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Actin Polymerization Controls the Organization of WASH Domains at the Surface of Endosomes
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Specific endosomal membrane sub-domains are enriched for either degradative components such as ESCRT or recycling machinery including Retromer, Retriever, the CCC complex, and WASH-dependent actin patches.
“A number of studies have shown that specific endosomal membrane sub-domains are enriched for either degradative components such as ESCRT or recycling machinery including Retromer, Retriever, the CCC complex, and WASH-dependent actin patches9,34–44”
From Mechanism and regulation of cargo entry into the Commander endosomal recycling pathway (2024) · cites this paper as [36]
The Results section (page unavailable) reports that Retromer/Vps35 and WASH colocalize in discrete endosomal domains, while HRS, an ESCRT-0 component, occupies distinct domains. This supports the contrast between ESCRT-associated and WASH/Retromer domains, but our copy does not address Retriever or the CCC complex. (LLM, conf=0.88)
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Cites
A High Precision Survey of the Molecular Dynamics of Mammalian Clathrin-Mediated Endocytosis
Taylor, M. J., Perrais, D., & Merrifield, C. J. (2011) · PLoS Biology · doi:10.1371/journal.pbio.1000604 · Cited by 754
McBride, H. M., Rybin, V., Murphy, C., Giner, A., Teasdale, R., & Zerial, M. (1999) · Cell · doi:10.1016/s0092-8674(00)81966-2 · Cited by 520
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Research works printed but not linked: 52
- TD Pollard, 2007, Regulation of actin filament assembly by Arp2/3 complex and formins., Annu Rev Biophys Biomol Struct, 36, 451, 10.1146/annurev.biophys.35.040405.101936 · DOI
- K Rottner, 2010, WASH, WHAMM and JMY: regulation of Arp2/3 complex and beyond., Trends Cell Biol, 20, 650, 10.1016/j.tcb.2010.08.014 · DOI
- E Derivery, 2010, Generation of branched actin networks: assembly and regulation of the N-WASP and WAVE molecular machines., BioEssays, 32, 119, 10.1002/bies.200900123 · DOI
- RH Insall, 2009, Actin dynamics at the leading edge: from simple machinery to complex networks., Dev Cell, 17, 310, 10.1016/j.devcel.2009.08.012 · DOI
- T Takenawa, 2007, The WASP-WAVE protein network: connecting the membrane to the cytoskeleton., Nat Rev Mol Cell Biol, 8, 37, 10.1038/nrm2069 · DOI · Paper page
- KG Campellone, 2008, WHAMM is an Arp2/3 complex activator that binds microtubules and functions in ER to Golgi transport., Cell, 134, 148, 10.1016/j.cell.2008.05.032 · DOI
- E Derivery, 2009, The Arp2/3 activator WASH controls the fission of endosomes through a large multiprotein complex., Dev Cell, 17, 712, 10.1016/j.devcel.2009.09.010 · DOI · Paper page
- TS Gomez, 2009, A FAM21-containing WASH complex regulates retromer-dependent sorting., Dev Cell, 17, 699, 10.1016/j.devcel.2009.09.009 · DOI · Paper page
- SN Duleh, 2010, WASH and the Arp2/3 complex regulate endosome shape and trafficking., Cytoskeleton, 67, 193, 10.1002/cm.20437 · DOI · Paper page
- ME Harbour, 2010, The cargo-selective retromer complex is a recruiting hub for protein complexes that regulate endosomal tubule dynamics., J Cell Sci, 123, 3703, 10.1242/jcs.071472 · DOI · Paper page
- M Carnell, 2011, Actin polymerization driven by WASH causes V-ATPase retrieval and vesicle neutralization before exocytosis., J Cell Biol, 193, 831, 10.1083/jcb.201009119 · DOI · Paper page
- T Zech, 2011, The Arp2/3 activator WASH regulates alpha5beta1-integrin-mediated invasive migration., Journal of cell science, 124, 3753, 10.1242/jcs.080986 · DOI · Paper page
- J Taunton, 2000, Actin-dependent propulsion of endosomes and lysosomes by recruitment of N-WASP., J Cell Biol, 148, 519, 10.1083/jcb.148.3.519 · DOI
- S Benesch, 2002, Phosphatidylinositol 4,5-biphosphate (PIP2)-induced vesicle movement depends on N-WASP and involves Nck, WIP, and Grb2., J Biol Chem, 277, 37771, 10.1074/jbc.M204145200 · DOI
- E Morel, 2009, Annexin A2-dependent polymerization of actin mediates endosome biogenesis., Dev Cell, 16, 445, 10.1016/j.devcel.2009.01.007 · DOI
- S Gasman, 2003, RhoD regulates endosome dynamics through Diaphanous-related Formin and Src tyrosine kinase., Nat Cell Biol, 5, 195, 10.1038/ncb935 · DOI
- BJ Wallar, 2007, RhoB and the mammalian Diaphanous-related formin mDia2 in endosome trafficking., Exp Cell Res, 313, 560, 10.1016/j.yexcr.2006.10.033 · DOI
- I Guerin, 2000, Disruption of the actin filament network affects delivery of endocytic contents marker to phagosomes with early endosome characteristics: the case of phagosomes with pathogenic mycobacteria., Eur J Cell Biol, 79, 735, 10.1078/0171-9335-00092 · DOI
- A Jahraus, 2001, ATP-dependent membrane assembly of F-actin facilitates membrane fusion., Mol Biol Cell, 12, 155, 10.1091/mbc.12.1.155 · DOI
- A Drengk, 2003, A coat of filamentous actin prevents clustering of late-endosomal vacuoles in vivo., Curr Biol, 13, 1814, 10.1016/j.cub.2003.09.037 · DOI
- R Kjeken, 2004, Fusion between phagosomes, early and late endosomes: a role for actin in fusion between late, but not early endocytic organelles., Mol Biol Cell, 15, 345, 10.1091/mbc.E03-05-0334 · DOI
- L Cai, 2008, Coronin 1B antagonizes cortactin and remodels Arp2/3-containing actin branches in lamellipodia., Cell, 134, 828, 10.1016/j.cell.2008.06.054 · DOI
- MA Puthenveedu, 2010, Sequence-dependent sorting of recycling proteins by actin-stabilized endosomal microdomains., Cell, 143, 761, 10.1016/j.cell.2010.10.003 · DOI · Paper page
- D Jia, 2010, WASH and WAVE actin regulators of the Wiskott-Aldrich syndrome protein (WASP) family are controlled by analogous structurally related complexes., Proc Natl Acad Sci U S A, 107, 10442, 10.1073/pnas.0913293107 · DOI · Paper page
- E Ohashi, 2011, Receptor sorting within endosomal trafficking pathway is facilitated by dynamic actin filaments., PLoS ONE, 6, e19942, 10.1371/journal.pone.0019942 · DOI
- S Benesch, 2005, N-WASP deficiency impairs EGF internalization and actin assembly at clathrin-coated pits., J Cell Sci, 118, 3103, 10.1242/jcs.02444 · DOI
- M Zerial, 2001, Rab proteins as membrane organizers., Nat Rev Mol Cell Biol, 2, 107, 10.1038/35052055 · DOI · Paper page
- FR Maxfield, 2004, Endocytic recycling., Nat Rev Mol Cell Biol, 5, 121, 10.1038/nrm1315 · DOI · Paper page
- B Sonnichsen, 2000, Distinct membrane domains on endosomes in the recycling pathway visualized by multicolor imaging of Rab4, Rab5, and Rab11., J Cell Biol, 149, 901, 10.1083/jcb.149.4.901 · DOI · Paper page
- J Gruenberg, 2001, The endocytic pathway: a mosaic of domains., Nat Rev Mol Cell Biol, 2, 721, 10.1038/35096054 · DOI
- H Stenmark, 1995, Rabaptin-5 is a direct effector of the small GTPase Rab5 in endocytic membrane fusion., Cell, 83, 423, 10.1016/0092-8674(95)90120-5 · DOI
- H Horiuchi, 1997, A novel Rab5 GDP/GTP exchange factor complexed to Rabaptin-5 links nucleotide exchange to effector recruitment and function., Cell, 90, 1149, 10.1016/S0092-8674(00)80380-3 · DOI
- A Simonsen, 1998, EEA1 links PI(3)K function to Rab5 regulation of endosome fusion., Nature, 394, 494, 10.1038/28879 · DOI · Paper page
- K Simons, 1997, Functional rafts in cell membranes., Nature, 387, 569, 10.1038/42408 · DOI · Paper page
- MF Carlier, 1986, Interaction of cytochalasin D with actin filaments in the presence of ADP and ATP., J Biol Chem, 261, 2041, 10.1016/S0021-9258(17)35894-5 · DOI
- S Bolte, 2006, A guided tour into subcellular colocalization analysis in light microscopy., J Microsc, 224, 213, 10.1111/j.1365-2818.2006.01706.x · DOI
- H Stenmark, 1994, Inhibition of rab5 GTPase activity stimulates membrane fusion in endocytosis., EMBO J, 13, 1287, 10.1002/j.1460-2075.1994.tb06381.x · DOI · Paper page
- ME Harbour, 2012, Recruitment of the endosomal WASH complex is mediated by the extended ‘tail’ of Fam21 binding to the retromer protein Vps35., Biochem J, 442, 209, 10.1042/BJ20111761 · DOI · Paper page
- MN Seaman, 2009, Membrane recruitment of the cargo-selective retromer subcomplex is catalysed by the small GTPase Rab7 and inhibited by the Rab-GAP TBC1D5., J Cell Sci, 122, 2371, 10.1242/jcs.048686 · DOI · Paper page
- JJ Gautier, 2011, Clathrin is required for Scar/Wave mediated lamellipodium formation., Journal Cell Sci, 124, 3414, 10.1242/jcs.081083 · DOI
- OD Weiner, 2007, An actin-based wave generator organizes cell motility., PLoS Biol, 5, e221, 10.1371/journal.pbio.0050221 · DOI
- I Weisswange, 2009, The rate of N-WASP exchange limits the extent of ARP2/3-complex-dependent actin-based motility., Nature, 458, 87, 10.1038/nature07773 · DOI
- V Delatour, 2008, Arp2/3 controls the motile behavior of N-WASP-functionalized GUVs and modulates N-WASP surface distribution by mediating transient links with actin filaments., Biophys J, 94, 4890, 10.1529/biophysj.107.118653 · DOI
- A Millius, 2012, Diffusion, capture and recycling of SCAR/WAVE and Arp2/3 complexes observed in cells by single-molecule imaging., 10.1242/jcs.091157 · DOI
- T Baumgart, 2003, Imaging coexisting fluid domains in biomembrane models coupling curvature and line tension., Nature, 425, 821, 10.1038/nature02013 · DOI
- K Bacia, 2005, Sterol structure determines the separation of phases and the curvature of the liquid-ordered phase in model membranes., Proc Natl Acad Sci U S A, 102, 3272, 10.1073/pnas.0408215102 · DOI
- J Solon, 2005, Membrane deformations induced by the matrix protein of vesicular stomatitis virus in a minimal system., J Gen Virol, 86, 3357, 10.1099/vir.0.81129-0 · DOI
- W Römer, 2007, Shiga toxin induces tubular membrane invaginations for its uptake into cells., Nature, 450, 670, 10.1038/nature05996 · DOI
- A Roux, 2005, Role of curvature and phase transition in lipid sorting and fission of membrane tubules., Embo J, 24, 1537, 10.1038/sj.emboj.7600631 · DOI
- AP Liu, 2006, Actin polymerization serves as a membrane domain switch in model lipid bilayers., Biophys J, 91, 4064, 10.1529/biophysj.106.090852 · DOI
- JM Allain, 2004, Fission of a multiphase membrane tube., Phys Rev Lett, 93, 158104, 10.1103/PhysRevLett.93.158104 · DOI
- W Römer, 2010, Actin dynamics drive membrane reorganization and scission in clathrin-independent endocytosis., Cell, 140, 540, 10.1016/j.cell.2010.01.010 · DOI
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Burd, C., & Cullen, P. J. (2014) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a016774 · Cited by 435
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Metadata
- Authors
- Derivery, E., Helfer, E., Henriot, V., & Gautreau, A.
- Venue
- PLoS ONE
- Publisher
- Public Library of Science (PLoS)
- Published
- 2012-06-21
- Volume
- 7
- Issue
- 6
- Pages
- e39774
- ISSN
- 1932-6203
- PMC
- PMC3380866
- Cited by
- 77
- References
- 2
- Language
- en
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