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Preparation of 3D Decellularized Matrices from Fetal Mouse Skeletal Muscle for Cell Culture
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Decellularized Human Skeletal Muscle as Biologic Scaffold for Reconstructive Surgery.
Andrea Porzionato1, Maria Martina Sfriso2, Alex Pontini3
1Section of Human Anatomy, Department of Molecular Medicine, University of Padova, Via Gabelli 65, Padova 35127, Italy. andrea.porzionato@unipd.it.
International Journal of Molecular Sciences
|July 4, 2015
Summary
Human skeletal muscle decellularization yields effective biologic scaffolds. These scaffolds preserve extracellular matrix architecture and show good integration in abdominal wall defects, though further research on cell recolonization is needed.
Area of Science:
- Biomaterials Science
- Tissue Engineering
- Regenerative Medicine
Background:
- Engineered skeletal muscle tissues offer solutions for volumetric muscle loss.
- Biologic scaffolds are typically derived from decellularized animal skeletal muscles.
Purpose of the Study:
- To characterize biologic scaffolds from decellularized human skeletal muscle.
- To compare decellularization protocols for human, rat, and rabbit muscle.
- To evaluate the integration of human scaffolds in rabbit abdominal wall defects.
Main Methods:
- Skeletal muscle samples (human, rat, rabbit) were decellularized using two protocols: Protocol 1 (sodium deoxycholate, DNase I) and Protocol 2 (trypsin-EDTA, Triton X-NH4OH).
- Scaffold characteristics were analyzed using transmission and scanning electron microscopy.
- Human scaffolds were implanted into rabbit abdominal wall defects to assess integration.
Main Results:
- Protocol 2 was more effective, removing cellular material while preserving the collagen and elastic fiber network.
- Ultrastructural analysis confirmed the preservation of collagen, elastic fibers, glycosaminoglycans, and proteoglycans.
- Implanted human scaffolds demonstrated good integration in rabbits, but complete muscle cell recolonization was not achieved.
Conclusions:
- Human skeletal muscle can be effectively decellularized to create scaffolds with preserved extracellular matrix architecture and suitable mechanical properties for implantation.
- These scaffolds show promise for integration into tissue defects.
- Further investigation is required to assess the efficacy of in vitro recolonization with autologous cells prior to in vivo application.

