Proangiogenic Effect of 2A-Peptide Based Multicistronic Recombinant Constructs Encoding VEGF and FGF2 Growth Factors

Dilara Z Gatina1, Ekaterina E Garanina1, Margarita N Zhuravleva1

  • 1Institute of Fundamental Medicine and Biology, Kazan Federal University, 420008 Kazan, Russia.

Insights

New gene therapy vectors using vascular endothelial growth factor (VEGF) and fibroblast growth factor 2 (FGF2) show promise for treating ischemic diseases by promoting blood vessel formation. These constructs enhance endothelial cell proliferation, offering a potential new therapeutic avenue.

Area of Science:

  • Biotechnology
  • Molecular Biology
  • Regenerative Medicine

Background:

  • Coronary artery disease presents a significant healthcare challenge due to high costs, patient numbers, poor outcomes, and limited effective therapies.
  • Current pharmacological and surgical treatments offer symptomatic relief but have a limited impact on overall disease outcomes.
  • Alternative therapeutic strategies for ischemic diseases, particularly decompensated forms, are urgently needed.

Purpose of the Study:

  • To develop novel multigenic vectors for therapeutic angiogenesis to treat ischemic diseases.
  • To engineer plasmid constructs encoding vascular endothelial growth factor (VEGF) and fibroblast growth factor 2 (FGF2) using picornavirus 2A peptide sequences.
  • To evaluate the expression and functional effects of these engineered constructs in vitro.

Main Methods:

  • Development of a multigenic plasmid vector (pVax1-based) encoding VEGF, FGF2, and DsRed using picornavirus 2A peptide sequences.
  • In vitro assessment of protein expression in genetically modified HEK293T cells.
  • Analysis of the secretome from modified cells for effects on human umbilical vein endothelial cell (HUVEC) capillary-like structure formation.

Main Results:

  • Genetically modified cells successfully expressed target proteins (VEGF, FGF2, DsRed) with increased recombinant protein levels.
  • The secretome of modified cells significantly stimulated capillary-like structure formation by HUVECs in vitro.
  • Co-expression of VEGF and FGF2 demonstrated synergistic effects on endothelial cell proliferation.

Conclusions:

  • Recombinant multicistronic multigenic vectors ensure transient transgene co-expression.
  • The combination of VEGF and FGF2 via these vectors shows synergistic effects on endothelial cell proliferation.
  • These engineered constructs represent a promising approach for developing safe and effective treatments for ischemic diseases.