Department of Laboratory Medicine, Affiliated Kunshan Hospital of Jiangsu University, Kunshan 215300, China.
J Zhejiang Univ Sci B. 2024 Aug 15;25(8):633-655. doi: 10.1631/jzus.B2300566.
Extracellular vesicles (EVs) are nano-sized bilayer vesicles that are shed or secreted by virtually every cell type. A variety of biomolecules, including proteins, lipids, coding and non-coding RNAs, and mitochondrial DNA, can be selectively encapsulated into EVs and delivered to nearby and distant recipient cells, leading to alterations in the recipient cells, suggesting that EVs play an important role in intercellular communication. EVs play effective roles in physiology and pathology and could be used as diagnostic and therapeutic tools. At present, although the mechanisms of exosome biogenesis and secretion in donor cells are well understood, the molecular mechanism of EV recognition and uptake by recipient cells is still unclear. This review summarizes the current understanding of the molecular mechanisms of EVs' biological journey in recipient cells, from recognition to uptake and cargo release. Furthermore, we highlight how EVs escape endolysosomal degradation after uptake and thus release cargo, which is crucial for studies applying EVs as drug-targeted delivery vehicles. Knowledge of the cellular processes that govern EV uptake is important to shed light on the functions of EVs as well as on related clinical applications.
细胞外囊泡(EVs)是由几乎所有细胞类型分泌或释放的纳米大小双层囊泡。各种生物分子,包括蛋白质、脂质、编码和非编码 RNA 以及线粒体 DNA,可以被选择性地包裹在 EV 中,并递送到附近和远处的受体细胞,导致受体细胞发生改变,这表明 EV 在细胞间通讯中发挥着重要作用。EV 在生理和病理中发挥着有效的作用,并可作为诊断和治疗工具。目前,尽管供体细胞中 exosome 生物发生和分泌的机制已经得到很好的理解,但 EV 被受体细胞识别和摄取的分子机制仍不清楚。本文综述了目前对 EV 在受体细胞中的生物学途径的分子机制的理解,从识别到摄取和货物释放。此外,我们强调了 EV 在摄取后如何逃避内体溶酶体降解从而释放货物,这对于将 EV 作为药物靶向递送载体的研究至关重要。了解控制 EV 摄取的细胞过程对于揭示 EV 的功能以及相关的临床应用都很重要。