Macrophage inflammatory protein-2 induced by TNF-alpha plays a pivotal role in concanavalin A-induced liver injury in mice

J Hepatol. 2001 Aug;35(2):217-24. doi: 10.1016/s0168-8278(01)00109-x.

Abstract

Background/aims: Macrophage inflammatory protein-2 (MIP-2), one of the CXC chemokines, is involved in the recruitment of neutrophils in several tissue injuries. In this study, we investigated the role of MIP-2 in concanavalin A (Con A)-induced liver injury in mice.

Methods: Liver injury was induced by intravenous injection of Con A (15 mg/kg) and plasma alanine aminotransferase (ALT), MIP-2 levels were determined and histological assessment of the liver was performed. Anti-mouse MIP-2 antibody was intravenously administered 30 min before Con A injection.

Results: The plasma ALT level significantly elevated and reached a maximum at 8 h after Con A injection. The plasma MIP-2 level was also elevated and reached a peak value at 2 h after Con A injection. The elevated ALT level by Con A injection was significantly inhibited by the MIP-2 antibody. The elevated plasma MIP-2 level after Con A injection was significantly reduced by the tumor necrosis factor alpha (TNF-alpha) antibody, and MIP-2 was induced in plasma after recombinant TNF-alpha injection. Hepatic necrosis and infiltration of neutrophils were observed after Con A injection, and these histological changes were attenuated by the MIP-2 antibody.

Conclusions: These findings suggest that Con A induces TNF-alpha release, and this TNF-alpha stimulates MIP-2 induction, at least partially contributing to the liver injury mediated through the recruitment of neutrophils.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alanine Transaminase / blood
  • Animals
  • Antibodies / pharmacology
  • Chemokine CXCL2
  • Chemokines / antagonists & inhibitors
  • Chemokines / biosynthesis*
  • Concanavalin A / toxicity*
  • Female
  • Interferon-gamma / antagonists & inhibitors
  • Interferon-gamma / blood
  • Interferon-gamma / pharmacology
  • Liver / drug effects*
  • Liver / injuries*
  • Liver / pathology
  • Liver / physiopathology
  • Mice
  • Mice, Inbred BALB C
  • Neutrophils / drug effects
  • Neutrophils / physiology
  • Recombinant Proteins / pharmacology
  • Tumor Necrosis Factor-alpha / antagonists & inhibitors
  • Tumor Necrosis Factor-alpha / pharmacology
  • Tumor Necrosis Factor-alpha / physiology*

Substances

  • Antibodies
  • Chemokine CXCL2
  • Chemokines
  • Cxcl2 protein, mouse
  • Recombinant Proteins
  • Tumor Necrosis Factor-alpha
  • Concanavalin A
  • Interferon-gamma
  • Alanine Transaminase