Chondrogenic differentiation of umbilical cord-derived mesenchymal stem cells in type I collagen-hydrogel for cartilage engineering

Injury. 2013 Apr;44(4):540-9. doi: 10.1016/j.injury.2012.09.024. Epub 2013 Jan 19.

Abstract

Introduction: A potent mesenchymal stem cell (MSC) population was recently isolated from the Wharton's jelly of human umbilical cord (UC). The aim of the current experiments was to determine the potential of human UC-derived MSC (UC-MSC) in cartilage healing.

Materials and methods: Chondrogenic differentiation of collagen hydrogel-embedded cells was induced in standard chondrocyte conditioning medium and further detected by real-time PCR, histochemistry and immunohistochemistry analyses. Cell viability and apoptosis of the MSCs in the collagen I hydrogels were monitored using apoptosis detection kit.

Results: Cells isolated from UC were positive for MSC biomarkers and negative for haematopoietic lineage and endothelial biomarkers and possess the capacity to differentiate along osteogenic lineage. UC-MSCs embedded in collagen hydrogel can undergo chondrogenesis characterised by significantly increased expressions of collagen II, aggrecan, COMP (cartilage oligomeric matrix protein) and sox9 after exposed cells-embedded hydrogels to chondrogenic factors. The most of cells remained viable throughout the hydrogels after 3 weeks of cultivation in chondrogenic differentiation medium.

Conclusions: Collagen hydrogel can provide an appropriate 3-D environment for the chondrogenesis of UC-MSCs. UC-MSCs embedded in biocompatible scaffold may have great potential for cartilage engineering.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cartilage / metabolism*
  • Cell Differentiation
  • Cells, Cultured
  • China
  • Chondrogenesis*
  • Collagen Type I / metabolism*
  • Female
  • Humans
  • Hydrogels / metabolism
  • Immunohistochemistry
  • Male
  • Mesenchymal Stem Cells / cytology
  • Mesenchymal Stem Cells / metabolism*
  • Real-Time Polymerase Chain Reaction
  • Tissue Engineering / methods*
  • Tissue Scaffolds / chemistry*
  • Wharton Jelly / cytology
  • Wharton Jelly / metabolism*

Substances

  • Collagen Type I
  • Hydrogels