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Detailed analysis of the plasma extracellular vesicle proteome after separation from lipoproteins

Karimi, Nasibeh (författare)
Gothenburg University,Göteborgs universitet,Krefting Research Centre
Cvjetkovic, Aleksander (författare)
Gothenburg University,Göteborgs universitet,Krefting Research Centre
Jang, Su Chul, 1984 (författare)
Gothenburg University,Göteborgs universitet,Krefting Research Centre
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Crescitelli, Rossella, 1985 (författare)
Gothenburg University,Göteborgs universitet,Krefting Research Centre
Feizi, M. A. H. (författare)
Nieuwland, R. (författare)
Lötvall, Jan, 1956 (författare)
Gothenburg University,Göteborgs universitet,Krefting Research Centre
Lässer, Cecilia, 1981 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för medicin, avdelningen för invärtesmedicin och klinisk nutrition,Krefting Research Centre,Institute of Medicine, Department of Internal Medicine and Clinical Nutrition
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 (creator_code:org_t)
2018-02-13
2018
Engelska.
Ingår i: Cellular and Molecular Life Sciences. - : Springer Science and Business Media LLC. - 1420-682X .- 1420-9071. ; 75:15, s. 2873-2886
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • The isolation of extracellular vesicles (EVs) from blood is of great importance to understand the biological role of circulating EVs and to develop EVs as biomarkers of disease. Due to the concurrent presence of lipoprotein particles, however, blood is one of the most difficult body fluids to isolate EVs from. The aim of this study was to develop a robust method to isolate and characterise EVs from blood with minimal contamination by plasma proteins and lipoprotein particles. Plasma and serum were collected from healthy subjects, and EVs were isolated by size-exclusion chromatography (SEC), with most particles being present in fractions 8-12, while the bulk of the plasma proteins was present in fractions 11-28. Vesicle markers peaked in fractions 7-11; however, the same fractions also contained lipoprotein particles. The purity of EVs was improved by combining a density cushion with SEC to further separate lipoprotein particles from the vesicles, which reduced the contamination of lipoprotein particles by 100-fold. Using this novel isolation procedure, a total of 1187 proteins were identified in plasma EVs by mass spectrometry, of which several proteins are known as EV-associated proteins but have hitherto not been identified in the previous proteomic studies of plasma EVs. This study shows that SEC alone is unable to completely separate plasma EVs from lipoprotein particles. However, combining SEC with a density cushion significantly improved the separation of EVs from lipoproteins and allowed for a detailed analysis of the proteome of plasma EVs, thus making blood a viable source for EV biomarker discovery.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine (hsv//eng)

Nyckelord

Exosomes
Extracellular vesicles
Lipoproteins
Plasma
Serum
Size-exclusion chromatography
Density cushion
Mass spectrometry
Proteomics
blood-plasma
exosomes
microvesicles
cells
density
rna
chromatography
subpopulations
micrornas
proteins
Biochemistry & Molecular Biology
Cell Biology

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