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

Adv Biosyst. 2019 Dec;3(12):e1900005. doi: 10.1002/adbi.201900005. Epub 2019 Nov 4.

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.

Keywords: 3D skeletal muscle tissue engineering; EGM-2 supplements; contractile forces; human pluripotent stem cells.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Cell Differentiation* / drug effects
  • Cell Differentiation* / physiology
  • Cells, Cultured
  • Culture Media, Conditioned / chemistry
  • Culture Media, Conditioned / metabolism
  • Culture Media, Conditioned / pharmacology*
  • Human Embryonic Stem Cells / metabolism
  • Humans
  • Muscle Contraction / drug effects
  • Muscle Contraction / physiology
  • Muscle Development* / drug effects
  • Muscle Development* / physiology
  • Muscle Fibers, Skeletal / cytology
  • Muscle, Skeletal* / cytology
  • Muscle, Skeletal* / drug effects
  • Muscle, Skeletal* / physiology
  • Tissue Engineering / methods*
  • Tissue Scaffolds

Substances

  • Culture Media, Conditioned