In-situ forming injectable GFOGER-conjugated BMSCs-laden hydrogels for osteochondral regeneration.
Mi Yeon HaDae Hyeok YangSu Jung YouHyun Joo KimHeung Jae ChunPublished in: NPJ Regenerative medicine (2023)
The collagen-mimetic peptide GFOGER possesses the chondrogenic potential and has been used as a cell adhesion peptide or chondrogenic inducer. Here, we prepared an injectable in situ forming composite hydrogel system comprising methoxy polyethylene glycol-b-polycaprolactone (MPEG-PCL) and GFOGER-conjugated PEG-PCL (GFOGER-PEG-PCL) with various GFOGER concentrations based on our recently patented technology. The conjugation of GFOGER to PEG-PCL was confirmed by 1 H NMR, and the particle size distribution and rheological properties for the sol-gel transition behavior of the samples with respect to the GFOGER content were evaluated systemically. In vitro experiments using rat bone marrow-derived mesenchymal stem cells (BMSCs) revealed that the GFOGER-PEG-PCL hydrogel significantly enhanced expression of integrins (β1, α2, and α11), increased expression of FAK, and induced downstream signaling of ERK and p38. Overexpression of chondrogenic markers suggested that BMSCs have the potential to differentiate into chondrogenic lineages within GFOGER-PEG-PCL samples. In vivo studies using a rat osteochondral defect model revealed that transplanted BMSCs with GFOGER 0.8 -PEG-PCL survived at the defect with strong chondrogenic expression after 4 weeks. The stem cell-laden GFOGER 0.8 -PEG-PCL hydrogel produced remarkable osteochondral regeneration at 8 weeks of transplantation, as determined by histological findings and micro-CT analysis. The histomorphological score in the GFOGER 0.8 -PEG-PCL + BMSCs group was ~1.7-, 2.6-, and 5.3-fold higher than that in the GFOGER 0.8 -PEG-PCL, MPEG-PCL, and defect groups, respectively. Taken together, these results provide an important platform for further advanced GFOGER-based stem cell research for osteochondral repair.
Keyphrases
- drug delivery
- stem cells
- mesenchymal stem cells
- tissue engineering
- hyaluronic acid
- bone marrow
- poor prognosis
- wound healing
- magnetic resonance
- oxidative stress
- binding protein
- mass spectrometry
- computed tomography
- magnetic resonance imaging
- photodynamic therapy
- cell therapy
- endothelial cells
- contrast enhanced
- pet ct
- case control