Enhanced intracellular translocation and biodistribution of gold nanoparticles functionalized with a cell-penetrating peptide (VG-21) from vesicular stomatitis virus

Biomaterials. 2014 Nov;35(35):9484-94. doi: 10.1016/j.biomaterials.2014.07.032. Epub 2014 Aug 22.

Abstract

Reduced toxicity and ease of modification make gold nanoparticles (GNPs) suitable for targeted delivery, bioimaging and theranostics by conjugating cell-penetrating peptides (CPPs). This study presents the biodistribution and enhanced intracellular uptake of GNPs functionalized with VG-21, a CPP derived from vesicular stomatitis virus glycoprotein (G). Cell penetrating efficiency of VG-21 was demonstrated using CellPPD web server, conjugated to GNPs and were characterized using, UV-visible and FTIR spectroscopy, transmission electron microscopy, dynamic light scattering and zeta potential. Uptake of VG-21 functionalized GNPs (fGNPs) was tested in eukaryotic cell lines, HEp-2, HeLa, Vero and Cos-7, using flow cytometry, fluorescence and transmission electron microscopy (TEM), and inductively coupled plasmon optical emission spectroscopy (ICP-OES). The effects of nanoparticles on stress and toxicity related genes were studied in HEp-2 cells. Cytokine response to fGNPs was studied in vitro and in vivo. Biodistribution of nanoparticles was studied in BALB/c mice using TEM and ICP-OES. VG-21, GNPs and fGNPs had little to no effect on cell viability. Upon exposure to fGNPs, HEp-2 cells revealed minimal down regulation of stress response genes. fGNPs displayed higher uptake than GNPs in all cell lines with highest internalization by HEp-2, HeLa and Cos-7 cells, in endocytotic vesicles and nuclei. Cytokine ELISA showed that mouse J774 cells exposed to fGNPs produced less IL-6 than did GNP-treated macrophage cells, whereas TNF-α levels were low in both treatment groups. Biodistribution studies in BALB/c mice revealed higher accumulation of fGNPs than GNPs in the liver and spleen. Histopathological analyses showed that fGNP-treated mice accumulated 35 ng/mg tissue and 20 ng/mg tissue gold in spleen and liver respectively, without any adverse effects. Likewise, serum cytokines were low in both GNP- and fGNP-treated mice. Thus, VG-21-conjugated GNPs have enhanced cellular internalization and are suitable for various biomedical applications as nano-conjugates.

Keywords: Cell-penetrating peptide; Drug delivery; Functionalized gold nanoparticles; Vesicular stomatitis virus.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • COS Cells
  • Cell Survival / drug effects
  • Cell-Penetrating Peptides / pharmacokinetics*
  • Chlorocebus aethiops
  • Female
  • Gold / chemistry
  • Gold / pharmacokinetics*
  • HeLa Cells
  • Humans
  • Interleukin-6 / metabolism
  • Membrane Glycoproteins / pharmacokinetics
  • Metal Nanoparticles / chemistry*
  • Mice
  • Mice, Inbred BALB C
  • Microscopy, Electron, Transmission
  • Tissue Distribution
  • Tumor Necrosis Factor-alpha / metabolism
  • Vero Cells
  • Vesiculovirus / metabolism
  • Viral Envelope Proteins / pharmacokinetics

Substances

  • Cell-Penetrating Peptides
  • G protein, vesicular stomatitis virus
  • Interleukin-6
  • Membrane Glycoproteins
  • Tumor Necrosis Factor-alpha
  • Viral Envelope Proteins
  • Gold