内体
细胞外小泡
纳米颗粒
纳米医学
材料科学
纳米技术
胞吐
细胞外
微泡
胞外囊泡
自噬
药物输送
细胞内
生物物理学
小泡
内吞作用
细胞生物学
化学
细胞
膜
生物化学
生物
细胞凋亡
小RNA
基因
作者
Lihuan Shang,Qi Xie,Conglian Yang,Li Kong,Zhiping Zhang
标识
DOI:10.1021/acsami.3c10237
摘要
The interaction between nanoparticles and cells is closely associated with the therapeutic effects of nanomedicine. Nanoparticles could be transported among cells, but the process-related mechanism remains to be further explored. In this study, it was found that endocytosed cationic polymer nanoparticles (cNPs) could be excreted in an extracellular vesicle (EV)-coated form (cNP@EVs). It was deduced that cNPs may pass through early endosomes, multivesicular bodies (MVBs), and autophagic MVBs within cells. Moreover, a high level of autophagy facilitated the exocytosis process. Since EVs were the effective vehicles for conveying biological information and substances, cNP@EVs were proved to be efficient forms for the intercellular transportation of nanoparticles and have the potential as efficient biomimetic drug delivery systems. These properties endowed cNP@EVs with deep penetration and enhanced antitumor activity. Our findings provided a proof-of-concept for understanding the transfer process of nanoparticles among cells and may help us to further utilize EV-mediated transportation of nanoparticles, therefore, expanding its clinical application.
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