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Meeting Report

Proceedings of the ISEV symposium on “HIV, NeuroAIDS, drug abuse & EVs”

, , , , , & ORCID Icon show all
Article: 1294360 | Received 13 Jan 2017, Accepted 06 Feb 2017, Published online: 10 Mar 2017

References

  • Thery C, Zitvogel L, Amigorena S. Exosomes: composition, biogenesis and function. Nat Reviews Immunol. 2002;2(8):1–8.
  • Valadi H, Ekstrom K, Bossios A, et al. Exosome-mediated transfer of mRNAs and microRNAs is a novel mechanism of genetic exchange between cells. Nat Cell Biol. 2007;9(6):654–659.
  • Hu G, Drescher KM, Chen XM. Exosomal miRNAs: biological properties and therapeutic potential. Front Genet. 2012;3:56.
  • Hu G, Gong AY, Roth AL, et al. Release of luminal exosomes contributes to TLR4-mediated epithelial antimicrobial defense. Plos Pathog. 2013;9(4):e1003261.
  • Trams EG, Lauter CJ, Salem N Jr., et al. Exfoliation of membrane ecto-enzymes in the form of micro-vesicles. Biochim Biophys Acta. 1981;645(1):63–70.
  • Pan BT, Teng K, Wu C, et al. Electron microscopic evidence for externalization of the transferrin receptor in vesicular form in sheep reticulocytes. J Cell Biol. 1985;101(3):942–948.
  • 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):9412–9420.
  • Gupta A, Pulliam L. Exosomes as mediators of neuroinflammation. J Neuroinflammation. 2014;11:68.
  • Schwab A, Meyering SS, Lepene B, et al. Extracellular vesicles from infected cells: potential for direct pathogenesis. Front Microbiol. 2015;6:1132.
  • Hu G, Yao H, Chaudhuri AD, et al. Exosome-mediated shuttling of microRNA-29 regulates HIV Tat and morphine-mediated neuronal dysfunction. Cell Death Dis. 2012;3:e381.
  • Tan IL, McArthur JC. HIV-associated neurological disorders: a guide to pharmacotherapy. CNS Drugs. 2012;26(2):123–134.
  • Gould SJ, Booth AM, Hildreth JE. The Trojan exosome hypothesis. Proc Natl Acad Sci U S A. 2003;100(19):10592–10597.
  • Mack M, Kleinschmidt A, Bruhl H, et al. Transfer of the chemokine receptor CCR5 between cells by membrane-derived microparticles: a mechanism for cellular human immunodeficiency virus 1 infection. Nat Med. 2000;6(7):769–775.
  • Simons M, Raposo G. Exosomes–vesicular carriers for intercellular communication. Curr Opin Cell Biol. 2009;21(4):575–581.
  • Svedberg T, Pedersen KO, Bauer JH. The ultracentrifuge. Oxford: The Clarendon Press; 1940. p. 478.
  • Stanley WM. Isolation and properties of tobacco mosaic and other virus proteins: harvey lecture, March 17, 1938. Bull N Y Acad Med. 1938;14(7):398–428.
  • Stanley WM, Wyckoff RW. The isolation of tobacco ring spot and other virus proteins by ultracentrifugation. Science. 1937;85(2198):181–183.
  • Chargaff E, West R. The biological significance of the thromboplastic protein of blood. J Biol Chem. 1946;166(1):189–197.
  • Wolf P. The nature and significance of platelet products in human plasma. Br J Haematol. 1967;13(3):269–288.
  • Thery C, Amigorena S, Raposo G, et al. Isolation and characterization of exosomes from cell culture supernatants and biological fluids. Curr Protoc Cell Biol. 2006 Chapter 3: Unit 3.22.
  • Witwer KW, Buzás EI, Bemis LT, et al. Standardization of sample collection, isolation and analysis methods in extracellular vesicle research: an ISEV position paper. J Extracell Vesicles. 2013;2:20360.
  • Anderson HC. Vesicles associated with calcification in the matrix of epiphyseal cartilage. J Cell Biol. 1969;41(1):59–72.
  • Brody I, Ronquist G, Gottfries A. Ultrastructural localization of the prostasome - an organelle in human seminal plasma. Ups J Med Sci. 1983;88(2):63–80.
  • Poutsiaka DD, Schroder EW, Taylor DD, et al. Membrane vesicles shed by murine melanoma cells selectively inhibit the expression of Ia antigen by macrophages. J Immunology. 1985;134(1):138–144.
  • Raposo G, Nijman HW, Stoorvogel W, et al. B lymphocytes secrete antigen-presenting vesicles. J Exp Med. 1996;183(3):1161–1172.
  • Dettenhofer M, Yu XF. Highly purified human immunodeficiency virus type 1 reveals a virtual absence of Vif in virions. J Virol. 1999;73(2):1460–1467.
  • Bess JW Jr., Gorelick RJ, Bosche WJ, et al. Microvesicles are a source of contaminating cellular proteins found in purified HIV-1 preparations. Virology. 1997;230(1):134–144.
  • Ott DE. Purification of HIV-1 virions by subtilisin digestion or CD45 immunoaffinity depletion for biochemical studies. Methods Mol Biol. 2009;485:15–25.
  • Cantin R, Diou J, Belanger D, et al. Discrimination between exosomes and HIV-1: purification of both vesicles from cell-free supernatants. J Immunol Methods. 2008;338(1–2):21–30.
  • Pegtel DM, Cosmopoulos K, Thorley-Lawson DA, et al. Functional delivery of viral miRNAs via exosomes. Proc Natl Acad Sci U S A. 2010;107(14):6328–6333.
  • Skog J, Wurdinger T, Van Rijn S, et al. Glioblastoma microvesicles transport RNA and proteins that promote tumour growth and provide diagnostic biomarkers. Nat Cell Biol. 2008;10(12):1470–1476.
  • Kliewer S, Forman B, Blumberg B, et al. Differential expression and activation of a family of murine peroxisome proliferator-activated receptors. Pnas. 1994;91(15):7355–7359.
  • Vega RB, Huss JM, Kelly DP. The coactivator PGC-1 cooperates with peroxisome proliferator-activated receptor α in transcriptional control of nuclear genes encoding mitochondrial fatty acid oxidation enzymes. Mol Cell Biol. 2000;20(5):1868–1876.
  • Staels B, Koenig W, Habib A, et al. Activation of human aortic smooth-muscle cells is inhibited by PPARα but not by PPARγ activators. Nature. 1998;393(6687):790–793.
  • Schnell L, Fearn S, Schwab ME, et al. Cytokine-induced acute inflammation in the brain and spinal cord. J Neuropathol Exp Neurol. 1999;58(3):245–254.
  • Wilcockson DC, Campbell SJ, Anthony DC, et al. The systemic and local acute phase response following acute brain injury. J Cereb Blood Flow Metab. 2002;22(3):318–326.
  • Campbell SJ, Hughes PM, Iredale JP, et al. CINC-1 is an acute-phase protein induced by focal brain injury causing leukocyte mobilization and liver injury. Faseb J. 2003;17(9):1168–1170.
  • Campbell SJ, Zahid I, Losey P, et al. Liver Kupffer cells control the magnitude of the inflammatory response in the injured brain and spinal cord. Neuropharmacology. 2008;55(5):780–787.
  • McCluskey L, Campbell S, Anthony D, et al. Inflammatory responses in the rat brain in response to different methods of intra-cerebral administration. J Neuroimmunol. 2008;194(1–2):27–33.
  • Losey P, Ladds E, Laprais M, et al. The role of PPAR activation during the systemic response to brain injury. J Neuroinflammation. 2015;12:99.
  • Sampey GC, Meyering SS, Asad Zadeh M, et al. Exosomes and their role in CNS viral infections. J Neurovirol. 2014;20(3):199–208.
  • Sampey GC, Saifuddin M, Schwab A, et al. Exosomes from HIV-1-infected cells stimulate production of pro-inflammatory cytokines through trans-activating response (TAR) RNA. J Biol Chem. 2016;291(3):1251–1266.
  • Ismail N, Wang Y, Dakhlallah D, et al. Macrophage microvesicles induce macrophage differentiation and miR-223 transfer. Blood. 2013;121(6):984–995.
  • Pulliam L, Gupta A. Modulation of cellular function through immune-activated exosomes. DNA Cell Biol. 2015;34(7):459–463.
  • Tang N, Sun B, Gupta A, et al. Monocyte exosomes induce adhesion molecules and cytokines via activation of NF-kappaB in endothelial cells. Faseb J. 2016;30(9):3097–3106.