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Advances in Manufacturing Cardiomyocytes from Human Pluripotent Stem Cells.
Floy, Martha E; Shabnam, Fathima; Simmons, Aaron D; Bhute, Vijesh J; Jin, Gyuhyung; Friedrich, Will A; Steinberg, Alexandra B; Palecek, Sean P.
Afiliación
  • Floy ME; Department of Chemical and Biological Engineering, University of Wisconsin-Madison, Madison, Wisconsin, USA; email: mefloy@wisc.edu, shabnam@wisc.edu, adsimmons2@wisc.edu, wfriedrich@wisc.edu, absteinberg4@wisc.edu, sppalecek@wisc.edu.
  • Shabnam F; Department of Chemical and Biological Engineering, University of Wisconsin-Madison, Madison, Wisconsin, USA; email: mefloy@wisc.edu, shabnam@wisc.edu, adsimmons2@wisc.edu, wfriedrich@wisc.edu, absteinberg4@wisc.edu, sppalecek@wisc.edu.
  • Simmons AD; Department of Chemical and Biological Engineering, University of Wisconsin-Madison, Madison, Wisconsin, USA; email: mefloy@wisc.edu, shabnam@wisc.edu, adsimmons2@wisc.edu, wfriedrich@wisc.edu, absteinberg4@wisc.edu, sppalecek@wisc.edu.
  • Bhute VJ; Department of Medical Genetics, University of Wisconsin-Madison, Madison, Wisconsin, USA.
  • Jin G; Department of Chemical Engineering, Imperial College London, London, United Kingdom; email: v.bhute@imperial.ac.uk.
  • Friedrich WA; Department of Chemical Engineering, Purdue University, West Lafayette, Indiana, USA; email: jin443@purdue.edu.
  • Steinberg AB; Department of Chemical and Biological Engineering, University of Wisconsin-Madison, Madison, Wisconsin, USA; email: mefloy@wisc.edu, shabnam@wisc.edu, adsimmons2@wisc.edu, wfriedrich@wisc.edu, absteinberg4@wisc.edu, sppalecek@wisc.edu.
  • Palecek SP; Department of Chemical and Biological Engineering, University of Wisconsin-Madison, Madison, Wisconsin, USA; email: mefloy@wisc.edu, shabnam@wisc.edu, adsimmons2@wisc.edu, wfriedrich@wisc.edu, absteinberg4@wisc.edu, sppalecek@wisc.edu.
Annu Rev Chem Biomol Eng ; 13: 255-278, 2022 06 10.
Article en En | MEDLINE | ID: mdl-35320695
ABSTRACT
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.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Miocitos Cardíacos / Células Madre Pluripotentes Límite: Humans Idioma: En Revista: Annu Rev Chem Biomol Eng Año: 2022 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Miocitos Cardíacos / Células Madre Pluripotentes Límite: Humans Idioma: En Revista: Annu Rev Chem Biomol Eng Año: 2022 Tipo del documento: Article