PPAR alpha
  • Sterol Regulatory Element Binding Protein 1
  • Alanine Transaminase
  • Caspase 1