Liang Luxin, Lin Zhengjun, Duan Ziqing, Agbedor Solomon-Oshioke, Li Ning, Baker Ian, Wang Bing, Liu Tang, Wu Hong
Department of Orthopedics, The Second Xiangya Hospital, Central South University, Changsha 410011, P. R. China.
Department of Spine Surgery, The Second Xiangya Hospital, Central South University, Changsha 410083, P. R. China.
Regen Biomater. 2024 Aug 29;11:rbae104. doi: 10.1093/rb/rbae104. eCollection 2024.
Facilitating an appropriate immune response is crucial for promoting bone tissue regeneration upon biomaterial implantation. In this study, the Mg-containing nanostructures on the surface of Ti-1.25Mg alloy were prepared by a one-step hydrothermal reaction method via regulating pH value to enhance the immunomodulatory osteogenic properties of Ti-Mg alloys. In neutral (HT7) or alkaline (HT9) hydrothermal treatment (HT) solution, the size of MgTiO nanostructures formed on the surface of Ti-1.25Mg alloy is smaller than that in acidic HT solution (HT5), and lamellar Mg(OH) nanostructures are found in HT7 and HT9. In addition, the sample surface has a lower roughness and higher wettability with increasing pH value. The Mg-containing nanostructures on the Ti-1.25Mg alloy inhibited inflammatory response by promoting the polarization of M2 macrophages, thereby promoting osteogenesis in vitro. The micro-CT and histological assessment proved that the regeneration of bone defect was faster in HT7 than the Ti-1.25Mg . Mechanically, Mg-containing nanostructures can mediate the immune response of macrophages via upregulating integrins α5β1 and inhibiting Toll-like receptors (TLR-4), subsequently inhibiting the NF-κB signaling pathway. Overall, osteoimmunity-regulating Mg-containing nanostructures on Ti-1.25Mg present a promising biomaterial for bone repair.
促进适当的免疫反应对于生物材料植入后促进骨组织再生至关重要。在本研究中,通过一步水热反应法,通过调节pH值制备了Ti-1.25Mg合金表面含镁纳米结构,以增强Ti-Mg合金的免疫调节成骨性能。在中性(HT7)或碱性(HT9)水热处理(HT)溶液中,Ti-1.25Mg合金表面形成的MgTiO纳米结构尺寸小于酸性HT溶液(HT5)中的尺寸,并且在HT7和HT9中发现了层状Mg(OH)纳米结构。此外,随着pH值的增加,样品表面粗糙度降低,润湿性提高。Ti-1.25Mg合金上的含镁纳米结构通过促进M2巨噬细胞极化抑制炎症反应,从而在体外促进成骨。显微CT和组织学评估证明,HT7中骨缺损的再生比Ti-1.25Mg更快。从机制上讲,含镁纳米结构可通过上调整合素α5β1和抑制Toll样受体(TLR-4)来介导巨噬细胞的免疫反应,随后抑制NF-κB信号通路。总体而言,Ti-1.25Mg上调节骨免疫的含镁纳米结构是一种很有前途的骨修复生物材料。