A Bioprinted Cardiac Patch Composed of Cardiac-Specific Extracellular Matrix and Progenitor Cells for Heart Repair

• Published in: Advanced healthcare materials Vol. 7; no. 23; p. e1800672
• Main Authors: Bejleri, Donald, Streeter, Benjamin W, Nachlas, Aline L Y, Brown, Milton E, Gaetani, Roberto, Christman, Karen L, Davis, Michael E
• Format: Journal Article
• Language: English
• Published: Germany 01.12.2018
• Subjects: Animals; Bioprinting; Cells, Cultured; Elastic Modulus; Extracellular Matrix - metabolism; Gelatin - chemistry; Heart Diseases - pathology; Heart Diseases - therapy; Heart Diseases - veterinary; Humans; Hydrogels - chemistry; Myocardium - cytology; Myocytes, Cardiac - cytology; Printing, Three-Dimensional; Rats; Rats, Sprague-Dawley; Stem Cell Transplantation; Stem Cells - cytology; Stem Cells - metabolism; Tissue Engineering; Tissue Scaffolds; pediatric heart failure; cardiac progenitor cells; cardiac extracellular matrix; bioprinting; cardiac patches
• ISSN: 2192-2659
• DOI: 10.1002/adhm.201800672

Congenital heart defects are present in 8 of 1000 newborns and palliative surgical therapy has increased survival. Despite improved outcomes, many children develop reduced cardiac function and heart failure requiring transplantation. Human cardiac progenitor cell (hCPC) therapy has potential to repair the pediatric myocardium through release of reparative factors, but therapy suffers from limited hCPC retention and functionality. Decellularized cardiac extracellular matrix hydrogel (cECM) improves heart function in animals, and human trials are ongoing. In the present study, a 3D-bioprinted patch containing cECM for delivery of pediatric hCPCs is developed. Cardiac patches are printed with bioinks composed of cECM, hCPCs, and gelatin methacrylate (GelMA). GelMA-cECM bioinks print uniformly with a homogeneous distribution of cECM and hCPCs. hCPCs maintain >75% viability and incorporation of cECM within patches results in a 30-fold increase in cardiogenic gene expression of hCPCs compared to hCPCs grown in pure GelMA patches. Conditioned media from GelMA-cECM patches show increased angiogenic potential (>2-fold) over GelMA alone, as seen by improved endothelial cell tube formation. Finally, patches are retained on rat hearts and show vascularization over 14 d in vivo. This work shows the successful bioprinting and implementation of cECM-hCPC patches for potential use in repairing damaged myocardium.