4.8 Article

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

Journal

BIOMATERIALS
Volume 35, Issue 36, Pages 9608-9619

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.biomaterials.2014.08.020

Keywords

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

Funding

  1. National Natural Science Foundation of China [90919022, 81101390]
  2. Specialized Research Fund for the Doctoral Program of Higher Education [20110001130001]
  3. Leading Academic Discipline Project of Beijing Education Bureau

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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. (C) 2014 Elsevier Ltd. All rights reserved.

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