Biological Evaluation of Thermosensitive Hydrogels of Chitosan/Hydrolyzed Collagen/β-GP in an In Vitro Model of Induced Cardiac Ischemia.
Lina Orozco MarínYulieth MontoyaJohn BustamantePublished in: Polymers (2024)
Ischemic events can culminate in acute myocardial infarction, which is generated by irreversible cardiac lesions that cannot be restored due to the limited regenerative capacity of the heart. Cardiac cell therapy aims to replace injured or necrotic cells with healthy and functional cells. Tissue engineering and cardiovascular regenerative medicine propose therapeutic alternatives using biomaterials that mimic the native extracellular environment and improve cellular and tissue functionality. This investigation evaluates the effect of thermosensitive hydrogels, and murine fetal ventricular cardiomyocytes encapsulated in thermosensitive hydrogels, on the contractile function of cardiomyocyte regeneration during an ischemic event. Chitosan and hydrolyzed collagen thermosensitive hydrogels were developed, and they were physically and chemically characterized. Likewise, their biocompatibility was evaluated through cytotoxicity assays by MTT, LDH, and their hemolytic capacity. The hydrogels, and cells inside the hydrogels, were used as an intervention for primary cardiomyocytes under hypoxic conditions to determine the restoration of the contractile capacity by measuring intracellular calcium levels and the expressions of binding proteins, such as a-actinin and connexin 43. These results evidence the potential of natural thermosensitive hydrogels to restore the bioelectrical functionality of ischemic cardiomyocytes.
Keyphrases
- tissue engineering
- wound healing
- induced apoptosis
- drug delivery
- hyaluronic acid
- cell therapy
- left ventricular
- cell cycle arrest
- acute myocardial infarction
- high glucose
- stem cells
- endoplasmic reticulum stress
- extracellular matrix
- drug release
- magnetic resonance imaging
- ischemia reperfusion injury
- body composition
- acute coronary syndrome
- mesenchymal stem cells
- subarachnoid hemorrhage
- cerebral ischemia
- bone marrow
- risk assessment
- atrial fibrillation
- stress induced
- climate change
- drug induced
- diabetic rats
- cell proliferation
- high throughput