CoChat
Sign Up
Cited by 1,424

The DOI matches its Crossref record; 4 of the 4 references it cites were found in a registry or an index.

Pathways and mechanisms of endocytic recycling

Grant, Barth D., Donaldson, Julie G.·2009·Nature Reviews Molecular Cell Biology
DOI 10.1038/nrm2755PMC PMC3038567
Open this paper in CoChat — free account

Overview

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1038/nrm2755

Cites

4 of 4 references verified0 citation errors · 0 not checkable

Statistics

Verification

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Citations

Cites

Flagged first, then by citations

Research works printed but not linked: 120

  1. Steinman, R. M., Mellman, I. S., Muller, W. A. & Cohn, Z. A. Endocytosis and the recycling of plasma membrane. J. Cell Biol. 96, 1–27 (1983). · DOI
  2. Conner, S. D. & Schmid, S. L. Regulated portals of entry into the cell. Nature 422, 37–44 (2003). · DOI
  3. Doherty, G. J. & McMahon, H. T. Mechanisms of endocytosis. Annu. Rev. Biochem. 78, 857–902 (2009). · DOI · Paper page
  4. Mayor, S. & Pagano, R. E. Pathways of clathrin-independent endocytosis. Nature Rev. Mol. Cell Biol. 8, 603–612 (2007). · DOI · Paper page
  5. Sandvig, K., Torgersen, M. L., Raa, H. A. & van Deurs, B. Clathrin-independent endocytosis: from nonexisting to an extreme degree of complexity. Histochem. Cell Biol. 129, 267–276 (2008). · DOI
  6. Donaldson, J. G., Porat-Shliom, N. & Cohen, L. A. Clathrin-independent endocytosis: a unique platform for cell signaling and PM remodeling. Cell Signal. 21, 1–6 (2009). · DOI
  7. Maxfield, F. R. & McGraw, T. E. Endocytic recycling. Nature Rev. Mol. Cell Biol. 5, 121–132 (2004). · DOI · Paper page
  8. Gruenberg, J. & Stenmark, H. The biogenesis of multivesicular endosomes. Nature Rev. Mol. Cell Biol. 5, 317–323 (2004). · DOI
  9. Woodman, P. G. & Futter, C. E. Multivesicular bodies: co-ordinated progression to maturity. Curr. Opin. Cell Biol. 20, 408–414 (2008). · DOI
  10. Johannes, L. & Popoff, V. Tracing the retrograde route in protein trafficking. Cell 135, 1175–1187 (2008). · DOI · Paper page
  11. Kumari, S. & Mayor, S. ARF1 is directly involved in dynamin-independent endocytosis. Nature Cell Biol. 10, 30–41 (2008). · DOI
  12. Radhakrishna, H. & Donaldson, J. G. ADP-ribosylation factor 6 regulates a novel plasma membrane recycling pathway. J. Cell Biol. 139, 49–61 (1997). · DOI
  13. Brown, F. D., Rozelle, A. L., Yin, H. L., Balla, T. & Donaldson, J. G. Phosphatidylinositol 4, 5-bisphosphate and Arf6-regulated membrane traffic. J. Cell Biol. 154, 1007–1017 (2001). · DOI
  14. Powelka, A. M. et al. Stimulation-dependent recycling of integrin β1 regulated by ARF6 and Rab11. Traffic 5, 20–36 (2004). · DOI
  15. Naslavsky, N., Weigert, R. & Donaldson, J. G. Characterization of a nonclathrin endocytic pathway: membrane cargo and lipid requirements. Mol. Biol. Cell 15, 3542–3552 (2004). · DOI
  16. Eyster, C. A. et al. Discovery of new cargo proteins that enter cells through clathrin-independent endocytosis. Traffic 10, 590–599 (2009). This study identified endogenous plasma membrane proteins that enter human cells by CIE, thereby providing new cargo proteins that can be examined in different cell types. · DOI
  17. Barral, D. C. et al. CD1a and MHC class I follow a similar endocytic recycling pathway. Traffic 9, 1446–1457 (2008). · DOI
  18. Scarselli, M. & Donaldson, J. G. Constitutive internalization of G protein-coupled receptors and G proteins via clathrin-independent endocytosis. J. Biol. Chem. 284, 3577–3585 (2009). · DOI
  19. Zimmermann, P. et al. Syndecan recycling is controlled by syntenin-PIP2 interaction and Arf6. Dev. Cell 9, 377–388 (2005). First report of specific intracellular sorting of the cargo protein syndecan in CIE by phosphoinositides, syntenin and ARF6. · DOI
  20. Walseng, E., Bakke, O. & Roche, P. A. MHC class II-peptide complexes internalize using a clathrin- and dynamin-independent endocytosis pathway. J. Biol. Chem. 283, 14717–14727 (2008). · DOI
  21. Gong, Q. et al. Identification and characterization of a new class of trafficking motifs for controlling clathrin-independent internalization and recycling. J. Biol. Chem. 282, 13087–13097 (2007). · DOI · Paper page
  22. Chen, C. C. et al. RAB-10 is required for endocytic recycling in the Caenorhabditis elegans intestine. Mol. Biol. Cell 17, 1286–1297 (2006). · DOI · Paper page
  23. Shi, A. et al. A novel requirement for C. elegans Alix/ALX-1 in RME-1-mediated membrane transport. Curr. Biol. 17, 1913–1924 (2007). New role for ALX-1 (homologous to Bro1 in yeast), previously implicated in MVB formation, in RME-1-regulated endocytic recycling. · DOI · Paper page
  24. D' Souza-Schorey, C. & Chavrier, P. ARF proteins: roles in membrane traffic and beyond. Nature Rev. Mol. Cell Biol. 7, 347–358 (2006). · DOI
  25. Grant, B. D. & Caplan, S. Mechanisms of EHD/RME-1 protein function in endocytic transport. Traffic 9, 2043–2052 (2008). · DOI · Paper page
  26. Daumke, O. et al. Architectural and mechanistic insights into an EHD ATPase involved in membrane remodelling. Nature 449, 923–927 (2007). · DOI · Paper page
  27. Balklava, Z., Pant, S., Fares, H. & Grant, B. D. Genome-wide analysis identifies a general requirement for polarity proteins in endocytic traffic. Nature Cell Biol. 9, 1066–1073 (2007). Genome-wide analysis of genes involved in endocytosis and recycling in C. elegans , finding a role for polarity proteins in CDE and for cargo recycling in CIE. · DOI
  28. Fares, H. & Greenwald, I. Genetic analysis of endocytosis in Caenorhabditis elegans: coelomocyte uptake defective mutants. Genetics 159, 133–145 (2001). · DOI
  29. Grant, B. & Hirsh, D. Receptor-mediated endocytosis in the Caenorhabditis elegans oocyte. Mol. Biol. Cell 10, 4311–4326 (1999). · DOI
  30. Shaw, J. D., Cummings, K. B., Huyer, G., Michaelis, S. & Wendland, B. Yeast as a model system for studying endocytosis. Exp. Cell Res. 271, 1–9 (2001). · DOI
  31. Choudhury, A., Sharma, D. K., Marks, D. L. & Pagano, R. E. Elevated endosomal cholesterol levels in Niemann–Pick cells inhibit rab4 and perturb membrane recycling. Mol. Biol. Cell 15, 4500–4511 (2004). · DOI
  32. van der Sluijs, P. et al. The small GTP-binding protein rab4 controls an early sorting event on the endocytic pathway. Cell 70, 729–740 (1992). · DOI
  33. Deneka, M. et al. Rabaptin-5α/rabaptin-4 serves as a linker between rab4 and γ1-adaptin in membrane recycling from endosomes. EMBO J. 22, 2645–2657 (2003). · DOI
  34. Yudowski, G. A., Puthenveedu, M. A., Henry, A. G. & von Zastrow, M. Cargo-mediated regulation of a rapid rab4-dependent recycling pathway. Mol. Biol. Cell 20, 2774–2784 (2009). · DOI
  35. Kouranti, I., Sachse, M., Arouche, N., Goud, B. & Echard, A. Rab35 regulates an endocytic recycling pathway essential for the terminal steps of cytokinesis. Curr. Biol. 16, 1719–1725 (2006). · DOI · Paper page
  36. Sato, M. et al. Regulation of endocytic recycling by C. elegans Rab35 and its regulator RME-4, a coated-pit protein. EMBO J. 27, 1183–1196 (2008). · DOI · Paper page
  37. Allaire, P. D. et al. Connecdenn, a novel DENN domain-containing protein of neuronal clathrin-coated vesicles functioning in synaptic vesicle endocytosis. J. Neurosci. 26, 13202–13212 (2006). · DOI
  38. Patino-Lopez, G. et al. Rab35 and its GAP EPI64C in T cells regulate receptor recycling and immunological synapse formation. J. Biol. Chem. 283, 18323–18330 (2008). · DOI
  39. Sonnichsen, B., De Renzis, S., Nielsen, E., Rietdorf, J. & Zerial, M. Distinct membrane domains on endosomes in the recycling pathway visualized by multicolor imaging of Rab4, Rab5 and Rab11. J. Cell Biol. 149, 901–913 (2000). · DOI · Paper page
  40. Sharma, M., Naslavsky, N. & Caplan, S. A role for EHD4 in the regulation of early endosomal transport. Traffic 9, 995–1018 (2008). · DOI · Paper page
  41. Naslavsky, N., Rahajeng, J., Sharma, M., Jovic, M. & Caplan, S. Interactions between EHD proteins and Rab11-FIP2: a role for EHD3 in early endosomal transport. Mol. Biol. Cell 17, 163–177 (2006). Reports on the interaction of EHD1 and EHD3 with the same RAB11 effector, RAB11FIP2, leading to spatially distinct functions of these scaffolding proteins. · DOI · Paper page
  42. Schonteich, E. et al. The Rip11/Rab11-FIP5 and kinesin II complex regulates endocytic protein recycling. J. Cell Sci. 121, 3824–3833 (2008). · DOI
  43. Horgan, C. P. et al. Rab11-FIP3 is critical for the structural integrity of the endosomal recycling compartment. Traffic 8, 414–430 (2007). · DOI
  44. Inoue, H., Ha, V. L., Prekeris, R. & Randazzo, P. A. Arf GTPase-activating protein ASAP1 interacts with Rab11 effector FIP3 and regulates pericentrosomal localization of transferrin receptor-positive recycling endosome. Mol. Biol. Cell 19, 4224–4237 (2008). · DOI
  45. Magadan, J. G., Barbieri, M. A., Mesa, R., Stahl, P. D. & Mayorga, L. S. Rab22a regulates the sorting of transferrin to recycling endosomes. Mol. Cell. Biol. 26, 2595–2614 (2006). · DOI
  46. Babbey, C. M. et al. Rab10 regulates membrane transport through early endosomes of polarized Madin–Darby canine kidney cells. Mol. Biol. Cell 17, 3156–3175 (2006). · DOI · Paper page
  47. Pelham, H. R. Insights from yeast endosomes. Curr. Opin. Cell Biol. 14, 454–462 (2002). · DOI
  48. Traer, C. J. et al. SNX4 coordinates endosomal sorting of TfnR with dynein-mediated transport into the endocytic recycling compartment. Nature Cell Biol. 9, 1370–1380 (2007). Reports that SNX4 promotes dynein minus end-directed movement of early endosomes towards the ERC. · DOI · Paper page
  49. Lau, A. W. & Chou, M. M. The adaptor complex AP-2 regulates post-endocytic trafficking through the non-clathrin Arf6-dependent endocytic pathway. J. Cell Sci. 121, 4008–4017 (2008). · DOI
  50. Naslavsky, N., Weigert, R. & Donaldson, J. G. Convergence of non-clathrin- and clathrin-derived endosomes involves Arf6 inactivation and changes in phosphoinositides. Mol. Biol. Cell 14, 417–431 (2003). · DOI
  51. Weigert, R., Yeung, A. C., Li, J. & Donaldson, J. G. Rab22a regulates the recycling of membrane proteins internalized independently of clathrin. Mol. Biol. Cell 15, 3758–3770 (2004). Shows that cargo recycling back to the plasma membrane in CIE requires RAB11, RAB22 and actin, distinguishing it from TFR recycling processes. · DOI
  52. Balasubramanian, N., Scott, D. W., Castle, J. D., Casanova, J. E. & Schwartz, M. A. Arf6 and microtubules in adhesion-dependent trafficking of lipid rafts. Nature Cell Biol. 9, 1381–1391 (2007). · DOI
  53. Jovanovic, O. A., Brown, F. D. & Donaldson, J. G. An effector domain mutant of Arf6 implicates phospholipase D in endosomal membrane recycling. Mol. Biol. Cell 17, 327–335 (2006). · DOI
  54. Robertson, S. E. et al. Extracellular signal-regulated kinase regulates clathrin-independent endosomal trafficking. Mol. Biol. Cell 17, 645–657 (2006). Provides evidence that ERK signalling stimulates cargo recycling back to the plasma membrane in CIE. · DOI
  55. Karacsonyi, C., Miguel, A. S. & Puertollano, R. Mucolipin-2 localizes to the Arf6-associated pathway and regulates recycling of GPI-APs. Traffic 8, 1404–1414 (2007). · DOI
  56. Li, J. et al. An ACAP1-containing clathrin coat complex for endocytic recycling. J. Cell Biol. 178, 453–464 (2007). · DOI
  57. Montagnac, G. et al. ARF6 interacts with JIP4 to control a motor switch mechanism regulating endosome traffic in cytokinesis. Curr. Biol. 19, 184–195 (2009). Evidence that ARF6 can control the direction of endosomal movement by binding to the JIP scaffolding proteins, which bind to either dynein or kinesin. · DOI · Paper page
  58. Prigent, M. et al. ARF6 controls post-endocytic recycling through its downstream exocyst complex effector. J. Cell Biol. 163, 1111–1121 (2003). · DOI
  59. Hattula, K. et al. Characterization of the Rab8-specific membrane traffic route linked to protrusion formation. J. Cell Sci. 119, 4866–4877 (2006). · DOI
  60. Folsch, H., Pypaert, M., Maday, S., Pelletier, L. & Mellman, I. The AP-1A and AP-1B clathrin adaptor complexes define biochemically and functionally distinct membrane domains. J. Cell Biol. 163, 351–362 (2003). · DOI
  61. Thompson, A. et al. Recycling endosomes of polarized epithelial cells actively sort apical and basolateral cargos into separate subdomains. Mol. Biol. Cell 18, 2687–2697 (2007). Provides evidence for the segregation of recycling cargoes into separate subdomains in the recycling endosome. · DOI
  62. Caplan, S. et al. A tubular EHD1-containing compartment involved in the recycling of major histocompatibility complex class I molecules to the plasma membrane. EMBO J. 21, 2557–2567 (2002). · DOI · Paper page
  63. Grant, B. et al. Evidence that RME-1, a conserved C. elegans EH-domain protein, functions in endocytic recycling. Nature Cell Biol. 3, 573–579 (2001). · DOI
  64. Lin, S. X., Grant, B., Hirsh, D. & Maxfield, F. R. Rme-1 regulates the distribution and function of the endocytic recycling compartment in mammalian cells. Nature Cell Biol. 3, 567–572 (2001). · DOI · Paper page
  65. Jovic, M., Kieken, F., Naslavsky, N., Sorgen, P. L. & Caplan, S. Eps15 homology domain 1-associated tubules contain phosphatidylinositol-4-phosphate and phosphatidylinositol-(4, 5)-bisphosphate and are required for efficient recycling. Mol. Biol. Cell 20, 2731–2743 (2009). · DOI · Paper page
  66. Braun, A. et al. EHD proteins associate with syndapin I and II and such interactions play a crucial role in endosomal recycling. Mol. Biol. Cell 16, 3642–3658 (2005). · DOI · Paper page
  67. Welsch, S. et al. Ultrastructural analysis of ESCRT proteins suggests a role for endosome-associated tubular-vesicular membranes in ESCRT function. Traffic 7, 1551–1566 (2006). · DOI
  68. Yan, Q. et al. mVps24p functions in EGF receptor sorting/trafficking from the early endosome. Exp. Cell Res. 304, 265–273 (2005). · DOI
  69. Boucrot, E. & Kirchhausen, T. Endosomal recycling controls plasma membrane area during mitosis. Proc. Natl Acad. Sci. USA 104, 7939–7944 (2007). Shows that reduced recycling occurs during mitosis, which contributes to a reduced plasma membrane area and the rounding up of dividing cells. · DOI
  70. Van Damme, D., Inze, D. & Russinova, E. Vesicle trafficking during somatic cytokinesis. Plant Physiol. 147, 1544–1552 (2008). · DOI
  71. Jantsch-Plunger, V. & Glotzer, M. Depletion of syntaxins in the early Caenorhabditis elegans embryo reveals a role for membrane fusion events in cytokinesis. Curr. Biol. 9, 738–745 (1999). · DOI
  72. Xu, H. et al. Syntaxin 5 is required for cytokinesis and spermatid differentiation in Drosophila. Dev. Biol. 251, 294–306 (2002). · DOI
  73. Low, S. H. et al. Syntaxin 2 and endobrevin are required for the terminal step of cytokinesis in mammalian cells. Dev. Cell 4, 753–759 (2003). · DOI
  74. Glotzer, M. The molecular requirements for cytokinesis. Science 307, 1735–1739 (2005). · DOI
  75. Montagnac, G., Echard, A. & Chavrier, P. Endocytic traffic in animal cell cytokinesis. Curr. Opin. Cell Biol. 20, 454–461 (2008). · DOI
  76. Skop, A. R., Bergmann, D., Mohler, W. A. & White, J. G. Completion of cytokinesis in C. elegans requires a brefeldin A-sensitive membrane accumulation at the cleavage furrow apex. Curr. Biol. 11, 735–746 (2001). · DOI
  77. Riggs, B. et al. Actin cytoskeleton remodeling during early Drosophila furrow formation requires recycling endosomal components Nuclear-fallout and Rab11. J. Cell Biol. 163, 143–154 (2003). · DOI
  78. Fielding, A. B. et al. Rab11-FIP3 and FIP4 interact with Arf6 and the exocyst to control membrane traffic in cytokinesis. EMBO J. 24, 3389–3399 (2005). · DOI
  79. Schweitzer, J. K. & D' Souza-Schorey, C. Localization and activation of the ARF6 GTPase during cleavage furrow ingression and cytokinesis. J. Biol. Chem. 277, 27210–27216 (2002). · DOI
  80. Dyer, N. et al. Spermatocyte cytokinesis requires rapid membrane addition mediated by ARF6 on central spindle recycling endosomes. Development 134, 4437–4447 (2007). · DOI
  81. Hickson, G. R. et al. Arfophilins are dual Arf/Rab11 binding proteins that regulate recycling endosome distribution and are related to Drosophila nuclear fallout. Mol. Biol. Cell 14, 2908–2920 (2003). · DOI
  82. Grosshans, J. et al. RhoGEF2 and the formin Dia control the formation of the furrow canal by directed actin assembly during Drosophila cellularisation. Development 132, 1009–1020 (2005). · DOI
  83. Padash Barmchi, M., Rogers, S. & Hacker, U. DRhoGEF2 regulates actin organization and contractility in the Drosophila blastoderm embryo. J. Cell Biol. 168, 575–585 (2005). · DOI
  84. Cao, J., Albertson, R., Riggs, B., Field, C. M. & Sullivan, W. Nuf, a Rab11 effector, maintains cytokinetic furrow integrity by promoting local actin polymerization. J. Cell Biol. 182, 301–313 (2008). · DOI
  85. Simon, G. C. et al. Sequential Cyk-4 binding to ECT2 and FIP3 regulates cleavage furrow ingression and abscission during cytokinesis. EMBO J. 27, 1791–1803 (2008). · DOI
  86. Arden, S. D., Puri, C., Au, J. S., Kendrick-Jones, J. & Buss, F. Myosin VI is required for targeted membrane transport during cytokinesis. Mol. Biol. Cell 18, 4750–4761 (2007). · DOI
  87. Roux, A., Uyhazi, K., Frost, A. & De Camilli, P. GTP-dependent twisting of dynamin implicates constriction and tension in membrane fission. Nature 441, 528–531 (2006). · DOI
  88. Lin, S. X., Gundersen, G. G. & Maxfield, F. R. Export from pericentriolar endocytic recycling compartment to cell surface depends on stable, detyrosinated (glu) microtubules and kinesin. Mol. Biol. Cell 13, 96–109 (2002). · DOI
  89. Paterson, A. D., Parton, R. G., Ferguson, C., Stow, J. L. & Yap, A. S. Characterization of E-cadherin endocytosis in isolated MCF-7 and chinese hamster ovary cells: the initial fate of unbound E-cadherin. J. Biol. Chem. 278, 21050–21057 (2003). · DOI
  90. Palacios, F., Price, L., Schweitzer, J., Collard, J. G. & D'Souza-Schorey, C. An essential role for ARF6-regulated membrane traffic in adherens junction turnover and epithelial cell migration. EMBO J. 20, 4973–4986 (2001). · DOI
  91. Lock, J. G. & Stow, J. L. Rab11 in recycling endosomes regulates the sorting and basolateral transport of E-cadherin. Mol. Biol. Cell 16, 1744–1755 (2005). · DOI
  92. Bryant, D. M. et al. EGF induces macropinocytosis and SNX1-modulated recycling of E-cadherin. J. Cell Sci. 120, 1818–1828 (2007). · DOI
  93. Langevin, J. et al. Drosophila exocyst components Sec5, Sec6, and Sec15 regulate DE-cadherin trafficking from recycling endosomes to the plasma membrane. Dev. Cell 9, 365–376 (2005). · DOI
  94. Ribeiro, C., Ebner, A. & Affolter, M. In vivo imaging reveals different cellular functions for FGF and Dpp signaling in tracheal branching morphogenesis. Dev. Cell 2, 677–683 (2002). · DOI
  95. Shaye, D. D., Casanova, J. & Llimargas, M. Modulation of intracellular trafficking regulates cell intercalation in the Drosophila trachea. Nature Cell Biol. 10, 964–970 (2008). Connects morphological events in development with the temporal and spatial regulation of the underlying recycling endosome machinery. · DOI
  96. Harris, K. P. & Tepass, U. Cdc42 and Par proteins stabilize dynamic adherens junctions in the Drosophila neuroectoderm through regulation of apical endocytosis. J. Cell Biol. 183, 1129–1143 (2008). · DOI
  97. Duncan, M. C. & Peifer, M. Regulating polarity by directing traffic: Cdc42 prevents adherens junctions from Crumblin' aPart. J. Cell Biol. 183, 971–974 (2008). · DOI
  98. Georgiou, M., Marinari, E., Burden, J. & Baum, B. Cdc42, Par6, and aPKC regulate Arp2/3-mediated endocytosis to control local adherens junction stability. Curr. Biol. 18, 1631–1638 (2008). · DOI
  99. Leibfried, A., Fricke, R., Morgan, M. J., Bogdan, S. & Bellaiche, Y. Drosophila Cip4 and WASp define a branch of the Cdc42-Par6-aPKC pathway regulating E-cadherin endocytosis. Curr. Biol. 18, 1639–1648 (2008). · DOI
  100. Erickson, M. R., Galletta, B. J. & Abmayr, S. M. Drosophila myoblast city encodes a conserved protein that is essential for myoblast fusion, dorsal closure, and cytoskeletal organization. J. Cell Biol. 138, 589–603 (1997). · DOI
  101. Pajcini, K. V., Pomerantz, J. H., Alkan, O., Doyonnas, R. & Blau, H. M. Myoblasts and macrophages share molecular components that contribute to cell–cell fusion. J. Cell Biol. 180, 1005–1019 (2008). · DOI
  102. Grassart, A., Dujeancourt, A., Lazarow, P. B., Dautry-Varsat, A. & Sauvonnet, N. Clathrin-independent endocytosis used by the IL-2 receptor is regulated by Rac1, Pak1 and Pak2. EMBO Rep. 9, 356–362 (2008). · DOI
  103. Chen, E. H., Pryce, B. A., Tzeng, J. A., Gonzalez, G. A. & Olson, E. N. Control of myoblast fusion by a guanine nucleotide exchange factor, loner, and its effector ARF6. Cell 114, 751–762 (2003). · DOI
  104. Palamidessi, A. et al. Endocytic trafficking of Rac is required for the spatial restriction of signaling in cell migration. Cell 134, 135–147 (2008). · DOI
  105. Doherty, K. R. et al. The endocytic recycling protein EHD2 interacts with myoferlin to regulate myoblast fusion. J. Biol. Chem. 283, 20252–20260 (2008). · DOI
  106. Wang, Z. et al. Myosin Vb mobilizes recycling endosomes and AMPA receptors for postsynaptic plasticity. Cell 135, 535–548 (2008). Elegant study that shows how NMDAR-stimulated calcium levels allow myosin Vb to associate with RAB11FIP2-positive endosomes bearing AMPARs, facilitating their delivery to dendritic spines. · DOI · Paper page
  107. Chung, H. J. et al. G protein-activated inwardly rectifying potassium channels mediate depotentiation of long-term potentiation. Proc. Natl Acad. Sci. USA 106, 635–640 (2009). · DOI
  108. Brown, T. C., Correia, S. S., Petrok, C. N. & Esteban, J. A. Functional compartmentalization of endosomal trafficking for the synaptic delivery of AMPA receptors during long-term potentiation. J. Neurosci. 27, 13311–13315 (2007). · DOI · Paper page
  109. Gerges, N. Z., Backos, D. S. & Esteban, J. A. Local control of AMPA receptor trafficking at the postsynaptic terminal by a small GTPase of the Rab family. J. Biol. Chem. 279, 43870–43878 (2004). · DOI
  110. Glodowski, D. R., Chen, C. C., Schaefer, H., Grant, B. D. & Rongo, C. RAB-10 regulates glutamate receptor recycling in a cholesterol-dependent endocytosis pathway. Mol. Biol. Cell 18, 4387–4396 (2007). · DOI · Paper page
  111. Ang, A. L. et al. Recycling endosomes can serve as intermediates during transport from the Golgi to the plasma membrane of MDCK cells. J. Cell Biol. 167, 531–543 (2004). · DOI
  112. Murray, R. Z., Kay, J. G., Sangermani, D. G. & Stow, J. L. A role for the phagosome in cytokine secretion. Science 310, 1492–1495 (2005). · DOI · Paper page
  113. Hao, M. M. et al. Vesicular and non-vesicular sterol transport in living cells. The endocytic recycling compartment is a major sterol storage organelle. J. Biol. Chem. 277, 609–617 (2002). · DOI · Paper page
  114. Padron, D., Tall, R. D. & Roth, M. G. Phospholipase D2 is required for efficient endocytic recycling of transferrin receptors. Mol. Biol. Cell 17, 598–606 (2006). · DOI
  115. Jordens, I., Marsman, M., Kuijl, C. & Neefjes, J. Rab proteins, connecting transport and vesicle fusion. Traffic 6, 1070–1077 (2005). · DOI
  116. Pfeffer, S. R. Structural clues to Rab GTPase functional diversity. J. Biol. Chem. 280, 15485–15488 (2005). · DOI
  117. Jones, M. C., Caswell, P. T. & Norman, J. C. Endocytic recycling pathways: emerging regulators of cell migration. Curr. Opin. Cell Biol. 18, 549–557 (2006). · DOI
  118. Cohen, L. A. et al. Active Arf6 recruits ARNO/cytohesin GEFs to the PM by binding their PH domains. Mol. Biol. Cell 18, 2244–2253 (2007). · DOI
  119. Chies, R. et al. Alterations in the Arf6-regulated plasma membrane endosomal recycling pathway in cells overexpressing the tetraspan protein Gas3/PMP22. J. Cell Sci. 116, 987–999 (2003). · DOI
  120. Lavezzari, G. & Roche, K. W. Constitutive endocytosis of the metabotropic glutamate receptor mGluR7 is clathrin-independent. Neuropharmacology 52, 100–107 (2007). · DOI

Cited by

Sorted by citations

Metadata

Authors
Grant, B. D., & Donaldson, J. G.
Venue
Nature Reviews Molecular Cell Biology
Publisher
Springer Science and Business Media LLC
Published
2009-09
Volume
10
Issue
9
Pages
597-608
ISSN
  • 1471-0072
  • 1471-0080
DOI
10.1038/nrm2755
PMC
PMC3038567
Cited by
1,424
References
4
Language
en
Licence

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review