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Journal of Zhejiang University SCIENCE B

ISSN 1673-1581(Print), 1862-1783(Online), Monthly

Extracellular vesicles (EVs)’ journey in recipient cells: from recognition to cargo release

Abstract: 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.

Key words: Extracellular vesicle (EV); Exosome; Endocytosis; Uptake; Release

Chinese Summary  <25> 胞外囊泡在受体细胞中的旅程:从识别到货物释放

相华苑, 包晨轩, 陈巧巧, 高庆, 王楠, 高乾乾, 茅凌翔
江苏大学附属昆山医院检验科, 中国昆山市, 215300
摘要:胞外囊泡(EVs)是几乎所有细胞均能分泌的纳米级脂质双层囊泡,可通过将其内含的多种包括蛋白质、脂质、编码和非编码RNA、线粒体DNA等在内的生物活性分子递送到邻近和远处的受体细胞中,以改变受体细胞功能,从而实现细胞间的信息交流。EVs在生理和病理过程中均发挥着重要作用,可用于疾病诊疗。尽管EVs在供体细胞中的生物发生和分泌机制已基本清晰,但受体细胞对EVs的识别和摄取的分子机制尚不清楚。本文对EVs进入受体细胞的生物过程包括受体细胞对EVs的识别、摄取以及EVs的货物释放进行综述,并重点关注了EVs在摄取后如何通过"溶酶体逃逸",从而释放货物,将有助于推进EVs作为药物递送载体的研究。此外,了解和控制EVs在受体细胞中的有效摄取,对阐明EVs的功能及其临床应用同样至关重要。

关键词组:胞外囊泡;外泌体;内吞作用;摄取;释放


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DOI:

10.1631/jzus.B2300566

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On-line Access:

2024-08-27

Received:

2023-10-17

Revision Accepted:

2024-05-08

Crosschecked:

2024-08-19

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