Ag2O‐TiO2‐NTs enhance osteogenic activity in vitro by modulating TNF‐α/β‐catenin signaling in bone marrow‐derived mesenchymal stem cells

碱性磷酸酶 乳酸脱氢酶 免疫印迹 化学 间充质干细胞 运行x2 肿瘤坏死因子α 分子生物学 骨桥蛋白 骨髓 细胞生物学 生物化学 生物 免疫学 基因
作者
Zhan‐Peng Zeng,Chang‐Rong Lai,Wei‐Jie Zheng
出处
期刊:Chemical Biology & Drug Design [Wiley]
卷期号:103 (3)
标识
DOI:10.1111/cbdd.14501
摘要

Abstract The toxic effects of nanoparticles‐silver oxide (Ag 2 O) limited its use. However, loading Ag 2 O nanoparticles into titanium dioxide (TiO 2 ) nanotubes (Ag 2 O‐TiO 2 ‐NTs) has more efficient biological activity and safety. The aim of this study was to observe the effect of Ag 2 O‐TiO 2 ‐NTs on osteogenic differentiation of bone marrow‐derived mesenchymal stem cells (BMSCs) and its mechanism. The enzyme activity of lactate dehydrogenase (LDH) and the expression of RUNX family transcription factor 2 (Runx2), OPN, OCN in BMSCs were detected by quantitative real time polymerase chain reaction. At 14 days of induction, the mineralization ability and alkaline phosphatase (ALP) activity of cells in each group were observed by Alizarin Red S staining and ALP staining. In addition, the protein levels of tumor necrosis factor‐α (TNF‐α) and β‐catenin in BMSCs of each group were observed by western blot. After 14 days of the induction, the mineralization ability and ALP activity of BMSCs in the Ag 2 O‐TiO 2 ‐NTs group were significantly enhanced compared with those in the Ag 2 O and TiO 2 groups. Western blot analysis showed that the BMSCs in the Ag 2 O‐TiO 2 ‐NTs group exhibited much lower protein level of TNF‐α and higher protein level of β‐catenin than those in the Ag 2 O and TiO 2 groups.Ag 2 O‐TiO 2 ‐NTs enhance the osteogenic activity of BMSCs by modulating TNF‐α/β‐catenin signaling.
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