| Literature DB >> 34220409 |
Jiantong Dong1, Ryan Y Zhang1, Na Sun1, Junhui Hu2, Matthew D Smalley1, Anqi Zhou1, Hua Yue1, Winston Rothermich1, Mengxiang Chen1, Jiayuan Chen1, Jinglei Ye1, Pai-Chi Teng1, Dongping Qi1, Jeffrey A Toretsky3, James S Tomlinson4, Mengyuan Li5, Paul S Weiss6, Steven J Jonas7, Noah Federman7, Lily Wu2, Meiping Zhao5, Hsian-Rong Tseng1, Yazhen Zhu1.
Abstract
Tumor-derived extracellular vesicles (EVs) play essential roles in intercellular communication during tumor growth and metastatic evolution. Currently, little is known about the possible roles of tumor-derived EVs in sarcoma because the lack of specific surface markers makes it technically challenging to purify sarcoma-derived EVs. In this study, a specific purification system is developed for Ewing sarcoma (ES)-derived EVs by coupling covalent chemistry-mediated EV capture/ release within a nanostructure-embedded microchip. The purification platform-ES-EV Click Chip-takes advantage of specific anti-LINGO-1 recognition and sensitive click chemistry-mediated EV capture, followed by disulfide cleavage-driven EV release. Since the device is capable of specific and efficient purification of intact ES EVs with high purity, ES-EV Click Chip is ideal for conducting downstream functional studies of ES EVs. Absolute quantification of the molecular hallmark of ES (i.e., EWS rearrangements) using reverse transcription Droplet Digital PCR enables specific quantification of ES EVs. The purified ES EVs can be internalized by recipient cells and transfer their mRNA cargoes, exhibiting their biological intactness and potential role as biological shuttles in intercellular communication.Entities:
Keywords: covalent chemistry; extracellular vesicles; microfluidics; nanostructured substrates; sarcoma
Year: 2020 PMID: 34220409 PMCID: PMC8248519 DOI: 10.1002/adfm.202003237
Source DB: PubMed Journal: Adv Funct Mater ISSN: 1616-301X Impact factor: 18.808