Large-sized bone defect repair by combining a decalcified bone matrix framework and bone regeneration units based on photo-crosslinkable osteogenic microgels.

Abstract

Physiological repair of large-sized bone defects is great challenging in clinic due to a lack of ideal grafts suitable for bone regeneration. Decalcified bone matrix (<b>DBM</b>) is considered as an ideal bone regeneration scaffold, but low cell seeding efficiency and a poor osteoinductive microenvironment greatly restrict its application in large-sized bone regeneration. To address these problems, we proposed a novel strategy of bone regeneration units (<b>BRUs</b>) based on microgels produced by photo-crosslinkable and microfluidic techniques, containing both the osteogenic ingredient <b>DBM</b> and vascular endothelial growth factor (<b>VEGF</b>) for accurate biomimic of an osteoinductive microenvironment. The physicochemical properties of microgels could be precisely controlled and the microgels effectively promoted adhesion, proliferation, and osteogenic differentiation of bone marrow mesenchymal stem cells (BMSCs) <i>in vitro</i>. <b>BRUs</b> were successfully constructed by seeding BMSCs onto microgels, which achieved reliable bone regeneration <i>in vivo</i>. Finally, by integrating the advantages of <b>BRUs</b> in bone regeneration and the advantages of <b>DBM</b> scaffolds in 3D morphology and mechanical strength, a <b>BRU</b>-loaded <b>DBM</b> framework successfully regenerated bone tissue with the desired 3D morphology and effectively repaired a large-sized bone defect of rabbit tibia. The current study developed an ideal bone biomimetic microcarrier and provided a novel strategy for bone regeneration and large-sized bone defect repair.