# Physical decellularization of fish skin utilizing electrical fields

**Authors:** Mengshi Chen, Siyi Chen, Yapei Song, Siran Wang, Qiaoyin Zheng, Zhifeng You, Weijie Peng, Huaqiong Li, Feng Wen

PMC · DOI: 10.1093/rb/rbag005 · Regenerative Biomaterials · 2026-01-22

## TL;DR

A new method using electrical fields to decellularize fish skin preserves tissue structure and biocompatibility better than traditional chemical methods.

## Contribution

Introduces a fast, chemical-free electrical decellularization method that preserves tissue integrity and reduces immunogenicity.

## Key findings

- Electrical decellularization achieved DNA levels below 50 ng/mg in 2 hours without toxic reagents.
- Electrically decellularized skin showed better microstructure and higher cell survival rates than chemical methods.
- The method caused minimal hemolysis and elicited fewer immune responses in implantation tests.

## Abstract

Decellularized tissues have attracted considerable attention in tissue engineering and regenerative medicine due to their diverse sources and excellent biocompatibility. However, current decellularization techniques often compromise the integrity of the extracellular matrix, leaving harmful chemical residues or inadequately removing immunogenic cellular components. Consequently, the biocompatibility and clinical efficacy of decellularized tissues are undermined. To address these issues, a novel decellularization technique employing an electrical field has been proposed. In the resulting decellularized tissue, the residual DNA concentration was measured at 27.44 ± 7.27 ng/mg, satisfying the evaluation criteria (<50 ng/mg) in a significantly shorter process compared to chemical/enzymatic decellularization (∼2 h vs. ∼15 h) and without the use of toxic reagents. The microstructure was better preserved in electrically decellularized skin than in chemically/enzymatically decellularized skin, maintaining an interconnected porous microstructure that facilitates neo-tissue ingrowth. Cytotoxicity assessments confirmed the non-cytotoxic nature of electrically decellularized fish skin, with a cell survival rate (115.84 ± 10.78%) higher than that of chemically/enzymatically decellularized and native skins (105.57 ± 3.43% and 118.69 ± 6.53%, respectively). The hemolysis rate of decellularized skin using electrical techniques was the lowest (0.35 ± 0.26%) compared to that of chemically/enzymatically decellularized and native skins (1.089 ± 0.03% and 1.11 ± 0.06%), indicating non-hemolytic material. Furthermore, subcutaneous implantation demonstrated that electrically decellularized skin did not elicit severe immune responses and exhibited faster tissue integration than chemically/enzymatically decellularized skin. Therefore, electrical decellularization effectively removes cellular components while preserving the natural architecture without the use of harmful reagents, establishing a secure foundation for extensive applications in tissue engineering and regenerative medicine using decellularized tissues in the future.

## Full-text entities

- **Genes:** Eln (elastin) [NCBI Gene 13717] {aka E030024M20Rik}, Cd86 (CD86 antigen) [NCBI Gene 12524] {aka B7, B7-2, B7.2, B70, CLS1, Cd28l2}, St3gal5 (ST3 beta-galactoside alpha-2,3-sialyltransferase 5) [NCBI Gene 20454] {aka 3S-T, Siat9, [a]2}, Pecam1 (platelet/endothelial cell adhesion molecule 1) [NCBI Gene 18613] {aka Cd31, PECAM-1, Pecam}, Brp1 (brain protein 1) [NCBI Gene 109667] {aka A1, Brp-1}, Mrc1 (mannose receptor, C type 1) [NCBI Gene 17533] {aka CD206, MR}
- **Diseases:** tumor (MESH:D009369), Cytotoxicity (MESH:D064420), inflammation (MESH:D007249), fractures (MESH:D050723), CD (MESH:D012871), DFS (MESH:D005393), necrosis (MESH:D009336), Hemolysis (MESH:D006461)
- **Chemicals:** Omega-3 fatty acids (MESH:D015525), MTT (MESH:C070243), Amino acid (MESH:D000596), nitrogen (MESH:D009584), Fastin (MESH:C013989), polycaprolactone (MESH:C016240), Triton X-100 (MESH:D017830), Coomassie brilliant blue (MESH:C004692), PC (MESH:C053518), ethylene oxide (MESH:D005027), streptomycin (MESH:D013307), Ala (MESH:D000409), acetone (MESH:D000096), Amino (-), Calcein AM (MESH:C085925), hydrogen peroxide (MESH:D006861), paraffin (MESH:D010232), Pro (MESH:D011392), gold (MESH:D006046), NaCl (MESH:D012965), H&amp;E (MESH:D006371), glycosaminoglycans (MESH:D006025), ethidium homodimer (MESH:C018533), phosphate (MESH:D010710), salt (MESH:D012492), penicillin (MESH:D010406), sulfate (MESH:D013431), alpha-Gal (MESH:C055075), polytetrafluoroethylene (MESH:D011138), 1-Ethyl-3-(3-dimethylaminopropyl) carbodiimide (MESH:D005022), poly (lactic-co-glycolic acid) (MESH:D000077182), SDS (MESH:D012967), acetic acid (MESH:D019342), Glu (MESH:D018698), HCl (MESH:D006851), formalin (MESH:D005557), Gly (MESH:D005998), sodium hydroxide (MESH:D012972), galactose (MESH:D005690), N-hydroxysuccinimide (MESH:C001426), water (MESH:D014867), CO2 (MESH:D002245), sGAG (MESH:C013786), lipid (MESH:D008055), isoflurane (MESH:D007530), agarose (MESH:D012685)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116], Mus musculus (house mouse, species) [taxon 10090], Gadus morhua (Atlantic cod, species) [taxon 8049], Homo sapiens (human, species) [taxon 9606], Oreochromis niloticus (Nile tilapia, species) [taxon 8128], Tilapia (genus) [taxon 8126], Actinopterygii (fishes, superclass) [taxon 7898]
- **Cell lines:** L929 — Mus musculus (Mouse), Spontaneously immortalized cell line (CVCL_AR58), HaCaT — Homo sapiens (Human), Spontaneously immortalized cell line (CVCL_0038), HSF — Homo sapiens (Human), Finite cell line (CVCL_A9FC)

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12947800/full.md

## References

52 references — full list in the complete paper: https://tomesphere.com/paper/PMC12947800/full.md

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Source: https://tomesphere.com/paper/PMC12947800