Department of Oral and Maxillofacial Head & Neck Oncology, Shanghai Key Laboratory Stomatology, Shanghai Research Institute of Stomatology, Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, 639 Zhizaoju Road, Shanghai, 200011, China.
Department of Plastic and Reconstructive Surgery, Shanghai Key Laboratory of Tissue Engineering, Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, National Tissue Engineering Center of China, 639 Zhizaoju Road, Shanghai, 200011, China.
Adv Healthc Mater. 2021 Jan;10(2):e2000631. doi: 10.1002/adhm.202000631. Epub 2020 Nov 9.
Tissue regeneration driven by immunomodulatory agents has emerged as a potential solution for repairing bone defects. However, the therapeutic benefits are compromised by disturbances in the pro- and anti-inflammatory balance. Here, using magnesium nanoparticles (MgNPs) as a template, magnesium-enriched graphene oxide nanoscrolls (MgNPs@GNSs) designed for combinational modulation of the inflammatory response are reported. First, the different effects of graphene oxide (GO) and magnesium ions (Mg ) on Raw264.7 macrophage phenotype transformation are screened. The results reveal that GO activates inflammatory M1 macrophages, and that Mg facilitates repolarization of M1 macrophages to the pro-healing M2 phenotype. With sustained release of Mg , the MgNPs@GNS nanoplatform can orchestrate harmonious type 1 and type 2 inflammatory responses. Mg decrease the internalization of GO and downregulate the nuclear factor kappa-B pathway, which is profoundly involved in the inflammatory process. A series of experiments show that the ordered inflammatory response induced by MgNPs@GNSs stimulates in vitro angiogenesis and osteogenesis through chemotactic, mitogenic, and morphogenic actions. Obvious vascularized bone regeneration is achieved in a rat cranial bone defect model via MgNPs@GNS deposited decellularized bone matrix scaffold. Therefore, the potential of using inherently therapeutic nanomedicine to modulate biomaterial-induced immune responses and thus enhance bone regeneration is demonstrated.
免疫调节剂驱动的组织再生已成为修复骨缺损的潜在解决方案。然而,由于促炎和抗炎平衡的失调,治疗效果受到了影响。在这里,我们使用镁纳米粒子(MgNPs)作为模板,设计了用于炎症反应的组合调节的富含镁的氧化石墨烯纳米卷(MgNPs@GNSs)。首先,筛选了氧化石墨烯(GO)和镁离子(Mg )对 Raw264.7 巨噬细胞表型转化的不同影响。结果表明,GO 激活了促炎 M1 巨噬细胞,而 Mg 促进 M1 巨噬细胞向促愈合的 M2 表型极化。随着 Mg 的持续释放,MgNPs@GNS 纳米平台可以协调和谐的 1 型和 2 型炎症反应。Mg 减少了 GO 的内化并下调了核因子 kappa-B 通路,该通路与炎症过程密切相关。一系列实验表明,MgNPs@GNSs 诱导的有序炎症反应通过趋化、有丝分裂和形态发生作用刺激体外血管生成和成骨。通过 MgNPs@GNS 沉积脱细胞骨基质支架在大鼠颅骨缺损模型中实现了明显的血管化骨再生。因此,证明了使用固有治疗性纳米医学来调节生物材料诱导的免疫反应并增强骨再生的潜力。