Skeletal muscle decellularization allows the generation of natural scaffolds that retain the extracellular matrix (ECM) mechanical integrity, biological activity, and three-dimensional (3D) architecture of the native tissue. Recent reports showed that in vivo implantation of decellularized muscles supports muscle regeneration in volumetric muscle loss models, including nervous system and neuromuscular junctional homing. Since the nervous system plays pivotal roles during skeletal muscle regeneration and in tissue homeostasis, support of reinnervation is a crucial aspect to be considered. However, the effect of decellularized muscles on reinnervation and on neuronal axon growth has been poorly investigated. Here, we characterized residual protein composition of decellularized muscles by mass spectrometry and we show that scaffolds preserve structural proteins of the ECM of both skeletal muscle and peripheral nervous system. To investigate whether decellularized scaffolds could per se attract neural axons, organotypic sections of spinal cord were cultured three dimensionally in vitro, in presence or in absence of decellularized muscles. We found that neural axons extended from the spinal cord are attracted by the decellularized muscles and penetrate inside the scaffolds upon 3D coculture. These results demonstrate that decellularized scaffolds possess intrinsic neurotrophic properties, supporting their potential use for the treatment of clinical cases where extensive functional regeneration of the muscle is required.

Raffa, P., Scattolini, V., Gerli, M., Perin, S., Cui, M., De Coppi, P., et al. (2020). Decellularized skeletal muscles display neurotrophic effects in three-dimensional organotypic cultures. STEM CELLS TRANSLATIONAL MEDICINE, 9(10), 1233-1243 [10.1002/sctm.20-0090].

Decellularized skeletal muscles display neurotrophic effects in three-dimensional organotypic cultures

De Coppi, Paolo;
2020-01-01

Abstract

Skeletal muscle decellularization allows the generation of natural scaffolds that retain the extracellular matrix (ECM) mechanical integrity, biological activity, and three-dimensional (3D) architecture of the native tissue. Recent reports showed that in vivo implantation of decellularized muscles supports muscle regeneration in volumetric muscle loss models, including nervous system and neuromuscular junctional homing. Since the nervous system plays pivotal roles during skeletal muscle regeneration and in tissue homeostasis, support of reinnervation is a crucial aspect to be considered. However, the effect of decellularized muscles on reinnervation and on neuronal axon growth has been poorly investigated. Here, we characterized residual protein composition of decellularized muscles by mass spectrometry and we show that scaffolds preserve structural proteins of the ECM of both skeletal muscle and peripheral nervous system. To investigate whether decellularized scaffolds could per se attract neural axons, organotypic sections of spinal cord were cultured three dimensionally in vitro, in presence or in absence of decellularized muscles. We found that neural axons extended from the spinal cord are attracted by the decellularized muscles and penetrate inside the scaffolds upon 3D coculture. These results demonstrate that decellularized scaffolds possess intrinsic neurotrophic properties, supporting their potential use for the treatment of clinical cases where extensive functional regeneration of the muscle is required.
2020
Pubblicato
Rilevanza internazionale
Articolo
Esperti anonimi
Settore MEDS-06/A - Chirurgia generale
English
3D culture
ECM
axons
decellularized muscle
innervation
neurons
organotypic culture
spinal cord
Raffa, P., Scattolini, V., Gerli, M., Perin, S., Cui, M., De Coppi, P., et al. (2020). Decellularized skeletal muscles display neurotrophic effects in three-dimensional organotypic cultures. STEM CELLS TRANSLATIONAL MEDICINE, 9(10), 1233-1243 [10.1002/sctm.20-0090].
Raffa, P; Scattolini, V; Gerli, Mfm; Perin, S; Cui, M; De Coppi, P; Elvassore, N; Caccin, P; Luni, C; Urciuolo, A
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/417265
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