Upregulation of Mer receptor tyrosine kinase signaling attenuated lipopolysaccharide-induced lung inflammation

J Pharmacol Exp Ther. 2013 Feb;344(2):447-58. doi: 10.1124/jpet.112.199778. Epub 2012 Nov 29.

Abstract

Mer receptor tyrosine kinase (Mer) signaling plays a central role in the intrinsic inhibition of the inflammatory response to Toll-like receptor activation. Previously, we found that lung Mer protein expression decreased after lipopolysaccharide (LPS) treatment due to enhanced Mer cleavage. The purpose of the present study was to examine whether pharmacologically restored membrane-bound Mer expression upregulates the Mer signaling pathways and suppresses lung inflammatory responses. Pretreatment with the ADAM17 (a disintegrin and metalloproteinase-17) inhibitor TAPI-0 (tumor necrosis factor alpha protease inhibitor-0) reduced LPS-induced production of soluble Mer protein in bronchoalveolar lavage (BAL) fluid, restored membrane-bound Mer expression, and increased Mer activation in alveolar macrophages and lungs after LPS treatment. TAPI-0 also enhanced Mer downstream signaling, including phosphorylation of protein kinase b, focal adhesion kinase, and signal transducer and activator of transcription 1. As expected from enhanced Mer signaling, TAPI-0 also augmented suppressor of cytokine signaling-1 and -3 mRNA and protein levels and inhibited nuclear factor κB activation at 4 and 24 hours after LPS treatment. TAPI-0 suppressed LPS-induced inflammatory cell accumulation, total protein level elevation in BAL fluid, and production of inflammatory mediators, including tumor necrosis factor-α, interleukin-1β, and macrophage inflammatory protein-2. Additionally, the effects of TAPI-0 on the activation of Mer signaling and the production of inflammatory responses could be reversed by cotreatment with specific Mer-neutralizing antibody. Restored Mer protein expression by treatment with TAPI-0 efficiently prevents the inflammatory cascade during acute lung injury.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • ADAM Proteins / antagonists & inhibitors
  • ADAM17 Protein
  • Animals
  • Blotting, Western
  • Bronchoalveolar Lavage Fluid / chemistry
  • Bronchoalveolar Lavage Fluid / cytology
  • Bronchoalveolar Lavage Fluid / immunology
  • Cell Count
  • Cells, Cultured
  • Dipeptides / administration & dosage
  • Dipeptides / therapeutic use*
  • Electrophoretic Mobility Shift Assay
  • Enzyme Activation
  • Enzyme Induction
  • Enzyme-Linked Immunosorbent Assay
  • Hydroxamic Acids / administration & dosage
  • Hydroxamic Acids / therapeutic use*
  • Lipopolysaccharides / pharmacology*
  • Lung / drug effects*
  • Lung / enzymology
  • Lung / metabolism
  • Lung / pathology
  • Macrophages, Alveolar / drug effects
  • Macrophages, Alveolar / enzymology
  • Macrophages, Peritoneal / drug effects
  • Macrophages, Peritoneal / enzymology
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Phosphorylation
  • Pneumonia, Bacterial / drug therapy*
  • Pneumonia, Bacterial / enzymology
  • Pneumonia, Bacterial / pathology
  • Proto-Oncogene Proteins / biosynthesis*
  • Proto-Oncogene Proteins / metabolism
  • RNA / metabolism
  • Receptor Protein-Tyrosine Kinases / biosynthesis*
  • Receptor Protein-Tyrosine Kinases / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction
  • Signal Transduction / drug effects*
  • Up-Regulation
  • c-Mer Tyrosine Kinase

Substances

  • Dipeptides
  • Hydroxamic Acids
  • Lipopolysaccharides
  • N-((2-(hydroxyaminocarbonyl)methyl)-4-methylpentanoyl)-3-(2'-naphthyl)alanylalanine, 2-aminoethylamide
  • Proto-Oncogene Proteins
  • lipopolysaccharide, E coli O55-B5
  • RNA
  • Mertk protein, mouse
  • Receptor Protein-Tyrosine Kinases
  • c-Mer Tyrosine Kinase
  • ADAM Proteins
  • ADAM17 Protein
  • Adam17 protein, mouse