In-situ forming injectable GFOGER-conjugated BMSCs-laden hydrogels for osteochondral regeneration

被引:14
作者
Ha, Mi Yeon [1 ,2 ]
Yang, Dae Hyeok [2 ]
You, Su Jung [2 ]
Kim, Hyun Joo [2 ]
Chun, Heung Jae [1 ,2 ,3 ]
机构
[1] Catholic Univ Korea, Coll Med, Dept Biomed & Hlth Sci, Seoul 06591, South Korea
[2] Catholic Univ Korea, Inst Cell & Tissue Engn, Coll Med, Seoul 06591, South Korea
[3] Catholic Univ Korea, Coll Med, Dept Med Life Sci, Seoul 06591, South Korea
关键词
MESENCHYMAL STEM-CELLS; DIBLOCK COPOLYMERS; CARTILAGE REPAIR; COLLAGEN; BONE; BIOMATERIALS; RGD; DIFFERENTIATION; OSTEOARTHRITIS; SCAFFOLD;
D O I
10.1038/s41536-022-00274-z
中图分类号
Q813 [细胞工程];
学科分类号
摘要
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 H-1 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 (beta 1, alpha 2, and alpha 11), 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 similar to 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.
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页数:13
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