Engineered Vesicles and Hydrogel Technologies for Myocardial Regeneration.
Kaitlyn GhassemiKeiko InouyeTatevik TakhmazyanVictor BonavidaJia-Wei YangNatan Roberto de BarrosFinosh G ThankamPublished in: Gels (Basel, Switzerland) (2023)
Increased prevalence of cardiovascular disease and potentially life-threatening complications of myocardial infarction (MI) has led to emerging therapeutic approaches focusing on myocardial regeneration and restoration of physiologic function following infarction. Extracellular vesicle (EV) technology has gained attention owing to the biological potential to modulate cellular immune responses and promote the repair of damaged tissue. Also, EVs are involved in local and distant cellular communication following damage and play an important role in initiating the repair process. Vesicles derived from stem cells and cardiomyocytes (CM) are of particular interest due to their ability to promote cell growth, proliferation, and angiogenesis following MI. Although a promising candidate for myocardial repair, EV technology is limited by the short retention time of vesicles and rapid elimination by the body. There have been several successful attempts to address this shortcoming, which includes hydrogel technology for the sustained bioavailability of EVs. This review discusses and summarizes current understanding regarding EV technology in the context of myocardial repair.
Keyphrases
- stem cells
- left ventricular
- cardiovascular disease
- wound healing
- immune response
- drug delivery
- risk factors
- heart failure
- type diabetes
- endothelial cells
- signaling pathway
- lymph node
- hyaluronic acid
- working memory
- vascular endothelial growth factor
- bone marrow
- tissue engineering
- atrial fibrillation
- inflammatory response
- climate change