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Small GTP Binding Proteins and the Control of Phagocytic Uptake

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Book cover Molecular Mechanisms of Phagocytosis

Part of the book series: Medical Intelligence Unit ((MIUN))

Abstract

Phagocytosis is a conserved cellular process in Eukaryotes. A multi-step process, it involves the recognition of paniculate material, e.g., microbes and apoptotic cells, their F-actin-driven engulfment and the subsequent destruction of the phagocytized material in phagolysosomes. Distinct sets of small GTP-binding proteins (Rap1, Arf6, Rho and Rab proteins) control and coordinate the successive steps of the phagocytic process. Moreover, these proteins are often targeted by microbial virulence factors. This review summarizes and discusses the evidence implicating Ras, Rho, Arf and Rab-family GTPases in the signalling pathways driving particle recognition and uptake.

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References

  1. Cardelli J. Phagocytosis and macropinocytosis in Dictyostelium: phosphoinositide-based processes, biochemically distinct. Traffic 2001; 2:311–320.

    PubMed  CAS  Google Scholar 

  2. Takai Y, Sasaki T, Matozaki T. Small GTP-binding proteins. Physiol Rev 2001; 81:153–208.

    PubMed  CAS  Google Scholar 

  3. Swanson JA, Baer SC. Phagocytosis by zippers and triggers. Trends Cell Biol 1995; 5:89–93.

    PubMed  CAS  Google Scholar 

  4. Etienne-Manneville S, Hall A. Rho GTPases in cell biology. Nature 2002; 420:629–635.

    PubMed  CAS  Google Scholar 

  5. Cox D, Chang P, Zhang Q et al. Requirements for both Rac1 and Cdc42 in membrane ruffling and phagocytosis in leukocytes. J Exp Med 1997; 186:1487–1494.

    PubMed  CAS  Google Scholar 

  6. Massol P, Montcourrier P, Guillemot JC et al. Fc receptor-mediated phagocytosis requires Cdc42 and Rac1. EMBO J 1998; 17:6219–6229.

    PubMed  CAS  Google Scholar 

  7. Caron E, Hall A. Identification of two distinct mechanisms of phagocytosis controlled by different Rho GTPases. Science 1998; 282:1717–1721.

    PubMed  CAS  Google Scholar 

  8. Patel JC, Hall A, Caron E. Vav regulates activation of Rac but not Cdc42 during FcgammaR-mediated phagocytosis. Mol Biol Cell 2002; 13:1215–1226.

    PubMed  CAS  Google Scholar 

  9. Kant AM, De P, Peng X, et al. SHP-1 regulates Fcgamma receptor-mediated phagocytosis and the activation of Rac. Blood 2002; 100:1852–1859.

    PubMed  CAS  Google Scholar 

  10. Niedergang F, Colucci-Guyon E, Dubois T et al. ADP ribosylation factor 6 is activated and controls membrane delivery during phagocytosis in macrophages. J Cell Biol 2003; 161:1143–1150.

    PubMed  CAS  Google Scholar 

  11. Billker O, Popp A, Brinkmann V, et al. Distinct mechanisms of internalization of Neisseria gonorrhoeae by members of the CEACAM receptor family involving Rac1-and Cdc42-dependent and-independent pathways. EMBO J 2002; 21:560–571.

    PubMed  CAS  Google Scholar 

  12. Hauck CR, Meyer TF, Lang F et al. CD66-mediated phagocytosis of Opa52 Neisseria gonorrhoeae requires a Src-like tyrosine kinase-and Rac1-dependent signalling pathway. EMBO J 1998; 17:443–454.

    PubMed  CAS  Google Scholar 

  13. Gruenheid S, Finlay BB. Microbial pathogenesis and cytoskeletal function. Nature 2003; 422:775–781.

    PubMed  CAS  Google Scholar 

  14. Zhou D, Galan J. Salmonella entry into host cells: the work in concert of type III secreted effector proteins. Microbes Infect 2001; 3:1293–1298.

    PubMed  CAS  Google Scholar 

  15. Buchwald G, Friebel A, Galan JE et al. Structural basis for the reversible activation of a Rho protein by the bacterial toxin SopE. EMBO J 2002; 21:3286–3295.

    PubMed  CAS  Google Scholar 

  16. Leverrier Y, Ridley AJ. Requirement for Rho GTPases and PI 3-kinases during apoptotic cell phagocytosis by macrophages. Curr Biol 2001; 11:195–199.

    PubMed  CAS  Google Scholar 

  17. Hoffmann PR, deCathelineau AM, Ogden CA et al. Phosphatidylserine (PS) induces PS receptor-mediated macropinocytosis and promotes clearance of apoptotic cells. J Cell Biol 2001; 155:649–659.

    PubMed  CAS  Google Scholar 

  18. Tosello-Trampont AC, Nakada-Tsukui K, Ravichandran KS. Engulfment of apoptotic cells is negatively regulated by Rho-mediated signaling. J Biol Chem 2003; 278:49911–49919.

    PubMed  CAS  Google Scholar 

  19. Albert ML, Kim JI, Birge RB. alphavbeta5 integrin recruits the CrkII-Dock180-rac1 complex for phagocytosis of apoptotic cells. Nat Cell Biol 2000; 2:899–905.

    PubMed  CAS  Google Scholar 

  20. Brugnera E, Haney L, Grimsley C, et al. Unconventional Rac-GEF activity is mediated through the Dock180-ELMO complex. Nat Cell Biol 2002; 4:574–582.

    PubMed  CAS  Google Scholar 

  21. Caron E. Rac and roll over the corpses. Curr Biol 2000; 10:R489–491.

    PubMed  CAS  Google Scholar 

  22. Reddien PW, Horvitz HR. CED-2/CrkII and CED-10/Rac control phagocytosis and cell migration in Caenorhabditis elegans. Nat Cell Biol 2000; 2:131–136.

    PubMed  CAS  Google Scholar 

  23. Gumienny TL, Brugnera E, Tosello-Trampont AC et al. CED-12/ELMO, a novel member of the CrkII/Dock180/Rac pathway, is required for phagocytosis and cell migration. Cell 2001; 107:27–41.

    PubMed  CAS  Google Scholar 

  24. Zhou Z, Caron E, Hartwieg E et al. The C. elegans PH domain protein CED-12 regulates cytoskeletal reorganization via a Rho/Rac GTPase signaling pathway. Dev Cell 2001; 1:477–489.

    PubMed  CAS  Google Scholar 

  25. Seastone DJ, Lee E, Bush J et al. Overexpression of a novel rho family GTPase, RacC, induces unusual actin-based structures and positively affects phagocytosis in Dictyostelium discoideum. Mol Biol Cell 1998; 9:2891–2904.

    PubMed  CAS  Google Scholar 

  26. Pearson AM, Baksa K, Ramet M et al. Identification of cytoskeletal regulatory proteins required for efficient phagocytosis in Drosophila. Microbes Infect 2003; 5:815–824.

    PubMed  CAS  Google Scholar 

  27. Kunda P, Craig G, Dominguez V et al. Abi, Sral, and Kette control the stability and localization of SCAR/WAVE to regulate the formation of actin-based protrusions. Curr Biol 2003; 13:1867–1875.

    PubMed  CAS  Google Scholar 

  28. Eden S, Rohatgi R, Podtelejnikov AV et al. Mechanism of regulation of WAVE1-induced actin nucleation by Rac1 and Nck. Nature 2002; 418:790–793.

    PubMed  CAS  Google Scholar 

  29. Rivero F, Somesh BP. Signal transduction pathways regulated by Rho GTPases in Dictyostelium. J Muscle Res Cell Motil 2002; 23:737–749.

    PubMed  CAS  Google Scholar 

  30. Chen W, Lim HH, Lim L. The CDC42 homologue from Caenorhabditis elegans. Complementation of yeast mutation. J Biol Chem 1993; 268:13280–13285.

    PubMed  CAS  Google Scholar 

  31. Castellano F, Montcourrier P, Guillemot JC et al. Inducible recruitment of Cdc42 or WASP to a cell-surface receptor triggers actin polymerization and filopodium formation. Curr Biol 1999; 9:351–360.

    PubMed  CAS  Google Scholar 

  32. Allen LA, Aderem A. Molecular definition of distinct cytoskeletal structures involved in complement-and Fc receptor-mediated phagocytosis in macrophages. J Exp Med 1996; 184:627–637.

    PubMed  CAS  Google Scholar 

  33. Olazabal IM, Caron E, May RC et al. Rho-kinase and myosin-II control phagocytic cup formation during CR, but not FcgammaR, phagocytosis. Curr Biol 2002; 12:1413–1418.

    PubMed  CAS  Google Scholar 

  34. Scott G, Leopardi S, Parker L et al. The proteinase-activated receptor-2 mediates phagocytosis in a Rho-dependent manner in human keratinocytes. J Invest Dermatol 2003; 121:529–541.

    PubMed  CAS  Google Scholar 

  35. Morehead J, Coppens I, Andrews NW. Opsonization modulates Rac-1 activation during cell entry by Leishmania amazonensis. Infect Immun 2002; 70:4571–4580.

    PubMed  CAS  Google Scholar 

  36. Eugene E, Hoffmann I, Pujol C et al. Microvilli-like structures are associated with the internalization of virulent capsulated Neisseria meningitidis into vascular endothelial cells. J Cell Sci 2002; 115:1231–1241.

    PubMed  CAS  Google Scholar 

  37. Cossart P, Pizarro-Cerda J, Lecuit M. Invasion of mammalian cells by Listeria monocytogenes: functional mimicry to subvert cellular functions. Trends Cell Biol 2003; 13:23–31.

    PubMed  CAS  Google Scholar 

  38. Mecsas J, Raupach B, Falkow S. The Yersinia Yops inhibit invasion of Listeria, Shigella and Edwardsiella but not Salmonella into epithelial cells. Mol Microbiol 1998; 28:1269–1281.

    PubMed  CAS  Google Scholar 

  39. Bierne H, Gouin E, Roux P et al. A role for cofilin and LIM kinase in Listeria-induced phagocytosis. J Cell Biol 2001; 155:101–112.

    PubMed  CAS  Google Scholar 

  40. Mounier J, Laurent V, Hall A et al. Rho family GTPases control entry of Shigella flexneri into epithelial cells but not intracellular motility. J Cell Sci 1999; 112:2069–2080.

    PubMed  CAS  Google Scholar 

  41. Tran Van Nhieu G, Caron E, Hall A et al. IpaC induces actin polymerisation and filopodia formation during Shigella entry into epithelial cells. EMBO J 1999; 18:3249–3262.

    PubMed  CAS  Google Scholar 

  42. Uchiya K, Tobe T, Komatsu K et al. Identification of a novel virulence gene, virA, on the large plasmid of Shigella, involved in invasion and intercellular spreading. Mol Microbiol 1995; 17:241–250.

    PubMed  CAS  Google Scholar 

  43. Yoshida S, Katayama E, Kuwae A et al. Shigella deliver an effector protein to trigger host microtubule destabilization, which promotes Rac1 activity and efficient bacterial internalization. EMBO J 2002; 21:2923–2935.

    PubMed  CAS  Google Scholar 

  44. Dumenil G, Sansonetti P, Tran Van Nhieu G. Src tyrosine kinase activity down-regulates Rho-dependent responses during Shigella entry into epithelial cells and stress fibre formation. J Cell Sci 2000; 113:71–80.

    PubMed  CAS  Google Scholar 

  45. Wiedemann A, Linder S, Grassl G et al. Yersinia enterocolitica invasin triggers phagocytosis via betal integrins, CDC42Hs and WASp in macrophages. Cell Microbiol 2001; 3:693–702.

    PubMed  CAS  Google Scholar 

  46. Guzman-Verri C, Chaves-Olarte E, von Eichel-Streiber C et al. GTPases of the Rho subfamily are required for Brucella abortus internalization in nonprofessional phagocytes: direct activation of Cdc42. J Biol Chem 2001; 276:44435–44443.

    PubMed  CAS  Google Scholar 

  47. Alrutz MA, Srivastava A, Wong KW et al. Efficient uptake of Yersinia pseudotuberculosis via integrin receptors involves a Rac1-Arp 2/3 pathway that bypasses N-WASP function. Mol Microbiol 2001; 42:689–703.

    PubMed  CAS  Google Scholar 

  48. McGee K, Zettl M, Way M et al. A role for N-WASP in invasin-promoted internalisation. FEBS Lett 2001; 509:59–65.

    PubMed  CAS  Google Scholar 

  49. Aepfelbacher M, Trasak C, Wiedemann A et al. Rho-GTP binding proteins in Yersinia target cell interaction. Adv Exp Med Biol 2003; 529:65–72.

    PubMed  Google Scholar 

  50. Boquet P, Lemichez E. Bacterial virulence factors targeting Rho GTPases: parasitism or symbiosis? Trends Cell Biol 2003; 13:238–246.

    PubMed  CAS  Google Scholar 

  51. Zumbihl R, Aepfelbacher M, Andor A et al. The cytotoxin YopT of Yersinia enterocolitica induces modification and cellular redistribution of the small GTP-binding protein RhoA. J Biol Chem 1999; 274:29289–29293.

    PubMed  CAS  Google Scholar 

  52. Shao F, Merritt PM, Bao Z et al. A Yersinia effector and a Pseudomonas avirulence protein define a family of cysteine proteases functioning in bacterial pathogenesis. Cell 2002; 109:575–588.

    PubMed  CAS  Google Scholar 

  53. Shao F, Vacratsis PO, Bao Z et al. Biochemical characterization of the Yersinia YopT protease: cleavage site and recognition elements in Rho GTPases. Proc Natl Acad Sci USA 2003; 100:904–909.

    PubMed  CAS  Google Scholar 

  54. Aepfelbacher M, Trasak C, Wilharm G et al. Characterization of YopT effects on Rho GTPases in Yersinia enterocolitica-infected cells. J Biol Chem 2003; 278:33217–33223.

    PubMed  CAS  Google Scholar 

  55. Von Pawel-Rammingen U, Telepnev MV, Schmidt G et al. GAP activity of the Yersinia YopE cytotoxin specifically targets the Rho pathway: a mechanism for disruption of actin microfilament structure. Mol Microbiol 2000; 36:737–748.

    Google Scholar 

  56. Kazmierczak BI, Engel JN. Pseudomonas aeruginosa ExoT acts in vivo as a GTPase-activating protein for RhoA, Rac1, and Cdc42. Infect Immun 2002; 70:2198–2205.

    PubMed  CAS  Google Scholar 

  57. Goehring UM, Schmidt G, Pederson KJ et al. The N-terminal domain of Pseudomonas aeruginosa exoenzyme S is a GTPase-activating protein for Rho GTPases. J Biol Chem 1999; 274(51):36369–36372.

    PubMed  CAS  Google Scholar 

  58. Gruenheid S, DeVinney R, Bladt F et al. Enteropathogenic E. coli Tir binds Nck to initiate actin pedestal formation in host cells. Nat Cell Biol 2001; 3:856–859.

    PubMed  CAS  Google Scholar 

  59. Ben-Ami G, Ozeri V, Hanski E et al. Agents that inhibit Rho, Rac, and Cdc42 do not block formation of actin pedestals in HeLa cells infected with enteropathogenic Escherichia coli. Infect Immun 1998; 66:1755–1758.

    PubMed  CAS  Google Scholar 

  60. Moreno SN, Docampo R. Calcium regulation in protozoan parasites. Curr Opin Microbiol 2003; 6:359–364.

    PubMed  CAS  Google Scholar 

  61. Ghosh SK, Samuelson J. Involvement of p21racA, phosphoinositide 3-kinase, and vacuolar ATPase in phagocytosis of bacteria and erythrocytes by Entamoeba histolytica: suggestive evidence for coincidental evolution of amebic invasiveness. Infect Immun 1997; 65:4243–4249.

    PubMed  CAS  Google Scholar 

  62. May RC, Caron E, Hall A et al. Involvement of the Arp2/3 complex in phagocytosis mediated by FcgammaR or CR3. Nat Cell Biol 2000; 2:246–248.

    PubMed  CAS  Google Scholar 

  63. Insall R, Muller-Taubenberger A, Machesky L et al. Dynamics of the Dictyostelium Arp2/3 complex in endocytosis, cytokinesis, and chemotaxis. Cell Motil Cytoskeleton 2001; 50:115–128.

    PubMed  CAS  Google Scholar 

  64. Olazabal IM, Machesky LM. Abplp and cortactin, new “hand-holds” for actin. J Cell Biol 2001; 154:679–682.

    PubMed  CAS  Google Scholar 

  65. Caron E. Regulation of Wiskott-Aldrich syndrome protein and related molecules. Curr Opin Cell Biol 2002; 14:82–87.

    PubMed  CAS  Google Scholar 

  66. Leverrier Y, Lorenzi R, Blundell MP et al. Cutting edge: the Wiskott-Aldrich syndrome protein is required for efficient phagocytosis of apoptotic cells. J Immunol 2001; 166:4831–4834.

    PubMed  CAS  Google Scholar 

  67. Lorenzi R, Brickell PM, Katz DR et al. Wiskott-Aldrich syndrome protein is necessary for efficient IgG-mediated phagocytosis. Blood 2000; 95:2943–2946.

    PubMed  CAS  Google Scholar 

  68. Popoff MR, Chaves-Olarte E, Lemichez E et al. Ras, Rap, and Rac small GTP-binding proteins are targets for Clostridium sordellii lethal toxin glucosylation. J Biol Chem 1996; 271:10217–10224.

    PubMed  CAS  Google Scholar 

  69. Chaves-Olarte E, Low P, Freer E et al. A novel cytotoxin from Clostridium difficile serogroup F is a functional hybrid between two other large clostridial cytotoxins. J Biol Chem 1999; 274:11046–11052.

    PubMed  CAS  Google Scholar 

  70. Chaves-Olarte E, Freer E, Parra A et al. R-Ras glucosylation and transient RhoA activation determine the cytopathic effect produced by toxin B variants from toxin A-negative strains of Clostridium difficile. J Biol Chem 2003; 278:7956–7963.

    PubMed  CAS  Google Scholar 

  71. Ehlers MR. CR3: a general purpose adhesion-recognition receptor essential for innate immunity. Microbes Infect 2000; 2:289–294.

    PubMed  CAS  Google Scholar 

  72. Caron E, Self AJ, Hall A. The GTPase Rap1 controls functional activation of macrophage integrin alphaMbeta2 by LPS and other inflammatory mediators. Curr Biol 2000; 10:974–978.

    PubMed  CAS  Google Scholar 

  73. Blom M, Tool AT, Roos D et al. Priming of human eosinophils by platelet-activating factor enhances the number of cells able to bind and respond to opsonized particles. J Immunol 1992; 149:3672–3677.

    PubMed  CAS  Google Scholar 

  74. Kinbara K, Goldfinger LE, Hansen M et al. Ras GTPases: integrins’ friends or foes? Nat Rev Mol Cell Biol 2003; 4:767–776.

    PubMed  CAS  Google Scholar 

  75. Ravetch JV, Kinet JP. Fc receptors. Annu Rev Immunol 1991; 9:457–492.

    PubMed  CAS  Google Scholar 

  76. Caron E. Cellular functions of the Rap1 GTP-binding protein: a pattern emerges. J Cell Sci 2003; 116:435–440.

    PubMed  CAS  Google Scholar 

  77. Albert ML, Pearce SF, Francisco LM et al. Immature dendritic cells phagocytose apoptotic cells via alphavbeta5 and CD36, and cross-present antigens to cytotoxic T lymphocytes. J Exp Med 1998; 188:1359–1368.

    PubMed  CAS  Google Scholar 

  78. Savill J, Dransfield I, Hogg N et al. Vitronectin receptor-mediated phagocytosis of cells undergoing apoptosis. Nature 1990; 343:170–173.

    PubMed  CAS  Google Scholar 

  79. Finnemann SC, Rodriguez-Boulan E. Macrophage and retinal pigment epithelium phagocytosis: apoptotic cells and photoreceptors compete for alphavbeta3 and alphavbeta5 integrins, and protein kinase C regulates alphavbeta5 binding and cytoskeletal linkage. J Exp Med 1999; 190:861–874.

    PubMed  CAS  Google Scholar 

  80. Robbins SM, Suttorp W, Weeks G et al. A ras-related gene from the lower eukaryote Dictyostelium that is highly conserved relative to the human rap genes. Nucleic Acids Res 1990; 18:5265–5269.

    PubMed  CAS  Google Scholar 

  81. Seastone DJ, Zhang L, Buczynski G et al. The small Mr Ras-like GTPase Rap1 and the phospholipase C pathway act to regulate phagocytosis in Dictyostelium discoideum. Mol Biol Cell 1999; 10:393–406.

    PubMed  CAS  Google Scholar 

  82. Fey P, Stephens S, Titus MA et al. SadA, a novel adhesion receptor in Dictyostelium. J Cell Biol 2002; 159:1109–1119.

    PubMed  CAS  Google Scholar 

  83. Yuan A, Siu CH, Chia CP. Calcium requirement for efficient phagocytosis by Dictyostelium discoideum. Cell Calcium 2001; 29:229–238.

    PubMed  CAS  Google Scholar 

  84. Cornillon S, Pech E, Benghezal M et al. Phglp is a nine-transmembrane protein superfamily member involved in Dictyostelium adhesion and phagocytosis. J Biol Chem 2000; 275:34287–34292.

    PubMed  CAS  Google Scholar 

  85. Kitayama H, Sugimoto Y, Matsuzaki T et al. A ras-related gene with transformation suppressor activity. Cell 1989; 56:77–84.

    PubMed  CAS  Google Scholar 

  86. Gulli MP, Peter M. Temporal and spatial regulation of Rho-type guanine-nucleotide exchange factors: the yeast perspective. Genes Dev 2001; 15:365–379.

    PubMed  CAS  Google Scholar 

  87. Park HO, Kang PJ, Rachfal AW. Localization of the Rsr1/Bud1 GTPase involved in selection of a proper growth site in yeast. J Biol Chem 2002; 277:26721–26724.

    PubMed  CAS  Google Scholar 

  88. Chubb JR, Wilkins A, Thomas GM et al. The Dictyostelium RasS protein is required for macropinocytosis, phagocytosis and the control of cell movement. J Cell Sci 2000; 113:709–719.

    PubMed  CAS  Google Scholar 

  89. Self AJ, Caron E, Paterson HF et al. Analysis of R-Ras signalling pathways. J Cell Sci 2001; 114:1357–1366.

    PubMed  CAS  Google Scholar 

  90. Zhang Z, Vuori K, Wang H et al. Integrin activation by R-ras. Cell 1996; 85:61–69.

    PubMed  CAS  Google Scholar 

  91. Keely PJ, Rusyn EV, Cox AD et al. R-Ras signals through specific integrin alpha cytoplasmic domains to promote migration and invasion of breast epithelial cells. J Cell Biol 1999; 145:1077–1088.

    PubMed  CAS  Google Scholar 

  92. Kinashi T, Katagiri K, Watanabe S et al. Distinct mechanisms of alpha 5beta 1 integrin activation by Ha-Ras and R-Ras. J Biol Chem 2000; 275:22590–22596.

    PubMed  CAS  Google Scholar 

  93. Cannon GJ, Swanson JA. The macrophage capacity for phagocytosis. J Cell Sci 1992; 101:907–913.

    PubMed  Google Scholar 

  94. Greenberg S, Grinstein S. Phagocytosis and innate immunity. Curr Opin Immunol 2002; 14:136–145.

    PubMed  CAS  Google Scholar 

  95. Lennartz MR, Yuen AF, Masi SM et al. Phospholipase A2 inhibition results in sequestration of plasma membrane into electronlucent vesicles during IgG-mediated phagocytosis. J Cell Sci 1997; 110:2041–2052.

    PubMed  CAS  Google Scholar 

  96. Desjardins M. ER-mediated phagocytosis: a new membrane for new functions. Nat Rev Immunol 2003; 3:280–291.

    PubMed  CAS  Google Scholar 

  97. Garin J, Diez R, Kieffer S et al. The phagosome proteome: insight into phagosome functions. J Cell Biol 2001; 152:165–180.

    PubMed  CAS  Google Scholar 

  98. Roberts RL, Barbieri MA, Ullrich J et al. Dynamics of rab5 activation in endocytosis and phagocytosis. J Leukoc Biol 2000; 68:627–632.

    PubMed  CAS  Google Scholar 

  99. Vieira OV, Bucci C, Harrison RE et al. Modulation of Rab5 and Rab7 recruitment to phagosomes by phosphatidylinositol 3-kinase. Mol Cell Biol 2003; 23:2501–2514.

    PubMed  CAS  Google Scholar 

  100. Harris E, Cardelli J. RabD, a Dictyostelium Rabl4-related GTPase, regulates phagocytosis and homotypic phagosome and lysosome fusion. J Cell Sci 2002; 115:3703–3713.

    PubMed  CAS  Google Scholar 

  101. Harris E, Yoshida K, Cardelli J et al. Rab11-like GTPase associates with and regulates the structure and function of the contractile vacuole system in Dictyostelium. J Cell Sci 2001; 114:3035–3045.

    PubMed  CAS  Google Scholar 

  102. Cox D, Lee DJ, Dale BM et al. A Rab11-containing rapidly recycling compartment in macrophages that promotes phagocytosis. Proc Natl Acad Sci USA 2000; 97:680–685.

    PubMed  CAS  Google Scholar 

  103. Donaldson JG. Multiple roles for Arf6: sorting, structuring, and signaling at the plasma membrane. J Biol Chem 2003; 278:41573–41576.

    PubMed  CAS  Google Scholar 

  104. Zhang Q, Cox D, Tseng CC et al. A requirement for ARF6 in Fcgamma receptor-mediated phagocytosis in macrophages. J Biol Chem 1998; 273:19977–19981.

    PubMed  CAS  Google Scholar 

  105. Allen LA, Yang C, Pessin JE. Rate and extent of phagocytosis in macrophages lacking vamp3. J Leukoc Biol 2002; 72:217–221.

    PubMed  CAS  Google Scholar 

  106. Knaus UG, Heyworth PG, Evans T et al. Regulation of phagocyte oxygen radical production by the GTP-binding protein Rac 2. Science 1991; 254:1512–1515.

    PubMed  CAS  Google Scholar 

  107. Abo A, Pick E, Hall A et al. Activation of the NADPH oxidase involves the small GTP-binding protein p21rac1. Nature 1991; 353:668–670.

    PubMed  CAS  Google Scholar 

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Wiedemann, A., Lim, J., Caron, E. (2005). Small GTP Binding Proteins and the Control of Phagocytic Uptake. In: Molecular Mechanisms of Phagocytosis. Medical Intelligence Unit. Springer, Boston, MA. https://doi.org/10.1007/978-0-387-28669-3_6

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