Tiopronin monolayer-protected silver nanoparticles modulate IL-6 secretion mediated by Toll-like receptor ligands

Nanomedicine (Lond). 2008 Oct;3(5):627-35. doi: 10.2217/17435889.3.5.627.

Abstract

Aims: Capped silver nanoparticles that can be coupled to a variety of molecules and biomolecules are of great interest owing to their potential applications in biomedicine. However, there are no data about their toxicity or functional effects on a key innate immune response, such as IL-6 secretion, after the engagement of the main group of pathogen-associated molecular patterns receptors, that is, the Toll-like receptors (TLRs).

Materials & methods: N-(2-mercaptopropionyl)glycine (tiopronin)-capped silver (Ag@tiopronin) nanoparticles of a narrow sized distribution ( approximately 5 nm) were synthesized and characterized by transmission electron microscopy, Fourier transform infrared spectroscopy, Raman, (1)H-NMR and total correlation spectroscopy. Cytotoxicity was determined by lactate deshidrogenase and 3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyl tetrazolium assays in Raw 264.7 macrophages. IL-6 was measured by ELISA.

Results & discussion: Ag@tiopronin nanoparticles have a narrow size distribution ( approximately 5 nm), high solubility and stability in aqueous environment with no cytotoxicity in terms of mitochondrial function or plasma-membrane integrity at concentrations as high as 200 microg/10(6) cells. Ag@tiopronin nanoparticles were not proinflammatory agents, but remarkably they specifically impaired the IL-6 secretion mediated by TLR2, TLR2/6, TLR3 or TLR9 stimulation in co-treatment experiments. However, in pretreatment experiments, nanoparticles enhanced the susceptibility of macrophages to inflammatory stimulation mediated by TLR2/1 and TLR2/6 specific ligands while severely impairing the IL-6 secretion activated by the TLR3 or TLR9 ligands.

Conclusions: Contrary to what is found for bare silver nanoparticles, Ag@tiopronin nanoparticles are noncytotoxic to macrophages. Ag@tiopronin nanoparticles showed differential effects on TLR signaling of a high degree of specificity, without proinflammatory effects by themselves. These effects have to be borne in mind when using bioconjugates of Ag@tiopronin nanoparticles for future medical applications.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line
  • Interleukin-6 / metabolism*
  • Macrophages / cytology
  • Macrophages / drug effects*
  • Macrophages / metabolism
  • Microscopy, Electron, Transmission
  • Nanoparticles / chemistry
  • Nanoparticles / ultrastructure
  • Silver / chemistry
  • Silver / pharmacology*
  • Spectroscopy, Fourier Transform Infrared
  • Tiopronin / pharmacology*
  • Toll-Like Receptor 2 / metabolism
  • Toll-Like Receptor 3 / metabolism
  • Toll-Like Receptor 9 / metabolism
  • Toll-Like Receptors / metabolism*

Substances

  • Interleukin-6
  • Toll-Like Receptor 2
  • Toll-Like Receptor 3
  • Toll-Like Receptor 9
  • Toll-Like Receptors
  • Silver
  • Tiopronin