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Skeletal Muscle Constructs Engineered from Human Embryonic Stem Cell Derived Myogenic Progenitors Exhibit Enhanced Contractile Forces When Differentiated in a Medium Containing EGM‐2 Supplements

Bin Xu

Department of Biomedical Engineering, University of Minnesota, Minneapolis, MN, 55455 USA

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Mengen Zhang

Department of Biomedical Engineering, University of Minnesota, Minneapolis, MN, 55455 USA

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Rita C. R. Perlingeiro

Department of Medicine, University of Minnesota, Minneapolis, MN, 55455 USA

Stem Cell Institute and Institute for Engineering in Medicine, University of Minnesota, Minneapolis, Minnesota, 55455 USA

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Wei Shen

Corresponding Author

E-mail address: shenx104@umn.edu

Department of Biomedical Engineering, University of Minnesota, Minneapolis, MN, 55455 USA

Stem Cell Institute and Institute for Engineering in Medicine, University of Minnesota, Minneapolis, Minnesota, 55455 USA

E‐mail: shenx104@umn.eduSearch for more papers by this author
First published: 04 November 2019
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Abstract

Three‐dimensional (3D) skeletal muscle constructs engineered from myogenic progenitors derived from human pluripotent stem cells (hPSCs) have a wide range of applications, but to date, such constructs generate lower specific tetanic force than adult human muscles. Methods enhancing functional muscle differentiation and force generation of these constructs are highly desirable. The finding of this study is that addition of the supplements in the endothelial cell growth medium‐2 (EGM‐2) to the myogenic differentiation medium can substantially enhance contractile force generation. For constructs differentiated for 4 weeks, addition of the EGM‐2 supplements in the first 2 weeks leads to tenfold and sevenfold increases in twitch and tetanic forces, respectively. The specific tetanic force generated by these constructs is 33 mN mm−2, which is significantly higher than previously reported. These constructs show wider myotubes and higher gene expression levels for all skeletal muscle‐specific myosin heavy chain isoforms, suggesting that a more mature differentiation stage of the cells underlies the greater contractile force generation. The constructs exposed to these supplements for 4 weeks do not generate as high contractile forces, suggesting that prolonged treatment is not beneficial. These results suggest that temporal conditioning with the EGM‐2 supplements assists functional development of hPSC‐derived skeletal muscle constructs.

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