Key result
Intramyocardial injection of a plasmid encoding PDGFBB after experimental myocardial infarction significantly increased the number of extravascular NG2-positive pericytes to 19.5 cells per field compared to 11.2 with saline.
Why the study?
Increasing ischemic disease rates and limited treatment options prompt interest in novel vascularization approaches, such as gene therapy activating the epicardium to generate vascular precursors and promote vessel assembly.
Absolute Event Rate: 19.5% vs 11.2%
p-value: p=<0.05
Intramyocardial injection of a plasmid encoding PDGFBB after experimental myocardial infarction stimulates arteriogenesis and pericyte migration in the peri-infarct zone, potentially via epicardial cell activation.
Gene therapy for epicardial activation may promote post-MI vascularization; leaves open clinical efficacy and safety.
Increasing incidence of ischemic diseases and limited resources for their treatment stimulate increased interest in studying the mechanisms of vascularization and finding new approaches for its promotion. One of these approaches is gene therapy aimed at activating the epicardium to produce the vascular precursor cells and microenvironment for the «assembly» of de novo vessels. The aim is to investigate the possibility of activating epicardial cells and post infarction cardiac vascularization by injecting a genetic construct encoding PDGFBB. Material and methods . A model of experimental myocardial infarction in a rat with subsequent intramyocardial injection of normal saline solution, control plasmid and plasmid encoding PDGFBB was used. The study of PDGFBB effect on epicardial cell activity was performed on the ex vivo model, as well as in vitro mesothelial cell culture. Results . Post infarction injection of plasmid encoding PDGFBB increases the density of the vascular network in the peri-infarct area as well as migration of pericytes to the injured zone. PDGFBB promotes activation of epicardial cell pool and expression of smooth muscle cell markers in them (shown on the ex vivo model), as well as stimulates activation of epithelial-mesenchymal transition (in vitro). Conclusion . Intramyocardial injection of a genetic construct encoding PDGFBB after an experimental myocardial infarction stimulated vascularization of the peri-infarction zone, which may have been partially due to the activation of the epicardial cell pool.
No takes yet. Share an insight, caveat, or question.
Дергилев et al. (2021) studied Experimental myocardial infarction. Plasmid encoding PDGFBB (pVAX1-PDGF-Bopt) vs. Normal saline solution and empty plasmid pVAX1 was evaluated on Number of extravascular NG2-positive cells (pericytes) per vision field in the myocardium (p=<0.05). Intramyocardial injection of a plasmid encoding PDGFBB after experimental myocardial infarction significantly increased the number of extravascular NG2-positive pericytes to 19.5 cells per field compared to 11.2 with saline.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: