Inhibition of Rac activity alleviates lipopolysaccharide-induced acute pulmonary injury in mice

Biochim Biophys Acta. 2011 Jul;1810(7):666-74. doi: 10.1016/j.bbagen.2011.03.020. Epub 2011 Apr 12.

Abstract

Background: Rac small GTPases play important roles in cytoskeleton and many cell functions including cell cycle, cell growth, cell adhesion and gene transcription. Here, we investigated the roles of Rac including Rac1 and Rac2 in lipopolysaccharide (LPS)-induced pulmonary injury.

Methods: After LPS was intratracheally instilled to lungs in mice, Rac, CDC42 and RhoA activation assay by pull-down and West blot, inflammatory cell infiltration assay by counting cell numbers and lung histological examination, pro-inflammatory mediator mRNA expression assay by quantitative RT-PCR, measurement of myeloperoxidase (MPO) activity, Evans Blue and albumin accumulation by spectrophotometry were performed to evaluate the roles of Rac in pulmonary injury by using its specific inhibitor, NSC23766.

Results: LPS challenge led to increases of both Rac1 and Rac2, but not CDC42 or RhoA activities in lungs, and intraperitoneal administration with NSC23766 inhibited both Rac1 and Rac2, but not CDC42 or RhoA activities. Treatment with NSC23766 at 1 or 3mg/kg not only reduced the inflammatory cells infiltration and MPO activities, but also inhibited pro-inflammatory mediators, tumor necrosis factor-α and interleukin-1β, mRNA expression. Moreover, in vitro neutrophil migration assay and in vivo microvascular permeability assay indicated that NSC23766 not only inhibited neutrophil transwell migration toward a chemoattractant, fMLP, but also reduced Evans Blue and albumin accumulation in LPS-challenged lungs. LPS activated both Rac1 and Rac2, but not CDC42 or RhoA activities in lungs, and specific inhibition of Rac activities by NSC23766 effectively alleviated LPS-induced injury.

General significance: Rac could be a potential target for therapeutic intervention of pulmonary inflammation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aminoquinolines / chemistry
  • Aminoquinolines / pharmacology*
  • Animals
  • Blotting, Western
  • Bronchoalveolar Lavage Fluid / cytology
  • Capillary Permeability / drug effects
  • Cell Movement / drug effects
  • Gene Expression Regulation / drug effects
  • Interleukin-10 / genetics
  • Interleukin-1beta / genetics
  • Lipopolysaccharides
  • Lung / drug effects
  • Lung / metabolism
  • Lung / pathology
  • Lung Injury / chemically induced
  • Lung Injury / metabolism
  • Lung Injury / prevention & control*
  • Male
  • Mice
  • Mice, Inbred ICR
  • Molecular Structure
  • Neutrophils / drug effects
  • Neutrophils / metabolism
  • Neutrophils / pathology
  • Peroxidase / metabolism
  • Pyrimidines / chemistry
  • Pyrimidines / pharmacology*
  • RAC2 GTP-Binding Protein
  • Reverse Transcriptase Polymerase Chain Reaction
  • Tumor Necrosis Factor-alpha / genetics
  • rac GTP-Binding Proteins / antagonists & inhibitors*
  • rac GTP-Binding Proteins / metabolism
  • rac1 GTP-Binding Protein / antagonists & inhibitors
  • rac1 GTP-Binding Protein / metabolism

Substances

  • Aminoquinolines
  • Interleukin-1beta
  • Lipopolysaccharides
  • NSC 23766
  • Pyrimidines
  • Tumor Necrosis Factor-alpha
  • Interleukin-10
  • Peroxidase
  • rac GTP-Binding Proteins
  • rac1 GTP-Binding Protein