A two-insult in vitro model of PMN-mediated pulmonary endothelial damage: requirements for adherence and chemokine release

Am J Physiol Cell Physiol. 2002 Dec;283(6):C1592-603. doi: 10.1152/ajpcell.00540.2001. Epub 2002 Jul 24.

Abstract

Lysophosphatidylcholines (lyso-PCs), generated during blood storage, are etiologic in a two-insult, sepsis-based model of transfusion-related acute lung injury (TRALI). Individually, endotoxin (LPS) and lyso-PCs prime but do not activate neutrophils (PMNs). We hypothesized that priming of PMNs alters their reactivity such that a second priming agent causes PMN activation and endothelial cell damage. PMNs were primed or not with LPS and then treated with lyso-PCs, and oxidase activation and elastase release were measured. For coculture experiments, activation of human pulmonary microvascular endothelial cells (HMVECs) was assessed by ICAM-1 expression and chemokine release. HMVECs were stimulated or not with LPS, PMNs were added, cells were incubated with lyso-PCs, and the number of viable HMVECs was counted. Lyso-PCs activated LPS-primed PMNs. HMVEC activation resulted in increased ICAM-1 and release of ENA-78, GRO alpha, and IL-8. PMN-mediated HMVEC damage was dependent on LPS activation of HMVECs, chemokine release, PMN adhesion, and lyso-PC activation of the oxidase. In conclusion, sequential exposure of PMNs to priming agents activates the microbicidal arsenal, and PMN-mediated HMVEC damage was the result of two insults: HMVEC activation and PMN oxidase assembly.

Publication types

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

MeSH terms

  • Cell Adhesion
  • Cell Count
  • Cells, Cultured
  • Chemokine CXCL1
  • Chemokine CXCL5
  • Chemokines / metabolism
  • Chemokines, CXC*
  • Chemotactic Factors / metabolism
  • Coculture Techniques
  • Endothelium, Vascular / pathology*
  • Endothelium, Vascular / physiopathology*
  • Enzyme Activation
  • Humans
  • Intercellular Adhesion Molecule-1 / metabolism
  • Intercellular Signaling Peptides and Proteins / metabolism
  • Interleukin-8 / analogs & derivatives*
  • Interleukin-8 / metabolism
  • Lipopolysaccharides / pharmacology
  • Lysophosphatidylcholines / pharmacology
  • Microcirculation
  • Neutrophil Activation
  • Neutrophils / drug effects
  • Neutrophils / physiology*
  • Oxidoreductases / metabolism
  • Pancreatic Elastase / metabolism
  • Pulmonary Circulation*

Substances

  • CXCL1 protein, human
  • CXCL5 protein, human
  • Chemokine CXCL1
  • Chemokine CXCL5
  • Chemokines
  • Chemokines, CXC
  • Chemotactic Factors
  • Intercellular Signaling Peptides and Proteins
  • Interleukin-8
  • Lipopolysaccharides
  • Lysophosphatidylcholines
  • Intercellular Adhesion Molecule-1
  • Oxidoreductases
  • Pancreatic Elastase