Involvement of Syk protein tyrosine kinase in LPS-induced responses in macrophages

J Endotoxin Res. 2007;13(2):117-25. doi: 10.1177/0968051907079125.

Abstract

Syk kinase is best known as a critical component of immunoreceptor signaling in leukocytes. Activation of Syk following cross-linking of Fcgamma and Fcepsilon receptors on macrophages, mast cells, and other cells induces various inflammatory events. We hypothesized that Syk is involved in inflammatory responses induced by the lipopolysaccharide (LPS). We studied the role of Syk using its inhibition by antisense oligonucleotides, or small interfering RNA. Our data demonstrated that in vivo inhibition of Syk caused down-regulation of LPS-induced responses in rat alveolar macrophages. In in vitro experiments, inhibition of Syk in rat peritoneal macrophages, as well as in human myelomonocyte cell line THP-1 also caused a decrease in LPS-induced cytokine release. Our data support the hypothesis that, in macrophages, Syk is involved in LPS-induced intracellular signaling pathways leading to the release of pro-inflammatory mediators. Understanding the role of Syk in LPS-induced signaling may help in developing new therapeutic tools for inflammatory disorders.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Blotting, Western
  • Cell Line
  • Cytokines / immunology
  • Cytokines / metabolism*
  • Enzyme-Linked Immunosorbent Assay
  • Humans
  • Inflammation Mediators / metabolism
  • Intracellular Signaling Peptides and Proteins / antagonists & inhibitors
  • Intracellular Signaling Peptides and Proteins / immunology
  • Intracellular Signaling Peptides and Proteins / metabolism*
  • Lipopolysaccharides / immunology
  • Lipopolysaccharides / metabolism*
  • Liposomes
  • Macrophages, Alveolar / enzymology
  • Macrophages, Alveolar / immunology
  • Macrophages, Alveolar / metabolism*
  • Macrophages, Peritoneal / enzymology
  • Macrophages, Peritoneal / immunology
  • Macrophages, Peritoneal / metabolism*
  • Male
  • Monocytes / immunology
  • Monocytes / metabolism
  • Nitric Oxide / metabolism
  • Oligonucleotides, Antisense / metabolism
  • Oligonucleotides, Antisense / pharmacology
  • Protein-Tyrosine Kinases / antagonists & inhibitors
  • Protein-Tyrosine Kinases / immunology
  • Protein-Tyrosine Kinases / metabolism*
  • RNA, Small Interfering / genetics
  • RNA, Small Interfering / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Reverse Transcriptase Polymerase Chain Reaction
  • Syk Kinase
  • Transfection
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Cytokines
  • Inflammation Mediators
  • Intracellular Signaling Peptides and Proteins
  • Lipopolysaccharides
  • Liposomes
  • Oligonucleotides, Antisense
  • RNA, Small Interfering
  • Tumor Necrosis Factor-alpha
  • Nitric Oxide
  • Protein-Tyrosine Kinases
  • SYK protein, human
  • Syk Kinase
  • Syk protein, rat