Effects of C-reactive protein on the neutrophil respiratory burst in vitro

Innate Immun. 2014 May;20(4):339-49. doi: 10.1177/1753425913493199. Epub 2013 Jul 9.

Abstract

This study determined the influence of physiologically relevant concentrations of C-reactive protein (CRP) on reactive oxygen species (ROS) production by neutrophils. Neutrophils from healthy individuals were incubated with soluble pentameric CRP prior to TLR stimulation with Fusobacterium nucleatum, or FcγR stimulation with IgG-opsonised Staphylococcus aureus or heat-aggregated IgG. ROS generation by unstimulated cells and those after stimulation were determined using luminol, isoluminol and lucigenin chemiluminescence, detecting predominantly intracellular hypochlorous acid (HOCl), extracellular hydrogen peroxide (detected as HOCl) and extracellular superoxide respectively. Baseline (unstimulated) neutrophil ROS generation and release was reduced compared with vehicle control by 10 µg/ml CRP. There was no consistent effect of CRP on FcγR-stimulated HOCl production, but the extracellular superoxide response was reduced by 10 µg/ml CRP. By contrast, CRP reduced intracellular (10 µg/ml) and extracellular (3 and 10 µg/ml) HOCl generation, but increased superoxide release (1-10 µg/ml) in response to TLR stimulation. Physiologically relevant concentrations of CRP inhibited baseline ROS generation and reduced FcγR-stimulated extracellular superoxide and TLR-stimulated HOCl release, suggesting that CRP may offer some degree of host protection from neutrophil-associated, low-level oxidative stress. However, CRP enhanced TLR-mediated superoxide release from neutrophils, potentially increasing oxidative stress but aiding host protection from infection.

Keywords: C-reactive protein; neutrophil; periodontitis; reactive oxygen species; respiratory burst.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • C-Reactive Protein / metabolism*
  • Cells, Cultured
  • Fusobacterium Infections / metabolism*
  • Fusobacterium nucleatum / physiology*
  • Humans
  • Hydrogen Peroxide / metabolism
  • Hypochlorous Acid / metabolism
  • In Vitro Techniques
  • Neutrophils / metabolism*
  • Oxidative Stress
  • Receptors, IgG / metabolism
  • Staphylococcal Infections / metabolism*
  • Staphylococcus aureus / physiology*
  • Superoxides / metabolism
  • Toll-Like Receptors / metabolism

Substances

  • Receptors, IgG
  • Toll-Like Receptors
  • Superoxides
  • Hypochlorous Acid
  • C-Reactive Protein
  • Hydrogen Peroxide