Applied Sciences (Feb 2025)

Decellularized Membrane Derived from the Cell-Produced Extracellular Matrix of 1-Day-Old Porcine Cartilage Can Be a Substitute for Periosteal Patches in Autologous Chondrocyte Implantation

  • Minh-Dung Truong,
  • Thanh-Tam Nguyen-Thi,
  • Thanh-Tan Nguyen-Ngoc,
  • Bich-Tram Vo-Ngoc,
  • Hoang-Yen Duong-Thi,
  • Hoang-Vinh Nguyen,
  • Duc-Quy Mai Hoang,
  • Phuong-Vy Bui,
  • Khanh Hong-Thien Bui,
  • Phuong Le Thi,
  • Dieu Linh Tran,
  • Vo Thi Xuyen

DOI
https://doi.org/10.3390/app15042237
Journal volume & issue
Vol. 15, no. 4
p. 2237

Abstract

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(1) Autologous chondrocyte implantation (ACI) is a prominent method for treating cartilage damage, but periosteal patches can cause chondrocyte leakage. This study evaluates the potential of a decellularized membrane derived from the cell-produced extracellular matrix of 1-day-old porcine cartilage (pcECM-DM) to act as a substitute for periosteal patches. (2) The interaction between young rabbit chondrocyte cells and pcECM-DM was assessed through cytotoxicity, differentiation, cell viability, cell migration, and adhesive ability. Rabbit chondrocyte cells, cultivated until passage two, were seeded onto a 6 mm diameter membrane. Assessments included DAPI-PKH26 staining, histological staining, live/dead assay, WST-1 assay, and proteomics analysis. (3) Results: DAPI-PKH26 staining showed successful adhesion and the uniform distribution of cells on the membrane. Safranin-O and H&E staining confirmed that the membrane supports chondrocyte adhesion and extracellular matrix production with high cell density and typical chondrocyte morphology. The live/dead assay demonstrated a high proportion of viable cells at 24 and 48 h, with increased cell proliferation over time. The WST-1 assay showed a significant increase in OD450 values, confirming cell proliferation and biocompatibility. Proteomic analysis revealed the significant enrichment of genes associated with extracellular matrix organization, cell adhesion, and cartilage development. (4) Conclusions: This novel biomaterial holds the potential to enhance cartilage regeneration and offer a viable alternative to periosteal patches.

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