Phagocytosis of Leishmania. Interaction with the host and intracellular trafficking

Advances in Cellular and Molecular Biology of Membranes and Organelles

Volumn 6, Issue C, 1999, Pages 297-316

  Desjardins, Michel ^a   Descoteaux, Albert ^b  

^a UNIVERSITÉ DE MONTRÉAL   (Canada)

^b INRS INSTITUT ARMAND FRAPPIER   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0343981513     PISSN: 18745172     EISSN: None     Source Type: Book Series    
DOI: 10.1016/S1874-5172(99)80017-0     Document Type: Review

References (80)

1. Alexander J. Effect of the antiphagocytic agent cytochalasin B on macrophage invasion by Leishmania mexicana promastigotes and Trypanosoma cruzi epimastigotes. J. Protozool. 22 (1975) 237-240
2. Alexander J., and Vickerman K. Fusion of host cell secondary lysosomes with the parasitophorous vacuoles of Leishmania mexicana-infected macrophages. J. Protozool. 22 (1975) 502-508
3. Alexander J., and Russell D.G. The interaction of Leishmania species with macrophages. Adv. Parasitol. 31 (1992) 175-254
4. Antoine J.C., Prina E., Jouanne C., and Bongrand P. Parasitophorous vacuoles of Leishmania amazonensis-infected macrophages maintain an acidic pH. Infect. Immun. 58 (1990) 779-787
5. Antoine J.C., Jouanne C., Lang T., Prina E., de Chastellier C., and Frehel C. Localization of major histocompatibility complex calss II molecules in phagolysosomes of murine macrophages infected with Leishmania amazonensis. Infect. Immun. 59 (1991) 764-775
6. Beebe A.M., Mauze S., Schork N.J., and Coffman R.L. Serial backcross mapping of multiple loci associated with resistance to Leishmania major in mice. Immun. 6 (1997) 551-557
7. Blackwell J.M., Black G.F., Peacock C.S., Miller E.N., Sibthorpe D., Gnananandha D., Shaw J.J., Silveira F., Lins-Lainson Z., Ramos F., Collins A., and Shaw M.A. Immunogenetics of leishmanial and mycobacterial infections: the Belem Family Study. Philos. Trans. R. Soc. Lond. B. Biol. Sci. 352 (1997) 1331-1345
8. Brittingham A., Morrison C.J., McMaster W.R., McGwire B.S., Chang K.P., and Mosser D.M. Role of the Leishmania surface protease gp63 in complement fixation, cell adhesion, and resistance to complement-mediated lysis. J. Immunol. 155 (1995) 3102-3111
9. Bradley D.J., Taylor B.A., Blackwell J., Evans E.P., and Freeman J. Regulation of Leishmania populations within the host. III. Mapping of the locus controlling susceptibility to visceral leishmaniasis in the mouse. Clin. Exp. Immunol. 37 (1979) 7-14
10. Butcher B.A., Turco S.J., Hilty B.A., Pimenta P.F., Panunzio M., and Sacks D.L. Deficiency in beta1,3-galactosyltransferase of a Leishmania major lipophosphoglycan mutant adversely influences the Leishmania-sand fly interaction. J. Biol. Chem. 271 (1996) 20573-20579
11. Button L.L., Russell D.G., Klein H.L., Medina-Acosta E., Karess R.E., and McMaster W.R. Genes encoding the major surface glycoprotein in Leishmania are tandemly linked at a single chromosomal locus and are constitutively transcribed. Mol. Biochem. Parasitol. 32 (1989) 271-283
12. Carrera L., Gazzinelli R.T., Badolato R., Hieny S., Muller W., Kuhn R., and Sacks D.L. Leishmania promastigotes selectively inhibit interleukin 12 induction in bone marrow-derived macrophages from susceptible and resistant mice. J. Exp. Med. 183 (1996) 515-526
13. Cellier M., Prive G., Belouchi A., Kwan T., Rodrigues V., Chia W., and Gros P. Nramp defines a family of membrane proteins. Proc. Natl. Acad. Sci. U.S.A. 92 (1995) 10089-10093
14. Chang K.-P., and Dwyer D.M. Multiplication of a human parasite (Leishmania donovani) in phagolysosomes of hamster macrophages in vitro. Science 193 (1976) 678-680
15. Chang K.P., Chaudhuri G., and Fong D. Molecular determinants of Leishmania virulence. Annu. Rev. Microbiol. 44 (1990) 499-529
16. Collins H., Schaible U., Ernst J., and Russell D. Transfer of phagocytosed particles to the parasitophorous vacuole of Leishmania mexicana is a transient phenomenon preceding the acquisition of annexin I by the phagosome. J. Cell Sci. 110 (1997) 191-200
17. Culley F.J., Harris R.A., Kaye P.M., McAdam K.P., and Raynes J.G. C-reactive protein binds to a novel ligand on Leishmania donovani and increases uptake into human macrophages. J. Immunol. 156 (1996) 4691-4696
18. Descoteaux A., and Matlashewski G. C-fos and tumor necrosis factor gene expression in Leishmania donovani-infected macrophages. Mol. Cell. Biol. 9 (1989) 5223-5227
19. Descoteaux A., Matlashewski G., and Turco S.J. Inhibition of macrophage protein kinase C-mediated protein phosphorylation by Leishmania donovani lipophosphoglycan. J. Immunol. 149 (1992) 3008-3015
20. Descoteaux A., and Turco S.J. The lipophosphoglycan of Leishmania and macrophage protein kinase C. Parasitol. Today 9 (1993) 468-471
21. Descoteaux A., Luo Y., Turco S.J., and Beverley S.M. A specialized pathway affecting virulence glycoconjugates of Leishmania. Science 269 (1995) 1869-1872
22. Desjardins M., Huber L.A., Parton R.G., and Griffiths G. Biogenesis of phagolysosomes proceeds through a sequential series of interactions with endocytic apparatus. J. Cell Biol. 124 (1994) 677-688
23. Desjardins M. Biogenesis of phagolysosomes: the 'kiss and run' hypothesis. Trends Cell Biol. 5 (1995) 183-186
24. Desjardins M., and Descoteaux A. Inhibition of phagolysosomal biogenesis by the Leishmania lipophosphoglycan. J. Exp. Med. 185 (1997) 2061-2068
25. Desjardins M., Nsumu N.N., Corsini R., and Rondeau C. Maturation of phagosomes is accompanied by changes in their fusion properties and size-selective acquisition of solute materials from endosomes. J. Cell Sci. 110 (1997) 2303-2314
26. De Souza Leao S., Lang T., Prina E., Hellio R., and Antoine J.C. Intracellular Leishmania amazonensis amastigotes internalize and degrade MHC class II molecules of their host cells. J. Cell Sci. 108 (1995) 3219-3231
27. Dobrowolski J.M., and Sibley L.D. Toxoplasma invasion of mammalian cells is powered by the actin cytoskeleton of the parasite. Cell 84 (1996) 933-939
28. Falkow S., Isberg R.R., and Portnoy D.A. The interaction of bacteria with mammalian cells. Annu. Rev. Cell. Biol. 8 (1992) 333-363
29. Finlay B.B., and Falkow S. Common themes in microbial pathogenicity revisited. Microbiol. Mol. Biol. Rev. 61 (1997) 136-169
30. Flohé S., Lang T., and Moll H. Synthesis, stability, and subcellular distribution of major histocompatibility complex class II molecules in Langerhans cells infected with Leishmania major. Infect. Immun. 65 (1997) 3444-3450
31. Frommel T.O., Button L.L., Fujikura Y., and McMaster W.R. The major surface glycoprotein (GP63) is present in both life stages of Leishmania. Mol. Biochem. Parasitol. 38 (1990) 25-32
32. Green P.J., Feizi T., Stoll M.S., Thiel S., Prescott A., and McConville M.J. Recognition of the major cell surface glycoconjugates of Leishmania parasites by the human serum manan-binding protein. Mol. Biochem. Parasitol. 66 (1994) 319-328
33. Gruenheid S., Pinner E., Desjardins M., and Gros P. Natural resistance to infection with intracellular parasites: the Nrampl protein is recruited to the membrane of the phagosome. J. Exp. Med. 185 (1997) 717-730
34. Handman E., Schnur L.F., Spithill T.W., and Mitchell G.F. Passive transfer of Leishmania lipopolysaccharide confers parasite survival in macrophages. J. Immunol. 137 (1986) 3608-3613
35. Joiner K.A., Fuhrman S.A., Miettinen H.M., Kasper L.H., and Mellman I. Toxoplasma gondii: fusion competence of parasitophorous vacuoles in Fc receptor-transfected fibroblasts. Science 249 (1990) 641-646
36. Joshi P.B., Sacks D.L., Modi G., and McMaster W.R. Targeted gene deletion of Leishmania major genes encoding developmental stage-specific leishmanolysin. Mol. Microbiol. 27 (1998) 519-530
37. Lang T., de Chastellier C., Frehel C., Hellio R., Metezeau P., De Souza Leao S., and Antoine J.C. Distribution of MHC class I and of MHC class II molecules in macrophages infected with Leishmania amazonensis. J. Cell Sci. 107 (1994) 69-82
38. Lang T., Hellio R., Kaye P.M., and Antoine J.C. Leishmania donovani-infected macrophages: characterization of the parasitophorous vacuole and potential role of this organelle in antigen presentation. J. Cell Sci. 107 (1994) 2137-2150
39. Lang T., Prina E., Sibthorpe D., and Blackwell J.M. Nrampl transfection transfers Ity/Lsh/Bcg-related pleiotropic effects on macrophage activation: influence on antigen processing and presentation. Infect. Immun. 65 (1997) 380-386
40. Marth T., and Kelsall B.L. Regulation of interleukin-12 by complement receptor 3 signaling. J. Exp. Med. 185 (1997) 1987-1995
41. McConville M.J., and Blackwell JM. Developmental changes in the glycosylated phosphatidylinositols of Leishmania donovani: characterization of the promastigote and amastigote glycolipids. J. Biol. Chem. 266 (1991) 15170-15179
42. McConville M.J., Turco SJ., Ferguson M.A., and Sacks D.L. Developmental modification of lipophosphoglycan during the differentiation of Leishmania major promastigotes to an infectious stage. EMBO J. 11 (1992) 3593-3600
43. McGwire B., and Chang K.-P. Genetic rescue of surface metalloproteinase (gp63)-deficiency in Leishmania amazonensis variants increases their infection of macrophages at the early phase. Mol. Biochem. Parasitol. 66 (1994) 345-347
44. McNeely T.B., and Turco SJ. Requirement of lipophosphoglycan for intracellular survival of Leishmania donovani within human monocytes. J. Immunol. 144 (1990) 2475-2750
45. McNeely T.B., Tolson DL., Pearson T.W., and Turco S.J. Characterization of Leishmania donovani variant clones using anti-lipophosphoglycan monoclonal antibodies. Glycobiol. 1 (1990) 63-69
46. Medina-Acosta E., Karess R.E., Schwartz H., and Russell D.G. The promastigote surface protease (gp63) of Leishmania is expressed but differentially processed and localized in the amastigote stage. Mol. Biochem. Parasitol. 37 (1989) 263-273
47. Medina-Acosta E., Beverley S.M., and Russell D.G. Evolution and expression of the Leishmania surface proteinase (gp63) gene locus. Infect. Agents Dis. 2 (1993) 25-34
48. Miao L., Stafford A., Nir S., Turco S.J., Flanagan T.D., and Epand R.M. Potent inhibition of viral fusion by the lipophosphoglycan of Leishmania donovani. Biochem. 34 (1995) 4676-4683
49. Mosser D.M., and Edelson P.J. The mouse macrophage receptor for C3bi (CR3) is a major mechanism in the phagocytosis of Leishmania promastigotes. J. Immunol. 135 (1985) 2785-2789
50. Mosser D.M., and Rosenthal L.A. Leishmania-macrophage interactions: multiple receptors, multiple ligands and diverse cellular responses. Semin. Cell Biol. 4 (1993) 315-322
51. Nandan D., and Reiner N.E. Attenuation of gamma interferon-induced tyrosine phosphorylation in mononuclear phagocytes infected with Leishmania donovani: selective inhibition of signaling through Janus kinases and Stat1. Infect. Immun. 63 (1995) 4495-4500
52. Pearson R.D., Harcus J.L., Symes P.H., Romito R., and Donowitz G.R. Failure of the phagocytic oxidative response to protect human monocyte-derived macrophages from infection by Leishmania donovani. J. Immunol. 129 (1982) 1282-1286
53. Pimenta P.F.P., Saraiva E.M.B., Rowton E., Modi G.B., Garraway L.A., Beverley S.M., Turco S.J., and Sacks D.L. Evidence that the vectorial competence of phlebotomine sand flies for different species of Leishmania is controlled by structural polymorphisms in the surface lipophosphoglycan. Proc. Natl. Acad. Sci. U.S.A. 91 (1994) 9155-9159
54. Pitt A., Mayorga L.S., Stahl P.D., and Schwartz A.L. Alterations in the protein composition of maturing phagosomes. J. Clin. Invest. 90 (1992) 1978-1983
55. Prina E., Antoine J.C., Wiederanders B., and Krischke H. Localization and activity of various lysosomal proteases in Leishmania amazonensis-infected macrophages. Infect. Immun. 58 (1990) 1730-1737
56. Prina E., Lang T., Glaichenhaus N., and Antoine J.C. Presentation of the protective parasite antigen LACK by Leishmania-infected macrophages. J. Immunol. 156 (1996) 4318-4327
57. Puentes S.M., Sacks D.L., da Silva R.P., and Joiner K.A. Complement binding by two developmental stages of Leishmania major promastigotes varying in expression of a surface lipophosphoglycan. J. Exp. Med. 167 (1988) 887-902
58. Puentes S.M., da Silva R.P., Sacks D.L., Hammer C.H., and Joiner K.A. Serum resistance of metacyclic stage Leishmania major promastigotes is due to release of C5b-9. J. Immunol. 145 (1990) 4311-4316
59. Rabinovitch M., Topper G., Cristello P., and Rich A. Receptor-mediated entry of peorxidases into the parasitophorous vacuoles of macrophages infected with Leishmania mexicana amazonensis. J. Leukoc. Biol. 37 (1985) 247-261
60. Rabinovitch M., and Veras P.S. Cohabitation of Leishmania amazonensis and Coxiella burnetii. Trends Microbiol. 4 (1996) 158-161
61. Reiner N.E. Altered cell signaling and mononuclear phagocyte deactivation during intracellular infection. Immunol. Today 15 (1994) 374-381
62. Reiner S.L., Zheng S., Wang Z.E., Stowring L., and Locksley R.M. Leishmania promastigotes evade interleukin 12 (IL-12) induction by macrophages and stimulate a broad range of cytokines from CD4+ T cells during initiation of infection. J. Exp. Med. 179 (1994) 447-456
63. Reiner S.L., and Locksley R.M. The regulation of immunity to Leishmania major. Annu. Rev. Immunol. 13 (1995) 151-177
64. Roberts L.J., Baldwin T.M., Curtis J.M., Handman E., and Foote S.J. Resistance to Leishmania major is linked to the H2 region on chromosome 17 and to chromosome 9. J. Exp. Med. 185 (1997) 1705-1710
65. Russell D.G. The macrophage-attachment glycoprotein gp63 is the predominant C3-acceptor site on Leishmania mexicana promastigotes. Eur. J. Biochem. 164 (1987) 213-221
66. Russell D.G., Xu S., and Chakraborty P. Intracellular trafficking and the parasitophorous vacuole of Leishmania mexicana-infected macrophages. J. Cell Sci. 103 (1992) 1120-1193
67. Sacks D.L. Metacyclogenesis in Leishmania promastigotes. Exp. Parasitol. 69 (1989) 100-103
68. Suppl. Sacks D.L., Saraiva E.M., Rowton E., Turco S.J., and Pimenta P.F. The role of the lipophosphoglycan of Leishmania in vector competence. Parasitol. 108 (1994) S55-S62
69. Sacks D.L., Pimenta P.F., McConville M.J., Schneider P., and Turco S.J. Stage-specific binding of Leishmania donovani to the sand fly vector midgut is regulated by conformational changes in the abundant surface lipophosphoglycan. J. Exp. Med. 181 (1995) 685-697
70. Shepherd V.L., Stahl P.D., Bernd P., and Rabinovitch M. Receptor-mediated entry of beta-glucuronidase into the parasitophorous vacuoles of macrophages infected with Leishmania mexicana amazonensis. J. Exp. Med. 157 (1983) 1471-1482
71. Skamene E., Schurr E., and Gros P. Infection genomics: Nrampl as a major determinant of natural resistance to intracellular infection. Ann. Rev. Med. 49 (1998) 275-287
72. Small P.L.C., Ramakrishnan L., and Falkow S. Remodeling schemes of intracellular pathogens. Science 263 (1994) 637-639
73. Sutterwala F., Noel G.J., Clynes R., and Mosser D.M. Selective suppression of interleukin-12 induction after macrophage receptor ligation. J. Exp. Med. 185 (1997) 1977-1985
74. Tolson D.L., Turco S.J., and Pearson T.W. Expression of a repeating phosphorylated disaccharide lipophosphoglycan epitope on the surface of macrophages infected with Leishmania donovani. Infect. Immun. 58 (1990) 3500-3507
75. Turco S.J., and Descoteaux A. The lipophosphoglycan of Leishmania parasites. Annu. Rev. Microbiol. 46 (1992) 65-94
76. Veras P.S.T., de Chastellier C., and Rabinovitch M. Transfer of zymosan (yeast cell walls) to the parasitophorous vacuoles of macrophages infected with Leishmania amazonensis. J. Exp. Med. 176 (1992) 639-646
77. Vidal S.M., Malo D., Vogan K., Skamene E., and Gros P. Natural resistance to infection with intracellular parasites: isolation of a candidate for Bcg. Cell 73 (1993) 469-485
78. Vidal S., Tremblay M.L., Govoni G., Gauthier S., Sebastiani G., Malo D., Skamene E., Olivier M., Jothy S., and Gros P. The Ity/Lsh/Bcg locus: natural resistance to infection with intracellular parasites is abrogated by disruption of the Nramp1 gene. J. Exp. Med. 182 (1995) 655-666
79. Wright S.D., and Silverstein S.C. Receptors for C3b and C3bi promote phagocytosis but not the release of toxic oxygen from human phagocytes. J. Exp. Med. 158 (1983) 2016-2023
80. Zilberstein D., and Shapira M. The role of pH and temperature in the development of Leishmania parasites. Annu. Rev. Microbiol. 48 (1994) 449-470