[Contamination of exosome preparations, isolated from biological fluids]

A E Grigor'eva1, N S Dyrkheeva1, O E Bryzgunova1

  • 1Institute of Chemical Biology and Fundamental Medicine, SB RAS, Novosibirsk, Russia.

Insights

Contamination is common in exosome preparations, with lipoproteins often mistaken for exosomes. Electron microscopy is crucial for identifying these non-vesicle contaminants in research samples.

Area of Science:

  • Biotechnology
  • Nanomedicine
  • Cell Biology

Background:

  • Exosomes are crucial biomarkers and therapeutic agents.
  • Current isolation methods may yield contaminated preparations.
  • Accurate characterization of exosomes is vital for reliable research.

Purpose of the Study:

  • To investigate contamination in exosome preparations.
  • To identify non-exosomal structures in isolated samples.
  • To highlight the importance of quality control in exosome research.

Main Methods:

  • Transmission electron microscopy (JEM-1400) used for structural analysis.
  • Immuno-electron microscopy with CD63/CD9 antibodies for exosome identification.
  • Isolation of exosomes from diverse biological fluids (plasma, urine, serum, cell culture).

Main Results:

  • All exosome preparations contained exosomes and contaminating "non-vesicles".
  • Two main types of non-vesicles (20-40 nm and 40-100 nm) identified as lipoproteins.
  • Highest contamination levels observed in plasma-derived exosome preparations.

Conclusions:

  • Exosome preparations frequently contain lipoprotein contaminants.
  • Electron microscopy is essential for distinguishing exosomes from non-vesicles.
  • Researchers must account for contaminants in experimental data analysis.