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Published on: March 15, 2016
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.
Abstract:
Coronary artery disease remains one of the primary healthcare problems due to the high cost of treatment, increased number of patients, poor clinical outcomes, and lack of effective therapy. Though pharmacological and surgical treatments positively affect symptoms and arrest the disease progression, they generally exhibit a limited effect on the disease outcome. The development of alternative therapeutic approaches towards ischemic disease treatment, especially of decompensated forms, is therefore relevant. Therapeutic angiogenesis, stimulated by various cytokines, chemokines, and growth factors, provides the possibility of restoring functional blood flow in ischemic tissues, thereby ensuring the regeneration of the damaged area. In the current study, based on the clinically approved plasmid vector pVax1, multigenic constructs were developed encoding vascular endothelial growth factor (VEGF), fibroblast growth factors (FGF2), and the DsRed fluorescent protein, integrated via picornaviruses' furin-2A peptide sequences. In vitro experiments demonstrated that genetically modified cells with engineered plasmid constructs expressed the target proteins. Overexpression of VEGF and FGF2 resulted in increased levels of the recombinant proteins. Concomitantly, these did not lead to a significant shift in the general secretory profile of modified HEK293T cells. Simultaneously, the secretome of genetically modified cells showed significant stimulating effects on the formation of capillary-like structures by HUVEC (endothelial cells) in vitro. Our results revealed that when the multicistronic multigene vectors encoding 2A peptide sequences are created, transient transgene co-expression is ensured. The results obtained indicated the mutual synergistic effects of the growth factors VEGF and FGF2 on the proliferation of endothelial cells in vitro. Thus, recombinant multicistronic multigenic constructs might serve as a promising approach for establishing safe and effective systems to treat ischemic diseases.
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