Effects of in vitro low oxygen tension preconditioning of buccal fat pad stem cells on in Vivo articular cartilage tissue repair

Life Sci. 2021 Sep 1:280:119728. doi: 10.1016/j.lfs.2021.119728. Epub 2021 Jun 16.

Abstract

Aims: Progenitor cells-based regenerative strategy has shown promise to repair cartilage, an avascular tissue in which cells experience hypoxia. Hypoxia is known to improve the early chondrogenic differentiation of stem cells. Therefore, this study aimed to determine whether hypoxia preconditioning could be used to enhance the regenerative potential of the combination of buccal fat pad stem cells (BFPSCs) and bilayer chitosan-based hydrogel scaffold for articular cartilage repair.

Materials and methods: Human BFPSCs were seeded on the bilayer chitosan-based hydrogel scaffolds in the culture medium. The viability and proliferation of cells on the scaffolds were monitored using scanning electron microscopy (SEM), MTT assay, and DAPI staining. Hypoxia preconditioned BFPSCs-seeded scaffolds were transplanted into rabbit articular cartilage knee defects for 12 weeks. The newly formed tissue was evaluated by cartilage-specific immunohistological analysis and histological staining.

Key findings: It was found that the chondrogenic differentiation and osteochondral conjunction in articular cartilage defect via BFPSCs-seeded bilayer scaffolds was enhanced by hypoxic preconditioning compared to a normoxic environment.

Significance: Based on our study, the integrity with subchondral bone in osteochondral defect was enhanced by BFPSCs on bilayer scaffold. Thus, this study provides evidence on the design of preconditioned cell-seeded bilayer hydrogels for articular cartilage regeneration.

Keywords: Bilayer chitosan scaffolds; Buccal fat pad stem cells (BFPSCs); Cartilage tissue engineering; Hypoxia preconditioning.

MeSH terms

  • Animals
  • Cartilage, Articular / cytology*
  • Cartilage, Articular / physiology
  • Cell Hypoxia
  • Cells, Cultured
  • Chitosan / chemistry*
  • Chondrogenesis
  • Humans
  • Male
  • Oxygen / metabolism*
  • Rabbits
  • Stem Cell Transplantation*
  • Stem Cells / cytology*
  • Stem Cells / metabolism
  • Tissue Engineering / methods
  • Tissue Scaffolds / chemistry*

Substances

  • Chitosan
  • Oxygen