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Background: Coordination between osteo-/angiogenesis and the osteoimmune microenvironment is essential for effective bone repair with biomaterials. As a highly personalized and precise biomaterial suitable for repairing complex bone defects in clinical practice, it is essential to endow 3D-printed scaffold the above key capabilities.
Results: Herein, by introducing xonotlite nanofiber (Ca(SiO) (OH), CS) into the 3D-printed silk fibroin/gelatin basal scaffold, a novel bone repair system named SGC was fabricated. It was noted that the incorporation of CS could greatly enhance the chemical and mechanical properties of the scaffold to match the needs of bone regeneration. Besides, benefiting from the addition of CS, SGC scaffolds could accelerate osteo-/angiogenic differentiation of bone mesenchymal stem cells (BMSCs) and meanwhile reprogram macrophages to establish a favorable osteoimmune microenvironment. In vivo experiments further demonstrated that SGC scaffolds could efficiently stimulate bone repair and create a regeneration-friendly osteoimmune microenvironment. Mechanistically, we discovered that SGC scaffolds may achieve immune reprogramming in macrophages through a decrease in the expression of Smad6 and Smad7, both of which participate in the transforming growth factor-β (TGF-β) signaling pathway.
Conclusion: Overall, this study demonstrated the clinical potential of the SGC scaffold due to its favorable pro-osteo-/angiogenic and osteoimmunomodulatory properties. In addition, it is a promising strategy to develop novel bone repair biomaterials by taking osteoinduction and osteoimmune microenvironment remodeling functions into account.
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http://dx.doi.org/10.1186/s12951-024-02323-9 | DOI Listing |
J Nanobiotechnology
September 2025
Hospital of Stomatology, Guanghua School of Stomatology, Guangdong Provincial Key Laboratory of Stomatology, Sun Yat-sen University, Guangzhou, 510055, Guangdong, China.
Irregular alveolar bone defects pose persistent clinical challenges due to their complex morphology and the lack of biomaterials that simultaneously provide structural integrity, biocompatibility, and dynamic osteoinductive potential. Herein, we report a fiber-reinforced, dual-network hydrogel system (OHADN fiber@Yoda1 hydrogel) engineered to recapitulate mechanobiological cues for enhanced bone regeneration. This injectable hydrogel integrates oxidized hyaluronic acid (OHA) crosslinked with Yoda1-loaded PLGA-collagen fiber fragments and stabilized via catechol-Fe³⁺ coordination, forming a robust and self-healing structure.
View Article and Find Full Text PDFBiomater Adv
August 2025
School of Materials Science and Engineering, National Key Laboratory of Silicon and Advanced Semiconductor Materials, Zhejiang University, Hangzhou 310058, China; Institute of Wenzhou, Zhejiang University, Wenzhou 325006, China. Electronic address:
The limited self-healing capacity of critical-sized bone defects presents significant challenges in healing. An effective approach is to regulate the physicochemical properties of biomaterials to mimic the natural bone regenerative microenvironment. In this work, we have prepared Chitosan-Gelatin (CS-Gel) based hydrogel/ Poly(vinylidene fluoride-co-trifluoroethylene) (P(VDF-TrFE)) systems, which provide biomimetic and electric cues for bone regeneration.
View Article and Find Full Text PDFCell Prolif
August 2025
Department of Orthodontics, The Affiliated Stomatological Hospital of Nanjing Medical University, Nanjing, China.
Macrophages and bone marrow mesenchymal stem cells (BMSCs) share a close relationship within the osteoimmune microenvironment. During mechanically induced bone formation, macrophages respond to stimuli and regulate this microenvironment, influencing BMSCs' proliferation and differentiation. However, the underlying mechanisms remain incompletely understood.
View Article and Find Full Text PDFMater Horiz
August 2025
National Key Laboratory of Advanced Polymer Materials, College of Polymer Science and Engineering, Sichuan University, Chengdu, Sichuan 610065, People's Republic of China.
Implantation is the most common strategy for treating large segment bone defects, while current implants mainly focus on osteogenic activity and early immune responses, ignoring their anti-infective capacity and late-stage immune cooperation. Herein, a unique asymmetric fluorine-containing structure was successfully designed and constructed on a poly-ether-ether-ketone (PEEK) surface a substitution reaction with fluorine gas. On the one hand, the unexpected hydrophilicity of fluorinated PEEK enhanced the adhesion of bone marrow stem cells (BMSCs) upregulation of focal adhesion-related signaling pathways, and the fluorine-rich surface simultaneously constructed an early osteoimmune microenvironment, collectively facilitating the early osteogenic process.
View Article and Find Full Text PDFBioact Mater
December 2025
School of Pharmacy, the Key Laboratory of Prescription Effect and Clinical Evaluation of State Administration of Traditional Chinese Medicine of China, Binzhou Medical University, Yantai, 264003, PR China.
Critical-sized calvarial defects remain a formidable clinical challenge due to dyssynchronous immunomodulation-osteogenesis coupling and unregulated growth factor release. Here, a bioinspired porous core-shell microsphere system (GCI@HPPS) is developed, integrating hydroxyapatite (HA)-loaded shell, surface-immobilized SDF-1α, and IGF-1-encapsulated cores to immunomodulate osteoimmune microenvironment and osteogenesis promotion. The hierarchical architecture achieved spatiotemporally programmed release: HA degradation-dependent mineralization, SDF-1α-mediated BMSC chemotaxis, and sustained IGF-1 delivery, mimicking natural bone repair cascades.
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