Abstract
Mesenchymal stem cells (MSC) are potentially a good material for transplantation in many diseases, including neurodegenerative diseases. The main problem with using them is the low percentage of surviving cells after the transplant procedure and the naturally poor ability of MSC to spontaneously differentiate into certain types of cells, which results in their poor integration with the host cells. The aim and the novelty of this work consists in the synergistic overexpression of two genes, BCL2 and BDNF, using lentiviral vectors. According to our hypothesis, the overexpression of the BCL2 gene is aimed at increasing the resistance of cells to stressors and toxic factors. In turn, the overexpression of the BDNF gene is suspected to direct the MSC into the neural differentiation pathway. As a result, it was shown that the overexpression of both genes and the overproduction of proteins is permanent and persists for at least 60 days. The synergistically transduced MSC were significantly more resistant to the action of staurosporine; 12 days after transduction, the synergistically transduced MSC had a six-times greater survival rate. The overexpression of the Bcl-2 and BDNF proteins was sufficient to stimulate a significant overexpression of the CHAT gene, and under specific conditions, the TH, TPH1, and SYP genes were also overexpressed. Modified MSC are able to differentiate into cholinergic and dopaminergic neurons, and the release of acetylcholine and dopamine may indicate their functionality.
Highlights
Mesenchymal stem cells (MSC) have great potential when it comes to using them in regenerative medicine, in cell therapy [1,2,3]
The study group was transduced with a pair of LeGO-iG2-Bcl-2 and LeGO-iT2BDNF vectors in order to undergo a synergistic overexpression (Figure 2C,D)
The addition of bFGF or resveratrol was investigated, and the group was indicated as full vectors (FV) + bFGF or FV + resveratrol
Summary
Mesenchymal stem cells (MSC) have great potential when it comes to using them in regenerative medicine, in cell therapy [1,2,3]. A big advantage of MSC is the fact that they are isolated from various tissues, from Wharton’s Jelly (WJ-MSC) among others; they have a low tumorigenic potential and are characterized by a high degree of plasticity [6]. Their low expression of MHC molecules makes it possible to use them in allogeneic transplants [7,8]. MSC differentiate into the different cell types from all three germ layers [6,9,10].
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