IRCCS Istituto Ortopedico Galeazzi, Cell and Tissue Engineering Laboratory, Milano, Italy; PhD School in Life Sciences, University of Milano Bicocca, Milano, Italy
Giovanni S. Ugolini
Department of Electronics, Information and Bioengineering, Politecnico di Milano, Milano, Italy
Veronica Sansoni
IRCCS Istituto Ortopedico Galeazzi, Laboratory of Experimental Biochemistry and Molecular Biology, Milano, Italy
IRCCS Istituto Ortopedico Galeazzi, Laboratory of Experimental Biochemistry and Molecular Biology, Milano, Italy
Simona Zanotti
Muscle Cell Biology Laboratory, Neuromuscular Diseases and Neuroimmunology Unit, Fondazione IRCCS Istituto Neurologico C. Besta, Milano, Italy
Paola Ostano
Cancer Genomics Laboratory, Fondazione Edo ed Elvo Tempia Valenta, Biella, Italy
Marina Mora
Muscle Cell Biology Laboratory, Neuromuscular Diseases and Neuroimmunology Unit, Fondazione IRCCS Istituto Neurologico C. Besta, Milano, Italy
Monica Soncini
Department of Electronics, Information and Bioengineering, Politecnico di Milano, Milano, Italy
Marco Vanoni
PhD School in Life Sciences, University of Milano Bicocca, Milano, Italy; SYSBIO Centre for Systems Biology, Department of Biotechnology and Biosciences, University of Milano Bicocca, Milano, Italy
Giovanni Lombardi
IRCCS Istituto Ortopedico Galeazzi, Laboratory of Experimental Biochemistry and Molecular Biology, Milano, Italy
Matteo Moretti
IRCCS Istituto Ortopedico Galeazzi, Cell and Tissue Engineering Laboratory, Milano, Italy; Regenerative Medicine Technologies Lab, Ente Ospedaliero Cantonale, Lugano, Switzerland; Swiss Institute for Regenerative Medicine, Lugano, Switzerland; Corresponding author
Summary: The integration of vascular structures into in vitro cultured tissues provides realistic models of complex tissue-vascular interactions. Despite the incidence and impact of muscle-wasting disorders, advanced in vitro systems are still far from recapitulating the environmental complexity of skeletal muscle. Our model comprises differentiated human muscle fibers enveloped by a sheath of human muscle-derived fibroblasts and supported by a vascular network with mural-like cells. Here, we demonstrate the induction of muscle-specific endothelium and the self-organization of endomysial muscle fibroblasts mediated by endothelial cells. We use this model to mimic the fibrotic environment characterizing muscular dystrophies and to highlight key signatures of fibrosis that are neglected or underestimated in traditional 2D monocultures. Overall, this vascularized meso-scale cellular construct finely recapitulates the human skeletal muscle environment and provides an advanced solution for in vitro studies of muscle physiology and pathology. : Bersini et al. demonstrate the generation of a mesoscale model of the human muscle environment and prove its application for the study of fibrosis. This engineered muscle environment promotes the organ-specific differentiation of endothelial cells and the self-assembly of myofibers spontaneously wrapped by a continuous endomysium-like structure. Keywords: endothelial specificity, 3D vascularized muscle model, fibrosis, muscle environment