Recombinant soluble CD14 mediates the activation of endothelial cells by lipopolysaccharide

J Immunol. 1993 Aug 1;151(3):1500-7.

Abstract

Recent studies have suggested that soluble CD14 found in serum is involved in the LPS-induced activation of endothelial cells (EC). To more fully investigate the relevance of sCD14 to LPS-induced activation of EC, we have used recombinant soluble CD14 (rsCD14) and have examined, under serum-free conditions, its role in the LPS-induced EC response in the presence of LPS alone as well as in the presence of LPS-binding protein. Our studies show that EC can be activated by high concentrations of LPS in the presence of rsCD14 alone. However, at low concentrations of LPS (5 and 10 ng/ml), the rsCD14-stimulated activation is strongly enhanced by LPS-binding protein. In addition, we show that LPS binds to rsCD14 directly; in the presence of low concentrations of LPS this binding is enhanced by the presence of LPS-binding protein. These results show that while the membrane form of CD14 can function as a receptor, its soluble form can function as a co-ligand with LPS in the EC-LPS response.

Publication types

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

MeSH terms

  • Acute-Phase Proteins*
  • Antigens, CD / chemistry
  • Antigens, CD / pharmacology*
  • Antigens, Differentiation, Myelomonocytic / chemistry
  • Antigens, Differentiation, Myelomonocytic / pharmacology*
  • Carrier Proteins / metabolism
  • Cell Adhesion Molecules / metabolism
  • Cells, Cultured
  • Endothelium, Vascular / drug effects*
  • Humans
  • In Vitro Techniques
  • Intercellular Adhesion Molecule-1
  • Lipopolysaccharide Receptors
  • Lipopolysaccharides / metabolism
  • Lipopolysaccharides / pharmacology*
  • Macromolecular Substances
  • Membrane Glycoproteins*
  • Recombinant Proteins
  • Solubility
  • Up-Regulation / drug effects

Substances

  • Acute-Phase Proteins
  • Antigens, CD
  • Antigens, Differentiation, Myelomonocytic
  • Carrier Proteins
  • Cell Adhesion Molecules
  • Lipopolysaccharide Receptors
  • Lipopolysaccharides
  • Macromolecular Substances
  • Membrane Glycoproteins
  • Recombinant Proteins
  • lipopolysaccharide-binding protein
  • Intercellular Adhesion Molecule-1