骨钙素
运行x2
化学
碱性磷酸酶
双膦酸盐
体内
体外
骨桥蛋白
癌症研究
生物化学
成骨细胞
医学
酶
生物
骨质疏松症
内科学
生物技术
作者
Qianming Du,Na Li,Ziwei Jing,Lianping Xue,Haojie Fu,Jiyun Liu,Qingquan Jia,Zhi Sun,Wei He,Xiaojian Zhang
标识
DOI:10.1016/j.apmt.2023.101787
摘要
The growing use of bisphosphonates (BPs) is a great challenge to the treatment of bisphosphonate-related osteonecrosis of the jaws (BRONJ), however effective treatment methods are currently lacking. Here, modified citraconic amide-functionalized chitosan (CAS) was selected to encapsulate the zeolite imidazolate framework 8 (ZIF-8) loaded with gold nanoparticles (Au NPs) to prepare Au@ZIF-8/CAS. Characterizations confirmed the successful synthesis of Au@ZIF-8/CAS. Mass spectrometry-based metabolomics detected the effects of Au@ZIF-8/CAS on significant metabolic pathways of macrophages in the presence of zoledronic acid (ZA). Twenty-three candidate key metabolites were identified, mainly focusing on the phenylalanine/tyrosine/tryptophan biosynthetic metabolic pathway in the amino acid metabolic pathway. In vitro experiments further confirmed that Au@ZIF-8/CAS could promote the polarization of macrophages from M1 pro-inflammatory phenotype to M2 anti-inflammatory phenotype, so as to produce a good immune microenvironment. In the co-culture system, Au@ZIF-8/CAS could also promote the expression of alkaline phosphatase (ALP), Osteocalcin (OCN), and Runt-related transcription factor 2 (Runx2), and synergistically increased the osteogenic differentiation ability of MC3T3-E1 cells through immunomodulatory effects and direct osteogenic stimulation. Furthermore, the antibacterial properties of Au@ZIF-8/CAS were also investigated. In vivo experiments further verified the potential role of Au@ZIF-8/CAS in treatment of BRONJ. These results will provide new directions and ideas for the treatment of inflammatory diseases.
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