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A Single Extracellular Vesicle (EV) Flow Cytometry Approach to Reveal EV Heterogeneity.


ABSTRACT: 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 nanostructures 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.

SUBMITTER: Shen W 

PROVIDER: S-EPMC6246790 | biostudies-literature | 2018 Nov

REPOSITORIES: biostudies-literature

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A Single Extracellular Vesicle (EV) Flow Cytometry Approach to Reveal EV Heterogeneity.

Shen Wen W   Guo Kaizhu K   Adkins Gary Brent GB   Jiang Qiaoshi Q   Liu Yang Y   Sedano Sabrina S   Duan Yaokai Y   Yan Wei W   Wang Shizhen Emily SE   Bergersen Kristina K   Worth Danielle D   Wilson Emma H EH   Zhong Wenwan W  

Angewandte Chemie (International ed. in English) 20181030 48


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 cyt  ...[more]

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