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Proteomic Analysis of Microglia-Derived Exosomes: Metabolic Role of the Aminopeptidase CD13 in Neuropeptide Catabolism
Abstract
Vesicle transport is a fundamental mechanism of communication in the CNS. In this study we characterized a novel type of vesicle released by murine brain microglial cells: microglial exosomes. Analysis of their protein content identified several enzymes, chaperones, tetraspanins, and membrane receptors previously reported in B cells and dendritic cell-derived exosomes. Additionally, microglia-derived exosomes expressed the aminopeptidase CD13 and the lactate transporter MCT-1. Exosomal CD13 was metabolically active in cleaving leucine- and methionine-enkephalins peptides by releasing the N-terminal tyrosine. Cleaved neuropeptides were unable to bind to the neuronal opioid receptor as assessed by cAMP response. Microglial exosomal vesicles may represent an important, previously unrecognized, cellular communication system in an organ in which cell motility is highly restricted.
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“Aminopeptidase CD13 is an important characteristic protein of exosomes derived from microglia,44”
From Microglia secrete miR-146a-5p-containing exosomes to regulate neurogenesis in depression (2022) · cites this paper as [44]
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Cites
Exosomes: composition, biogenesis and function
Théry, C., Zitvogel, L., & Amigorena, S. (2002) · Nature reviews. Immunology · doi:10.1038/nri855 · Cited by 5,355
B lymphocytes secrete antigen-presenting vesicles.
Raposo, G., Nijman, H. W., Stoorvogel, W., Liejendekker, R., Harding, C. V., Melief, C. J., & Geuze, H. J. (1996) · The Journal of experimental medicine · doi:10.1084/jem.183.3.1161 · Cited by 3,546
14-3-3 Proteins: Structure, Function, and Regulation
Fu, H., Subramanian, R. R., & Masters, S. C. (2000) · The Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev.pharmtox.40.1.617 · Cited by 1,596
Théry, C., Boussac, M., Véron, P., Ricciardi‐Castagnoli, P., Raposo, G., Garin, J., & Amigorena, S. (2001) · The Journal of Immunology · doi:10.4049/jimmunol.166.12.7309 · Cited by 1,564
Molecular Characterization of Dendritic Cell-Derived Exosomes
Théry, C., Régnault, A., Garin, J., Wolfers, J., Zitvogel, L., Ricciardi‐Castagnoli, P., Raposo, G., & Amigorena, S. (1999) · The Journal of Cell Biology · doi:10.1083/jcb.147.3.599 · Cited by 1,065
Proteomic and Biochemical Analyses of Human B Cell-derived Exosomes
Wubbolts, R., Leckie, R. S., Veenhuizen, P. T. M., Schwarzmann, G., Möbius, W., Hoernschemeyer, J., Slot, J.-W., Geuze, H. J., & Stoorvogel, W. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m207550200 · Cited by 886
Ford, A. L., Goodsall, A. L., Hickey, W. F., & Sedgwick, J. D. (1995) · The Journal of Immunology · doi:10.4049/jimmunol.154.9.4309 · Cited by 631
Riese, R. J., Wolf, P. R., Brömme, D., Natkin, L. W., Villadangos, J. A., Ploegh, H. L., & Chapman, H. A. (1996) · Immunity · doi:10.1016/s1074-7613(00)80249-6 · Cited by 536
Self-citationBasic principles of immunological surveillance of the normal central nervous system
Hickey, W. F. (2001) · Glia · doi:10.1002/glia.1101 · Cited by 476
Amigorena, S., Drake, J. R., Webster, P. C., & Mellman, I. (1994) · Nature · doi:10.1038/369113a0 · Cited by 439
Flagged first, then by citations
Research works printed but not linked: 37
- 2001, Glia, 118
- 1995, J. Immunol., 4309
- 1997, Mol. Psychiatry, 96
- 2002, Glia, 218
- 2002, J. Immunol., 2264
- 1996, Eur. J. Neurosci., 2582
- 1998, Proc. Natl. Acad. Sci. USA, 5779
- 1983, Biochem. J., 37
- 1996, J. Exp. Med., 1161
- 1999, J. Cell Biol., 599
- 2001, J. Immunol., 7309
- 2002, Nat. Rev. Immunol., 569
- 2003, J. Biol. Chem., 10963
- 1993, Glia, 255
- 2001, Proc. Natl. Acad. Sci. USA, 6295
- 1996, Immunity, 357
- 2000, J. Cell Sci., 997
- 1999, Mol. Biol. Cell., 119
- 1999, Mol. Biol. Cell, 3891
- 2000, Eur. J. Cell Biol., 771
- 2002, Eur. J. Cell Biol., 273
- 2004, Mol. Biol. Cell, 3530
- 2002, Trends Biochem. Sci., 257
- 2001, Curr. Opin. Cell. Biol., 454
- 1994, Nature, 113
- 1994, Nature, 120
- 1994, Curr. Opin. Immunol., 57
- 2000, Annu. Rev. Pharmacol. Toxicol., 617
- 2002, Immunogenetics, 87
- 1997, Neurosci. Lett., 127
- 1995, J. Neurochem., 1841
- 1997, J. Biol. Chem., 30096
- 2001, J. Biol. Chem., 37779
- 1984, Prog. Neuropsychopharmacol. Biol. Psychiatry, 719
- 2003, Science, 1070
- 1993, FEBS Lett., 61
- 1998, J. Biol. Chem., 31053
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Sorted by citations
Valadi, H., Ekström, K., Bossios, A., Sjöstrand, M., Lee, J. J., & Lötvall, J. O. (2007) · Nature Cell Biology · doi:10.1038/ncb1596 · Cited by 12,834
Membrane vesicles as conveyors of immune responses
Théry, C., Ostrowski, M., & Segura, É. (2009) · Nature reviews. Immunology · doi:10.1038/nri2567 · Cited by 3,996
Extracellular vesicles: biology and emerging therapeutic opportunities
EL Andaloussi, S., Mäger, I., Breakefield, X. O., & Wood, M. J. A. (2013) · Nature Reviews Drug Discovery · doi:10.1038/nrd3978 · Cited by 3,571
Exosomes: Extracellular organelles important in intercellular communication
Mathivanan, S., Ji, H. L., & Simpson, R. J. (2010) · Journal of Proteomics · doi:10.1016/j.jprot.2010.06.006 · Cited by 2,581
Exosomes: proteomic insights and diagnostic potential
Simpson, R. J., Lim, J. W., Moritz, R. L., & Mathivanan, S. (2009) · Expert Review of Proteomics · doi:10.1586/epr.09.17 · Cited by 1,119
Exosome Secretion: Molecular Mechanisms and Roles in Immune Responses
Bobrie, A., Colombo, M., Raposo, G., & Théry, C. (2011) · Traffic · doi:10.1111/j.1600-0854.2011.01225.x · Cited by 1,148
Exosomes: secreted vesicles and intercellular communications
Théry, C. (2011) · F1000 Biology Reports · doi:10.3410/b3-15 · Cited by 989
Exosomes: A Common Pathway for a Specialized Function
van Niel, G., Porto-Carreiro, I., Simoes, S., & Raposo, G. (2006) · The Journal of Biochemistry · doi:10.1093/jb/mvj128 · Cited by 922
Microautophagy of Cytosolic Proteins by Late Endosomes
Sahu, R., Kaushik, S., Clement, C. C., Cannizzo, E. S., Scharf, B., Follenzi, A., Potolicchio, I., Nieves, E., Cuervo, A. M., & Santambrogio, L. (2011) · Developmental Cell · doi:10.1016/j.devcel.2010.12.003 · Cited by 902
Self-citationProteomic profiling of exosomes: Current perspectives
Simpson, R. J., Jensen, S. S., & Lim, J. W. E. (2008) · PROTEOMICS · doi:10.1002/pmic.200800109 · Cited by 872
Extracellular vesicles round off communication in the nervous system
Budnik, V., Ruiz-Cañada, C., & Wendler, F. (2016) · Nature Reviews Neuroscience · doi:10.1038/nrn.2015.29 · Cited by 712
Tetraspanins: push and pull in suppressing and promoting metastasis
Zöller, M. (2008) · Nature reviews. Cancer · doi:10.1038/nrc2543 · Cited by 687
Characterization and Comprehensive Proteome Profiling of Exosomes Secreted by Hepatocytes
Conde‐Vancells, J., Rodríguez‐Suárez, E., Embade, N., Gil‐Carton, D., Matthiesen, R., Valle, M., Elortza, F., Lu, S. C.-L., Mato, J. M., & Falcón‐Pérez, J. M. (2008) · Journal of Proteome Research · doi:10.1021/pr8004887 · Cited by 662
San-Millán, I., & Brooks, G. A. (2016) · Carcinogenesis · doi:10.1093/carcin/bgw127 · Cited by 640
Brites, D., & Fernandes, A. (2015) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2015.00476 · Cited by 599
“preparations derived from N9 microglial cells (Potolicchio et al., 2005).”
BackgroundLachenal, G. M., Pernet‐Gallay, K., Chivet, M., Hemming, F. J., Belly, A., Bodon, G., Blot, B., Haase, G., Goldberg, Y., & Sadoul, R. (2010) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2010.11.004 · Cited by 617
Acid sphingomyelinase activity triggers microparticle release from glial cells
Bianco, F., Perrotta, C., Novellino, L., Francolini, M., Riganti, L., Menna, E., Saglietti, L., Schuchman, E. H., Furlan, R., Clementi, E., et al. (2009) · The EMBO Journal · doi:10.1038/emboj.2009.45 · Cited by 615
Exosomes: immune properties and potential clinical implementations
Chaput, N., & Théry, C. (2010) · Seminars in Immunopathology · doi:10.1007/s00281-010-0233-9 · Cited by 590
Rodrigues, M. L., Nakayasu, E. S., Oliveira, D. L., Nimrichter, L., Nosanchuk, J. D., Almeida, I. C., & Casadevall, A. (2008) · Eukaryotic Cell · doi:10.1128/ec.00370-07 · Cited by 558
Krämer‐Albers, E., Bretz, N. P., Tenzer, S., Winterstein, C., Möbius, W., Berger, H., Nave, K., Schild, H., & Trotter, J. (2007) · PROTEOMICS - CLINICAL APPLICATIONS · doi:10.1002/prca.200700522 · Cited by 574
Exosome mimetics: a novel class of drug delivery systems
Schiffelers, R. M., Kooijmans, S. A. A., Vader, P., van Dommelen, & van Solinge, W. W. (2012) · International Journal of Nanomedicine · doi:10.2147/ijn.s29661 · Cited by 531
Proteomics, transcriptomics and lipidomics of exosomes and ectosomes
Choi, D., Kim, D., Kim, Y., & Gho, Y. S. (2013) · PROTEOMICS · doi:10.1002/pmic.201200329 · Cited by 528
Identification and proteomic profiling of exosomes in human cerebrospinal fluid
Street, J. M., Barran, P. E., Mackay, C. L., Weidt, S. K., Balmforth, C., Walsh, T. S., Chalmers, R. T. A., Webb, D. J., & Dear, J. W. (2012) · Journal of Translational Medicine · doi:10.1186/1479-5876-10-5 · Cited by 508
Schwann cell‐derived exosomes enhance axonal regeneration in the peripheral nervous system
Lopez‐Verrilli, M. A., Picou, F., & Court, F. A. (2013) · Glia · doi:10.1002/glia.22558 · Cited by 453
Proteomic and immunologic analyses of brain tumor exosomes
Graner, M. W., Álzate, Ó., Dechkovskaia, A. M., Keene, J. D., Sampson, J. H., Mitchell, D. A., & Bigner, D. D. (2008) · The FASEB Journal · doi:10.1096/fj.08-122184 · Cited by 440
Huang, S., Ge, X., Yu, J., Han, Z., Yin, Z., Li, Y., Chen, F., Wang, H., Zhang, J., & Lei, P. (2018) · The FASEB Journal · doi:10.1096/fj.201700673r · Cited by 388
Mesenchymal stem cell derived-exosomes: a modern approach in translational medicine
Nikfarjam, S., Rezaie, J., Zolbanin, N. M., & Jafari, R. (2020) · Journal of Translational Medicine · doi:10.1186/s12967-020-02622-3 · Cited by 428
Layé, S., Nadjar, A., Joffre, C., & Bazinet, R. P. (2018) · Pharmacological Reviews · doi:10.1124/pr.117.014092 · Cited by 420
Ridder, K., Keller, S., Dams, M., Rupp, A.-K., Schlaudraff, J., Del Turco, D., Starmann, J., Macas, J., Karpova, D., Devraj, K., et al. (2014) · PLoS Biology · doi:10.1371/journal.pbio.1001874 · Cited by 412
Exosomes: Vehicles for the Transfer of Toxic Proteins Associated with Neurodegenerative Diseases?
Bellingham, S. A., Guo, B. B., Coleman, B. M., & Hill, A. F. (2012) · Frontiers in Physiology · doi:10.3389/fphys.2012.00124 · Cited by 412
Corrado, C., Raimondo, S., Chiesi, A., Ciccia, F., Leo, G. D., & Alessandro, R. (2013) · International Journal of Molecular Sciences · doi:10.3390/ijms14035338 · Cited by 402
Proteomics Analysis of Bladder Cancer Exosomes
Welton, J. L., Khanna, S., Giles, P. J., Brennan, P., Brewis, I. A., Staffurth, J. N., Mason, M. D., & Clayton, A. (2010) · Molecular & Cellular Proteomics · doi:10.1074/mcp.m000063-mcp201 · Cited by 393
Extracellular vesicles as mediators of neuron-glia communication
Frühbeis, C., Fröhlich, D., Kuo, W. P., & Krämer‐Albers, E. (2013) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2013.00182 · Cited by 397
Cell-to-cell Communication by Extracellular Vesicles: Focus on Microglia
Paolicelli, R. C., Bergamini, G., & Rajendran, L. (2019) · Neuroscience · doi:10.1016/j.neuroscience.2018.04.003 · Cited by 338
Albuquerque, P. C., Nakayasu, E. S., Rodrigues, M. L., Frasés, S., Casadevall, A., Zancopé‐Oliveira, R. M., de Almeida, I. C., & Nosanchuk, J. D. (2008) · Cellular Microbiology · doi:10.1111/j.1462-5822.2008.01160.x · Cited by 347
Kesimer, M., Scull, M., Brighton, B., DeMaria, G., Burns, K., O'Neal, W., Pickles, R. J., & Sheehan, J. K. (2009) · The FASEB Journal · doi:10.1096/fj.08-119131 · Cited by 346
Tumor cell-derived exosomes: A message in a bottle
Kharaziha, P., Ceder, S., Li, Q., & Panaretakis, T. (2012) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2012.03.006 · Cited by 347
Exosomes: Mediators of Neurodegeneration, Neuroprotection and Therapeutics
Kalani, A., Tyagi, A. A., & Tyagi, N. (2013) · Molecular Neurobiology · doi:10.1007/s12035-013-8544-1 · Cited by 339
Chivet, M., Javalet, C., Laulagnier, K., Blot, B., Hemming, F. J., & Sadoul, R. (2014) · Journal of Extracellular Vesicles · doi:10.3402/jev.v3.24722 · Cited by 340
Role of Exosomes/Microvesicles in the Nervous System and Use in Emerging Therapies
Lai, C. P., & Breakefield, X. O. (2012) · Frontiers in Physiology · doi:10.3389/fphys.2012.00228 · Cited by 323
Iraci, N., Leonardi, T., Gessler, F., Vega, B., & Pluchino, S. (2016) · International Journal of Molecular Sciences · doi:10.3390/ijms17020171 · Cited by 301
Exosomes: vesicular carriers for intercellular communication in neurodegenerative disorders
Schneider, A., & Simons, M. (2012) · Cell and Tissue Research · doi:10.1007/s00441-012-1428-2 · Cited by 301
Understanding wiring and volume transmission
Agnati, L. F., Guidolin, D., Guescini, M., Genedani, S., & Fuxé, K. (2010) · Brain Research Reviews · doi:10.1016/j.brainresrev.2010.03.003 · Cited by 295
Dickens, A. M., Tovar-y-Romo, L. B., Yoo, S.-W., Trout, A. L., Bae, M., Kanmogne, M., Megra, B., Williams, D. W., Witwer, K. W., Gacias, M., et al. (2017) · Science Signaling · doi:10.1126/scisignal.aai7696 · Cited by 285
Stimulation of P2 receptors causes release of IL-1β–loaded microvesicles from human dendritic cells
Pizzirani, C., Ferrari, D., Chiozzi, P., Adinolfi, E., Sandonà, D., Savaglio, E., & Virgilio, F. D. (2006) · Blood · doi:10.1182/blood-2005-06-031377 · Cited by 280
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Segura, É., Guérin, C. L., Hogg, N., Amigorena, S., & Théry, C. (2007) · The Journal of Immunology · doi:10.4049/jimmunol.179.3.1489 · Cited by 278
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Frühbeis, C., Fröhlich, D., & Krämer-Albers, E.-M. (2012) · Frontiers in Physiology · doi:10.3389/fphys.2012.00119 · Cited by 275
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Zappulli, V., Friis, K. P., Fitzpatrick, Z., Maguire, C. A., & Breakefield, X. O. (2016) · Journal of Clinical Investigation · doi:10.1172/jci81134 · Cited by 262
Sharples, R. A., Vella, L. J., Nisbet, R. M., Naylor, R., Perez, K. A., Barnham, K. J., Masters, C. L., & Hill, A. F. (2008) · The FASEB Journal · doi:10.1096/fj.07-9357com · Cited by 253
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Smalheiser, N. R. (2007) · Biology Direct · doi:10.1186/1745-6150-2-35 · Cited by 256
Exosomes are endogenous nanoparticles that can deliver biological information between cells
Sun, D., Zhuang, X., Zhang, S., Deng, Z., Grizzle, W. E., Miller, D., & Zhang, H. (2012) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2012.07.002 · Cited by 250
Exosomes as nano-theranostic delivery platforms for gene therapy
Tan, A., Rajadas, J., & Seifalian, A. M. (2012) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2012.06.014 · Cited by 246
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Aryani, A., & Denecke, B. (2014) · Molecular Neurobiology · doi:10.1007/s12035-014-9054-5 · Cited by 242
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Hornung, S., Dutta, S., & Bitan, G. (2020) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2020.00038 · Cited by 244
Pironti, G., Strachan, R. T., Abraham, D., Yu, S. M.-W., Chen, M., Chen, W., Hanada, K., Mao, L., Watson, L. J., & Rockman, H. A. (2015) · Circulation · doi:10.1161/circulationaha.115.015687 · Cited by 245
The role of exosomes in the processing of proteins associated with neurodegenerative diseases
Vella, L. J., Sharples, R. A., Nisbet, R. M., Cappai, R., & Hill, A. F. (2007) · European Biophysics Journal · doi:10.1007/s00249-007-0246-z · Cited by 235
Extracellular vesicles as modulators of cell-to-cell communication in the healthy and diseased brain
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Janas, A., Sapoń, K., Janas, T., Stowell, M. H. B., & Janas, T. (2016) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/j.bbamem.2016.02.011 · Cited by 235
Exosomes in stroke pathogenesis and therapy
Zhang, Z. G., & Chopp, M. (2016) · Journal of Clinical Investigation · doi:10.1172/jci81133 · Cited by 228
Beheshti, E. H., Pham, S., Adomat, H. H., Li, N., & Guns, E. S. T. (2012) · Molecular & Cellular Proteomics · doi:10.1074/mcp.m111.014845 · Cited by 224
Active endocannabinoids are secreted on extracellular membrane vesicles
Gabrielli, M., Battista, N., Riganti, L., Prada, I., Antonucci, F., Cantone, L., Matteoli, M., Maccarrone, M., & Verderio, C. (2015) · The EMBO Reports · doi:10.15252/embr.201439668 · Cited by 231
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Kanninen, K. M., Korvenlaita, N., Koıstınaho, J., & Malm, T. (2015) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2015.09.020 · Cited by 226
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Microglia centered pathogenesis in ALS: insights in cell interconnectivity
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Multivesicular bodies in neurons: Distribution, protein content, and trafficking functions
von Bartheld, C. S., & Altick, A. L. (2011) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2011.01.003 · Cited by 207
Inclusion Biogenesis, Methods of Isolation and Clinical Application of Human Cellular Exosomes
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Delpech, J.-C., Herron, S., Botros, M. B., & Ikezu, T. (2019) · Trends in Neurosciences · doi:10.1016/j.tins.2019.02.007 · Cited by 193
Inflammation leads to distinct populations of extracellular vesicles from microglia
Yang, Y., Boza‐Serrano, A., Dunning, C. J. R., Clausen, B. H., Lambertsen, K. L., & Deierborg, T. (2018) · Journal of Neuroinflammation · doi:10.1186/s12974-018-1204-7 · Cited by 194
Li, J., Lee, Y., Johansson, H. J., Mäger, I., Vader, P., Nordin, J. Z., Wiklander, O. P. B., Lehtiö, J., Wood, M. J. A., & Andaloussi, S. E. (2015) · Journal of Extracellular Vesicles · doi:10.3402/jev.v4.26883 · Cited by 190
Koniusz, S., Andrzejewska, A., Muraca, M., Srivastava, A. K., Janowski, M., & Łukomska, B. (2016) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2016.00109 · Cited by 191
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Crotti, A., Sait, H. R., McAvoy, K. M., Estrada, K., Ergun, A., Szak, S., Marsh, G., Jandreski, L., Peterson, M., Reynolds, T. L., et al. (2019) · Scientific Reports · doi:10.1038/s41598-019-45676-0 · Cited by 171
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Basso, M., & Bonetto, V. (2016) · Frontiers in Neuroscience · doi:10.3389/fnins.2016.00127 · Cited by 161
Staubach, S., Razawi, H., & Hanisch, F. (2009) · PROTEOMICS · doi:10.1002/pmic.200800793 · Cited by 175
Zăgrean, A., Hermann, D. M., Opriș, I. C., Zăgrean, L., & Popa‐Wagner, A. (2018) · Frontiers in Neuroscience · doi:10.3389/fnins.2018.00811 · Cited by 173
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Turola, E. (2012) · Frontiers in Physiology · doi:10.3389/fphys.2012.00149 · Cited by 174
Laulagnier, K., Javalet, C., Hemming, F. J., Chivet, M., Lachenal, G., Blot, B., Chatellard, C., & Sadoul, R. (2018) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-017-2664-0 · Cited by 164
Silverman, J. M., Christy, D., Shyu, C. C., Moon, K., Fernando, S. M., Gidden, Z., Cowan, C. M., Ban, Y., Stacey, R. G., Grad, L. I., et al. (2019) · Journal of Biological Chemistry · doi:10.1074/jbc.ra118.004825 · Cited by 176
TREM2/DAP12 Signal Elicits Proinflammatory Response in Microglia and Exacerbates Neuropathic Pain
Kobayashi, M., Konishi, H., Sayo, A., Takai, T., & Kiyama, H. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.1238-16.2016 · Cited by 162
Large Extracellular Vesicles: Have We Found the Holy Grail of Inflammation?
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Chang, Y.-H., Wu, K.-C., Harn, H.-J., Lin, S.-Z., & Ding, D.-C. (2018) · Cell Transplantation · doi:10.1177/0963689717723636 · Cited by 159
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Metadata
- Authors
- Potolicchio, I., Carven, G. J., Xu, X., Stipp, C., Riese, R. J., Stern, L. J., & Santambrogio, L.
- Affiliations
- Albert Einstein College of Medicine (US)
- University of Massachusetts Chan Medical School (US)
- Dana-Farber Cancer Institute (US)
- Brigham and Women's Hospital (US)
- Venue
- The Journal of Immunology
- Publisher
- Oxford University Press (OUP)
- Published
- 2005-08
- Volume
- 175
- Issue
- 4
- Pages
- 2237-2243
- ISSN
- 0022-1767 (ISSN-L)
- 1550-6606
- OpenAlex
- W1524589668
- Cited by
- 365
- References
- 37
- Citations by year
- 2026: 11 · 2025: 6 · 2024: 18 · 2023: 22 · 2022: 32 · 2021: 31 · 2020: 30 · 2019: 29 · 2018: 16 · 2017: 18 · 2016: 29 · 2015: 13 · 2014: 16 · 2013: 14 · 2012: 22
- FWCI
- 3.39
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- The Journal of Immunology (publishedVersion)
- PubMed (publishedVersion)
- IRIS (submittedVersion)
- SERVAL (Université de Lausanne) (submittedVersion)
- Funders
- National Institutes of Health (5k08ai001555-03)
- National Cancer Institute (CA 86712, R01CA086712)
- National Institute of Allergy and Infectious Diseases (K08AI01555, R01-AI38996, R01AI048832, R01AI038996)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Extracellular vesicles in disease
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular transport and secretion
- Keywords
- CD13, aminopeptidase, enkephalin, opioid receptors, MCT1, lactate transporters, tetraspanins, cell surface receptors, molecular chaperones
- MeSH terms
- Animals, Antigens, Differentiation, B-Lymphocyte, Histocompatibility Antigens Class II, Cathepsins, Cell Communication, Cell Line, Neuropeptides, Endosomes, Biomarkers, Microglia, CD13 Antigens, Proteome, Cytoplasmic Vesicles, Cell Line, Tumor, Mice
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