Arche de Noé immunologique
Accès gratuit
Med Sci (Paris)
Volume 25, Numéro 4, Avril 2009
Arche de Noé immunologique
Page(s) 405 - 411
Section M/S revues
Publié en ligne 15 avril 2009
  1. Manning, MJ. Fishes, in Immunology. A comparative approach, R. Turner, Editor. 1994, John Wiley & Sons: Chichester. p. 69–100.
  2. Kobayashi I, Kuniyoshi S, Saito K, et al. Long-term hematopoietic reconstitution by transplantation of kidney hematopoietic stem cells in lethally irradiated clonal gibuna crucian carp (Carassius auratus langsdorfii). Dev Comp Immunol 2008; 32 : 957–65.
  3. Yaniv K, Isogai S, Castranova D, et al. Live imaging of lymphatic development in the zebrafish. Nat Med 2006; 12 : 711–6.
  4. Bernard D, Riteau B, Hansen JD, et al. Phenotypic and functional similarity of gut intraepithelial and systemic T cells in a teleost fish. J Immunol 2006; 176 : 3942–9.
  5. Subramanian S, MacKinnon SL, Ross NW. A comparative study on innate immune parameters in the epidermal mucus of various fish species. Comparative Biochemistry and Physiology Part B: Biochem Mol Biol 2007; 148 : 256–63.
  6. Miller N, Wilson M, Bengtén E, et al. Functional and molecular characterization of teleost leukocytes. Immunol Rev 1998; 166 :187–97.
  7. Bleyzac P, Exbrayat JM, Fellah JS. Emergence dy système immunitaire adaptatif. Med Sci (Paris) 2005; 21 : 210–5.
  8. Wienholds E, Schulte-Merker S, Walderich B, Plasterk RH. Target-selected inactivation of the zebrafish rag1 gene. Science 2002; 297 : 99–102.
  9. Danilova N, Bussmann J, Jekosch K, Steiner LA. The immunoglobulin heavy-chain locus in zebrafish: identification and expression of a previously unknown isotype, immunoglobulin Z. Nat Immunol 2005; 6 : 295–302.
  10. Hansen JD, Landis ED, Phillips RB. Discovery of a unique Ig heavy-chain isotype (IgT) in rainbow trout: Implications for a distinctive B cell developmental pathway in teleost fish. Proc Natl Acad Sci U S A 2005; 102 : 6919–24.
  11. Kaattari SL, Zhang HL, Khor IW, Kaattari IM, Shapiro DA. Affinity maturation in trout: clonal dominance of high affinity antibodies late in the immune response. Dev Comp Immunol 2002; 26 : 191–200.
  12. Yang F, Waldbieser GC, Lobb CJ. The nucleotide targets of somatic mutation and the role of selection in immunoglobulin heavy chains of a teleost fish. J Immunol 2006; 176 : 1655–67.
  13. Li J, Barreda DR, Zhang YA, et al. B lymphocytes from early vertebrates have potent phagocytic and microbicidal activities. Nat Immunol 2006; 7 : 1116–24.
  14. Herbomel, P., B. Thisse, and C. Thisse, Ontogeny and behaviour of early macrophages in the zebrafish embryo. Development 1999; 126 : 3735–45.
  15. Le Guyader D, Redd MJ, Colucci-Guyon E, et al. Origins and unconventional behavior of neutrophils in developing zebrafish. Blood 2008; 111.
  16. Cuesta A, Angeles Esteban M, Meseguer J. Cloning, distribution and up-regulation of the teleost fish MHC class II alpha suggests a role for granulocytes as antigen-presenting cells. Mol Immunol 2006; 43 : 1275–85.
  17. Yoder JA. Investigating the morphology, function and genetics of cytotoxic cells in bony fish. Comp Biochem Physiol C Toxicol Pharmacol 2004; 138 : 271–80.
  18. Vandepoele K, De Vos W, Taylor JS, et al. Major events in the genome evolution of vertebrates: paranome age and size differ considerably between ray-finned fishes and land vertebrates. Proc Natl Acad Sci USA 2004; 101 :1638–43.
  19. Hansen JD, Strassburger P, Thorgaard GH, Young WP, Du Pasquier L. Expression, linkage, and polymorphism of MHC-related genes in rainbow trout, Oncorhynchus mykiss. J Immunol 1999; 163 : 774–86.
  20. Nakao M, Mutsuro J, Nakahara M, Kato Y, Yano T. Expansion of genes encoding complement components in bony fish: biological implications of the complement diversity. Dev Comp Immunol 2003; 27 : 749–62.
  21. Roach JC, Glusman G, Rowen L, et al. The evolution of vertebrate Toll-like receptors. Proc Natl Acad Sci USA 2005; 102 : 9577–82.
  22. Matsuo A, Oshiumi H, Tsujita T, et al. Teleost TLR22 recognizes RNA duplex to induce IFN and protect cells from birnaviruses. J Immunol 200; 181 : 3474–85.
  23. Lutfalla G, Roest Crollius H, Stange-Thomann N, et al. Comparative genomic analysis reveals independent expansion of a lineage-specific gene family in vertebrates: the class II cytokine receptors and their ligands in mammals and fish. BMC Genomics 2003; 4 : 29.
  24. Huising MO, Kruiswijk CP, Flik G. Phylogeny and evolution of class-I helical cytokines. J Endocrinol 2006; 189 : 1–25.
  25. Stein C, Caccamo M, Laird G, Leptin M. Conservation and divergence of gene families encoding components of innate immune response systems in zebrafish. Genome Biol 2007; 8 : R251.
  26. Huising MO, Stet RJ, Savelkoul HF, et al. The molecular evolution of the interleukin-1 family of cytokines ; IL-18 in teleost fish. Dev Comp Immunol 2004; 28 : 395–413.
  27. Nomiyama H, Hieshima K, Osada N, et al. Extensive expansion and diversification of the chemokine genefamily in zebrafish: Identification of a novel chemokine subfamily CX. BMC Genomics 2008; 9 : 222.
  28. de Kinkelin P, Dorson M. Interferon production in rainbow trout (Salmo gairdneri) experimentally infected with Egtved virus. J Gen Virol 1973; 19 : 125–7.
  29. Robertsen B, Bergan V, Røkenes T, Larsen R, Albuquerque A. Atlantic salmon interferon genes: cloning, sequence analysis, expression, and biological activity. J Interferon Cytokine Res 2003; 23 : 601–12.
  30. Sun B, Robertsen B, Wang Z, Liu B. Identification of an Atlantic salmon IFN multigene cluster encoding three IFN subtypes with very different expression properties. Dev Comp Immunol 2009; 33 : 547–58.
  31. Levraud JP, Boudinot P, Colin I, et al. Identification of the zebrafish IFN receptor: implications for the origin of the vertebrate IFN system. J Immunol 2007; 178 : 4385–94.
  32. Zou J, Yoshiura Y, Dijkstra JM, et al. Identification of an interferon gamma homologue in Fugu, Takifugu rubripes. Fish Shellfish Immunol 2004; 17 : 403–9.
  33. Haller O, Kochs G, Weber F. The interferon response circuit: induction and suppression by pathogenic viruses. Virology 2006; 344 : 119–30.
  34. Staeheli P, Yu YX, Grob R, Haller O. A double-stranded RNA-inducible fish gene homologous to the murine influenza virus resistance gene Mx. Mol Cell Biol 1989; 9 : 3117–21.
  35. Boudinot P, Salhi S, Blanco M, Benmansour A. Viral haemorrhagic septicaemia virus induces vig-2, a new interferon-responsive gene in rainbow trout. Fish Shellfish Immunol 2001; 11 : 383–97.
  36. Boudinot P, Massin P, Blanco M, Riffault S, Benmansour A. vig-1, a new fish gene induced by the rhabdovirus glycoprotein, has a virus-induced homologue in humans and shares motifs with the MoaA family. J Virol 1999; 73 : 1846–52.
  37. van der Aa LM, Levraud JP, Yahmi M, et al. A large new subset of TRIM genes highly diversified by duplication and positive selection in teleost fish. BMC Biology, 2009. 7: p. 7.
  38. DuPasquier L. Diversification des immuno-récepteurs au cours de l’évolution des Métazoaires. Med Sci 2009 sous presse.
  39. Bisbal C, Salehzada T. RNase L, a crucial mediator of innate immunity and other cell functions. Med Sci (Paris) 2008; 24 : 859–64.

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