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The power of imaging to understand extracellular vesicle biology in vivo.
Verweij, Frederik J; Balaj, Leonora; Boulanger, Chantal M; Carter, David R F; Compeer, Ewoud B; D'Angelo, Gisela; El Andaloussi, Samir; Goetz, Jacky G; Gross, Julia Christina; Hyenne, Vincent; Krämer-Albers, Eva-Maria; Lai, Charles P; Loyer, Xavier; Marki, Alex; Momma, Stefan; Nolte-'t Hoen, Esther N M; Pegtel, D Michiel; Peinado, Hector; Raposo, Graça; Rilla, Kirsi; Tahara, Hidetoshi; Théry, Clotilde; van Royen, Martin E; Vandenbroucke, Roosmarijn E; Wehman, Ann M; Witwer, Kenneth; Wu, Zhiwei; Wubbolts, Richard; van Niel, Guillaume.
  • Verweij FJ; Université de Paris, Institute of Psychiatry and Neuroscience of Paris (IPNP), INSERM U1266, Paris, France. frederikverweij@gmail.com.
  • Balaj L; GHU Paris Psychiatrie et Neurosciences, Hôpital Sainte Anne, Paris, France. frederikverweij@gmail.com.
  • Boulanger CM; Department of Neurosurgery, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.
  • Carter DRF; Université de Paris, PARCC, INSERM, Paris, France.
  • Compeer EB; Department of Biological and Medical Sciences, Faculty of Health and Life Sciences, Oxford Brookes University, Oxford, UK.
  • D'Angelo G; Evox Therapeutics Limited, Oxford Science Park, Oxford, UK.
  • El Andaloussi S; Kennedy Institute of Rheumatology, NDORMS, University of Oxford, Oxford, UK.
  • Goetz JG; Institut Curie, PSL Research University, CNRS, UMR144 Cell Biology and Cancer, Paris, France.
  • Gross JC; Evox Therapeutics Limited, Oxford Science Park, Oxford, UK.
  • Hyenne V; Clinical Research Center, Department of Laboratory Medicine, Karolinska Institutet, Stockholm, Sweden.
  • Krämer-Albers EM; INSERM UMR_S1109, Tumor Biomechanics Lab, Université de Strasbourg, Fédération de Médecine Translationnelle de Strasbourg (FMTS), Equipe Labellisée Ligue contre le Cancer, Strasbourg, France.
  • Lai CP; Health and Medical University, Potsdam, Germany.
  • Loyer X; INSERM UMR_S1109, Tumor Biomechanics Lab, Université de Strasbourg, Fédération de Médecine Translationnelle de Strasbourg (FMTS), Equipe Labellisée Ligue contre le Cancer, Strasbourg, France.
  • Marki A; CNRS SNC5055, Strasbourg, France.
  • Momma S; Johannes Gutenberg-Universität Mainz, Institute of Developmental Biology and Neurobiology, Mainz, Germany.
  • Nolte-'t Hoen ENM; Institute of Atomic and Molecular Sciences, Academia Sinica, Taipei, Taiwan.
  • Pegtel DM; Université de Paris, PARCC, INSERM, Paris, France.
  • Peinado H; La Jolla Institute for Allergy and Immunology, La Jolla, CA, USA.
  • Raposo G; Institute of Neurology (Edinger Institute), Goethe-University, Frankfurt am Main, Germany.
  • Rilla K; Department of Biomolecular Health Sciences, Faculty of veterinary medicine, Utrecht University, Utrecht, the Netherlands.
  • Tahara H; Amsterdam UMC, Vrije Universiteit Amsterdam, Pathology, Cancer Center Amsterdam, Amsterdam, the Netherlands.
  • Théry C; Microenvironment and Metastasis Laboratory, Molecular Oncology Programme, Spanish National Cancer Research Center (CNIO), Madrid, Spain.
  • van Royen ME; Institut Curie, PSL Research University, CNRS, UMR144 Cell Biology and Cancer, Paris, France.
  • Vandenbroucke RE; University of Eastern Finland, Institute of Biomedicine, Kuopio, Finland.
  • Wehman AM; Department of Cellular and Molecular Biology, Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima, Japan.
  • Witwer K; Institut Curie, PSL Research University, INSERM U932, Immunity and Cancer, Paris, France.
  • Wu Z; Erasmus MC, Department of Pathology, Rotterdam, the Netherlands.
  • Wubbolts R; VIB Center for Inflammation Research and Department of Biomedical Molecular Biology, Ghent University, Ghent, Belgium.
  • van Niel G; Department of Biological Sciences, University of Denver, Denver, CO, USA.
Nat Methods ; 18(9): 1013-1026, 2021 09.
Article en En | MEDLINE | ID: mdl-34446922
Extracellular vesicles (EVs) are nano-sized lipid bilayer vesicles released by virtually every cell type. EVs have diverse biological activities, ranging from roles in development and homeostasis to cancer progression, which has spurred the development of EVs as disease biomarkers and drug nanovehicles. Owing to the small size of EVs, however, most studies have relied on isolation and biochemical analysis of bulk EVs separated from biofluids. Although informative, these approaches do not capture the dynamics of EV release, biodistribution, and other contributions to pathophysiology. Recent advances in live and high-resolution microscopy techniques, combined with innovative EV labeling strategies and reporter systems, provide new tools to study EVs in vivo in their physiological environment and at the single-vesicle level. Here we critically review the latest advances and challenges in EV imaging, and identify urgent, outstanding questions in our quest to unravel EV biology and therapeutic applications.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Vesículas Extracelulares / Microscopía Límite: Animals / Humans Idioma: En Año: 2021 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Vesículas Extracelulares / Microscopía Límite: Animals / Humans Idioma: En Año: 2021 Tipo del documento: Article