Molecular determinants for the interaction between AMPA receptors and the clathrin adaptor complex AP-2
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α-Amino-3-hydroxy-5-methylisoxazole-4-propionic acid (AMPA)-type glutamate receptors undergo constitutive and ligand-induced internalization that requires dynamin and the clathrin adaptor complex AP-2. We report here that an atypical basic motif within the cytoplasmic tails of AMPA-type glutamate receptors directly associates with μ2-adaptin by a mechanism similar to the recognition of the presynaptic vesicle protein synaptotagmin 1 by AP-2. A synaptotagmin 1-derived AP-2 binding peptide competes the interaction of the AMPA receptor subunit GluR2 with AP-2μ and increases the number of surface active glutamate receptors in living neurons. Moreover, fusion of the GluR2-derived tail peptide with a synaptotagmin 1 truncation mutant restores clathrin/AP-2-dependent internalization of the chimeric reporter protein. These data suggest that common mechanisms regulate AP-2-dependent internalization of pre- and postsynaptic membrane proteins.
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GluA2 can directly interact with AP-2 clathrin adapter complex, which allows GluA2-containing receptors to be rapidly depleted from the cell-surface.
“GluA2 can directly interact with AP-2 clathrin adapter complex, which allows GluA2-containing receptors to be rapidly depleted from the cell-surface (Kastning et al., 2007, Lee et al., 2002).”
From The AMPA Receptor Code of Synaptic Plasticity (2018) · cites this paper as Kastning et al., 2007
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AMPA Receptor Trafficking and Synaptic Plasticity
Malinow, R., & Malenka, R. C. (2002) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.25.112701.142758 · Cited by 2,588 · see citing works
AMPA receptor trafficking at excitatory synapses
Bredt, D. S., & Nicoll, R. A. (2003) · Neuron · doi:10.1016/s0896-6273(03)00640-8 · Cited by 1,150 · see citing works
PKA phosphorylation of AMPA receptor subunits controls synaptic trafficking underlying plasticity
Esteban, J. A., Shi, S.-H., Wilson, C., Nuriya, M., Huganir, R. L., & Malinow, R. (2003) · Nature Neuroscience · doi:10.1038/nn997 · Cited by 894 · see citing works
Regulation of AMPA receptor endocytosis by a signaling mechanism shared with LTD
Beattie, E. C., Carroll, R. C., Yu, X., Morishita, W., Yasuda, H., von Zastrow, M., & Malenka, R. C. (2000) · Nature Neuroscience · doi:10.1038/81823 · Cited by 745 · see citing works
Adaptable adaptors for coated vesicles.
Robinson, M. (2004) · Trends in Cell Biology · doi:10.1016/j.tcb.2004.02.002 · Cited by 741 · see citing works
Postsynaptic signaling and plasticity mechanisms
Sheng, M., & Kim, M. J. (2002) · Science · doi:10.1126/science.1075333 · Cited by 731 · see citing works
Self-citationRecycling Endosomes Supply AMPA Receptors for LTP
Park, M., Penick, E. C., Edwards, J. G., Kauer, J. A., & Ehlers, M. D. (2004) · Science · doi:10.1126/science.1102026 · Cited by 730 · see citing works
Clathrin-mediated endocytosis in AP-2–depleted cells
Motley, A. M., Bright, N. A., Seaman, M. N. J., & Robinson, M. S. (2003) · The Journal of Cell Biology · doi:10.1083/jcb.200305145 · Cited by 699 · see citing works
Man, H., Lin, J., Ju, W. H., Ahmadian, G., Liu, L., Becker, L. E., Sheng, M., & Wang, Y. T. (2000) · Neuron · doi:10.1016/s0896-6273(00)81067-3 · Cited by 698 · see citing works
Self-citationRole of AMPA Receptor Cycling in Synaptic Transmission and Plasticity
Lüscher, C., Xia, H., Beattie, E. C., Carroll, R. C., von Zastrow, M., Malenka, R. C., & Nicoll, R. A. (1999) · Neuron · doi:10.1016/s0896-6273(00)81119-8 · Cited by 692 · see citing works
Lakadamyali, M., Rust, M., & Zhuang, X. (2006) · Cell · doi:10.1016/j.cell.2005.12.038 · Cited by 589 · see citing works
Distinct molecular mechanisms and divergent endocytotic pathways of AMPA receptor internalization
Lin, J., Ju, W. H., Foster, K. A., Lee, S. H., Ahmadian, G., Wyszynski, M. W., Wang, Y. T., & Sheng, M. (2000) · Nature Neuroscience · doi:10.1038/81814 · Cited by 554 · see citing works
Self-citationLee, S. H., Liu, L., Wang, Y. T., & Sheng, M. (2002) · Neuron · doi:10.1016/s0896-6273(02)01024-3 · Cited by 441 · see citing works
Self-citationHomeostatic plasticity and NMDA receptor trafficking
Pérez-Otaño, I., & Ehlers, M. D. (2005) · Trends in Neurosciences · doi:10.1016/j.tins.2005.03.004 · Cited by 356 · see citing works
Ahmadian, G., Ju, W., Liu, L., Wyszynski, M., Lee, S. H., Dunah, A. W., Taghibiglou, C., Wang, Y., Lu, J., Wong, T. P., et al. (2004) · The EMBO Journal · doi:10.1038/sj.emboj.7600126 · Cited by 296 · see citing works
Self-citationBurbea, M., Dreier, L., Dittman, J. S., Grunwald, M. E., & Kaplan, J. M. (2002) · Neuron · doi:10.1016/s0896-6273(02)00749-3 · Cited by 294 · see citing works
Subunit Rules Governing the Sorting of Internalized AMPA Receptors in Hippocampal Neurons
Lee, S. H., Simonetta, A., & Sheng, M. (2004) · Neuron · doi:10.1016/j.neuron.2004.06.015 · Cited by 268 · see citing works
Self-citationPotentiation of NMDA receptor currents by dopamine D 1 receptors in prefrontal cortex
Chen, G., Greengard, P., & Yan, Z. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0308618100 · Cited by 243 · see citing works
Self-citationLateral organization of endocytic machinery in dendritic spines
Rácz, B., Blanpied, T. A., Ehlers, M., & Weinberg, R. J. (2004) · Nature Neuroscience · doi:10.1038/nn1303 · Cited by 227 · see citing works
Evolving nature of the AP2 α‐appendage hub during clathrin‐coated vesicle endocytosis
Praefcke, G. J. K., Ford, M. G. J., Schmid, E. M., Olesen, L. E., Gallop, J. L., Peak‐Chew, S., Vallis, Y., Babu, M. M., Mills, I. G., & McMahon, H. T. (2004) · The EMBO Journal · doi:10.1038/sj.emboj.7600445 · Cited by 200 · see citing works
Kittler, J. T., Chen, G., Honing, S., Bogdanov, Y. D., McAinsh, K., Arancibia‐Cárcamo, I. L., Jovanovic, J. N., Pangalos, M. N., Haucke, V., Yan, Z., et al. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0506653102 · Cited by 192 · see citing works
Self-citationDiril, M. K., Wienisch, M., Jung, N., Klingauf, J., & Haucke, V. (2006) · Developmental Cell · doi:10.1016/j.devcel.2005.12.011 · Cited by 172 · see citing works
Self-citationDual interaction of synaptotagmin with μ2‐ and α‐adaptin facilitates clathrin‐coated pit nucleation
Haucke, V., Wenk, M. R., Chapman, E. R., Farsad, K., & Camilli, P. V. D. (2000) · The EMBO Journal · doi:10.1093/emboj/19.22.6011 · Cited by 135 · see citing works
Self-citationMetzler, M., Li, B., Gan, L., Georgiou, J., Gutekunst, C., Wang, Y., Torre, E. R., Devon, R. S., Oh-McGinnis, R., Legendre‐Guillemin, V., et al. (2003) · The EMBO Journal · doi:10.1093/emboj/cdg334 · Cited by 123 · see citing works
Molecular constituents of neuronal AMPA receptors
Fukata, Y., Tzingounis, A. V., Trinidad, J. C., Fukata, M., Burlingame, A. L., Nicoll, R. A., & Bredt, D. S. (2005) · The Journal of Cell Biology · doi:10.1083/jcb.200501121 · Cited by 121 · see citing works
Grass, I., Thiel, S., Höning, S., & Haucke, V. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m409995200 · Cited by 72 · see citing works
Self-citationRegulation of AP-2-Synaptotagmin Interaction by Inositol High Polyphosphates
Mizutani, A., Fukuda, M., Niinobe, M., & Mikoshiba, K. (1997) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.1997.7578 · Cited by 30 · see citing works
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Traynelis, S. F., Wollmuth, L. P., McBain, C. J., Menniti, F. S., Vance, K. M., Ogden, K. K., Hansen, K. B., Yuan, H., Myers, S. J., & Dingledine, R. (2010) · Pharmacological Reviews · doi:10.1124/pr.109.002451 · Cited by 3,568 · see citing works
Synaptic Plasticity: Multiple Forms, Functions, and Mechanisms
Citri, A., & Malenka, R. C. (2008) · Neuropsychopharmacology · doi:10.1038/sj.npp.1301559 · Cited by 2,323 · see citing works
The AMPA Receptor Code of Synaptic Plasticity
Diering, G. H., & Huganir, R. L. (2018) · Neuron · doi:10.1016/j.neuron.2018.10.018 · Cited by 844 · see citing works
The role of the GluR2 subunit in AMPA receptor function and synaptic plasticity
Isaac, J. T. R., Ashby, M. C., & McBain, C. J. (2007) · Neuron · doi:10.1016/j.neuron.2007.06.001 · Cited by 802 · see citing works
Regulation of AMPA receptor trafficking and synaptic plasticity
Anggono, V., & Huganir, R. L. (2012) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2011.12.006 · Cited by 588 · see citing works
Glutamate receptor dynamics in dendritic microdomains.
Newpher, T. M., & Ehlers, M. D. (2008) · Neuron · doi:10.1016/j.neuron.2008.04.030 · Cited by 356 · see citing works
Prefrontal cortex AMPA receptor plasticity is crucial for cue-induced relapse to heroin-seeking
Van den Oever, M. C., Goriounova, N. A., Wan Li, K., Van der Schors, R. C., Binnekade, R., Schoffelmeer, A. N. M., Mansvelder, H. D., Smit, A. B., Spijker, S., & De Vries, T. J. (2008) · Nature Neuroscience · doi:10.1038/nn.2165 · Cited by 206 · see citing works
Adaptor protein complexes and intracellular transport
Park, S., & Guo, X. (2014) · Bioscience Reports · doi:10.1042/bsr20140069 · Cited by 197 · see citing works
Survey of the year 2007 commercial optical biosensor literature
Rich, R. L., & Myszka, D. G. (2008) · Journal of Molecular Recognition · doi:10.1002/jmr.928 · Cited by 177 · see citing works
Montpetit, A., Côté, S., Brustein, E., Drouin, C. A., Lapointe, L., Boudreau, M., Meloche, C., Drouin, R., Hudson, T. J., Drapeau, P., et al. (2008) · PLoS Genetics · doi:10.1371/journal.pgen.1000296 · Cited by 171 · see citing works
AMPA receptor signaling through BRAG2 and Arf6 critical for long-term synaptic depression
Scholz, R., Berberich, S., Rathgeber, L., Kolleker, A., Köhr, G., & Kornau, H.-C. (2010) · Neuron · doi:10.1016/j.neuron.2010.05.003 · Cited by 161 · see citing works
Protein aggregation can inhibit clathrin-mediated endocytosis by chaperone competition
Yu, A., Shibata, Y., Shah, B., Calamini, B., Lo, D. C., & Morimoto, R. I. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1321811111 · Cited by 149 · see citing works
Corticosterone Alters AMPAR Mobility and Facilitates Bidirectional Synaptic Plasticity
Martin, S., Henley, J. M., Holman, D., Zhou, M., Wiegert, O., van Spronsen, M., Joëls, M., Hoogenraad, C. C., & Krugers, H. J. (2009) · PLoS ONE · doi:10.1371/journal.pone.0004714 · Cited by 130 · see citing works
Kittler, J. T., Chen, G., Kukhtina, V., Vahedi‐Faridi, A., Gu, Z., Tretter, V. E., Smith, K. R., McAinsh, K., Arancibia‐Cárcamo, I. L., Saenger, W., et al. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0707920105 · Cited by 129 · see citing works
Self-citationClathrin‐Mediated Endocytosis at Synapses
Jung, N., & Haucke, V. (2007) · Traffic · doi:10.1111/j.1600-0854.2007.00595.x · Cited by 118 · see citing works
Self-citationEndocytosis of synaptic ADAM10 in neuronal plasticity and Alzheimer’s disease
Marcello, E. E., Saraceno, C., Musardo, S., Vara, H., de la Fuente, A. G., Pelucchi, S., Marino, D. D., Borroni, B., Tramontano, A. L., Pérez‐Otaño, I., et al. (2013) · Journal of Clinical Investigation · doi:10.1172/jci65401 · Cited by 117 · see citing works
Williams, C., Mehrian Shai, R., Wu, Y., Hsu, Y.-H., Sitzer, T., Spann, B., McCleary, C., Mo, Y., & Miller, C. A. (2009) · PLoS ONE · doi:10.1371/journal.pone.0004936 · Cited by 116 · see citing works
Calpains and neuronal damage in the ischemic brain: The swiss knife in synaptic injury
Curcio, M., Salazar, I. L., Mele, M., Canzoniero, L. M. T., & Duarte, C. B. (2016) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2016.06.001 · Cited by 96 · see citing works
AMPAR trafficking in synapse maturation and plasticity
Bassani, S., Folci, A., Zapata, J., & Passafaro, M. (2013) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-013-1309-1 · Cited by 81 · see citing works
Matsuda, S., Kakegawa, W., Budisantoso, T., Nomura, T., Kohda, K., & Yuzaki, M. (2013) · Nature Communications · doi:10.1038/ncomms3759 · Cited by 79 · see citing works
Neuronal functions of adaptor complexes involved in protein sorting
Guardia, C. M. A., Pace, R. D., Mattera, R., & Bonifacino, J. S. (2018) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2018.02.021 · Cited by 78 · see citing works
Regulation of postsynaptic AMPA responses by synaptojanin 1
Gong, L., & Camilli, P. V. D. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0809221105 · Cited by 75 · see citing works
AP2 hemicomplexes contribute independently to synaptic vesicle endocytosis
Gu, M., Liu, Q., Watanabe, S., Sun, L., Hollopeter, G., Grant, B. D., & Jørgensen, E. M. (2013) · eLife · doi:10.7554/elife.00190 · Cited by 75 · see citing works
daSilva, L. L. P., Wall, M. J., de Almeida, L. P., Wauters, S. C., Januário, Y. C., Müller, J., & Corrêa, S. A. L. (2016) · eNeuro · doi:10.1523/eneuro.0144-15.2016 · Cited by 74 · see citing works
AMPA Receptors in Synaptic Plasticity, Memory Function, and Brain Diseases
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Fiuza, M., Rostosky, C. M., Parkinson, G. T., Bygrave, A. M., Halemani, N., Baptista, M., Milosevic, I., & Hanley, J. G. (2017) · Journal of Cell Biology · doi:10.1083/jcb.201701034 · Cited by 71 · see citing works
Molecular basis of synaptic vesicle cargo recognition by the endocytic sorting adaptor stonin 2
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Hanley, J. G. (2018) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2018.00362 · Cited by 67 · see citing works
Endocytosis and recycling of AMPA receptors lacking GluR2/3
Biou, V., Bhattacharyya, S., & Malenka, R. C. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0711412105 · Cited by 66 · see citing works
Smith, K. R., Muir, J., Rao, Y., Browarski, M., Gruenig, M. C., Sheehan, D. F., Haucke, V., & Kittler, J. T. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.1622-11.2011 · Cited by 64 · see citing works
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Martinelli, D., & Dionisi‐Vici, C. (2014) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.12426 · Cited by 63 · see citing works
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Regulation of GABAA receptor membrane trafficking and synaptic localization
Arancibia‐Cárcamo, I. L., & Kittler, J. T. (2009) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2009.03.012 · Cited by 59 · see citing works
Self-citationMorita, I., Kakuda, S., Takeuchi, Y., Itoh, S., Kawasaki, N., Kizuka, Y., Kawasaki, T., & Oka, S. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.024208 · Cited by 56 · see citing works
Fred, S. M., Laukkanen, L., Brunello, C. A., Vesa, L., Göös, H., Cardon, I., Moliner, R., Maritzen, T., Varjosalo, M., Casarotto, P. C., et al. (2019) · Journal of Biological Chemistry · doi:10.1074/jbc.ra119.008837 · Cited by 52 · see citing works
Endosomal trafficking of AMPA-type glutamate receptors
Hirling, H. (2008) · Neuroscience · doi:10.1016/j.neuroscience.2008.02.057 · Cited by 50 · see citing works
Role of Phosphoinositides at the Neuronal Synapse
Frère, S. G. A., Chang-Ileto, B., & Paolo, G. D. (2012) · Sub-cellular biochemistry/Subcellular biochemistry · doi:10.1007/978-94-007-3015-1_5 · Cited by 48 · see citing works
Vithlani, M., & Moss, S. J. (2009) · Biochemical Society Transactions · doi:10.1042/bst0371355 · Cited by 46 · see citing works
Rudinskiy, N., Grishchuk, Y., Vaslin, A., Puyal, J., Delacourte, A., Hirling, H., Clarke, P. G. H., & Luthi‐Carter, R. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m804740200 · Cited by 45 · see citing works
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The mechanistic link between Arc/Arg3.1 expression and AMPA receptor endocytosis
Wall, M. J., & Corrêa, S. A. L. (2017) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2017.09.005 · Cited by 40 · see citing works
Zaręba-Kozioł, M., Szwajda, A., Dadlez, M., Wysłouch-Cieszyńska, A., & Lalowski, M. (2014) · Molecular & Cellular Proteomics · doi:10.1074/mcp.m113.036079 · Cited by 39 · see citing works
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Overhoff, M., Bruyckere, E. D., & Kononenko, N. L. (2020) · Journal of Neurochemistry · doi:10.1111/jnc.15194 · Cited by 38 · see citing works
The early steps of endocytosis: From cargo selection to membrane deformation
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Liu, K., Lei, R., Li, Q., Wang, X., Wu, Q., An, P., Zhang, J., Zhu, M., Xu, Z., Hong, Y., et al. (2016) · Scientific Reports · doi:10.1038/srep21019 · Cited by 32 · see citing works
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Cao, Y., Ling-Ling, W., Li, X., Yuan, Y.-L., Zhao, W., Qi, J., Zhao, X.-Y., Ward, N., & Wang, J. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms25010111 · Cited by 31 · see citing works
Mattera, R., Williamson, C. D., Ren, X., & Bonifacino, J. S. (2020) · Molecular Biology of the Cell · doi:10.1091/mbc.e19-11-0658 · Cited by 31 · see citing works
Davidson, H. T., Xiao, J., Dai, R., & Bergson, C. M. (2008) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2008.06563.x · Cited by 31 · see citing works
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Tehran, D. A., Kochlamazashvili, G., Pampaloni, N. P., Sposini, S., Shergill, J. K., Lehmann, M., Pashkova, N., Schmidt, C., Löwe, D., Napieczyńska, H., et al. (2022) · Science Advances · doi:10.1126/sciadv.abl5032 · Cited by 29 · see citing works
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Self-citationLin, A. W., & Man, H. (2014) · Journal of Biological Chemistry · doi:10.1074/jbc.m114.582114 · Cited by 23 · see citing works
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Czöndör, K., & Thoumine, O. R. (2012) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2012.11.001 · Cited by 20 · see citing works
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Hu, T., den Bergh, G. V., Thorrez, L., Heylen, K., Eysel, U. T., & Arckens, L. (2011) · Cerebral Cortex · doi:10.1093/cercor/bhr079 · Cited by 19 · see citing works
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Shen, K., & Limón, A. (2021) · Neuroscience Letters · doi:10.1016/j.neulet.2021.135938 · Cited by 11 · see citing works
ABHD6 drives endocytosis of AMPA receptors to regulate synaptic plasticity and learning flexibility
Wei, M., Yang, L., Su, F., Liu, Y., Zhao, X., Luo, L., Sun, X., Liu, S., Dong, Z., Zhang, Y., et al. (2023) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2023.102559 · Cited by 10 · see citing works
Chen, K. H., Yang, J., Liu, B., Jiang, C., Koylass, N., Zhang, Z., Sun, S., Huganir, R. L., & Qiu, Z. (2025) · Cell Reports · doi:10.1016/j.celrep.2025.115302 · Cited by 9 · see citing works
Selvakumar, D., Drescher, M. J., Deckard, N. A., Ramakrishnan, N. A., Morley, B. J., & Drescher, D. G. (2016) · Biochemical Journal · doi:10.1042/bcj20160690 · Cited by 9 · see citing works
Hormonal regulation of AMPA receptor trafficking and memory formation
Krugers, H. J. (2009) · Frontiers in Synaptic Neuroscience · doi:10.3389/neuro.19.002.2009 · Cited by 8 · see citing works
The lemur tail kinase family in neuronal function and disfunction in neurodegenerative diseases
Larose, A., Miller, C. C. J., & Mórotz, G. M. (2024) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-024-05480-0 · Cited by 7 · see citing works
Matsuda, S., & Yuzaki, M. (2021) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2021.100949 · Cited by 6 · see citing works
Lertpeerapan, P., Kanlayaprasit, S., Thongkorn, S., Kasitipradit, K., Panjabud, P., Songsritaya, K., Jantheang, T., Morita, M., Akaike, T., Hu, V. W., et al. (2025) · Biology of Sex Differences · doi:10.1186/s13293-025-00744-1 · Cited by 5 · see citing works
Zhang, J., Cheng, Y., & Xing, Q. (2023) · Journal of Bio-X Research · doi:10.34133/jbioxresearch.0003 · Cited by 4 · see citing works
Li, B., Wang, C., Yu, A., Chen, Y., & Zuo, Z. (2010) · Aquatic Toxicology · doi:10.1016/j.aquatox.2010.05.002 · Cited by 4 · see citing works
Neuronal functions of clathrin-associated endocytic sorting adaptors – from molecules to disease
Kononenko, N. L., & Haucke, V. (2020) · e-Neuroforum · doi:10.1515/nf-2020-0023 · Cited by 2 · see citing works
Self-citationBanerjee, B., MEDDA, B. K., Zhang, J., Tuchscherer, V. J., Babygirija, R., Kannampalli, P., Sengupta, J. N., & Shaker, R. (2016) · Neurogastroenterology & Motility · doi:10.1111/nmo.12834 · Cited by 1 · see citing works
Dendritic Organelles for Postsynaptic Trafficking
Hanus, C., & Ehlers, M. (2008) · Springer eBooks · doi:10.1007/978-0-387-77232-5_8 · Cited by 1 · see citing works
Requirement for AMPA receptor endocytosis and long-term depression in ocular dominance plasticity
Smith, G. B. (2010) · DSpace@MIT (Massachusetts Institute of Technology)
Taraska, J. W., & Sochacki, K. A. (2013) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.718010602.793476802
Gu, X., & Lin, L. (2024) · Acta Oto-Laryngologica · doi:10.1080/00016489.2024.2341126
Киселев, А. В., Titova, N., Arseenkova, O. Y., Vedenkin, A. S., & Хохлов, А. Л. (2026) · S S Korsakov Journal of Neurology and Psychiatry · doi:10.17116/jnevro202612606159
- Authors
- Kastning, K., Kukhtina, V., Kittler, J. T., Chen, G., Pechstein, A., Enders, S., Lee, S. H., Sheng, M., Yan, Z., & Haucke, V.
- Affiliations
- Freie Universität Berlin (DE)
- University College London (GB)
- University at Buffalo, State University of New York (US)
- Howard Hughes Medical Institute (US)
- Corresponding author
- Haucke, Volker
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 2007-02-20
- Volume
- 104
- Issue
- 8
- Pages
- 2991-2996
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- PMC
- PMC1815294
- OpenAlex
- W1975658980
- Cited by
- 88
- References
- 27
- Citations by year
- 2026: 1 · 2025: 3 · 2024: 3 · 2023: 3 · 2022: 3 · 2021: 3 · 2020: 4 · 2019: 2 · 2018: 5 · 2017: 2 · 2016: 6 · 2015: 2 · 2014: 6 · 2013: 5 · 2012: 6
- FWCI
- 4.28
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Proceedings of the National Academy of Sciences (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- UCL Discovery (University College London) (submittedVersion)
- Funders
- European Molecular Biology Organization
- Yale University
- Deutsche Forschungsgemeinschaft (GRK1123, TP-A11)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular transport and secretion
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Receptor Mechanisms and Signaling
- Keywords
- AMPA receptors, receptor internalization, synaptotagmin-1, dynamin, clathrin-mediated endocytosis, receptor trafficking
- MeSH terms
- Amino Acid Sequence, Animals, Cell Survival, Chlorocebus aethiops, Clathrin, Endocytosis, Humans, Molecular Sequence Data, Neurons, Peptides, Protein Binding, Recombinant Fusion Proteins, Synaptic Vesicles, Receptors, AMPA, COS Cells, Excitatory Postsynaptic Potentials, Amino Acid Motifs, Amino Acids, Basic, Adaptor Protein Complex mu Subunits, Synaptotagmin I, Rats
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.
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