细胞外小泡
骨质疏松症
胞外囊泡
小泡
细胞外
骨形态发生蛋白2
微泡
微生物学
计算生物学
医学
细胞生物学
生物信息学
生物
病理
生物化学
体外
微泡
膜
基因
小RNA
作者
Han Liu,Peiran Song,Hao Zhang,Fengjin Zhou,Ning Ji,Mingkai Wang,Guangyin Zhou,Ruina Han,Xinru Liu,Weizong Weng,Haoqi Tan,Sicheng Wang,Lei Zheng,Yingying Jing,Jiacan Su
摘要
Osteoporosis (OP) is a systematic bone disease characterized by low bone mass and fragile bone microarchitecture. Conventional treatment for OP has limited efficacy and long-term toxicity. Synthetic biology makes bacterial extracellular vesicle (BEVs)-based therapeutic strategies a promising alternative for the treatment of OP. Here, we constructed a recombinant probiotics Escherichia coli Nissle 1917-pET28a-ClyA-BMP-2-CXCR4 (ECN-pClyA-BMP-2-CXCR4), in which BMP-2 and CXCR4 were overexpressed in fusion with BEVs surface protein ClyA. Subsequently, we isolated engineered BEVs-BMP-2-CXCR4 (BEVs-BC) for OP therapy. The engineered BEVs-BC exhibited great bone targeting in vivo. In addition, BEVs-BC had good biocompatibility and remarkable ability to promote osteogenic differentiation of BMSCs. Finally, the synthetic biology-based BEVs-BC significantly prevented the OP in an ovariectomized (OVX) mouse model. In conclusion, we constructed BEVs-BC with both bone-targeting and bone-forming in one-step using synthetic biology, which provides an effective strategy for OP and has great potential for industrialization.
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