Myocardial infarction (MI) often results in significant damage to heart tissues, leading to cardiac dysfunction, fibrosis, and diminished cell-cell communication. Exosomes (EXOs) from stem cells show great potential in promoting tissue repair and angiogenesis, but their rapid clearance and degradation in vivo limit therapeutic efficacy. Here, we introduce a 3D-printed in vitro scaffold using a conductive biomaterial ink composed of chitosan (CS) and polyaniline (PANI). This scaffold combines the bioactivity of EXOs with the conductive properties of PANI to protect cardiac cells under ischemic stress. Using an in vitro hypoxia/reoxygenation (H/R) model with HL-1 cardiomyocytes, we simulated key aspects of myocardial ischemia-reperfusion injury. The addition of PANI improved the electrical conductivity of the scaffold, which was essential for enhancing cardiomyocyte viability and intercellular connectivity under hypoxic conditions. EXOs significantly promoted angiogenic activity in vitro, as evidenced by enhanced human umbilical vein endothelial cell (HUVEC) migration and robust tube formation, highlighting their role in stimulating new blood vessel growth. Molecular analyses revealed that EXOs positively influence processes such as angiogenesis and inflammation regulation in HL-1 cells. Additionally, EXOs improved HUVEC migration, emphasizing their pro-angiogenic role. These findings indicate that combining PANI and EXOs in a 3D-printed scaffold yields synergistic benefits, improving cardiomyocyte function and promoting endothelial angiogenesis in vitro, thereby providing insights for future cardiac repair strategies.

• Publikační typ
• časopisecké články MeSH

Regenerating skin tissue remains a major challenge in medical science, especially due to the risk of scarring and prolonged healing, which becomes even more complicated in people with diabetes. Recent advancements have led to the creation of therapeutic dressings incorporating drug-delivery systems to tackle these issues. Exosomes (Exos) derived from mesenchymal stem cells (MSCs) have gained significant attention for mediating therapy without directly using cells, thanks to their natural anti-inflammatory and tissue repair properties mirroring those of MSCs. In this study, an advanced wound dressing combines chitosan (CS) and polyethylene glycol (PEG) hydrogel with adipose MSCs-derived Exos (ADMSCs-Exos). This composite, formed using a straightforward blending technique, is engineered to improve the healing process of severe skin injuries by steadily releasing Exos as the hydrogel degrades. The in vitro studies demonstrate that this hydrogel-exosome dressing greatly enhances endothelial cell migration, reduces oxidative stress, and promotes angiogenesis, crucial for effective wound healing. Additionally, real time-polymerase chain reaction (RT-PCR) analysis revealed significant upregulation of key genes involved in these processes, supporting the therapeutic potential of the hydrogel-Exo combination. These findings emphasize the potential of this hydrogel-Exos combination as an innovative and promising solution for advanced wound care.

• Klíčová slova
• angiogenesis, cell migration, chitosan‐polyethylene glycol hydrogel, mesenchymal stem cells derived exosomes, wound healing,
• MeSH
• chitosan * chemie   farmakologie   MeSH
• endoteliální buňky pupečníkové žíly (lidské) metabolismus   MeSH
• exozómy * metabolismus   chemie   MeSH
• hojení ran * účinky léků   MeSH
• hydrogely * chemie   farmakologie   MeSH
• lidé MeSH
• mezenchymální kmenové buňky * metabolismus   cytologie   MeSH
• pohyb buněk účinky léků   MeSH
• polyethylenglykoly * chemie   farmakologie   MeSH
• zvířata MeSH
• Check Tag
• lidé MeSH
• zvířata MeSH
• Publikační typ
• časopisecké články MeSH
• Názvy látek
• chitosan * MeSH
• hydrogely * MeSH
• polyethylenglykoly * MeSH