计算生物学
微泡
化学
非编码RNA
核糖核酸
适体
细胞生物学
分子生物学
生物
遗传学
小RNA
基因
作者
Emily E. Bonacquisti,Scott Ferguson,Gable M. Wadsworth,Natalie E. Jasiewicz,Jinli Wang,Ameya Chaudhari,Caden C. Kussatz,Ana T. Nogueira,Daniel P. Keeley,Michelle S. Itano,Matthew L. Bolton,Klaus M. Hahn,Priya R. Banerjee,Juliane Nguyen
标识
DOI:10.1016/j.jconrel.2024.07.043
摘要
Extracellular vesicles (EVs), or exosomes, play important roles in physiological and pathological cellular communication and have gained substantial traction as biological drug carriers. EVs contain both short and long non-coding RNAs that regulate gene expression and epigenetic processes. To fully capitalize on the potential of EVs as drug carriers, it is important to study and understand the intricacies of EV function and EV RNA-based communication. Here we developed a genetically encodable RNA-based biomaterial, termed EXO-Probe, for tracking EV RNAs. The EXO-Probe comprises an EV-loading RNA sequence (EXO-Code), fused to a fluorogenic RNA Mango aptamer for RNA imaging. This fusion construct allowed the visualization and tracking of EV RNA and colocalization with markers of multivesicular bodies; imaging RNA within EVs, and non-destructive quantification of EVs. Overall, the new RNA-based biomaterial provides a useful and versatile means to interrogate the role of EVs in cellular communication via RNA trafficking to EVs and to study cellular sorting decisions. The system will also help lay the foundation to further improve the therapeutic efficacy of EVs as drug carriers.
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