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Fish Acellular Dermal Matrix Promotes Repair of Full-Thickness Skin Defects in Mice and Bama Pigs
Zi-Yi Wang1, Zi-Hao Lin1, Ruo-Tao Liu1
1Department of Orthopedic Surgery, Shanghai Sixth People's Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Summary
Tilapia skin can be transformed into a biocompatible dermal matrix for skin repair. This fish-derived scaffold promotes faster wound healing and better tissue regeneration than porcine matrices.
Area of Science:
- Biomaterials Science
- Tissue Engineering
- Regenerative Medicine
Background:
- Acellular dermal matrices (ADMs) are crucial for skin wound repair.
- Developing novel, cost-effective, and biocompatible scaffolds is essential for clinical applications.
Purpose of the Study:
- To develop an acellular dermal matrix from tilapia skin.
- To evaluate its efficacy as a bioscaffold for skin wound repair in preclinical models.
Main Methods:
- Decellularization of tilapia skin.
- Histological, electron microscopy, and immunological analyses.
- In vitro cell culture assays (proliferation, migration, tube formation).
- In vivo studies using full-thickness skin defects in mice and pigs.
- Transcriptomic profiling of wound tissue.
Main Results:
- The tilapia-derived matrix demonstrated low immunogenicity and preserved extracellular matrix structure.
- In vitro studies showed enhanced endothelial cell and fibroblast activity.
- In vivo studies in mice and pigs accelerated wound closure and improved tissue regeneration (collagen deposition, vascularization).
- The fish-derived scaffold outperformed a commercial porcine-derived matrix.
- Transcriptomic analysis revealed modulation of immune regulation, ECM remodeling, and angiogenesis pathways.
Conclusions:
- Tilapia-derived acellular dermal matrix is a promising, biocompatible, and effective bioscaffold for skin wound repair.
- It offers superior regenerative outcomes compared to porcine matrices.
- The scaffold has potential as a safe, economical, and sustainable option for clinical use, supported by large animal model data and mechanistic insights from transcriptomics.

