4.6 Article

Gold Nanocluster Extracellular Vesicle Supraparticles: Self-Assembled Nanostructures for Three-Dimensional Uptake Visualization

期刊

LANGMUIR
卷 36, 期 14, 页码 3912-3923

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.langmuir.9b03479

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资金

  1. Deutsche Forschungsgemeinschaft [KA 4370/1-1]
  2. NanoMed Marie Sklodowska-Curie ITN from the H2020 program [676137]
  3. GlaxoSmithKline Engineered Medicines Laboratory
  4. Swiss National Science Foundation [P300PA_171540]
  5. FP7Marie Curie Intra-European Fellowship SMase LIPOSOME [626766]
  6. Swedish Foundation of Strategic Research in the Industrial Research Centre, FoRmulaEx - Nucleotide Functional Drug Delivery [IRC15-0065]
  7. Ermenegildo Zegna Founder's Scholarship Program
  8. Rosetrees Trust
  9. European Union [642414]
  10. Department of Medicine and the Department of Bioengineering, Imperial College London
  11. EPSRC
  12. Wellcome Trust [098411/Z/12/Z]
  13. Swiss National Science Foundation (SNF) [P300PA_171540] Funding Source: Swiss National Science Foundation (SNF)
  14. Marie Curie Actions (MSCA) [676137] Funding Source: Marie Curie Actions (MSCA)

向作者/读者索取更多资源

Extracellular vesicles (EVs) are secreted by the vast majority of cells and are being intensively studied due to their emerging involvement in a variety of cellular communication processes. However, the study of their cellular uptake and fate has been hampered by difficulty in imaging EVs against the cellular background. Here, we show that EVs combined with hydrophobic gold nanoclusters (AuNCs) can self-assemble into supraparticles, offering an excellent labeling strategy for high-resolution electron microscopic imaging in vitro. We have tracked and visualized the reuptake of breast cancer cell-derived EV AuNC supraparticles into their parent cells, from early endocytosis to lysosomal degradation, using focused ion beam-scanning electron microscopy (FIB-SEM). The presence of gold within the EVs and lysosomes was confirmed via DF-STEM EDX analysis of lift-out sections. The demonstrated formation of AuNC EV supraparticles will facilitate future applications in EV imaging as well as the EV-assisted cellular delivery of AuNCs.

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