Heart Institute, University of South Florida, Tampa, FL 33602, USA.
Department of Internal Medicine, University of South Florida, Tampa, FL 33602, USA.
Cells. 2024 Jan 29;13(3):250. doi: 10.3390/cells13030250.
The human heart lacks significant regenerative capacity; thus, the solution to heart failure (HF) remains organ donation, requiring surgery and immunosuppression. The demand for constructed cardiac tissues (CCTs) to model and treat disease continues to grow. Recent advances in induced pluripotent stem cell (iPSC) manipulation, CRISPR gene editing, and 3D tissue culture have enabled a boom in iPSC-derived CCTs (iPSC-CCTs) with diverse cell types and architecture. Compared with 2D-cultured cells, iPSC-CCTs better recapitulate heart biology, demonstrating the potential to advance organ modeling, drug discovery, and regenerative medicine, though iPSC-CCTs could benefit from better methods to faithfully mimic heart physiology and electrophysiology. Here, we summarize advances in iPSC-CCTs and future developments in the vascularization, immunization, and maturation of iPSC-CCTs for study and therapy.
人类心脏缺乏显著的再生能力;因此,心力衰竭(HF)的解决方案仍然是器官捐献,这需要手术和免疫抑制。对用于模拟和治疗疾病的构建型心脏组织(CCT)的需求持续增长。诱导多能干细胞(iPSC)操作、CRISPR 基因编辑和 3D 组织培养方面的最新进展,使得具有不同细胞类型和结构的 iPSC 衍生的 CCT(iPSC-CCT)蓬勃发展。与 2D 培养的细胞相比,iPSC-CCT 更好地再现了心脏生物学,具有推进器官建模、药物发现和再生医学的潜力,尽管 iPSC-CCT 可以通过更好的方法来真实模拟心脏生理学和电生理学而受益。在这里,我们总结了 iPSC-CCT 的进展以及 iPSC-CCT 的血管化、免疫和成熟方面的未来发展,用于研究和治疗。