Tolerant and Rapid Endochondral Bone Regeneration Using Framework-Enhanced 3D Biomineralized Matrix Hydrogels.
Baoshuai BaiYanhan LiuJinyi HuangSinan WangHongying ChenYingying HuoHengxing ZhouYu LiuShiqing FengGuangdong ZhouYujie HuaPublished in: Advanced science (Weinheim, Baden-Wurttemberg, Germany) (2023)
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.
Keyphrases
- bone regeneration
- stem cells
- early stage
- mesenchymal stem cells
- drug delivery
- bone mineral density
- bone marrow
- squamous cell carcinoma
- transforming growth factor
- lymph node
- tissue engineering
- oxidative stress
- high intensity
- radiation therapy
- cell proliferation
- soft tissue
- neoadjuvant chemotherapy
- drug release
- combination therapy
- ionic liquid
- endoplasmic reticulum stress
- sentinel lymph node
- induced apoptosis
- locally advanced