Maturing differentiated human pluripotent stem cells in vitro: methods and challenges

被引:19
作者
Ottaviani, Daniele [1 ,5 ]
ter Huurne, Menno [2 ,3 ]
Elliott, David A. [2 ,3 ]
Bellin, Milena [1 ,3 ,4 ,5 ]
Mummery, Christine L. [3 ,4 ,6 ]
机构
[1] Univ Padua, Dept Biol, I-35131 Padua, Italy
[2] Murdoch Childrens Res Inst, Melbourne 3052, Australia
[3] Novo Nord Fdn, Ctr Stem Cell Med reNEW, DK-2200 Copenhagen, Denmark
[4] Leiden Univ, Dept Anat & Embryol, Med Ctr, NL-2333 ZC Leiden, Netherlands
[5] Veneto Inst Mol Med, I-35129 Padua, Italy
[6] Univ Twente, Dept Appl Stem Cell Technol, NL-7522 Enschede, Netherlands
来源
DEVELOPMENT | 2023年 / 150卷 / 11期
基金
欧洲研究理事会;
关键词
hiPSC-derived cardiomyocytes; Cardiac maturation; Cardiac organoids; Engineered heart tissue; Cardiac microtissues; CARDIOMYOCYTE MATURATION; ORGANOIDS; DISEASE; ADULT; PROLIFERATION; CONTRACTILITY; CONTRIBUTES; METABOLISM; RESOLUTION; EXPRESSION;
D O I
10.1242/dev.201103
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Human pluripotent stem cells (hPSCs), derived from individuals or genetically modified with disease-related mutations and variants, have revolutionised studies of human disease. Researchers are beginning to exploit the extraordinary potential of stem cell technology to screen for new drugs to treat intractable diseases, ideally without side -effects. However, a major problem is that the differentiated cell types on which these models are based are immature; they resemble fetal and not adult cells. Here, we discuss the nature and hurdles of hPSC maturation, using cardiomyocytes as an example. We review methods used to induce cardiomyocyte maturation in culture and consider remaining challenges for their integration into research on human disease and drug development pipelines.
引用
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页数:9
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