Functionally Mature Bioengineered Human Skeletal Muscle Tissues Capture Essential Aspects of Glucose Metabolism

Henriquez-Olguin, C.; Hojfeldt, M. K.; Lewis, C. T. A.; Birk, J. B.; Wang, T.; Li, Z.; Jensen, P.; Clemmens, P. L. B.; Hansen, B. F.; Meneses-Valdes, R.; Toledo, E.; Hogan, J.; Wang, Z.; Segeritz, C.-P.; Wojtaszewski, J. F. P.; Jensen, T. E.; Blois, A.; Pehmoller, C.; Knudsen, J. R.

doi:10.64898/2026.01.16.698404

bioRxiv · 10.64898/2026.01.16.698404

Functionally Mature Bioengineered Human Skeletal Muscle Tissues Capture Essential Aspects of Glucose Metabolism

Henriquez-Olguin, C.·Hojfeldt, M. K.·Lewis, C. T. A.·Birk, J. B.·Wang, T.·Li, Z.·Jensen, P.·Clemmens, P. L. B.·Hansen, B. F.·Meneses-Valdes, R.·Toledo, E.·Hogan, J.·Wang, Z.·Segeritz, C.-P.·Wojtaszewski, J. F. P.·Jensen, T. E.·Blois, A.·Pehmoller, C.·Knudsen, J. R.

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Abstract

Human skeletal muscle is a major regulator of whole-body metabolic homeostasis, yet mechanistic insight into human muscle plasticity is limited by the lack of in vitro models with adult-like metabolic and functional maturity. Here, we develop a workflow for generating bioengineered human skeletal muscle tissues that undergo coordinated structural, molecular, and functional maturation and stabilize in an adult-like state by day 21. Time-resolved RNA-seq and protein profiling reveal consolidation of contractile programs alongside progressive metabolic maturation, including increased mitochondrial electron transport chain content, mature mitochondrial network organization, and upregulation of glucose- and glycogen-handling proteins as well as muscle-enriched AMPK isoforms. Functionally, the tissues develop physiological force-frequency behavior, post-tetanic potentiation, and reproducible fatigue responses that are exacerbated by hypoxia and glucose withdrawal. Exercise-like chronic stimulation increases force and endurance with hypertrophy-like remodeling, and these adaptations reverse with detraining. The model also captures pharmacological responsiveness. {beta}2-adrenergic stimulation activates canonical signaling, increases force, limits disuse-related decline, and improves endurance in a glucose-dependent manner. Under physiological insulin and IGF-1 conditions, tissues show robust insulin-stimulated glucose uptake and glycogen synthesis, with punctate glucose transporter 4 (GLUT4) localization. Finally, knockdown of muscle glycogen synthase (GYS1) preserves peak tetanic force but impairs endurance and force recovery under fuel stress, indicating that glycogen metabolism is a key determinant of human muscle resilience.

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Henriquez-Olguin, C., Hojfeldt, M. K., Lewis, C. T. A., Birk, J. B., Wang, T., Li, Z., Jensen, P., Clemmens, P. L. B., Hansen, B. F., Meneses-Valdes, R., Toledo, E., Hogan, J., Wang, Z., Segeritz, C.-P., Wojtaszewski, J. F. P., Jensen, T. E., Blois, A., Pehmoller, C., Knudsen, J. R.. 2026-01-16. Functionally Mature Bioengineered Human Skeletal Muscle Tissues Capture Essential Aspects of Glucose Metabolism. https://doi.org/10.64898/2026.01.16.698404

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