Effective methods for isolation and purification of extracellular vesicles from plants

被引:48
|
作者
Huang, Yifan [1 ,2 ]
Wang, Shumei [3 ,4 ]
Cai, Qiang [1 ,2 ]
Jin, Hailing [3 ,4 ]
机构
[1] Wuhan Univ, State Key Lab Hybrid Rice, Coll Life Sci, Wuhan 430072, Peoples R China
[2] Hubei Hongshan Lab, Wuhan 430072, Peoples R China
[3] Univ Calif Riverside, Dept Microbiol & Plant Pathol, Inst Integrat Genome Biol, Riverside, CA 92507 USA
[4] Univ Calif Riverside, Ctr Plant Cell Biol, Riverside, CA 92507 USA
基金
美国农业部; 美国国家科学基金会; 中国国家自然科学基金; 澳大利亚研究理事会;
关键词
cell-to-cell communication; extracellular vesicles; isolation methods; plants interacting with pathogens; SMALL RNAS; EXOSOMES; TRAFFICKING; PATHOGEN; ARABIDOPSIS; CELLS; BIOGENESIS; MICRORNAS; SECRETION; INHIBIT;
D O I
10.1111/jipb.13181
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Plant extracellular vesicles (EVs) play critical roles in the cross-kingdom trafficking of molecules from hosts to interacting microbes, most notably in plant defense responses. However, the isolation of pure, intact EVs from plants remains challenging. A variety of methods have been utilized to isolate plant EVs from apoplastic washing fluid (AWF). Here, we compare published plant EV isolation methods, and provide our recommended method for the isolation and purification of plant EVs. This method includes a detailed protocol for clean AWF collection from Arabidopsis thaliana leaves, followed by EV isolation via differential centrifugation. To further separate and purify specific subclasses of EVs from heterogeneous vesicle populations, density gradient ultracentrifugation and immunoaffinity capture are then utilized. We found that immunoaffinity capture is the most precise method for specific EV subclass isolation when suitable specific EV biomarkers and their corresponding antibodies are available. Overall, this study provides a guide for the selection and optimization of EV isolation methods for desired downstream applications.
引用
收藏
页码:2020 / 2030
页数:11
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