CCAAT/enhancer binding protein epsilon is critical for effective neutrophil-mediated response to inflammatory challenge

Blood. 1999 May 1;93(9):3096-105.

Abstract

Targeted mutation of CCAAT/enhancer binding protein (C/EBP) epsilon in mice results in early death, primarily due to spontaneous infection with Pseudomonas aeruginosa. Functional analysis of C/EBPepsilon-deficient neutrophils, in an in vivo model of peritoneal inflammation, shows multiple defects. Reduction of phagocytotic killing by C/EBPepsilon-deficient neutrophils is a result of decreased uptake of opsonized bacteria as well as little to no expression of secondary granule proteins. Abnormalities in neutrophil migration detected in a chemical peritonitis model are likely secondary to abnormal CD11b integrin and L-selectin expression on C/EBPepsilon-deficient neutrophils. Alterations in neutrophil cytokine expression in response to inflammation show decreased levels of interleukin-1 receptor antagonist (IL-1Ra) and increased levels of tumor necrosis factor-alpha (TNF-alpha) expression by C/EBPepsilon-deficient neutrophils. Additionally, TNF-alpha expression is increased in nonactivated, circulating C/EBPepsilon-deficient neutrophils. Overall, C/EBPepsilon-deficient neutrophils are severely functionally impaired, evoking an abnormal microenvironment, which may contribute to the loss of normal responses to inflammatory stimuli. Similarities between the C/EBPepsilon-deficient mouse model and the human disease, specific granule deficiency, will be discussed.

MeSH terms

  • Animals
  • CCAAT-Enhancer-Binding Proteins
  • Chemotaxis, Leukocyte / drug effects
  • Chemotaxis, Leukocyte / physiology*
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / metabolism*
  • Enhancer Elements, Genetic*
  • Gene Expression Regulation
  • Humans
  • Inflammation / blood
  • Inflammation / immunology
  • Interleukin 1 Receptor Antagonist Protein
  • L-Selectin / genetics
  • Macrophage-1 Antigen / genetics
  • Mice
  • Mice, Knockout
  • Neutrophils / immunology
  • Neutrophils / physiology*
  • Nuclear Proteins / genetics
  • Nuclear Proteins / metabolism*
  • Peritoneal Cavity
  • Phagocytosis*
  • Sialoglycoproteins / genetics
  • Thioglycolates / pharmacology
  • Tumor Necrosis Factor-alpha / genetics

Substances

  • CCAAT-Enhancer-Binding Proteins
  • DNA-Binding Proteins
  • IL1RN protein, human
  • Il1rn protein, mouse
  • Interleukin 1 Receptor Antagonist Protein
  • Macrophage-1 Antigen
  • Nuclear Proteins
  • Sialoglycoproteins
  • Thioglycolates
  • Tumor Necrosis Factor-alpha
  • L-Selectin