Surfactant protein A directly interacts with TLR4 and MD-2 and regulates inflammatory cellular response. Importance of supratrimeric oligomerization

J Biol Chem. 2006 Aug 4;281(31):21771-21780. doi: 10.1074/jbc.M513041200. Epub 2006 Jun 5.

Abstract

The purpose of the current study was to examine the binding of pulmonary surfactant protein A (SP-A) to TLR4 and MD-2, which are critical signaling receptors for lipopolysaccharides (LPSs). The direct binding of SP-A to the recombinant soluble form of extracellular TLR4 domain (sTLR4) and MD-2 was detected using solid-phase binding, immunoprecipitation, and BIAcore. SP-A bound to sTLR4 and MD-2 in a Ca2+-dependent manner, and an anti-SP-A monoclonal antibody whose epitope lies in the region Thr184-Gly194 blocked the SP-A binding to sTLR4 and MD-2, indicating the involvement of the carbohydrate recognition domain (CRD) in the binding. SP-A avidly bound to the deglycosylated forms of sTLR4 and MD-2, suggesting a protein/protein interaction. In addition, SP-A attenuated cell surface binding of smooth LPS and smooth LPS-induced NF-kappaB activation in TLR4/MD-2-expressing cells. To know the role of oligomerization in the interaction of SP-A with TLR4 and MD-2, the collagenase-resistant fragment (CRF), which consisted of CRD plus neck domain of SP-A, was isolated. CRF assembled as a trimer, whereas SP-A assembled as a higher order oligomer. Although CRD was suggested to be involved in the binding, CRF exhibited approximately 600- and 155-fold higher KD for the binding to TLR4 and MD-2, respectively, when compared with SP-A. Consistently significantly higher molar concentrations of CRF were required to inhibit smooth LPS-induced NF-kappaB activation and tumor necrosis factor-alpha secretion. These results demonstrate for the first time the direct interaction between SP-A and TLR4/MD-2 and suggest the importance of supratrimeric oligomerization in the immunomodulatory function of SP-A.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Binding Sites
  • Calcium
  • Carbohydrates
  • Cell Line
  • Dimerization
  • Humans
  • Inflammation / metabolism
  • Inflammation / pathology*
  • Lipopolysaccharides / metabolism
  • Lipopolysaccharides / pharmacology
  • Lymphocyte Antigen 96 / metabolism*
  • Macrophages / cytology
  • Macrophages / metabolism
  • NF-kappa B / metabolism
  • Peptide Fragments
  • Protein Binding
  • Protein Structure, Tertiary
  • Pulmonary Surfactant-Associated Protein A / chemistry*
  • Pulmonary Surfactant-Associated Protein A / metabolism*
  • Pulmonary Surfactant-Associated Protein A / physiology
  • Toll-Like Receptor 4 / metabolism*
  • Transfection
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Carbohydrates
  • LY96 protein, human
  • Lipopolysaccharides
  • Lymphocyte Antigen 96
  • NF-kappa B
  • Peptide Fragments
  • Pulmonary Surfactant-Associated Protein A
  • Toll-Like Receptor 4
  • Tumor Necrosis Factor-alpha
  • Calcium