A functional biphasic biomaterial homing mesenchymal stem cells for in vivo cartilage regeneration

作者：Huang, Hongjie; Zhang, Xin; Hu, Xiaoqing; Shao, Zhenxing; Zhu, Jingxian; Dai, Linghui; Man, Zhentao; Yuan, Lan; Chen, Haifeng; Zhou, Chunyan; Ao, Yingfang^*

来源：Biomaterials, 2014, 35(36): 9608-9619.

DOI：10.1016/j.biomaterials.2014.08.020

• Affinity peptide
• Cartilage repair
• Functional biomaterials
• Mesenchymal stem cells homing
• Tissue engineering

Cartilage regeneration after trauma is still a great challenge for clinicians and researchers due to many reasons, such as joint load-bearing, synovial movement and the paucity of endogenous repair cells. To overcome these limitations, we constructed a functional biomaterial using a biphasic scaffold platform and a bone-derived mesenchymal stem cells (BMSCs)-specific affinity peptide. The biphasic scaffold platform retains more cells homogeneously within the sol-gel transition of chitosan and provides sufficient solid matrix strength. This biphasic scaffold platform is functionalized with an affinity peptide targeting a cell source of interest, BMSCs. The presence of conjugated peptide gives this system a biological functionality towards BMSC-specific homing both in vitro and in vivo. The functional biomaterial can stimulate stem cell proliferation and chondrogenic differentiation during in vitro culture. Six months after in vivo implantation, compared with routine surgery or control scaffolds, the functional biomaterials induced superior cartilage repair without complications, as indicated by histological observations, magnetic resonance imaging and biomechanical properties. Beyond cartilage repair, this functional biphasic scaffold may provide a biomaterial framework for one-step tissue engineering strategy by homing endogenous cells to stimulate tissue regeneration.

• 出版日期2014-12
• 单位北京大学