Expression and function of endothelial monocyte-activating polypeptide-II in acute lung inflammation

Inflamm Res. 2007 May;56(5):175-81. doi: 10.1007/s00011-006-6162-3.

Abstract

Objective and design: We tested the hypothesis that total endothelial monocyte-activating polypeptide-II (EMAP-II) expression (proEMAP/p43 and mature EMAP-II) is up-regulated in lipopolysaccharide (LPS)-induced acute lung inflammation (ALI) and that mature EMAP-II induces monocyte/macrophage and granulocyte recruitment in vivo.

Materials: Thirty-five 10 week old, male Sprague-Dawley rats.

Treatment: Animals were instilled intratracheally with 250 microg of E. coli LPS (N = 15) or saline (N = 5) or 20 microg of mature EMAP-II (N = 5).

Methods: Total EMAP-II was quantified using ELISA and the protein was localized with light and electron microscopic immunocytochemistry in lungs of rats at 1, 3 and 12 h (n = 5/group).

Results: ELISA showed increased total EMAP-II concentrations (p < 0.05) in lungs from LPS-treated rats compared to control animals. Compared to the controls, light and electron microscopic imunocytochemistry localized total EMAP-II in monocytes/macrophages and alveolar septa at 1 and 3 h and in vascular smooth muscles at 12 h post-LPS treatment. Instillation of mature EMAP-II increased lung monocytes/macrophages and granulocytes compared with control animals (p < 0.05). However, compared to the LPS treatment, mature EMAP-II instillation did not induce expression of IL-1beta and MIP-2 (p < 0.05) and provoked less vigorous recruitment of monocytes/macrophages.

Conclusion: EMAP-II expression is increased in LPS-induced ALI, and that intra-tracheal instillation of mature EMAP-II induces recruitment of monocytes/macrophages and granulocytes into the lungs without stimulating IL-1beta or MIP-2 expression.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute Disease
  • Animals
  • Chemokine CXCL2
  • Cytokines / genetics
  • Cytokines / metabolism*
  • Disease Models, Animal
  • Gene Expression Regulation
  • Granulocytes / metabolism
  • Granulocytes / pathology
  • Granulocytes / ultrastructure
  • Interleukin-1beta / genetics
  • Interleukin-1beta / metabolism
  • Lipopolysaccharides
  • Lung / metabolism
  • Lung / pathology
  • Lung / ultrastructure
  • Macrophages / metabolism
  • Macrophages / pathology
  • Macrophages / ultrastructure
  • Male
  • Monokines / genetics
  • Monokines / metabolism
  • Neoplasm Proteins / genetics
  • Neoplasm Proteins / metabolism*
  • Pneumonia / chemically induced
  • Pneumonia / metabolism*
  • Pneumonia / pathology
  • RNA-Binding Proteins / genetics
  • RNA-Binding Proteins / metabolism*
  • Rats
  • Rats, Sprague-Dawley

Substances

  • Chemokine CXCL2
  • Cytokines
  • Interleukin-1beta
  • Lipopolysaccharides
  • Monokines
  • Neoplasm Proteins
  • RNA-Binding Proteins
  • small inducible cytokine subfamily E, member 1