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Accueil Tous les numéros Volume 37 / Numéro 12 (Décembre 2021) Med Sci (Paris), 37 12 (2021) 1089-1091 Références
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Numéro
Med Sci (Paris)
Volume 37, Numéro 12, Décembre 2021
Vésicules extracellulaires
Page(s) 1089 - 1091
Section Vésicules extracellulaires
DOI https://doi.org/10.1051/medsci/2021200
Publié en ligne 20 décembre 2021
  1. Cocozza F, Grisard E, Martin-Jaular L, et al. SnapShot : Extracellular Vesicles. Cell 2020 ; 182(1) : 262–e1. [CrossRef] [PubMed] [Google Scholar]
  2. van Niel G, D’Angelo G, Raposo G. Shedding light on the cell biology of extracellular vesicles. Nat Rev Mol Cell Biol 2018 ; 19(4) : 213–28. [CrossRef] [PubMed] [Google Scholar]
  3. Raposo G, van Niel G, Stahl PD. Extracellular vesicles and homeostasis-An emerging field in bioscience research. FASEB Bioadv 2021 ; 3(6) : 456–8. [CrossRef] [PubMed] [Google Scholar]
  4. Gyorgy B, Szabo TG, Pasztoi M, et al. Membrane vesicles, current state-of-the-art : emerging role of extracellular vesicles. Cell Mol Life Sci 2011 ; 68 : 2667–88. [CrossRef] [PubMed] [Google Scholar]
  5. Wolf P. The nature and significance of platelet products in human plasma. Br J Haematol 1967 ; 13(3) : 269–88. [CrossRef] [PubMed] [Google Scholar]
  6. Dachary-Prigent J, Freyssinet JM, Pasquet JM, et al. Annexin V as a probe of aminophospholipid exposure and platelet membrane vesiculation : a flow cytometry study showing a role for free sulfhydryl groups. Blood 1993 ; 81(10) : 2554–65. [CrossRef] [PubMed] [Google Scholar]
  7. Aupeix K, Hugel B, Martin T, et al. The significance of shed membrane particles during programmed cell death in vitro, and in vivo, in HIV-1 infection. J Clin Invest 1997 ; 99(7) : 1546–54. [CrossRef] [PubMed] [Google Scholar]
  8. Satta N, Toti F, Feugeas O, Bohbot A, et al. Monocyte vesiculation is a possible mechanism for dissemination of membrane-associated procoagulant activities and adhesion molecules after stimulation by lipopolysaccharide. J Immunol 1994 ; 153(7) : 3245–55. [PubMed] [Google Scholar]
  9. Mallat Z, Benamer H, Hugel B, et al. Elevated levels of shed membrane microparticles with procoagulant potential in the peripheral circulating blood of patients with acute coronary syndromes. Circulation 2000 ; 101(8) : 841–3. [CrossRef] [PubMed] [Google Scholar]
  10. Boulanger CM, Scoazec A, Ebrahimian T, et al. Circulating microparticles from patients with myocardial infarction cause endothelial dysfunction. Circulation 2001 ; 104(22) : 2649–52. [CrossRef] [PubMed] [Google Scholar]
  11. Combes V, Simon AC, Grau GE, et al. In vitro generation of endothelial microparticles and possible prothrombotic activity in patients with lupus anticoagulant. J Clin Invest 1999 ; 104(1) : 93–102. [CrossRef] [PubMed] [Google Scholar]
  12. Sabatier F, Roux V, Anfosso F, et al. Interaction of endothelial microparticles with monocytic cells in vitro induces tissue factor-dependent procoagulant activity. Blood 2002 ; 99(11) : 3962–70. [CrossRef] [PubMed] [Google Scholar]
  13. Raposo G, Nijman HW, Stoorvogel W, et al. B lymphocytes secrete antigen-presenting vesicles. J Exp Med 1996 ; 183(3) : 1161–72. [CrossRef] [PubMed] [Google Scholar]
  14. Harding C, Heuser J, Stahl P. Receptor-mediated endocytosis of transferrin and recycling of the transferrin receptor in rat reticulocytes. J Cell Biol 1983 ; 97(2) : 329–39. [CrossRef] [PubMed] [Google Scholar]
  15. Pan BT, Johnstone RM. Fate of the transferrin receptor during maturation of sheep reticulocytes in vitro : selective externalization of the receptor. Cell 1983 ; 33(3) : 967–78. [CrossRef] [PubMed] [Google Scholar]
  16. Johnstone RM, Adam M, Hammond JR, et al. Vesicle formation during reticulocyte maturation. Association of plasma membrane activities with released vesicles (exosomes). J Biol Chem 1987 ; 262(19) : 9412–20. [CrossRef] [PubMed] [Google Scholar]
  17. Trams EG, Lauter CJ, Salem N Jr, Heine U. Exfoliation of membrane ecto-enzymes in the form of micro-vesicles. Biochim Biophys Acta 1981 ; 645(1) : 63–70. [CrossRef] [PubMed] [Google Scholar]
  18. Vidal M, Sainte-Marie J, Philippot JR, Bienvenue A. Asymmetric distribution of phospholipids in the membrane of vesicles released during in vitro maturation of guinea pig reticulocytes: evidence precluding a role for “aminophospholipid translocase”. J Cell Physiol 1989 ; 140(3) : 455–62. [CrossRef] [PubMed] [Google Scholar]
  19. Zitvogel L, Regnault A, Lozier A, et al. Eradication of established murine tumors using a novel cell-free vaccine : dendritic cell-derived exosomes. Nat Med 1998 ; 4(5) : 594–600. [CrossRef] [PubMed] [Google Scholar]
  20. Witwer KW, Thery C. Extracellular vesicles or exosomes? On primacy, precision, and popularity influencing a choice of nomenclature. J Extracell Vesicles 2019 ; 8(1) : 1648167. [CrossRef] [PubMed] [Google Scholar]
  21. Raposo G, Tenza D, Mecheri S, et al. Accumulation of major histocompatibility complex class II molecules in mast cell secretory granules and their release upon degranulation. Mol Biol Cell 1997 ; 8(12) : 2631–45. [CrossRef] [PubMed] [Google Scholar]
  22. Aline F, Bout D, Amigorena S, et al. Toxoplasma gondii antigen-pulsed-dendritic cell-derived exosomes induce a protective immune response against T. gondii infection. Infect Immun 2004 ; 72(7) : 4127–37. [CrossRef] [PubMed] [Google Scholar]
  23. Peche H, Heslan M, Usal C, et al. Presentation of donor major histocompatibility complex antigens by bone marrow dendritic cell-derived exosomes modulates allograft rejection. Transplantation 2003 ; 76(10) : 1503–10. [CrossRef] [PubMed] [Google Scholar]
  24. Thery C, Regnault A, Garin J, et al. Molecular characterization of dendritic cell-derived exosomes. Selective accumulation of the heat shock protein hsc73. J Cell Biol 1999 ; 147(3) : 599–610. [CrossRef] [PubMed] [Google Scholar]
  25. van Niel G, Raposo G, Candalh C, et al. Intestinal epithelial cells secrete exosome-like vesicles. Gastroenterology 2001 ; 121(2) : 337–49. [CrossRef] [PubMed] [Google Scholar]
  26. Blanchard N, Lankar D, Faure F, et al. TCR activation of human T cells induces the production of exosomes bearing the TCR/CD3/zeta complex. J Immunol 2002 ; 168(7) : 3235–41. [CrossRef] [PubMed] [Google Scholar]
  27. Wolfers J, Lozier A, Raposo G, et al. Tumor-derived exosomes are a source of shared tumor rejection antigens for CTL cross-priming. Nat Med 2001 ; 7(3) : 297–303. [CrossRef] [PubMed] [Google Scholar]
  28. Fevrier B, Vilette D, Archer F, et al. Cells release prions in association with exosomes. Proc Natl Acad Sci U S A 2004 ; 101(26) : 9683–8. [CrossRef] [PubMed] [Google Scholar]
  29. Faure J, Lachenal G, Court M, et al. Exosomes are released by cultured cortical neurones. Mol Cell Neurosci 2006 ; 31(4) : 642–8. [CrossRef] [PubMed] [Google Scholar]

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