核糖核酸
细胞内
体内
小泡
细胞生物学
纳米技术
细胞
细菌
膜
细菌外膜
生物物理学
化学
生物
材料科学
生物化学
基因
生物技术
遗传学
大肠杆菌
作者
Dawei Sun,Yize Li,Xiaoxuan Yin,Yali Fan,Jing Liu,Yaxin Wang,Xinyu Liu,Guijie Bai,Ke Li,Yanyan Shi,Peiyuan Liu,Yingying Zhang,Hanjie Wang
出处
期刊:ACS Nano
[American Chemical Society]
日期:2024-12-18
卷期号:18 (52): 35296-35309
被引量:1
标识
DOI:10.1021/acsnano.4c11412
摘要
Delivery systems play a crucial role in RNA therapy. However, the current RNA delivery system involves complex preparation and transport processes, requiring RNA preassembly in vitro, transportation at low temperatures throughout, and possibly multiple injections for improved therapeutic efficacy. To address these challenges, we developed a simple and efficient RNA delivery system. This system only requires the injection of engineered bacteria, which serve as in vivo "cell factories" for continuous production of the target RNA. The RNA can self-assemble with engineered bacteria's outer membrane vesicles (OMVs), facilitating in vivo RNA delivery. Experimental results demonstrated that this system allowed effective delivery with excellent stability and continuity for various types of RNA, including mRNA, miRNA, and siRNA. And the relative abundance of target RNA in the OMVs was 104-107 times higher than that in the mock group. We took the delivery of PD-L1 siRNA for tumor treatment as an example and found that this system could effectively downregulate the gene expression of PD-L1 by approximately twofold. Notably, a single injection of engineered bacteria achieved a significant tumor suppression of 49.37% in vivo. This research provides promising insights into the RNA delivery system for tumor therapy.
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