Cited by 174

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

Lysosome-related organelles as functional adaptations of the endolysosomal system

Delevoye, Cédric, Marks, Michael S, Raposo, Graça·2019·Current Opinion in Cell Biology

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 · 10.1016/j.ceb.2019.05.003

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?

  • Iridosome biogenesis depends on a similar molecular machinery that governs the formation of canonical LROs such as melanosomes, platelet dense granules, and Weibel-Palade bodies.

    “By integrating transcriptomic profiling, gene perturbation, cryo-TEM, and comparative evolutionary analyses, we reveal that iridosome biogenesis depends on a similar molecular machinery that governs the formation of canonical LROs such as melanosomes, platelet dense granules, and Weibel-Palade bodies (31, 32) (Fig. 4E).”

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: 75

  1. Klumperman, 2014, The complex ultrastructure of the endolysosomal system, Cold Spring Harb Perspect Biol, 6, 10.1101/cshperspect.a016857 · DOI
  2. Dell’Angelica, 2000, Lysosome-related organelles, FASEB J, 14, 1265
  3. Marks, 2013, Lysosome-related organelles: unusual compartments become mainstream, Curr Opin Cell Biol, 25, 495, 10.1016/j.ceb.2013.04.008 · DOI
  4. van Niel, 2018, Shedding light on the cell biology of extracellular vesicles, Nat Rev Mol Cell Biol, 19, 213, 10.1038/nrm.2017.125 · DOI · Paper page
  5. Griffiths, 2016, Secretion from myeloid cells: secretory lysosomes, Microbiol Spectr, 4, 10.1128/microbiolspec.MCHD-0030-2016 · DOI · Paper page
  6. Andrews, 2014, Damage control: cellular mechanisms of plasma membrane repair, Trends Cell Biol, 24, 734, 10.1016/j.tcb.2014.07.008 · DOI
  7. Hao, 2015, Impaired maturation of large dense-core vesicles in muted-deficient adrenal chromaffin cells, J Cell Sci, 128, 1365, 10.1242/jcs.161414 · DOI
  8. Sirkis, 2013, Widespread dysregulation of peptide hormone release in mice lacking adaptor protein AP-3, PLoS Genet, 9, 10.1371/journal.pgen.1003812 · DOI
  9. Watt, 2013, PMEL: a pigment cell-specific model for functional amyloid formation, Pigm Cell Melanoma Res, 26, 300, 10.1111/pcmr.12067 · DOI
  10. van Niel, 2015, Apolipoprotein E regulates amyloid formation within endosomes of pigment cells, Cell Rep, 13, 43, 10.1016/j.celrep.2015.08.057 · DOI
  11. Bissig, 2019, The PIKfyve complex regulates the early melanosome homeostasis required for physiological amyloid formation, J Cell Sci, 132, 10.1242/jcs.231746 · DOI
  12. Patwardhan, 2017, Routing of the RAB6 secretory pathway towards the lysosome related organelle of melanocytes, Nat Commun, 8, 10.1038/ncomms15835 · DOI
  13. Pols, 2013, hVps41 and VAMP7 function in direct TGN to late endosome transport of lysosomal membrane proteins, Nat Commun, 4, 10.1038/ncomms2360 · DOI
  14. Ferraro, 2014, A two-tier Golgi-based control of organelle size underpins the functional plasticity of endothelial cells, Dev Cell, 29, 292, 10.1016/j.devcel.2014.03.021 · DOI
  15. Ferraro, 2016, Weibel-Palade body size modulates the adhesive activity of its von Willebrand factor cargo in cultured endothelial cells, Sci Rep, 6
  16. Lopes da Silva, 2016, von Willebrand factor multimerization and the polarity of secretory pathways in endothelial cells, Blood, 128, 277, 10.1182/blood-2015-10-677054 · DOI
  17. Harrison-Lavoie, 2006, P-selectin and CD63 use different mechanisms for delivery to Weibel-Palade bodies, Traffic, 7, 647, 10.1111/j.1600-0854.2006.00415.x · DOI
  18. Karampini, 2019, Defective AP-3-dependent VAMP8 trafficking impairs Weibel-palade body exocytosis in Hermansky-Pudlak syndrome type 2 blood outgrowth endothelial cells, Haematologica, 10.3324/haematol.2018.207787 · DOI
  19. Wei, 2013, Hermansky-Pudlak syndrome: pigmentary and non-pigmentary defects and their pathogenesis, Pigment Cell Melanoma Res, 26, 176, 10.1111/pcmr.12051 · DOI
  20. Bowman, 2019, The road to LROs: insights into lysosome-related organelles from Hermansky-Pudlak syndrome and other rare diseases, Traffic, 20, 404, 10.1111/tra.12646 · DOI · Paper page
  21. Delevoye, 2016, BLOC-1 brings together the actin and microtubule cytoskeletons to generate recycling endosomes, Curr Biol, 26, 1, 10.1016/j.cub.2015.11.020 · DOI
  22. Delevoye, 2009, AP-1 and KIF13A coordinate endosomal sorting and positioning during melanosome biogenesis, J Cell Biol, 187, 247, 10.1083/jcb.200907122 · DOI
  23. Delevoye, 2014, Recycling endosome tubule morphogenesis from sorting endosomes requires the kinesin motor KIF13A, Cell Rep, 6, 445, 10.1016/j.celrep.2014.01.002 · DOI
  24. Dennis, 2016, BLOC-1 and BLOC-3 regulate VAMP7 cycling to and from melanosomes via distinct tubular transport carriers, J Cell Biol, 214, 293, 10.1083/jcb.201605090 · DOI
  25. Dennis, 2015, BLOC-2 targets recycling endosomal tubules to melanosomes for cargo delivery, J Cell Biol, 209, 563, 10.1083/jcb.201410026 · DOI
  26. Ryder, 2013, The WASH complex, and endosomal Arp2/3 activator, interacts with the Hermansky-Pudlak syndrome complex BLOC-1 and its cargo phosphatidylinositol-4 kinase type II alpha, Mol Biol Cell, 24, 2269, 10.1091/mbc.e13-02-0088 · DOI · Paper page
  27. Ripoll, 2018, Myosin VI and branched actin filaments mediate membrane constriction and fission of melanosomal tubule carriers, J Cell Biol, 217, 2709, 10.1083/jcb.201709055 · DOI
  28. Gokhale, 2016, The proteome of BLOC-1 genetic defects identifies the Arp2/3 actin polymerization complex to function downstream of the schizophrenia susceptibility factor dysbindin at the synapse, J Neurosci, 36, 12393, 10.1523/JNEUROSCI.1321-16.2016 · DOI
  29. Yang, 2018, Central role of autophagic UVRAG in melanogenesis and the suntan response, Proc Natl Acad Sci U S A, 115, E7728, 10.1073/pnas.1803303115 · DOI
  30. Monis, 2017, BLOC-1 is required for selective membrane protein trafficking from endosomes to primary cilia, J Cell Biol, 216, 2131, 10.1083/jcb.201611138 · DOI
  31. Shakya, 2018, Rab22A recruits BLOC-1 and BLOC-2 to promote the biogenesis of recycling endosomes, EMBO Rep, 19, 10.15252/embr.201845918 · DOI
  32. Ma, 2016, BLOC-2 subunit HPS6 deficiency affects the tubulation and secretion of von Willebrand factor from mouse endothelial cells, J Genet Genomics, 43, 686, 10.1016/j.jgg.2016.09.007 · DOI
  33. Sharda, 2015, Defective PDI release from platelets and endothelial cells impairs thrombus formation in Hermansky-Pudlak syndrome, Blood, 125, 1633, 10.1182/blood-2014-08-597419 · DOI
  34. Gerondopoulos, 2012, BLOC-3 mutated in Hermansky-Pudlak syndrome is a Rab32/38 guanine nucleotide exchange factor, Curr Biol, 22, 2135, 10.1016/j.cub.2012.09.020 · DOI
  35. Tamura, 2011, Structure-function analysis of VPS9-ankyrin-repeat protein (Varp) in the trafficking of tyrosinase-related protein 1 in melanocytes, J Biol Chem, 286, 7507, 10.1074/jbc.M110.191205 · DOI
  36. Salazar, 2006, BLOC-1 complex deficiency alters the targeting of adaptor protein complex-3 cargoes, Mol Biol Cell, 17, 4014, 10.1091/mbc.e06-02-0103 · DOI
  37. Ohishi, 2019, The BLOC-3 subunit HPS4 is required for activation of Rab32/38 GTPases in melanogenesis, but its Rab9 activity is dispensable for melanogenesis, J Biol Chem, 294, 6912, 10.1074/jbc.RA119.007345 · DOI
  38. Morris, 2018, Function and regulation of the C. elegans Rab32 family member GLO-1 in lysosome-related organelle biogenesis, PLoS Genet, 14, 10.1371/journal.pgen.1007772 · DOI
  39. Sieni, 2014, Familial hemophagocytic lymphohistiocytosis: when rare diseases shed light on immune system functioning, Front Immunol, 5, 167, 10.3389/fimmu.2014.00167 · DOI
  40. Tang, 2015, A unique SNARE machinery for exocytosis of cytotoxic granules and platelets granules, Mol Membr Biol, 32, 120, 10.3109/09687688.2015.1079934 · DOI
  41. Spessott, 2017, SM protein Munc18-2 facilitates transition of syntaxin 11-mediated lipid mixing to complete fusion for T-lymphocyte cytotoxicity, Proc Natl Acad Sci U S A, 114, E2176, 10.1073/pnas.1617981114 · DOI
  42. Marshall, 2015, VAMP8-dependent fusion of recycling endosomes with the plasma membrane facilitates T lymphocyte cytotoxicity, J Cell Biol, 210, 135, 10.1083/jcb.201411093 · DOI
  43. Spessott, 2017, Syntaxin 4 mediates endosome recycling for lytic granule exocytosis in cytotoxic T-lymphocytes, Traffic, 18, 442, 10.1111/tra.12490 · DOI
  44. Dieckmann, 2015, Munc18-2 is required for Syntaxin 11 localization on the plasma membrane in cytotoxic T-lymphocytes, Traffic, 16, 1330, 10.1111/tra.12337 · DOI
  45. Muller, 2014, An N-terminal missense mutation in STX11 causative of FHL4 abrogates syntaxin-11 binding to munc18-2, Front Immunol, 4, 515, 10.3389/fimmu.2013.00515 · DOI
  46. Spessott, 2015, Hemophagocytic lymphohistiocytosis caused by dominant negative mutations in STXBP2 that inhibit SNARE-mediated membrane fusion, Blood, 125, 1566, 10.1182/blood-2014-11-610816 · DOI
  47. Ye, 2014, Platelet secretion and hemostasis require syntaxin-binding protein STXBP5, J Clin Invest, 124, 4517, 10.1172/JCI75572 · DOI
  48. Zhu, 2014, Syntaxin-binding protein STXBP5 inhibits endothelial exocytosis and promotes platelet secretion, J Clin Invest, 124, 4503, 10.1172/JCI71245 · DOI
  49. Elstak, 2011, The Munc13-4-rab27 complex is specifically required for tethering secretory lysosomes at the plasma membrane, Blood, 118, 1570, 10.1182/blood-2011-02-339523 · DOI
  50. Chicka, 2016, Role of Munc13-4 as a Ca2+-dependent tether during platelet secretion, Biochem J, 473, 627, 10.1042/BJ20151150 · DOI
  51. Boswell, 2012, Munc13-4 reconstitutes calcium-dependent SNARE-mediated membrane fusion, J Cell Biol, 197, 301, 10.1083/jcb.201109132 · DOI
  52. Woo, 2017, Munc13-4 functions as a Ca2+ sensor for homotypic secretory granule fusion to generate endosomal exocytic vacuoles, Mol Biol Cell, 28, 792, 10.1091/mbc.e16-08-0617 · DOI
  53. Cetica, 2015, Patients with Griscelli syndrome and normal pigmentation identify RAB27A mutations that selectively disrupt MUNC13-4 binding, J Allergy Clin Immunol, 135, 1310, 10.1016/j.jaci.2014.08.039 · DOI
  54. Netter, 2016, A novel Rab27a mutation binds melanophilin, but not Munc13-4, causing immunodeficiency without albinism, J Allergy Clin Immunol, 138, 599, 10.1016/j.jaci.2015.12.1337 · DOI
  55. He, 2016, Munc13-4 interacts with syntaxin 7, regulates late endosomal maturation, endosomal signaling and TLR9-initiated cellular responses, Mol Biol Cell, 27, 572, 10.1091/mbc.e15-05-0283 · DOI
  56. Johnson, 2016, Munc13-4 is a Rab11-binding protein that regulates Rab11-positive vesicle trafficking and docking at the plasma membrane, J Biol Chem, 291, 3423, 10.1074/jbc.M115.705871 · DOI
  57. Chehab, 2017, A novel Munc13-4/S100A10/annexin A2 complex promotes Weibel-Palade body exocytosis in endothelial cells, Mol Biol Cell, 28, 1688, 10.1091/mbc.e17-02-0128 · DOI
  58. Wu, 2014, Melanosome transfer: it is best to give and receive, Curr Opin Cell Biol, 29, 1, 10.1016/j.ceb.2014.02.003 · DOI
  59. Correia, 2018, Melanin transferred to keratinocytes resides in nondegradative endocytic compartments, J Invest Dermatol, 138, 637, 10.1016/j.jid.2017.09.042 · DOI · Paper page
  60. Tarafder, 2014, Rab11b mediates melanin transfer between donor melanocytes and acceptor keratinocytes via coupled exo/endocytosis, J Invest Dermatol, 134, 1056, 10.1038/jid.2013.432 · DOI · Paper page
  61. Hurbain, 2018, Melanosome distribution in keratinocytes in different skin types: melanosome clusters are not degradative organelles, J Invest Dermatol, 138, 647, 10.1016/j.jid.2017.09.039 · DOI · Paper page
  62. Kanayama, 2016, Roles of autophagy and autophagy-related proteins in antifungal immunity, Front Immunol, 7, 47, 10.3389/fimmu.2016.00047 · DOI
  63. Spano, 2016, A bacterial pathogen targets a host Rab-family GTPase defense pathway with a GAP, Cell Host Microbe, 19, 216, 10.1016/j.chom.2016.01.004 · DOI
  64. Li, 2016, Analysis of the rab GTPase interactome in dendritic cells reveals anti-microbial functions of the Rab32 complex in bacterial containment, Immunity, 44, 422, 10.1016/j.immuni.2016.01.027 · DOI
  65. Seto, 2011, Rab GTPases regulating phagosome maturation are differentially recruited to mycobacterial phagosomes, Traffic, 12, 407, 10.1111/j.1600-0854.2011.01165.x · DOI
  66. Cheng, 2018, Characterization of LAMP1-labeled nondegradative lysosomal and endocytic compartments in neurons, J Cell Biol, 217, 3127, 10.1083/jcb.201711083 · DOI · Paper page
  67. Yap, 2018, Degradation of dendritic cargos requires Rab7-dependent transport to somatic lysosomes, J Cell Biol, 217, 3141, 10.1083/jcb.201711039 · DOI
  68. Farías, 2017, BORC/kinesin-1 ensemble drives polarized transport of lysosomes into the axon, Proc Natl Acad Sci U S A, 114, E2955, 10.1073/pnas.1616363114 · DOI · Paper page
  69. Niwa, 2017, BORC regulates the axonal transport of synaptic vesicle precursors by activating ARL-8, Curr Biol, 27, 2569, 10.1016/j.cub.2017.07.013 · DOI · Paper page
  70. Pu, 2015, BORC, a multisubunit complex that regulates lysosome positioning, Dev Cell, 33, 176, 10.1016/j.devcel.2015.02.011 · DOI · Paper page
  71. Guardia, 2016, BORC functions upstream of kinesins 1 and 3 to coordinate regional movement of lysosomes along different microtubule tracks, Cell Rep, 17, 1950, 10.1016/j.celrep.2016.10.062 · DOI · Paper page
  72. Snouwaert, 2018, A mutation in the Borcs7 subunit of the lysosome regulatory BORC complex results in motor deficits and dystrophic axonopathy in mice, Cell Rep, 24, 1254, 10.1016/j.celrep.2018.06.118 · DOI · Paper page
  73. Messenger, 2018, A Ca2+-stimulated exosome release pathway in cancer cells is regulated by Munc13-4, J. Cell Biol, 217, 2877, 10.1083/jcb.201710132 · DOI
  74. Verweij, 2019, Live tracking of inter-organ communication by endogenous exosomes in vivo, Dev Cell, 48, 573, 10.1016/j.devcel.2019.01.004 · DOI
  75. Hyenne, 2019, Studying the fate of tumor extracellular vesicles at high spatiotemporal resolution using the zebrafish embryo, Dev Cell, 48, 554, 10.1016/j.devcel.2019.01.014 · DOI

Cited by

Sorted by citations

Metadata

Authors
Delevoye, C., Marks, M. S., & Raposo, G.
Venue
Current Opinion in Cell Biology
Publisher
Elsevier BV
Published
2019-08
Volume
59
Pages
147-158
ISSN
0955-0674
Cited by
174
References
4
Language
en
Update notices
erratum (2019-12-01)
Funders
  • National Institutes of Health
  • National Eye Institute
  • National Heart, Lung and Blood Institute
  • Fondation pour la Recherche Médicale
  • Fondation ARC pour la Recherche sur le Cancer
  • ANR
  • L'Oréal Research and Development
  • Clarins Research and Development
  • Institut Curie
  • INSERM
  • Centre National de la Recherche Scientifique

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