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. Author manuscript; available in PMC: 2021 Jun 1.
Published in final edited form as: Expert Opin Drug Discov. 2020 Mar 3;15(6):643–645. doi: 10.1080/17460441.2020.1736031

Figure 1.

Figure 1.

In vitro tissue-engineered models of human skeletal muscle. (a) Components and platforms for engineering human skeletal muscle tissues for drug testing. Free-floating, dynamic culture improves muscle maturation and enables measurement of force–length relationships; micro-tissue platforms allow for high-throughput drug screening in individual muscle tissues; muscle-on-a-chip platforms have microfluidic feeds for interfacing with other organ-on-a-chip systems. MPC, myogenic progenitor cell. (b-c) Transverse (b) and longitudinal (c) sections of cylindrically shaped engineered human skeletal muscles showing viable myotubes throughout the entirety of the tissue; myotubes are aligned and cross-striated as characteristic of native skeletal muscle. SAA, sarcomeric-actinin; F-actin, filamentous actin; DAPI, nuclei. Tissues in b and c are cultured within free-floating frames on a rocker.