IL-10 mediated regulation of liver inflammation during acute murine cytomegalovirus infection

PLoS One. 2012;7(8):e42850. doi: 10.1371/journal.pone.0042850. Epub 2012 Aug 3.

Abstract

Various cell types in both lymphoid and non-lymphoid tissues produce the anti-inflammatory cytokine interleukin (IL)-10 during murine cytomegalovirus (MCMV) infection. The functions of IL-10 in the liver during acute infection and the cells that generate this cytokine at this site have not been extensively investigated. In this study, we demonstrate that the production of IL-10 in the liver is elevated in C57BL/6 mice during late acute MCMV infection. Using IL-10 green fluorescence protein (GFP) reporter knock-in mice, designated IL-10-internal ribosomal entry site (IRES)-GFP-enhanced reporter (tiger), NK cells are identified as major IL-10 expressing cells in the liver after infection, along with T cells and other leukocytes. In the absence of IL-10, mice exhibit marked elevations in proinflammatory cytokines and in the numbers of mononuclear cells and lymphocytes infiltrating the liver during this infection. IL-10-deficiency also enhances liver injury without improving viral clearance from this site. Collectively, the results indicate that IL-10-producing cells in the liver provide protection from collateral injury by modulating the inflammatory response associated with MCMV infection.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute Disease
  • Alanine Transaminase / blood
  • Animals
  • CD8-Positive T-Lymphocytes
  • Chemokines / biosynthesis
  • Cytomegalovirus Infections / blood
  • Cytomegalovirus Infections / immunology*
  • Cytomegalovirus Infections / pathology*
  • Cytomegalovirus Infections / virology
  • Inflammation / blood
  • Inflammation / complications
  • Inflammation / microbiology
  • Inflammation / pathology*
  • Inflammation Mediators / metabolism
  • Interferon-gamma / metabolism
  • Interleukin-10 / biosynthesis
  • Interleukin-10 / deficiency
  • Interleukin-10 / metabolism*
  • Leukocytes / metabolism
  • Liver / immunology*
  • Liver / pathology*
  • Liver / virology
  • Mice
  • Mice, Inbred C57BL
  • Muromegalovirus / physiology*
  • Tumor Necrosis Factor-alpha / metabolism
  • Viral Load

Substances

  • Chemokines
  • IL10 protein, mouse
  • Inflammation Mediators
  • Tumor Necrosis Factor-alpha
  • Interleukin-10
  • Interferon-gamma
  • Alanine Transaminase