Neutralization of the CXC chemokine, macrophage inflammatory protein-2, attenuates bleomycin-induced pulmonary fibrosis

J Immunol. 1999 May 1;162(9):5511-8.

Abstract

Few studies have addressed the importance of vascular remodeling in the lung during the development of bleomycin-induced pulmonary fibrosis. For fibroplasia and deposition of extracellular matrix to occur, there must be a geometric increase in neovascularization. We hypothesized that net angiogenesis during the pathogenesis of fibroplasia and deposition of extracellular matrix during bleomycin-induced pulmonary fibrosis are dependent in part upon an overexpression of the angiogenic CXC chemokine, macrophage inflammatory protein-2 (MIP-2). To test this hypothesis, we measured MIP-2 by specific ELISA in whole lung homogenates in either bleomycin-treated or control CBA/J mice and correlated these levels with lung hydroxyproline. We found that lung tissue from mice treated with bleomycin, compared with that from saline-treated controls, demonstrated a significant increase in the presence of MIP-2 that was correlated to a greater angiogenic response and total lung hydroxyproline content. Neutralizing anti-MIP-2 Abs inhibited the angiogenic activity of day 16 bleomycin-treated lung specimens using an in vivo angiogenesis bioassay. Furthermore, when MIP-2 was depleted in vivo by passive immunization, bleomycin-induced pulmonary fibrosis was significantly reduced without a change in the presence of pulmonary neutrophils, fibroblast proliferation, or collagen gene expression. This was also paralleled by a reduction in angiogenesis. These results demonstrate that the angiogenic CXC chemokine, MIP-2, is an important factor that regulates angiogenesis/fibrosis in pulmonary fibrosis.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Bleomycin / toxicity*
  • Cell Differentiation / immunology
  • Cell Movement / immunology
  • Chemokine CXCL2
  • Chemokines, CXC / biosynthesis
  • Chemokines, CXC / immunology*
  • Chemokines, CXC / physiology
  • Collagen / biosynthesis
  • Collagen / genetics
  • Female
  • Fibroblasts / pathology
  • Gene Expression Regulation / immunology
  • Immune Sera / administration & dosage
  • Immunization, Passive
  • Immunohistochemistry
  • Lung / blood supply
  • Lung / drug effects
  • Lung / metabolism
  • Mice
  • Mice, Inbred CBA
  • Monokines / biosynthesis
  • Monokines / immunology*
  • Monokines / physiology
  • Neovascularization, Pathologic / immunology
  • Neovascularization, Pathologic / physiopathology
  • Neovascularization, Pathologic / prevention & control
  • Neutrophils / pathology
  • Pulmonary Fibrosis / chemically induced*
  • Pulmonary Fibrosis / immunology*
  • Pulmonary Fibrosis / metabolism
  • Pulmonary Fibrosis / physiopathology
  • Rats
  • Rats, Long-Evans

Substances

  • Chemokine CXCL2
  • Chemokines, CXC
  • Immune Sera
  • Monokines
  • Bleomycin
  • Collagen