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首页> 外文期刊>Angewandte Chemie >A Single Extracellular Vesicle (EV) Flow Cytometry Approach to Reveal EV Heterogeneity
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A Single Extracellular Vesicle (EV) Flow Cytometry Approach to Reveal EV Heterogeneity

机译:单个细胞外囊泡(EV)流式细胞术方法,以显示EV异质性

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摘要

Extracellular vesicles (EVs) actively participate in intercellular communication and pathological processes. Studying the molecular signatures of EVs is key to reveal their biological functions and clinical values, which, however, is greatly hindered by their sub-100 nm dimensions, the low quantities of biomolecules each EV carries, and the large population heterogeneity. Now, single-EV flow cytometry analysis is introduced to realize single EV counting and phenotyping in a conventional flow cytometer for the first time, enabled by target-initiated engineering (TIE) of DNA nano-structures on each EV. By illuminating multiple markers on single EVs, statistically significant differences are revealed among the molecular signatures of EVs originating from several breast cancer cell lines, and the cancer cell-derived EVs among the heterogeneous EV populations are successfully recognized. Thus, our approach holds great potential for various biological and biomedical applications.
机译:细胞外囊(EVS)积极参与细胞间通信和病理过程。 研究EVS的分子签名是揭示其生物学功能和临床价值的关键,然而,由于它们的亚100nm尺寸大大阻碍了,每次EV携带的低量生物分子和群体异质性大量阻碍。 现在,引入单eV流式细胞术分析,首次通过对每个EV上的DNA纳米结构的目标发起的工程(TIE)实现的常规流式细胞仪中的单个EV计数和表型。 通过在单个EV上照射多个标记,统计上显着的差异在源自几种乳腺癌细胞系的EVS的分子鉴定中,并且成功地认识到异质性EV群体中的癌细胞衍生的EV。 因此,我们的方法对各种生物和生物医学应用具有很大的潜力。

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