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[基于亲和相互作用的外泌体高效分离方法的典型策略与研究进展]

[Typical strategy and research progress of efficient isolation methods of exosomes based on affinity interaction].

作者信息

Wang Hai-Yan, Xie Pei-Juan, Qiao Xiao-Qiang, Zhang Li-Yuan

机构信息

School of Pharmacy, Hebei University, Baoding 071002, China.

Institute of Advanced Science Facilities, Shenzhen 518107, China.

出版信息

Se Pu. 2025 May;43(5):413-423. doi: 10.3724/SP.J.1123.2024.11004.

DOI:10.3724/SP.J.1123.2024.11004
PMID:40331606
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12059992/
Abstract

Exosomes form a subclass of extracellular vesicle that are secreted by most cells and found in nearly all body fluids, including blood, urine, saliva, amniotic fluid, and milk, as well as in various tissues and intercellular spaces. Exosomes have recently been recognized as crucial intercellular communication mediators, and an increasing number of studies have shown that exosomes are important liquid-biopsy tools that play irreplaceable roles in the diagnosis, prognosis, and treatment of diseases. The ability to isolate high-quality exosomes is a prerequisite for diagnosing and subsequently treating diseases in an accurate and repeatable manner. However, efficiently isolating exosomes from complex biological samples is challenging owing to their relatively low abundances and interference from non-vesicular macromolecules (such as cell debris and proteins). To date, various isolation techniques based on the physical, chemical, and biological characteristics of exosomes have been developed. Indeed, efficient affinity-interaction-based methods have recently overcome the limitations and drawbacks of traditional exosome isolation methods and are widely used in scientific research and clinical applications. This review focuses on exosome isolation and enrichment, and systematically reviews recent research progress on efficient isolation methods based on affinity interactions. Developmental prospects of exosome isolation and enrichment directions are analyzed with the aim of providing a reference for the construction and use of new exosome-isolation strategies.

摘要

外泌体是细胞外囊泡的一个亚类,由大多数细胞分泌,存在于几乎所有体液中,包括血液、尿液、唾液、羊水和乳汁,以及各种组织和细胞间隙中。外泌体最近被认为是关键的细胞间通讯介质,越来越多的研究表明,外泌体是重要的液体活检工具,在疾病的诊断、预后和治疗中发挥着不可替代的作用。分离高质量外泌体的能力是以准确且可重复的方式诊断和后续治疗疾病的先决条件。然而,由于外泌体丰度相对较低且受到非囊泡大分子(如细胞碎片和蛋白质)的干扰,从复杂生物样品中有效分离外泌体具有挑战性。迄今为止,已经开发了基于外泌体物理、化学和生物学特性的各种分离技术。事实上,基于高效亲和相互作用的方法最近克服了传统外泌体分离方法的局限性和缺点,并广泛应用于科学研究和临床应用。本综述聚焦于外泌体的分离和富集,并系统地综述了基于亲和相互作用的高效分离方法的最新研究进展。分析了外泌体分离和富集方向的发展前景,旨在为构建和使用新的外泌体分离策略提供参考。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef57/12059992/42da1eb216af/img_6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef57/12059992/da33ff490f87/img_1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef57/12059992/06295af57e5d/img_2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef57/12059992/8dd4fde0b750/img_3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef57/12059992/6588acecba0b/img_4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef57/12059992/7383ad3373e8/img_5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef57/12059992/42da1eb216af/img_6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef57/12059992/da33ff490f87/img_1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef57/12059992/06295af57e5d/img_2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef57/12059992/8dd4fde0b750/img_3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef57/12059992/6588acecba0b/img_4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef57/12059992/7383ad3373e8/img_5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef57/12059992/42da1eb216af/img_6.jpg

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1
Metabolic landscaping of extracellular vesicles from body fluids by phosphatidylserine imprinted polymer enrichment and mass spectrometry analysis.通过磷脂酰丝氨酸印迹聚合物富集和质谱分析对体液外泌体进行代谢轮廓分析。
Talanta. 2025 Jan 1;282:126940. doi: 10.1016/j.talanta.2024.126940. Epub 2024 Sep 26.
2
High-throughput proteomic analysis of extracellular vesicles from saliva by chemical probe-based array.基于化学探针的阵列对唾液外泌体进行高通量蛋白质组学分析。
Anal Chim Acta. 2024 Jun 22;1309:342699. doi: 10.1016/j.aca.2024.342699. Epub 2024 May 7.
3
Bilateral efforts to improve SERS detection efficiency of exosomes by Au/NaPMoO Combined with Phospholipid Epitope Imprinting.
通过 Au/NaPMoO 与磷脂表位印迹的联合作用,改善外泌体 SERS 检测效率的双边努力。
Biosens Bioelectron. 2024 Aug 15;258:116349. doi: 10.1016/j.bios.2024.116349. Epub 2024 Apr 29.
4
Plant-derived exosomes: a green approach for cancer drug delivery.植物来源的外泌体:癌症药物传递的绿色方法。
J Mater Chem B. 2024 Feb 28;12(9):2236-2252. doi: 10.1039/d3tb02752j.
5
Tumor-derived small extracellular vesicles in cancer invasion and metastasis: molecular mechanisms, and clinical significance.肿瘤来源的小细胞外囊泡在癌症侵袭和转移中的作用:分子机制及临床意义。
Mol Cancer. 2024 Jan 19;23(1):18. doi: 10.1186/s12943-024-01932-0.
6
Investigation of rare earth-based magnetic nanocomposites for specific enrichment of exosomes from human plasma.用于从人血浆中特异性富集外泌体的基于稀土的磁性纳米复合材料的研究。
J Chromatogr A. 2024 Jan 11;1714:464543. doi: 10.1016/j.chroma.2023.464543. Epub 2023 Nov 28.
7
High Throughput and Noninvasive Exosomal PD-L1 Detection for Accurate Immunotherapy Response Prediction via Tim4-Functionalized Magnetic Core-Shell Metal-Organic Frameworks.通过Tim4功能化的磁性核壳金属有机框架进行高通量无创外泌体PD-L1检测以准确预测免疫治疗反应
Anal Chem. 2023 Dec 12;95(49):18268-18277. doi: 10.1021/acs.analchem.3c04117. Epub 2023 Nov 27.
8
Functional surfaces for exosomes capturing and exosomal microRNAs analysis.用于外泌体捕获和外泌体 microRNAs 分析的功能表面。
Colloids Surf B Biointerfaces. 2024 Jan;233:113627. doi: 10.1016/j.colsurfb.2023.113627. Epub 2023 Oct 31.
9
Rapid and Highly Efficient Purification of Extracellular Vesicles Enabled by a TiO Hybridized Spongy-like Polymer.TiO 杂化海绵状聚合物实现了细胞外囊泡的快速高效纯化。
Anal Chem. 2023 Sep 26;95(38):14502-14510. doi: 10.1021/acs.analchem.3c03411. Epub 2023 Sep 13.
10
The ins-and-outs of exosome biogenesis, secretion, and internalization.外泌体的生物发生、分泌和内化的细节。
Trends Cell Biol. 2024 Feb;34(2):90-108. doi: 10.1016/j.tcb.2023.06.006. Epub 2023 Jul 26.