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人诱导多能干细胞衍生心肌细胞的代谢成熟:诱导成年心脏表型的新兴策略

Metabolic Maturation in hiPSC-Derived Cardiomyocytes: Emerging Strategies for Inducing the Adult Cardiac Phenotype.

作者信息

Malan Daniela, Gallo Maria Pia, Geddo Federica, Levi Renzo, Querio Giulia

机构信息

Institute of Physiology I, Medical Faculty, University of Bonn, 53127 Bonn, Germany.

Department of Life Sciences and Systems Biology, University of Turin, Via Accademia Albertina 13, 10123 Turin, Italy.

出版信息

Pharmaceuticals (Basel). 2025 Jul 29;18(8):1133. doi: 10.3390/ph18081133.

Abstract

Human induced pluripotent stem cells (hiPSCs) are widely used in basic research because of their versatility and ability to differentiate into multiple cell types. In particular, differentiating hiPSCs into cardiac cells (hiPSC-CMs) has been an important milestone in cardiac pathophysiology studies. Although hiPSC-CMs offer a model for human cardiomyocytes, they still exhibit characteristics linked to the fetal cardiac cell phenotype. One important feature that prevents hiPSC-CMs from being identified as adult cells relates to their metabolism, which is a key factor in defining a mature phenotype capable of sustaining the workload requirements characteristic of fully differentiated cardiomyocytes. This review aims to present the most relevant strategies in terms of culture medium composition, culture times, and 3D culture methods that have been developed to promote the metabolic maturation of hiPSC-CMs, which are now widely used. Defining a standardized and universally accepted protocol would enable the creation of a cellular model for studies of cardiac pathophysiology from a patient-specific perspective and for drug screening.

摘要

人类诱导多能干细胞(hiPSC)因其多功能性和分化为多种细胞类型的能力而被广泛应用于基础研究。特别是,将hiPSC分化为心肌细胞(hiPSC-CM)已成为心脏病理生理学研究中的一个重要里程碑。尽管hiPSC-CM为人类心肌细胞提供了一个模型,但它们仍表现出与胎儿心脏细胞表型相关的特征。阻碍hiPSC-CM被认定为成熟细胞的一个重要特征与其代谢有关,代谢是定义能够维持完全分化心肌细胞特征性工作负荷要求的成熟表型的关键因素。本综述旨在介绍在培养基组成、培养时间和3D培养方法方面已开发出的最相关策略,这些策略用于促进hiPSC-CM的代谢成熟,目前已被广泛应用。定义一个标准化且被普遍接受的方案将能够从患者特异性角度创建一个用于心脏病理生理学研究和药物筛选的细胞模型。

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