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The emerging role of retromer in neuroprotection
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Perturbed endosomal transport is a contributing factor and, in some cases, a causative factor in human diseases, including neurodegenerative and neurological, and metabolic syndromes and cardiovascular disease.
“An increasing body of evidence points to perturbed endosomal transport being a contributing factor and, in some cases, a causative factor in human diseases, including neurodegenerative and neurological2–4, and metabolic syndromes and cardiovascular disease5.”
From Mapping of endosomal proximity proteomes reveals Retromer as a hub for RAB GTPase regulation (2025) · cites this paper as [2]
Sub-domain dysfunction is associated with human disease.
“Sub-domain dysfunction is associated with human disease, but our mechanistic understanding of its function remains poorly described.”
From Mapping of endosomal proximity proteomes reveals Retromer as a hub for RAB GTPase regulation (2025) · cites this paper as [2]
Functional retrieval sub-domains are essential for development and homeostasis, and disease-associated sub-domain dysregulation is associated with human disease.
“Analysis in cells and organisms have established the essential importance of functional retrieval sub-domains for development and homeostasis, and disease-associated sub-domain dysregulation is associated with human disease2–5.”
From Mapping of endosomal proximity proteomes reveals Retromer as a hub for RAB GTPase regulation (2025) · cites this paper as [2]
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Vogiatzi, T., Xilouri, M., Vekrellis, K., & Stefanis, L. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m801992200 · Cited by 683
Retromer: A Master Conductor of Endosome Sorting
Burd, C., & Cullen, P. J. (2014) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a016774 · Cited by 435
Self-citationVPS35 haploinsufficiency increases Alzheimer’s disease neuropathology
Wen, L., Tang, F.-L., Hong, Y., Luo, S.-W., Wang, C.-L., He, W., Shen, C., Jung, J.-U., Xiong, F., Lee, D.-H., et al. (2011) · Journal of Cell Biology · doi:10.1083/jcb.201105109 · Cited by 270
Tang, F.-L., Erion, J. R., Tian, Y., Liu, W., Yin, D.-M., Ye, J., Tang, B., Mei, L., & Xiong, W.-C. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.0042-15.2015 · Cited by 269
Huang, T. Y., Zhao, Y., Li, X., Wang, X., Tseng, I.-C., Thompson, R., Tu, S., Willnow, T. E., Zhang, Y.-W., & Xu, H. (2016) · The Journal of Neuroscience · doi:10.1523/jneurosci.0206-16.2016 · Cited by 69
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Research works printed but not linked: 82
- Huotari, 2011, Endosome maturation, EMBO J., 30, 3481, 10.1038/emboj.2011.286 · DOI
- Wang, 2015, The retromer complex in development and disease, Development, 142, 2392, 10.1242/dev.123737 · DOI
- Henne, 2013, Molecular mechanisms of the membrane sculpting ESCRT pathway, Cold Spring Harb. Perspect. Biol., 5, 10.1101/cshperspect.a016766 · DOI
- Hsu, 2012, Getting active: protein sorting in endocytic recycling, Nat. Rev. Mol. Cell Biol., 13, 323, 10.1038/nrm3332 · DOI
- Seaman, 2012, The retromer complex—endosomal protein recycling and beyond, J. Cell Sci., 125, 4693
- Small, 2015, Retromer in Alzheimer disease, Parkinson disease and other neurological disorders, Nat. Rev. Neurosci., 16, 126, 10.1038/nrn3896 · DOI · Paper page
- Cullen, 2011, Sorting nexins provide diversity for retromer-dependent trafficking events, Nat. Cell Biol., 14, 29, 10.1038/ncb2374 · DOI · Paper page
- Ehringer, 1960, Distribution of noradrenaline and dopamine (3-hydroxytyramine) in the human brain and their behavior in diseases of the extrapyramidal system, Klin. Wochenschr., 38, 1236, 10.1007/BF01485901 · DOI
- Bernheimer, 1973, Brain dopamine and the syndromes of Parkinson and Huntington Clinical, morphological and neurochemical correlations, J. Neurol. Sci., 20, 415, 10.1016/0022-510X(73)90175-5 · DOI
- Ferrer, 2011, Neuropathology of sporadic Parkinson disease before the appearance of parkinsonism: preclinical Parkinson disease, J. Neural Transm. (Vienna), 118, 821, 10.1007/s00702-010-0482-8 · DOI
- Vilarino-Guell, 2011, VPS35 mutations in Parkinson disease, Am. J. Hum. Genet., 89, 162, 10.1016/j.ajhg.2011.06.001 · DOI · Paper page
- Zimprich, 2011, A mutation in VPS35, encoding a subunit of the retromer complex, causes late-onset Parkinson disease, Am. J. Hum. Genet., 89, 168, 10.1016/j.ajhg.2011.06.008 · DOI · Paper page
- Shannon, 2014, Genetic variation of the retromer subunits VPS26A/B-VPS29 in Parkinson’s disease, Neurobiol. Aging, 35, 1958, 10.1016/j.neurobiolaging.2014.03.004 · DOI · Paper page
- Gustavsson, 2015, Genetic variability of the retromer cargo recognition complex in parkinsonism, Mov. Disord., 30, 580, 10.1002/mds.26104 · DOI · Paper page
- Deng, 2013, The VPS35 gene and Parkinson’s disease, Mov. Disord., 28, 569, 10.1002/mds.25430 · DOI
- Bandres-Ciga, 2016, Analysis of the genetic variability in Parkinson’s disease from Southern Spain, Neurobiol. Aging, 37, 210, 10.1016/j.neurobiolaging.2015.09.020 · DOI
- Nuytemans, 2013, Whole exome sequencing of rare variants in EIF4G1 and VPS35 in Parkinson disease, Neurology, 80, 982, 10.1212/WNL.0b013e31828727d4 · DOI
- Trinh, 2014, Disease penetrance of late-onset parkinsonism: a meta-analysis, JAMA Neurol., 71, 1535, 10.1001/jamaneurol.2014.1909 · DOI
- McMillan, 2016, Atypical parkinsonism-associated retromer mutant alters endosomal sorting of specific cargo proteins, J. Cell Biol., 214, 389, 10.1083/jcb.201604057 · DOI
- Follett, 2016, Parkinson disease-linked Vps35 R524W mutation impairs the endosomal association of retromer and induces alpha-synuclein aggregation, J. Biol. Chem., 291, 18283, 10.1074/jbc.M115.703157 · DOI · Paper page
- MacLeod, 2013, RAB7L1 interacts with LRRK2 to modify intraneuronal protein sorting and Parkinson’s disease risk, Neuron, 77, 425, 10.1016/j.neuron.2012.11.033 · DOI · Paper page
- Linhart, 2014, Vacuolar protein sorting 35 (Vps35) rescues locomotor deficits and shortened lifespan in Drosophila expressing a Parkinson’s disease mutant of Leucine-Rich Repeat Kinase 2 (LRRK2), Mol. Neurodegener., 9, 23, 10.1186/1750-1326-9-23 · DOI
- Bi, 2013, Pathogenic mutation in VPS35 impairs its protection against MPP(+) cytotoxicity, Int. J. Biol. Sci., 9, 149, 10.7150/ijbs.5617 · DOI
- Tsika, 2014, Parkinson’s disease-linked mutations in VPS35 induce dopaminergic neurodegeneration, Hum. Mol. Genet., 23, 4621, 10.1093/hmg/ddu178 · DOI · Paper page
- Trinh, 2013, Advances in the genetics of Parkinson disease, Nat. Rev. Neurol., 9, 445, 10.1038/nrneurol.2013.132 · DOI
- Seaman, 1998, A membrane coat complex essential for endosome-to-Golgi retrograde transport in yeast, J. Cell Biol., 142, 665, 10.1083/jcb.142.3.665 · DOI · Paper page
- Seaman, 2004, Cargo-selective endosomal sorting for retrieval to the Golgi requires retromer, J. Cell Biol., 165, 111, 10.1083/jcb.200312034 · DOI · Paper page
- Arighi, 2004, Role of the mammalian retromer in sorting of the cation-independent mannose 6-phosphate receptor, J. Cell Biol., 165, 123, 10.1083/jcb.200312055 · DOI · Paper page
- Cullen, 2009, Cathepsin D expression level affects alpha-synuclein processing, aggregation, and toxicity in vivo, Mol. Brain, 2, 5, 10.1186/1756-6606-2-5 · DOI
- Sevlever, 2008, Cathepsin D is the main lysosomal enzyme involved in the degradation of alpha-synuclein and generation of its carboxy-terminally truncated species, Biochemistry, 47, 9678, 10.1021/bi800699v · DOI · Paper page
- Spillantini, 1997, Alpha-synuclein in Lewy bodies, Nature, 388, 839, 10.1038/42166 · DOI · Paper page
- Dehay, 2013, Lysosomal impairment in Parkinson’s disease, Mov. Disord., 28, 725, 10.1002/mds.25462 · DOI · Paper page
- Zavodszky, 2014, Mutation in VPS35 associated with Parkinson’s disease impairs WASH complex association and inhibits autophagy, Nat. Commun., 5, 3828, 10.1038/ncomms4828 · DOI · Paper page
- Miura, 2014, VPS35 dysfunction impairs lysosomal degradation of alpha-synuclein and exacerbates neurotoxicity in a Drosophila model of Parkinson’s disease, Neurobiol. Dis., 71, 1, 10.1016/j.nbd.2014.07.014 · DOI
- Dhungel, 2015, Parkinson’s disease genes VPS35 and EIF4G1 interact genetically and converge on alpha-synuclein, Neuron, 85, 76, 10.1016/j.neuron.2014.11.027 · DOI
- McGough, 2014, Retromer binding to FAM21 and the WASH complex is perturbed by the Parkinson disease-linked VPS35(D620N) mutation, Curr. Biol., 24, 1670, 10.1016/j.cub.2014.06.024 · DOI · Paper page
- Follett, 2014, The Vps35 D620N mutation linked to Parkinson’s disease disrupts the cargo sorting function of retromer, Traffic, 15, 230, 10.1111/tra.12136 · DOI
- Dahms, 2008, Strategies for carbohydrate recognition by the mannose 6-phosphate receptors, Glycobiology, 18, 664, 10.1093/glycob/cwn061 · DOI
- Zhao, 2014, Lysosome sorting of beta-glucocerebrosidase by LIMP-2 is targeted by the mannose 6-phosphate receptor, Nat. Commun., 5, 4321, 10.1038/ncomms5321 · DOI
- Coutinho, 2012, A shortcut to the lysosome: the mannose-6-phosphate-independent pathway, Mol. Genet. Metab., 107, 257, 10.1016/j.ymgme.2012.07.012 · DOI
- Manzoni, 2013, Dysfunction of the autophagy/lysosomal degradation pathway is a shared feature of the genetic synucleinopathies, FASEB J., 27, 3424, 10.1096/fj.12-223842 · DOI
- Sidransky, 2012, The link between the GBA gene and parkinsonism, Lancet Neurol., 11, 986, 10.1016/S1474-4422(12)70190-4 · DOI
- Reitz, 2015, The role of the retromer complex in aging-related neurodegeneration: a molecular and genomic review, Mol. Genet. Genom., 290, 413, 10.1007/s00438-014-0939-9 · DOI
- Cuervo, 1996, A receptor for the selective uptake and degradation of proteins by lysosomes, Science, 273, 501, 10.1126/science.273.5274.501 · DOI · Paper page
- 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
- 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
- Seaman, 2013, Retromer-mediated endosomal protein sorting: all WASHed up!, Trends Cell Biol., 23, 522, 10.1016/j.tcb.2013.04.010 · DOI
- Vilarino-Guell, 2014, DNAJC13 mutations in Parkinson disease, Hum. Mol. Genet., 23, 1794, 10.1093/hmg/ddt570 · DOI
- Freeman, 2014, RME-8 coordinates the activity of the WASH complex with the function of the retromer SNX dimer to control endosomal tubulation, J. Cell Sci., 127, 2053
- King, 2013, WASH is required for lysosomal recycling and efficient autophagic and phagocytic digestion, Mol. Biol. Cell, 24, 2714, 10.1091/mbc.e13-02-0092 · DOI
- Xia, 2013, WASH inhibits autophagy through suppression of Beclin 1 ubiquitination, EMBO J., 32, 2685, 10.1038/emboj.2013.189 · DOI
- Temkin, 2011, SNX27 mediates retromer tubule entry and endosome-to-plasma membrane trafficking of signalling receptors, Nat. Cell Biol., 13, 715, 10.1038/ncb2252 · DOI · Paper page
- Zech, 2011, The Arp2/3 activator WASH regulates alpha5beta1-integrin-mediated invasive migration, J. Cell Sci., 124, 3753, 10.1242/jcs.080986 · DOI · Paper page
- Wang, 2016, VPS35 regulates cell surface recycling and signaling of dopamine receptor D1, Neurobiol. Aging, 46, 22, 10.1016/j.neurobiolaging.2016.05.016 · DOI
- Ishizu, 2016, Impaired striatal dopamine release in homozygous Vps35 D620N knock-in mice, Hum. Mol. Genet., 25, 4507
- Berwick, 2014, The regulation and deregulation of Wnt signaling by PARK genes in health and disease, J. Mol. Cell Biol., 6, 3, 10.1093/jmcb/mjt037 · DOI
- Munsie, 2015, Retromer-dependent neurotransmitter receptor trafficking to synapses is altered by the Parkinson’s disease VPS35 mutation p. D620N, Hum. Mol. Genet., 24, 1691, 10.1093/hmg/ddu582 · DOI · Paper page
- Sowada, 2016, Increased copper toxicity in Saccharomyces cerevisiae lacking VPS35, a component of the retromer and monogenic Parkinson disease gene in humans, Biochem. Biophys. Res. Commun., 476, 528, 10.1016/j.bbrc.2016.05.157 · DOI
- Steinberg, 2013, A global analysis of SNX27-retromer assembly and cargo specificity reveals a function in glucose and metal ion transport, Nat. Cell Biol., 15, 461, 10.1038/ncb2721 · DOI · Paper page
- Davies, 2016, Copper dyshomoeostasis in Parkinson’s disease: implications for pathogenesis and indications for novel therapeutics, Clin. Sci. (Lond.), 130, 565, 10.1042/CS20150153 · DOI
- Piotrowski, 2013, WASH knockout T cells demonstrate defective receptor trafficking, proliferation, and effector function, Mol. Cell. Biol., 33, 958, 10.1128/MCB.01288-12 · DOI · Paper page
- Clairfeuille, 2016, A molecular code for endosomal recycling of phosphorylated cargos by the SNX27-retromer complex, Nat. Struct. Mol. Biol., 23, 921, 10.1038/nsmb.3290 · DOI · Paper page
- Joubert, 2004, New sorting nexin (SNX27) and NHERF specifically interact with the 5-HT4a receptor splice variant: roles in receptor targeting, J. Cell Sci., 117, 5367, 10.1242/jcs.01379 · DOI
- Gallon, 2014, A unique PDZ domain and arrestin-like fold interaction reveals mechanistic details of endocytic recycling by SNX27-retromer, Proc. Natl. Acad. Sci. U. S. A., 111, E3604, 10.1073/pnas.1410552111 · DOI · Paper page
- Lee, 2016, FAM21 directs SNX27-retromer cargoes to the plasma membrane by preventing transport to the Golgi apparatus, Nat. Commun., 7, 10939, 10.1038/ncomms10939 · DOI · Paper page
- Cai, 2011, Deficiency of sorting nexin 27 (SNX27) leads to growth retardation and elevated levels of N-methyl-d-aspartate receptor 2C (NR2C), Mol. Cell. Biol., 31, 1734, 10.1128/MCB.01044-10 · DOI
- Wang, 2013, Loss of sorting nexin 27 contributes to excitatory synaptic dysfunction by modulating glutamate receptor recycling in Down’s syndrome, Nat. Med., 19, 473, 10.1038/nm.3117 · DOI · Paper page
- Damseh, 2015, A defect in the retromer accessory protein, SNX27, manifests by infantile myoclonic epilepsy and neurodegeneration, Neurogenetics, 16, 215, 10.1007/s10048-015-0446-0 · DOI · Paper page
- Hussain, 2014, Sorting Nexin 27 regulates basal and activity-dependent trafficking of AMPARs, Proc. Natl. Acad. Sci. U. S. A., 111, 11840, 10.1073/pnas.1412415111 · DOI · Paper page
- Loo, 2014, A role for sorting nexin 27 in AMPA receptor trafficking, Nat. Commun., 5, 3176, 10.1038/ncomms4176 · DOI · Paper page
- Davis, 1979, Chronic Parkinsonism secondary to intravenous injection of meperidine analogues, Psychiatry Res., 1, 249, 10.1016/0165-1781(79)90006-4 · DOI
- Langston, 1983, Chronic Parkinsonism in humans due to a product of meperidine-analog synthesis, Science, 219, 979, 10.1126/science.6823561 · DOI · Paper page
- Braschi, 2010, Vps35 mediates vesicle transport between the mitochondria and peroxisomes, Curr. Biol., 20, 1310, 10.1016/j.cub.2010.05.066 · DOI
- Tang, 2015, VPS35 deficiency or mutation causes dopaminergic neuronal loss by impairing mitochondrial fusion and function, Cell Rep., 12, 1631, 10.1016/j.celrep.2015.08.001 · DOI
- Wang, 2016, Parkinson’s disease-associated mutant VPS35 causes mitochondrial dysfunction by recycling DLP1 complexes, Nat. Med., 22, 54, 10.1038/nm.3983 · DOI
- Wang, 2016, A conserved retromer sorting motif is essential for mitochondrial DLP1 recycling by VPS35 in Parkinson’s disease model, Hum. Mol. Genet., 10.1093/hmg/ddw430 · DOI
- Prudent, 2015, MAPL SUMOylation of Drp1 stabilizes an ER/mitochondrial platform required for cell death, Mol. Cell, 59, 941, 10.1016/j.molcel.2015.08.001 · DOI
- McLelland, 2014, Parkin and PINK1 function in a vesicular trafficking pathway regulating mitochondrial quality control, EMBO J., 33, 282
- Chen, 2013, PINK1-phosphorylated mitofusin 2 is a Parkin receptor for culling damaged mitochondria, Science, 340, 471, 10.1126/science.1231031 · DOI · Paper page
- Malik, 2015, VPS35 pathogenic mutations confer no dominant toxicity but partial loss of function in Drosophila and genetically interact with parkin, Hum. Mol. Genet., 24, 6106, 10.1093/hmg/ddv322 · DOI
- Mecozzi, 2014, Pharmacological chaperones stabilize retromer to limit APP processing, Nat. Chem. Biol., 10, 443, 10.1038/nchembio.1508 · DOI · Paper page
- Lucas, 2016, Structural mechanism for cargo recognition by the retromer complex, Cell, 1623, 10.1016/j.cell.2016.10.056 · DOI · Paper page
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To degrade or not to degrade: Mechanisms and significance of endocytic recycling
Cullen, P. J., & Steinberg, F. (2018) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-018-0053-7 · Cited by 590
Self-citationEndosomal retrieval of cargo: Retromer is not alone
McNally, K. E., & Cullen, P. J. (2018) · Trends in Cell Biology · doi:10.1016/j.tcb.2018.06.005 · Cited by 169
Self-citationMapping of endosomal proximity proteomes reveals Retromer as a hub for RAB GTPase regulation
Antón-Plágaro, C., Chen, K.-E., Guo, Q., Liu, M., Evans, A. J., Lewis, P. A., Heesom, K. J., Wilkinson, K. A., Collins, B. M., & Cullen, P. J. (2025) · Nature Communications · doi:10.1038/s41467-025-61802-1 · Cited by 14
Self-citationJones, E., Adams, H., Chen, K.-E., Maroof, F., Ibbotson, T. M., Nakamura, Y., Banks, P. J., Healy, M. D., Lewis, P. A., Heesom, K. J., et al. (2026) · doi:10.64898/2026.05.14.724903
Self-citation
Metadata
- Authors
- McMillan, K. J., Korswagen, H. C., & Cullen, P. J.
- Venue
- Current Opinion in Cell Biology
- Publisher
- Elsevier BV
- Published
- 2017-08
- Volume
- 47
- Pages
- 72-82
- ISSN
- 0955-0674
- PMC
- PMC5677836
- Cited by
- 66
- References
- 5
- Language
- en
- Licence
- Funders
- Medical Research Council (MR/K018299/1)
- Wellcome Trust (104568, 089928)
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