Author:
Kahn-Krell Asher,Pretorius Danielle,Guragain Bijay,Lou Xi,Wei Yuhua,Zhang Jianhua,Qiao Aijun,Nakada Yuji,Kamp Timothy J.,Ye Lei,Zhang Jianyi
Abstract
Cardiomyocytes (CMs), endothelial cells (ECs), smooth-muscle cells (SMCs), and cardiac fibroblasts (CFs) differentiated from human induced-pluripotent stem cells (hiPSCs) are the fundamental components of cell-based regenerative myocardial therapy and can be used as in-vitro models for mechanistic studies and drug testing. However, newly differentiated hiPSC-CMs tend to more closely resemble fetal CMs than the mature CMs of adult hearts, and current techniques for improving CM maturation can be both complex and labor-intensive. Thus, the production of CMs for commercial and industrial applications will require more elementary methods for promoting CM maturity. CMs tend to develop a more mature phenotype when cultured as spheroids in a three-dimensional (3D) environment, rather than as two-dimensional monolayers, and the activity of ECs, SMCs, and CFs promote both CM maturation and electrical activity. Here, we introduce a simple and reproducible 3D-culture–based process for generating spheroids containing all four cardiac-cell types (i.e., cardiac spheroids) that is compatible with a wide range of applications and research equipment. Subsequent experiments demonstrated that the inclusion of vascular cells and CFs was associated with an increase in spheroid size, a decline in apoptosis, an improvement in sarcomere maturation and a change in CM bioenergetics.
Funder
National Heart, Lung, and Blood Institute
American Heart Association
National Institute of General Medical Sciences
National Institute of Biomedical Imaging and Bioengineering
Subject
Biomedical Engineering,Histology,Bioengineering,Biotechnology
Cited by
25 articles.
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