4.6 Article

Sizing and phenotyping of cellular vesicles using Nanoparticle Tracking Analysis

Journal

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.nano.2011.04.003

Keywords

Microvesicles; Microparticles; Exosomes; Nanoparticle Tracking Analysis; Flow Cytometry

Funding

  1. Wellcome Trust [GR087730, GR079862MA]
  2. Oxford Partnership Comprehensive Biomedical Research Centre
  3. Department of Health's NIHR Biomedical Research Centre

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Cellular microvesicles and nanovesicles (exosomes) are involved in many disease processes and have major potential as biomarkers. However, developments in this area are constrained by limitations in the technology available for their measurement. Here we report on the use of fluorescence nanoparticle tracking analysis (NTA) to rapidly size and phenotype cellular vesicles. In this system vesicles are visualized by light scattering using a light microscope. A video is taken, and the NTA software tracks the brownian motion of individual vesicles and calculates their size and total concentration. Using human placental vesicles and plasma, we have demonstrated that NTA can measure cellular vesicles as small as similar to 50 nm and is far more sensitive than conventional flow cytometry (lower limit similar to 300 nm). By combining NTA with fluorescence measurement we have demonstrated that vesicles can be labeled with specific antibody-conjugated quantum dots, allowing their phenotype to be determined. From the Clinical Editor: The authors of this study utilized fluorescence nanoparticle tracking analysis (NTA) to rapidly size and phenotype cellular vesicles, demonstrating that NTA is far more sensitive than conventional flow cytometry. (C) 2011 Elsevier Inc. All rights reserved.

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