Development of Injectable Polydactyly-Derived Chondrocyte Sheets

Int J Mol Sci. 2021 Mar 21;22(6):3198. doi: 10.3390/ijms22063198.

Abstract

We are conducting a clinical study of the use of allogeneic polydactyly-derived chondrocyte sheets (PD sheets) for the repair of articular cartilage damage caused by osteoarthritis. However, the transplantation of PD sheets requires highly invasive surgery. To establish a less invasive treatment, we are currently developing injectable fragments of PD sheets (PD sheets-mini). Polydactyly-derived chondrocytes were seeded in RepCell™ or conventional temperature-responsive inserts and cultured. Cell counts and viability, histology, enzyme-linked immunosorbent assay (ELISA), quantitative real-time polymerase chain reaction (qPCR), and flow cytometry were used to characterize PD sheets-mini and PD sheets collected from each culture. To examine the effects of injection on cell viability, PD sheets-mini were tested in four experimental conditions: non-injection control, 18 gauge (G) needle, 23G needle, and syringe only. PD sheets-mini produced similar amounts of humoral factors as PD sheets. No histological differences were observed between PD sheets and PD sheets-mini. Except for COL2A1, expression of cartilage-related genes did not differ between the two types of PD sheet. No significant differences were observed between injection conditions. PD sheets-mini have characteristics that resemble PD sheets. The cell viability of PD sheets-mini was not significantly affected by needle gauge size. Intra-articular injection may be a feasible, less invasive method to transplant PD sheets-mini.

Keywords: cartilage regeneration; cell sheet; minimally invasive treatment; osteoarthritis.

MeSH terms

  • Animals
  • Biomarkers
  • Cartilage, Articular
  • Cell Count
  • Cell Survival
  • Chondrocytes / cytology*
  • Chondrocytes / metabolism
  • Gene Expression
  • Humans
  • Immunohistochemistry
  • Immunophenotyping
  • Osteoarthritis / therapy
  • Polydactyly*
  • Regeneration
  • Tissue Scaffolds*

Substances

  • Biomarkers