间质细胞
骨髓
骨质疏松症
生物相容性
小泡
骨细胞
骨重建
化学
药物输送
细菌外膜
细胞生物学
骨愈合
微生物学
医学
药理学
癌症研究
生物
免疫学
膜
病理
内科学
生物化学
解剖
有机化学
大肠杆菌
基因
作者
Sanfu Lin,Chonggang Chen,Yuhui Zheng,Baofang Wu,Wenhua Wu
出处
期刊:Biomedicines
[Multidisciplinary Digital Publishing Institute]
日期:2025-04-02
卷期号:13 (4): 847-847
标识
DOI:10.3390/biomedicines13040847
摘要
Introduction: Osteoporosis (OP) is a prevalent condition marked by reduced bone density and a heightened risk of fractures. Current treatments often have side effects, underscoring the need for safer alternatives. Recent research highlights the significant role of gut microbiota and their metabolites in maintaining bone health. Notably, bacterial outer membrane vesicles (OMVs) have emerged as a promising platform due to their nanoscale sizes, low toxicity, drug-loading capabilities, and excellent biocompatibility. Methods: In this study, we developed a delivery system using OMVs derived from Pseudomonas mirabilis (PM). By anchoring bone-targeting peptides to the PM-OMVs membrane, we equipped these vesicles to deliver endogenous miRNAs to the bone microenvironment effectively. Results and Discussion: The bone-targeted PM-OMVs (PM-OMVs-BT) demonstrated exceptional bone-targeting abilities and exhibited a favorable safety profile in vivo. Additionally, LGG-OMVs-BT were successfully internalized by bone marrow stromal cells (BMSCs) without significant cytotoxicity, effectively promoting their osteogenic differentiation and mineralization. In conclusion, our study indicates that PM-OMVs-BT could offer a safe and effective treatment option for OP.
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