Kahn-Krell Asher, Pretorius Danielle, Guragain Bijay, Lou Xi, Wei Yuhua, Zhang Jianhua, Qiao Aijun, Nakada Yuji, Kamp Timothy J, Ye Lei, Zhang Jianyi
Department of Biomedical Engineering, School of Medicine and School of Engineering, University of Alabama at Birmingham, Birmingham, AL, United States.
Department of Medicine, School of Medicine and Public Health, University of Wisconsin-Madison, Madison, WI, United States.
Front Bioeng Biotechnol. 2022 Jul 22;10:908848. doi: 10.3389/fbioe.2022.908848. eCollection 2022.
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 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.
从人诱导多能干细胞(hiPSC)分化而来的心肌细胞(CM)、内皮细胞(EC)、平滑肌细胞(SMC)和心脏成纤维细胞(CF)是基于细胞的再生心肌治疗的基本组成部分,可作为机制研究和药物测试的模型。然而,新分化的hiPSC-CM往往更类似于胎儿CM,而不是成年心脏的成熟CM,目前改善CM成熟度的技术既复杂又费力。因此,用于商业和工业应用的CM生产将需要更基本的方法来促进CM成熟。当在三维(3D)环境中作为球体培养时,CM往往会形成更成熟的表型,而不是作为二维单层培养,并且EC、SMC和CF的活性促进CM成熟和电活动。在这里,我们介绍了一种基于3D培养的简单且可重复的方法,用于生成包含所有四种心脏细胞类型的球体(即心脏球体),该方法与广泛的应用和研究设备兼容。随后的实验表明,加入血管细胞和CF与球体大小增加、细胞凋亡减少、肌节成熟改善以及CM生物能量学变化有关。