Advances in Manufacturing Cardiomyocytes from Human Pluripotent Stem Cells

被引:9
作者
Floy, Martha E. [1 ]
Shabnam, Fathima [1 ]
Simmons, Aaron D. [1 ]
Bhute, Vijesh J. [2 ,3 ]
Jin, Gyuhyung [4 ]
Friedrich, Will A. [1 ]
Steinberg, Alexandra B. [1 ]
Palecek, Sean P. [1 ]
机构
[1] Univ Wisconsin, Dept Chem & Biol Engn, Madison, WI 53706 USA
[2] Univ Wisconsin, Dept Med Genet, Madison, WI 53706 USA
[3] Imperial Coll London, Dept Chem Engn, London, England
[4] Purdue Univ, Dept Chem Engn, W Lafayette, IN 47907 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
hPSC; cardiomyocytes; manufacturing; stem cells; human pluripotent stem cells; scale-up; quality attributes; bioreactors; ENGINEERED HEART-TISSUE; CARDIAC DIFFERENTIATION; ELECTROPHYSIOLOGIC CHARACTERISTICS; FUNCTIONAL MATURATION; IN-VITRO; REVEALS; CULTURE; PURIFICATION; GENERATION; ENRICHMENT;
D O I
10.1146/annurev-chembioeng-092120-033922
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The emergence of human pluripotent stem cell (hPSC) technology over the past two decades has provided a source of normal and diseased human cells for a wide variety of in vitro and in vivo applications. Notably, hPSC-derived cardiomyocytes (hPSC-CMs) are widely used to model human heart development and disease and are in clinical trials for treating heart disease. The success of hPSC-CMs in these applications requires robust, scalable approaches to manufacture large numbers of safe and potent cells. Although significant advances have been made over the past decade in improving the purity and yield of hPSC-CMs and scaling the differentiation process from 2D to 3D, efforts to induce maturation phenotypes during manufacturing have been slow. Process monitoring and closed-loop manufacturing strategies are just being developed. We discuss recent advances in hPSC-CM manufacturing, including differentiation process development and scaling and downstream processes as well as separation and stabilization.
引用
收藏
页码:255 / 278
页数:24
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