Compatibility and function of human induced pluripotent stem cell derived cardiomyocytes on an electrospun nanofibrous scaffold, generated from an ionomeric polyurethane composite. Issue 12 (19th July 2022)

• Record Type: Journal Article
• Authors: Chen, Yizhou; Chan, Jennifer P. Y.; Wu, Jun; Li, Ren‐Ke; Santerre, J. Paul
• Is Part Of: Journal of biomedical materials research. Volume 110:Issue 12(2022)
• Page Start: 1932
• Page End: 1943
• Publication Date: 2022-07-19
• Subjects: cardiac tissue engineering -- electrospun scaffold -- hiPSC derived cardiomyocytes -- ionomeric polyurethane; Biomedical materials -- Periodicals; 610.28
• DOI: 10.1002/jbm.a.37428
• Languages: English
• ISSNs: 1549-3296

Abstract

Abstract: Synthetic scaffolds are needed for generating organized neo‐myocardium constructs to promote functional tissue repair. This study investigated the biocompatibility of an elastomeric electrospun degradable polar/hydrophobic/ionic polyurethane (D‐PHI) composite scaffold with human‐induced pluripotent stem cell‐derived cardiomyocytes (hiPSC‐CMs). The composite material was electrospun to generate scaffolds, with nanofibres oriented in aligned or random directions. These features enabled the authors to evaluate the effect of characteristic elements which mimic that of the native extracellular matrix (alignment, chemical heterogeneity, and fiber topography) on hiPSC‐CMs activity. The functional nature of the hiPSC‐CM cultured on gelatin and Matrigel‐coated scaffolds were assessed, investigating the influence of protein interactions with the synthetic substrate on subsequent cell phenotype. After 7 days of culture, high hiPSC‐CM viability was observed on the scaffolds. The cells on the aligned scaffold were elongated and demonstrated aligned sarcomeres that oriented parallel to the direction of the fibers, while the cells on random scaffolds and a tissue culture polystyrene (TCPS) control did not exhibit such an organized morphology. The hiPSC‐CMs cultured on the scaffolds and TCPS expressed similar levels of cardiac troponin‐T, but there was a higher expression of ventricular myosin light chain‐2 on the D‐PHI composite scaffolds versus TCPS, indicating a higher proportion of hiPSC‐CM exhibiting a ventricular cardiomyocyte like phenotype. Within 7 days, the hiPSC‐CMs on aligned scaffolds and TCPS beat synchronously and had similar conductive velocities. These preliminary results show that aligned D‐PHI elastomeric scaffolds allow hiPSC‐CMs to demonstrate important cardiomyocytes characteristics, critical to enabling their future potential use for cardiac tissue regeneration.