In vitro and in vivo co-culture of chondrocytes and bone marrow stem cells in photocrosslinked PCL–PEG–PCL hydrogels enhances cartilage formation

  • Chao Yin Ko
  • , Kuan Lin Ku
  • , Shu Rui Yang
  • , Tsai Yu Lin
  • , Sydney Peng
  • , Yu Shiang Peng
  • , Ming Huei Cheng
  • , I. Ming Chu*
  • *Corresponding author for this work

Research output: Contribution to journalJournal Article peer-review

52 Scopus citations

Abstract

Chondrocytes (CH) and bone marrow stem cells (BMSCs) are sources that can be used in cartilage tissue engineering. Co-culture of CHs and BMSCs is a promising strategy for promoting chondrogenic differentiation. In this study, articular CHs and BMSCs were encapsulated in PCL–PEG–PCL photocrosslinked hydrogels for 4 weeks. Various ratios of CH:BMSC co-cultures were investigated to identify the optimal ratio for cartilage formation. The results thus obtained revealed that co-culturing CHs and BMSCs in hydrogels provides an appropriate in vitro microenvironment for chondrogenic differentiation and cartilage matrix production. Co-culture with a 1:4 CH:BMSC ratio significantly increased the synthesis of GAGs and collagen. In vivo cartilage regeneration was evaluated using a co-culture system in rabbit models. The co-culture system exhibited a hyaline chondrocyte phenotype with excellent regeneration, resembling the morphology of native cartilage. This finding suggests that the co-culture of these two cell types promotes cartilage regeneration and that the system, including the hydrogel scaffold, has potential in cartilage tissue engineering.

Original languageEnglish
Pages (from-to)E485-E496
JournalJournal of Tissue Engineering and Regenerative Medicine
Volume10
Issue number10
DOIs
StatePublished - 01 10 2016
Externally publishedYes

Bibliographical note

Publisher Copyright:
Copyright © 2013 John Wiley & Sons, Ltd.

Keywords

  • autologous cell
  • bone marrow stem cells
  • cartilage
  • co-culture
  • hydrogels
  • tissue engineering

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