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      Current methods for the isolation of extracellular vesicles

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          Abstract

          Extracellular vesicles (EVs), including microvesicles and exosomes, are nano- to micron-sized vesicles, which may deliver bioactive cargos that include lipids, growth factors and their receptors, proteases, signaling molecules, as well as mRNA and non-coding RNA, released from the cell of origin, to target cells. EVs are released by all cell types and likely induced by mechanisms involved in oncogenic transformation, environmental stimulation, cellular activation, oxidative stress, or death. Ongoing studies investigate the molecular mechanisms and mediators of EVs-based intercellular communication at physiological and oncogenic conditions with the hope of using this information as a possible source for explaining physiological processes in addition to using them as therapeutic targets and disease biomarkers in a variety of diseases. A major limitation in this evolving discipline is the hardship and the lack of standardization for already challenging techniques to isolate EVs. Technical advances have been accomplished in the field of isolation with improving knowledge and emerging novel technologies, including ultracentrifugation, microfluidics, magnetic beads and filtration-based isolation methods. In this review, we will discuss the latest advances in methods of isolation methods and production of clinical grade EVs as well as their advantages and disadvantages, and the justification for their support and the challenges that they encounter.

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          Author and article information

          Contributors
          Journal
          9700112
          20453
          Biol Chem
          Biol. Chem.
          Biological chemistry
          1431-6730
          1437-4315
          6 March 2020
          October 2013
          16 March 2020
          : 394
          : 10
          : 1253-1262
          Affiliations
          Laboratory for Innovative Translational Technologies, Harvard Medical School, 77 Louis Pasteur Avenue, Harvard Medical School, Boston, MA 02115, USA
          Department of Neurology and Radiology, Massachusetts General Hospital, 149 13th Street, Charlestown, MA 02129, USA
          Biopolymers Facility, Harvard Medical School, 77 Louis Pasteur Avenue, Boston, MA 02115, USA
          Department of Immunology and Infectious Diseases, Harvard School of Public Health, 665 Huntington Avenue, Boston, MA 02120, USA
          Laboratory for Innovative Translational Technologies, Harvard Medical School, 77 Louis Pasteur Avenue, Harvard Medical School, Boston, MA 02115, USA
          Laboratory for Innovative Translational Technologies, Harvard Medical School, 77 Louis Pasteur Avenue, Harvard Medical School, Boston, MA 02115, USA
          University of New Mexico, 1 University Blvd NE, Albuquerque, NM 87131, USA
          University of North Texas, 1155 Union Circle, Denton, TX 76203, USA
          Harvard School of Dental Medicine, 188 Longwood Avenue, Boston, MA 02115, USA
          Faculty of Dentistry, Istanbul University, Turgut Özal Caddesi (Millet Cd.), 34390 Istanbul, Turkey
          Exosome Diagnostic Inc., 3960 Broadway, New York, NY 10032, USA
          Harvard Catalyst Laboratory for Innovative Translational Technologies, Harvard Medical School, Boston, MA 02115, USA; and Department of Developmental Biology, Harvard School of Dental Medicine, Boston, MA 02115, USA
          Author notes
          [a]

          These authors contributed equally to this work.

          [* ] Corresponding author: Winston Patrick Kuo, Harvard Catalyst Laboratory for Innovative Translational Technologies, Harvard Medical School, Boston, MA 02115, USA; and Department of Developmental Biology, Harvard School of Dental Medicine, Boston, MA 02115, USA, wkuo@ 123456genetics.med.harvard.edu
          Article
          PMC7075462 PMC7075462 7075462 nihpa1570537
          10.1515/hsz-2013-0141
          7075462
          23770532
          f59ec9a5-5126-4c50-aa60-4e0890a54864
          History
          Categories
          Article

          ultracentrifugation,microvesicles,clinical grade EVs,magnetic beads,sedimentation efficiency,exosomes

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