Understanding muscle responses to external stimuli is critical for advancing therapeutic strategies and vaccine delivery, yet human-based models remain limited. To emulate muscle responses to immunological and delivery-related stimuli in vitro, we developed a human 3D muscle-like tissue model. Upon exposure to immunostimulatory agents, the system supported the recruitment and modulation of antigen-presenting cells, including monocytes and macrophages, while stromal elements promoted dendritic cell expansion and activation. To further explore muscle responses to delivery stimuli, we assessed the internalization and modulatory effects of solid lipid nanoparticles (SLN) and poly(lactic-co-glycolic acid) (PLGA) nanoparticles within the 3D muscle constructs. Both nanoparticle types were progressively internalized by myofibers, exhibiting distinct localization and accumulation near nuclei. Additionally, we tested the capability of SLN and PLGA nanoparticles to modulate inflammatory cytokines (IL-1β, IL-6, TNF-α) under inflammatory stimulation, indicating their potential for controlled delivery and local immune modulation within muscle tissue. In summary, this human 3D muscle-based in vitro model effectively emulates muscle responses to immunological and delivery stimuli, offering a versatile platform to study muscle immunobiology and evaluate advanced delivery strategies, while reducing the reliance on animal models in preclinical research.
In vitro study emulating muscle response to stimuli exploiting 3D tissue model / Guarnaccia, E., De Paolis, F., Deodati, R., Corci, B., Maretti, E., Molinari, S., Fuoco, C., Gargioli., C.. - (2025). (22nd IIM Meeting Assisi 11-14 September 2025).
In vitro study emulating muscle response to stimuli exploiting 3D tissue model
Eleonora Maretti;Susanna Molinari;
2025
Abstract
Understanding muscle responses to external stimuli is critical for advancing therapeutic strategies and vaccine delivery, yet human-based models remain limited. To emulate muscle responses to immunological and delivery-related stimuli in vitro, we developed a human 3D muscle-like tissue model. Upon exposure to immunostimulatory agents, the system supported the recruitment and modulation of antigen-presenting cells, including monocytes and macrophages, while stromal elements promoted dendritic cell expansion and activation. To further explore muscle responses to delivery stimuli, we assessed the internalization and modulatory effects of solid lipid nanoparticles (SLN) and poly(lactic-co-glycolic acid) (PLGA) nanoparticles within the 3D muscle constructs. Both nanoparticle types were progressively internalized by myofibers, exhibiting distinct localization and accumulation near nuclei. Additionally, we tested the capability of SLN and PLGA nanoparticles to modulate inflammatory cytokines (IL-1β, IL-6, TNF-α) under inflammatory stimulation, indicating their potential for controlled delivery and local immune modulation within muscle tissue. In summary, this human 3D muscle-based in vitro model effectively emulates muscle responses to immunological and delivery stimuli, offering a versatile platform to study muscle immunobiology and evaluate advanced delivery strategies, while reducing the reliance on animal models in preclinical research.Pubblicazioni consigliate

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