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Cryo‐electron microscopy of extracellular vesicles in fresh plasma

Yuana Yuana, Roman I. Koning, Maxim E. Kuil and 4 more

Journal of Extracellular Vesicles · 2013 · CC BY-NC

doi:10.3402/jev.v2i0.21494

Abstract

Introduction Extracellular vesicles (EV) are phospholipid bilayer‐enclosed vesicles recognized as new mediators in intercellular communication and potential biomarkers of disease. They are found in many body fluids and mainly studied in fractions isolated from blood plasma in view of their potential in medicine. Due to the limitations of available analytical methods, morphological information on EV in fresh plasma is still rather limited. Objectives To image EV and determine the morphology, structure and size distribution in fresh plasma by cryo‐electron microscopy (cryo‐EM). Methods Fresh citrate‐ and ethylenediaminetetraacetic acid (EDTA)‐anticoagulated plasma or EV isolated from these plasmas were rapidly cryo‐immobilized by vitrification and visualized by cryo‐EM. Results EV isolated from fresh plasma were highly heterogeneous in morphology and size and mostly contain a discernible lipid bilayer (lipid vesicles). In fresh plasma there were 2 types of particles with a median diameter of 30 nm (25–260 nm). The majority of these particles are electron dense particles which most likely represent lipoproteins. The minority are lipid vesicles, either electron dense or electron lucent, which most likely represent EV. Lipid vesicles were occasionally observed in close proximity of platelets in citrate and EDTA‐anticoagulated platelet‐rich plasma. Cryo‐electron tomography (cryo‐ET) was employed to determine the 3D structure of platelet secretory granules. Conclusions Cryo‐EM is a powerful technique that enables the characterization of EV in fresh plasma revealing structural details and considerable morphological heterogeneity. Only a small proportion of the submicron structures in fresh plasma are lipid vesicles representing EV.

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References 23

  1. 1.

    Yuana Y, Sturk A, Nieuwland R. Extracellular vesicles in physiological and pathological conditions. Blood Rev. 2013;27:31-9.

    Not in our library10.1016/j.blre.2012.12.002

  2. 2.

    Anderson HC, Mulhall D, Garimella R. Role of extracellular membrane vesicles in the pathogenesis of various diseases, including cancer, renal diseases, atherosclerosis, and arthritis. Lab Invest. 2010;90:1549-57.

    Not in our library10.1038/labinvest.2010.152

  3. 3.

    György B, Szabó TG, Pásztói M, Pál Z, Misják P, Aradi B, et al. Membrane vesicles, current state-of-the-art: emerging role of extracellular vesicles. Cell Mol Life Sci. 2011;68:2667-88.

    Not in our library10.1007/s00018-011-0689-3

  4. 4.

    van der Pol E, van Gemert MJ, Sturk A, Nieuwland R, van Leeuwen TG. Single vs. swarm detection of microparticles and exosomes by flow cytometry. J Thromb Haemost. 2012;10:919-30.

    Not in our library10.1111/j.1538-7836.2012.04683.x

  5. 5.

    Yuana Y, Bertina RM, Osanto S. Pre-analytical and analytical issues in the analysis of blood microparticles. Thromb Haemost. 2010;105:396-408.

    Not in our library10.1160/th10-09-0595

  6. 6.

    Ayers L, Kohler M, Harrison P, Sargent I, Dragovic R, Schaap M, et al. Measurement of circulating cell-derived microparticles by flow cytometry: sources of variability within the assay. Thromb Res. 2011;127:370-7.

    Not in our library10.1016/j.thromres.2010.12.014

  7. 7.

    Lee RD, Barcel DA, Williams JC, Wang JG, Boles JC, Manly DA, et al. Pre-analytical and analytical variables affecting the measurement of plasma-derived microparticle tissue factor activity. Thromb Res. 2012;129:80-5.

    Not in our library10.1016/j.thromres.2011.06.004

  8. 8.

    Yuana Y, Oosterkamp TH, Bahatyrova S, Ashcroft B, Garcia Rodriguez P, Bertina RM, et al. Atomic force microscopy: a novel approach to the detection of nanosized blood microparticles. J Thromb Haemost. 2010;8:315-23.

    Not in our library10.1111/j.1538-7836.2009.03654.x

  9. 9.
  10. 10.

    Aras O, Shet A, Bach RR, Hysjulien JL, Slungaard A, Hebbel RP, et al. Induction of microparticle- and cell-associated intravascular tissue factor in human endotoxemia. Blood. 2004;103:4545-53.

    Not in our library10.1182/blood-2003-03-0713

  11. 11.

    Heijnen HF, Schiel AE, Fijnheer R, Geuze HJ, Sixma JJ. Activated platelets release two types of membrane vesicles: microvesicles by surface shedding and exosomes derived from exocytosis of multivesicular bodies and alpha-granules. Blood. 1999;94:3791-9.

    Not in our library

  12. 12.

    Grigorieff N, Harrison SC. Near-atomic resolution reconstructions of icosahedral viruses from electron cryo-microscopy. Curr Opin Struct Biol. 2011;21:265-73.

    Not in our library10.1016/j.sbi.2011.01.008

  13. 13.

    Koning RI, Koster AJ. Cryo-electron tomography in biology and medicine. Ann Anat. 2009;191:427-45.

    Not in our library10.1016/j.aanat.2009.04.003

  14. 14.
  15. 15.

    Redgrave TG, Roberts DC, West CE. Separation of plasma lipoproteins by density-gradient ultracentrifugation. Anal Biochem. 1975;65:42-9.

    Not in our library10.1016/0003-2697(75)90488-1

  16. 16.

    Faas FG, Avramut MC, van den Berg BM, Mommaas AM, Koster AJ, Ravelli RB. Virtual nanoscopy: generation of ultra-large high resolution electron microscopy maps. J Cell Biol. 2012;198:457-69.

    Not in our library10.1083/jcb.201201140

  17. 17.

    Liu Y, Atkinson D. Immuno-electron cryo-microscopy imaging reveals a looped topology of apoB at the surface of human LDL. J Lipid Res. 2011;52:1111-16.

    Not in our library10.1194/jlr.m013946

  18. 18.

    Han M, Gillard BK, Courtney HS, Ward K, Rosales C, Khant H, et al. Disruption of human plasma high-density lipoproteins by streptococcal serum opacity factor requires labile apolipoprotein A-I. Biochemistry. 2009;48:1481-7.

    Not in our library10.1021/bi802287q

  19. 19.

    Zhang L, Yan F, Zhang S, Lei D, Charles MA, Cavigiolio G, et al. Structural basis of transfer between lipoproteins by cholesteryl ester transfer protein. Nat Chem Biol. 2012;8:342-9.

    Not in our library10.1038/nchembio.796

  20. 20.

    van Nispen tot Pannerden H, de Haas F, Geerts W, Posthuma G, van Dijk S, Heijnen HF. The platelet interior revisited: electron tomography reveals tubular alpha-granule subtypes. Blood. 2010;116:1147-56.

    Not in our library10.1182/blood-2010-02-268680

  21. 21.

    Raposo G, Stoorvogel W. Extracellular vesicles: exosomes, microvesicles, and friends. J Cell Biol. 2013;200:373-83.

    Not in our library10.1083/jcb.201211138

  22. 22.

    Brisson AR, Tan S, Arraud N, Gounou C. Plasmatic microvesicles: their size, morphology, phenotype revealed by cryo-electron microscopy and specific gold labeling. J Extracell Vesicles. 2013;2.

    Not in our library

  23. 23.

    de Vrij J, Maas SL, van Nispen M, Sena-Esteves M, Limpens RW, Koster AJ, et al. Quantification of nanosized extracellular membrane vesicles with scanning ion occlusion sensing. Nanomedicine. 2013;8:1443-58.

    Not in our library10.2217/nnm.12.173

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