The DOI matches its Crossref record; 16 of the 16 references it cites were found in a registry or an index.
Amyloid precursor protein products concentrate in a subset of exosomes specifically endocytosed by neurons.
Abstract
Amyloid beta peptide (Aβ), the main component of senile plaques of Alzheimer's disease brains, is produced by sequential cleavage of amyloid precursor protein (APP) and of its C-terminal fragments (CTFs). An unanswered question is how amyloidogenic peptides spread throughout the brain during the course of the disease. Here, we show that small lipid vesicles called exosomes, secreted in the extracellular milieu by cortical neurons, carry endogenous APP and are strikingly enriched in CTF-α and the newly characterized CTF-η. Exosomes from N2a cells expressing human APP with the autosomal dominant Swedish mutation contain Aβ peptides as well as CTF-α and CTF-η, while those from cells expressing the non-mutated form of APP only contain CTF-α and CTF-η. APP and CTFs are sorted into a subset of exosomes which lack the tetraspanin CD63 and specifically bind to dendrites of neurons, unlike exosomes carrying CD63 which bind to both neurons and glial cells. Thus, neuroblastoma cells secrete distinct populations of exosomes carrying different cargoes and targeting specific cell types. APP-carrying exosomes can be endocytosed by receiving cells, allowing the processing of APP acquired by exosomes to give rise to the APP intracellular domain (AICD). Thus, our results show for the first time that neuronal exosomes may indeed act as vehicles for the intercellular transport of APP and its catabolites.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
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?
In the citing paper
“The vesicles were uptaken by neurons”
From Emerging Alternative Proteinases in APP Metabolism and Alzheimer’s Disease Pathogenesis: A Focus on MT1-MMP and MT5-MMP (2019) · cites this paper as Laulagnier et al., 2018
In the citing paper
“η-CTF was detected in extracellular vesicles released by N2a neuroblastoma cells expressing APP Swedish.”
From Emerging Alternative Proteinases in APP Metabolism and Alzheimer’s Disease Pathogenesis: A Focus on MT1-MMP and MT5-MMP (2019) · cites this paper as Laulagnier et al., 2018
Citations
Cites
Kowal, J., Arras, G., Colombo, M., Jouve, M., Morath, J. P., Primdal-Bengtson, B., Dingli, F., Loew, D., Tkach, M., & Théry, C. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1521230113 · Cited by 3,426
Naj, A. C., Jun, G., Beecham, G. W., Wang, L.-S., Vardarajan, B. N., Buros, J., Gallins, P. J., Buxbaum, J. D., Jarvik, G. P., Crane, P. K., et al. (2011) · Nature Genetics · doi:10.1038/ng.801 · Cited by 1,901
Citron, M., Oltersdorf, T., Haass, C., McConlogue, L., Hung, A. Y., Seubert, P., Vigo-Pelfrey, C., Lieberburg, I., & Selkoe, D. J. (1992) · Nature · doi:10.1038/360672a0 · Cited by 1,757
Self-propagation of pathogenic protein aggregates in neurodegenerative diseases
Jucker, M., & Walker, L. C. (2013) · Nature · doi:10.1038/nature12481 · Cited by 1,663
Emmanouilidou, E., Melachroinou, K., Roumeliotis, T., Garbis, S. D., Ntzouni, M., Margaritis, L. H., Stefanis, L., & Vekrellis, K. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.5699-09.2010 · Cited by 1,115
Release of Excess Amyloid β Protein from a Mutant Amyloid β Protein Precursor
Cai, X.-D., Golde, T. E., & Younkin, S. G. (1993) · Science · doi:10.1126/science.8424174 · Cited by 913
Exosomes are released by cultured cortical neurones
Fauré, J., Lachenal, G., Court, M., Hirrlinger, J., Chatellard-Causse, C., Blot, B., Grange, J., Schoehn, G., Goldberg, Y., Boyer, V., et al. (2006) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2005.12.003 · Cited by 896
Self-citationMolecular mechanism of multivesicular body biogenesis by ESCRT complexes
Wollert, T., & Hurley, J. H. (2010) · Nature · doi:10.1038/nature08849 · Cited by 804
Tian, T., Zhu, Y.-L., Zhou, Y.-Y., Liang, G.-F., Wang, Y.-Y., Hu, F.-H., & Xiao, Z.-D. (2014) · Journal of Biological Chemistry · doi:10.1074/jbc.m114.588046 · Cited by 726
Role of LBPA and Alix in Multivesicular Liposome Formation and Endosome Organization
Matsuo, H., Chevallier, J., Mayran, N., Le Blanc, I., Ferguson, C., Fauré, J., Blanc, N. S., Matile, S., Dubochet, J., Sadoul, R., et al. (2004) · Science · doi:10.1126/science.1092425 · Cited by 705
Self-citationη-Secretase processing of APP inhibits neuronal activity in the hippocampus
Willem, M., Tahirovic, S., Busche, M. A., Ovsepian, S. V., Chafai, M., Kootar, S., Hornburg, D., Evans, L. D. B., Moore, S., Daria, A., et al. (2015) · Nature · doi:10.1038/nature14864 · Cited by 398
Potolicchio, I., Carven, G. J., Xu, X., Stipp, C., Riese, R. J., Stern, L. J., & Santambrogio, L. (2005) · The Journal of Immunology · doi:10.4049/jimmunol.175.4.2237 · Cited by 365
TDP-43 is intercellularly transmitted across axon terminals
Feiler, M. S., Strobel, B., Freischmidt, A., Helferich, A. M., Kappel, J., Brewer, B. M., Li, D., Thal, D. R., Walther, P., Ludolph, A. C., et al. (2015) · Journal of Cell Biology · doi:10.1083/jcb.201504057 · Cited by 329
Almeida, C. G., Takahashi, R. H., & Gouras, G. K. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.5078-05.2006 · Cited by 316
Coleman, B. M., & Hill, A. F. (2015) · Seminars in Cell & Developmental Biology · doi:10.1016/j.semcdb.2015.02.007 · Cited by 208
Edgar, J. R., Willén, K., Gouras, G. K., & Futter, C. E. (2015) · Journal of Cell Science · doi:10.1242/jcs.170233 · Cited by 70
Research works printed but not linked: 56
- Gruenberg J, Stenmark H (2004) The biogenesis of multivesicular endosomes. Nat Rev Mol Cell Biol 5:317–323. doi: 10.1038/nrm1360 · DOI
- Denzer K, Kleijmeer MJ, Heijnen HF et al (2000) Exosome: from internal vesicle of the multivesicular body to intercellular signaling device. J Cell Sci 113:3365–3374 · DOI
- Laulagnier K, Schieber NL, Maritzen T et al (2011) Role of AP1 and Gadkin in the traffic of secretory endo-lysosomes. Mol Biol Cell 22:2068–2082. doi: 10.1091/mbc.E11-03-0193 · DOI
- White IJ, Bailey LM, Aghakhani MR et al (2006) EGF stimulates annexin 1-dependent inward vesiculation in a multivesicular endosome subpopulation. EMBO J 25:1–12. doi: 10.1038/sj.emboj.7600759 · DOI
- Subra C, Laulagnier K, Perret B, Record M (2007) Exosome lipidomics unravels lipid sorting at the level of multivesicular bodies. Biochimie 89:205–212. doi: 10.1016/j.biochi.2006.10.014 · DOI
- Trajkovic K, Hsu C, Chiantia S et al (2008) Ceramide triggers budding of exosome vesicles into multivesicular endosomes. Science 319:1244–1247. doi: 10.1126/science.1153124 · DOI
- Colombo M, Raposo G, Théry C (2014) Biogenesis, secretion, and intercellular interactions of exosomes and other extracellular vesicles. Annu Rev Cell Dev Biol 30:255–289. doi: 10.1146/annurev-cellbio-101512-122326 · DOI · Paper page
- Nanbo A, Kawanishi E, Yoshida R, Yoshiyama H (2013) Exosomes derived from Epstein-Barr virus-infected cells are internalized via caveola-dependent endocytosis and promote phenotypic modulation in target cells. J Virol 87:10334–10347. doi: 10.1128/JVI.01310-13 · DOI
- Valadi H, Ekström K, Bossios A et al (2007) Exosome-mediated transfer of mRNAs and microRNAs is a novel mechanism of genetic exchange between cells. Nat Cell Biol 9:654–659. doi: 10.1038/ncb1596 · DOI · Paper page
- Perez-Gonzalez R, Gauthier SA, Kumar A, Levy E (2012) The exosome secretory pathway transports amyloid precursor protein carboxyl-terminal fragments from the cell into the brain extracellular space. J Biol Chem 287:43108–43115. doi: 10.1074/jbc.M112.404467 · DOI
- Street JM, Barran PE, Mackay CL et al (2012) Identification and proteomic profiling of exosomes in human cerebrospinal fluid. J Transl Med 10:5. doi: 10.1186/1479-5876-10-5 · DOI
- Fitzner D, Schnaars M, van Rossum D et al (2011) Selective transfer of exosomes from oligodendrocytes to microglia by macropinocytosis. J Cell Sci 124:447–458. doi: 10.1242/jcs.074088 · DOI · Paper page
- Wang G, Dinkins M, He Q et al (2012) Astrocytes secrete exosomes enriched with proapoptotic ceramide and prostate apoptosis response 4 (PAR-4): potential mechanism of apoptosis induction in Alzheimer disease (AD). J Biol Chem 287:21384–21395. doi: 10.1074/jbc.M112.340513 · DOI
- Chivet M, Hemming F, Pernet-Gallay K et al (2012) Emerging role of neuronal exosomes in the central nervous system. Front Physiol 3:145. doi: 10.3389/fphys.2012.00145 · DOI
- Chivet M, Javalet C, Hemming F et al (2013) Exosomes as a novel way of interneuronal communication. Biochem Soc Trans 41:241–244. doi: 10.1042/BST20120266 · DOI
- Lachenal G, Pernet-Gallay K, Chivet M et al (2011) Release of exosomes from differentiated neurons and its regulation by synaptic glutamatergic activity. Mol Cell Neurosci 46:409–418. doi: 10.1016/j.mcn.2010.11.004 · DOI
- Chivet M, Javalet C, Laulagnier K et al (2014) Exosomes secreted by cortical neurons upon glutamatergic synapse activation specifically interact with neurons. J Extracell Vesicles 3:24722. doi: 10.3402/jev.v3.24722 · DOI · Paper page
- Février B, Vilette D, Laude H, Raposo G (2005) Exosomes: a bubble ride for prions? Traffic 6:10–17. doi: 10.1111/j.1600-0854.2004.00247.x · DOI
- Haass C, Kaether C, Thinakaran G, Sisodia S (2012) Trafficking and proteolytic processing of APP. Cold Spring Harb Perspect Med 2:a006270. doi: 10.1101/cshperspect.a006270 · DOI · Paper page
- Xu W, Weissmiller AM, White JA et al (2016) Amyloid precursor protein–mediated endocytic pathway disruption induces axonal dysfunction and neurodegeneration. J Clin Invest 126:1815–1833. doi: 10.1172/JCI82409 · DOI
- Kim S, Sato Y, Mohan PS et al (2016) Evidence that the rab5 effector APPL1 mediates APP-βCTF-induced dysfunction of endosomes in Down syndrome and Alzheimer’s disease. Mol Psychiatry 21:707–716. doi: 10.1038/mp.2015.97 · DOI · Paper page
- Baranger K, Marchalant Y, Bonnet AE et al (2016) MT5-MMP is a new pro-amyloidogenic proteinase that promotes amyloid pathology and cognitive decline in a transgenic mouse model of Alzheimer’s disease. Cell Mol Life Sci 73:217–236. doi: 10.1007/s00018-015-1992-1 · DOI · Paper page
- Das U, Scott DA, Ganguly A et al (2013) Activity-induced convergence of APP and BACE-1 in acidic microdomains via an endocytosis-dependent pathway. Neuron 79:447–460. doi: 10.1016/j.neuron.2013.05.035 · DOI
- Takahashi RH, Milner TA, Li F et al (2002) Intraneuronal Alzheimer abeta42 accumulates in multivesicular bodies and is associated with synaptic pathology. Am J Pathol 161:1869–1879 · DOI · Paper page
- Sannerud R, Esselens C, Ejsmont P et al (2016) Restricted location of PSEN2/γ-secretase determines substrate specificity and generates an intracellular Aβ pool. Cell 166:193–208. doi: 10.1016/j.cell.2016.05.020 · DOI · Paper page
- Rajendran L, Honsho M, Zahn TR et al (2006) Alzheimer’s disease beta-amyloid peptides are released in association with exosomes. Proc Natl Acad Sci USA 103:11172–11177. doi: 10.1073/pnas.0603838103 · DOI · Paper page
- Vingtdeux V, Hamdane M, Loyens A et al (2007) Alkalizing drugs induce accumulation of amyloid precursor protein by-products in luminal vesicles of multivesicular bodies. J Biol Chem 282:18197–18205. doi: 10.1074/jbc.M609475200 · DOI
- Sharples RA, Vella LJ, Nisbet RM et al (2008) Inhibition of gamma-secretase causes increased secretion of amyloid precursor protein C-terminal fragments in association with exosomes. FASEB J 22:1469–1478. doi: 10.1096/fj.07-9357com · DOI
- Belly A, Bodon G, Blot B et al (2010) CHMP2B mutants linked to frontotemporal dementia impair maturation of dendritic spines. J Cell Sci 123:2943–2954. doi: 10.1242/jcs.068817 · DOI
- Chatellard-Causse C, Blot B, Cristina N et al (2002) Alix (ALG-2-interacting protein X), a protein involved in apoptosis, binds to endophilins and induces cytoplasmic vacuolization. J Biol Chem 277:29108–29115. doi: 10.1074/jbc.M204019200 · DOI
- Laulagnier K, Javalet C, Hemming FJ, Sadoul R (2017) Purification and analysis of exosomes released by mature cortical neurons following synaptic activation. Methods Mol Biol 1545:129–138. doi: 10.1007/978-1-4939-6728-5_9 · DOI
- Schagger H (2006) Tricine-SDS-PAGE. Nat Protoc 1:16–22. doi: 10.1038/nprot.2006.4 · DOI
- Bolte S, Cordelières FP (2006) A guided tour into subcellular colocalization analysis in light microscopy. J Microsc 224:213–232. doi: 10.1111/j.1365-2818.2006.01706.x · DOI
- Hoey SE, Williams RJ, Perkinton MS (2009) Synaptic NMDA receptor activation stimulates alpha-secretase amyloid precursor protein processing and inhibits amyloid-beta production. J Neurosci 29:4442–4460. doi: 10.1523/JNEUROSCI.6017-08.2009 · DOI · Paper page
- Forman MS, Cook DG, Leight S et al (1997) Differential effects of the swedish mutant amyloid precursor protein on β-amyloid accumulation and secretion in neurons and nonneuronal cells. J Biol Chem 272:32247–32253. doi: 10.1074/jbc.272.51.32247 · DOI
- Huotari J, Helenius A (2011) Endosome maturation. EMBO J 30:3481–3500. doi: 10.1038/emboj.2011.286 · DOI
- Stenmark H, Parton RG, Steele-Mortimer O et al (1994) Inhibition of rab5 GTPase activity stimulates membrane fusion in endocytosis. EMBO J 13:1287–1296 · DOI · Paper page
- Cao X, Südhof TC (2004) Dissection of amyloid-beta precursor protein-dependent transcriptional transactivation. J Biol Chem 279:24601–24611. doi: 10.1074/jbc.M402248200 · DOI
- Sullivan CP, Jay AG, Stack EC et al (2011) Retromer disruption promotes amyloidogenic APP processing. Neurobiol Dis 43:338–345. doi: 10.1016/j.nbd.2011.04.002 · DOI
- Langui D, Girardot N, El Hachimi KH et al (2004) Subcellular topography of neuronal Abeta peptide in APPxPS1 transgenic mice. Am J Pathol 165:1465–1477 · DOI · Paper page
- Hoey SE, Buonocore F, Cox CJ et al (2013) AMPA receptor activation promotes non-amyloidogenic amyloid precursor protein processing and suppresses neuronal amyloid-β production. PLoS One 8:e78155. doi: 10.1371/journal.pone.0078155 · DOI
- Lesné S, Ali C, Gabriel C et al (2005) NMDA receptor activation inhibits alpha-secretase and promotes neuronal amyloid-beta production. J Neurosci 25:9367–9377. doi: 10.1523/JNEUROSCI.0849-05.2005 · DOI
- Stoeck A, Keller S, Riedle S et al (2006) A role for exosomes in the constitutive and stimulus-induced ectodomain cleavage of L1 and CD44. Biochem J 393:609–618. doi: 10.1042/BJ20051013 · DOI
- Jämsä A, Belda O, Edlund M, Lindström E (2011) BACE-1 inhibition prevents the γ-secretase inhibitor evoked Aβ rise in human neuroblastoma SH-SY5Y cells. J Biomed Sci 18:76. doi: 10.1186/1423-0127-18-76 · DOI
- Lu X, Deng Y, Yu D et al (2014) Histone acetyltransferase p300 mediates histone acetylation of PS1 and BACE1 in a cellular model of Alzheimer’s disease. PLoS One 9:e103067. doi: 10.1371/journal.pone.0103067 · DOI
- Mucke L, Masliah E, Yu GQ et al (2000) High-level neuronal expression of abeta 1-42 in wild-type human amyloid protein precursor transgenic mice: synaptotoxicity without plaque formation. J Neurosci 20:4050–4058 · DOI · Paper page
- Falker C, Hartmann A, Guett I et al (2016) Exosomal cellular prion protein drives fibrillization of amyloid beta and counteracts amyloid beta-mediated neurotoxicity. J Neurochem 137:88–100. doi: 10.1111/jnc.13514 · DOI
- An K, Klyubin I, Kim Y et al (2013) Exosomes neutralize synaptic-plasticity-disrupting activity of Aβ assemblies in vivo. Mol Brain 6:47. doi: 10.1186/1756-6606-6-47 · DOI
- Cataldo AM, Peterhoff CM, Troncoso JC et al (2000) Endocytic pathway abnormalities precede amyloid beta deposition in sporadic Alzheimer’s disease and Down syndrome: differential effects of APOE genotype and presenilin mutations. Am J Pathol 157:277–286 · DOI · Paper page
- Hollingworth P, Harold D, Sims R et al (2011) Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer’s disease. Nat Genet 43:429–435. doi: 10.1038/ng.803 · DOI · Paper page
- Ubelmann F, Burrinha T, Salavessa L et al (2017) Bin1 and CD2AP polarise the endocytic generation of beta-amyloid. EMBO Rep 18:102–122. doi: 10.15252/embr.201642738 · DOI · Paper page
- van Niel G, Charrin S, Simoes S et al (2011) The tetraspanin CD63 regulates ESCRT-independent and -dependent endosomal sorting during melanogenesis. Dev Cell 21:708–721. doi: 10.1016/j.devcel.2011.08.019 · DOI · Paper page
- Deyts C, Thinakaran G, Parent AT (2016) APP Receptor. To Be or Not To Be. Trends Pharmacol Sci. doi: 10.1016/j.tips.2016.01.005 · DOI
- Sisodia SS, Koo EH, Hoffman PN et al (1993) Identification and transport of full-length amyloid precursor proteins in rat peripheral nervous system. J Neurosci 13:3136–3142 · DOI
- Wang Y, Ha Y (2004) The X-ray structure of an antiparallel dimer of the human amyloid precursor protein E2 domain. Mol Cell 15:343–353. doi: 10.1016/j.molcel.2004.06.037 · DOI
- Le Blanc I, Luyet P-P, Pons V et al (2005) Endosome-to-cytosol transport of viral nucleocapsids. Nat Cell Biol 7:653–664. doi: 10.1038/ncb1269 · DOI
Cited by
Sorted by citations
Shedding light on the cell biology of extracellular vesicles
van Niel, G., D'Angelo, G., & Raposo, G. (2018) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm.2017.125 · Cited by 8,369
Therapeutically harnessing extracellular vesicles
Cheng, L., & Hill, A. F. (2022) · Nature Reviews Drug Discovery · doi:10.1038/s41573-022-00410-w · Cited by 737
Engineering strategies for customizing extracellular vesicle uptake in a therapeutic context
Esmaeili, A., Alini, M., Baghaban Eslaminejad, M., & Hosseini, S. (2022) · Stem Cell Research & Therapy · doi:10.1186/s13287-022-02806-2 · Cited by 94
García-González, L., Pilat, D., Baranger, K., & Rivera, S. (2019) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2019.00244 · Cited by 88
The Dichotomous Role of Extracellular Vesicles in the Central Nervous System
Graykowski, D. R., Wang, Y.-Z., Upadhyay, A., & Savas, J. N. (2020) · iScience · doi:10.1016/j.isci.2020.101456 · Cited by 39
Metadata
- Authors
- Laulagnier, K., Javalet, C., Hemming, F. J., Chivet, M., Lachenal, G., Blot, B., Chatellard, C., & Sadoul, R.
- Venue
- Cellular and Molecular Life Sciences
- Published
- 2017-09-27
- Volume
- 75
- Issue
- 4
- Pages
- 757-773
- ISSN
- 1420-682X
- 1420-9071
- Cited by
- 164
- References
- 16
- Language
- en
- Funders
- Association France Alzheimer
- Agence Nationale de la Recherche (MALZ)
- Fondation Plan Alzheimer
- Ministère de l'Education Nationale, de l'Enseignement Superieur et de la Recherche
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