Tolerant and Rapid Endochondral Bone Regeneration Using Framework‐Enhanced 3D Biomineralized Matrix Hydrogels

• Published in: Advanced science 2024-03, Vol.11 (9), p.e2305580-n/a
• Main Authors: Bai, Baoshuai, Liu, Yanhan, Huang, Jinyi, Wang, Sinan, Chen, Hongying, Huo, Yingying, Zhou, Hengxing, Liu, Yu, Feng, Shiqing, Zhou, Guangdong, Hua, Yujie
• Format: Article
• Language: English
• Subjects: biomineralization; Bone marrow; bone regeneration; endochondral ossification; Fourier transforms; Hydrogels; Hydroxyapatite; Hypoxia; hypoxic microenvironment; Magnesium; Mineralization; Scanning electron microscopy; Stem cells; Zinc
• ISSN: 2198-3844; 2198-3844
• DOI: 10.1002/advs.202305580

Tissue‐engineered bone has emerged as a promising alternative for bone defect repair due to the advantages of regenerative bone healing and physiological functional reconstruction. However, there is very limited breakthrough in achieving favorable bone regeneration due to the harsh osteogenic microenvironment after bone injury, especially the avascular and hypoxic conditions. Inspired by the bone developmental mode of endochondral ossification, a novel strategy is proposed for tolerant and rapid endochondral bone regeneration using framework‐enhanced 3D biomineralized matrix hydrogels. First, it is meticulously designed 3D biomimetic hydrogels with both hypoxic and osteoinductive microenvironment, and then integrated 3D‐printed polycaprolactone framework to improve their mechanical strength and structural fidelity. The inherent hypoxic 3D matrix microenvironment effectively activates bone marrow mesenchymal stem cells self‐regulation for early‐stage chondrogenesis via TGFβ/Smad signaling pathway due to the obstacle of aerobic respiration. Meanwhile, the strong biomineralized microenvironment, created by a hybrid formulation of native‐constitute osteogenic inorganic salts, can synergistically regulate both bone mineralization and osteoclastic differentiation, and thus accelerate the late‐stage bone maturation. Furthermore, both in vivo ectopic osteogenesis and in situ skull defect repair successfully verified the high efficiency and mechanical maintenance of endochondral bone regeneration mode, which offers a promising treatment for craniofacial bone defect repair. In this study, a tolerant and rapid endochondral bone regeneration strategy is proposed using 3D‐printed PCL framework‐enhanced biomineralized matrix hydrogels with both hypoxic and osteoinductive microenvironment, which can effectively regulate BMSC‐based endochondral ossification (ECO) for tissue‐engineered bone construction. The current study eventually realized satisfactory ectopic osteogenesis in nude mice and skull defect repair in rabbits by the high‐efficiency ECO mode.