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Coordinated PKA and PKC phosphorylation suppresses RXR-mediated ER retention and regulates the surface delivery of NMDA receptors
Abstract
Endoplasmic reticulum (ER) retention mediated by the RXR (Arg-X-Arg) motif is an important quality control mechanism used by G-protein coupled receptors and ion channels, including N-methyl-D-aspartate (NMDA) receptors, to ensure the proper assembly and trafficking of multimeric complexes. During assembly, RXR motifs are masked by intersubunit interactions thereby allowing ER release. Here, we find that PKA and PKC phosphorylation sites flanking the RXR motif of the NMDA receptor NR1 subunit suppress ER retention and regulate receptor forward trafficking. These sites are differentially phosphorylated during the trafficking of NR1 subunits in vivo, and phosphorylation at these sites occurs in early secretory compartments. In addition, residues near the RXR motif not involved in phosphorylation are also required for ER retention. These results indicate that ER retention of NMDA receptors is tightly regulated, and suggest that coordinated phosphorylation by PKA and PKC mediates release of receptors from the ER for subsequent traffic to synapses. Phosphorylation-induced ER export of RXR-containing channels and receptors may serve as a novel quality control mechanism for creating a readily releasable pool of receptors sensitive to the activation of intracellular signaling pathways.
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“RXR motifs enhance the ER localization of ion channels (Scott et al., 2003; Gassmann et al., 2005).”
From Nicotine up-regulates α4β2 nicotinic receptors and ER exit sites via stoichiometry-dependent chaperoning (2011) · cites this paper as Scott et al., 2003
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Cites
Long-Term Potentiation--A Decade of Progress?
Malenka, R. C., & Nicoll, A. R. A. (1999) · Science · doi:10.1126/science.285.5435.1870 · Cited by 2,729
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
Quality control in the endoplasmic reticulum
Ellgaard, L., & Helenius, A. (2003) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm1052 · Cited by 2,171
The molecular basis of CaMKII function in synaptic and behavioural memory
Lisman, J., Schulman, H., & Cline, H. (2002) · Nature Reviews Neuroscience · doi:10.1038/nrn753 · Cited by 1,860
NMDA receptor subunits: diversity, development and disease
Cull-Candy, S., Brickley, S., & Farrant, M. (2001) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(00)00215-4 · Cited by 1,694
A New ER Trafficking Signal Regulates the Subunit Stoichiometry of Plasma Membrane KATP Channels
Zerangue, N., Schwappach, B., Jan, Y. N., & Jan, L. Y. (1999) · Neuron · doi:10.1016/s0896-6273(00)80708-4 · Cited by 1,025
Hebb and homeostasis in neuronal plasticity
Turrigiano, G. G., & Nelson, S. B. (2000) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(00)00091-x · Cited by 693
A Trafficking Checkpoint Controls GABAB Receptor Heterodimerization
Margeta, M., Jan, Y. N., & Jan, L. Y. (2000) · Neuron · doi:10.1016/s0896-6273(00)00012-x · Cited by 680
Long-Term Depression in Hippocampus
Bear, M. F., & Abraham, W. C. (1996) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.19.030196.002253 · Cited by 616
Hirschberg, K., Miller, C. M., Ellenberg, J., Presley, J. F., Siggia, E. D., Phair, R. D., & Lippincott‐Schwartz, J. (1998) · The Journal of Cell Biology · doi:10.1083/jcb.143.6.1485 · Cited by 610
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Mayer, M. L. (2005) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2005.05.004 · Cited by 3,655
Glutamate Receptor Ion Channels: Structure, Regulation, and Function
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
NMDA receptor trafficking in synaptic plasticity and neuropsychiatric disorders
Lau, C. G., & Zukin, R. S. (2007) · Nature Reviews Neuroscience · doi:10.1038/nrn2153 · Cited by 1,159
Structure, Function, and Pharmacology of Glutamate Receptor Ion Channels
Hansen, K. B., Wollmuth, L. P., Bowie, D., Furukawa, H., Menniti, F. S., Sobolevsky, A. I., Swanson, G. T., Swanger, S. A., Greger, I. H., Nakagawa, T., et al. (2021) · Pharmacological Reviews · doi:10.1124/pharmrev.120.000131 · Cited by 686
Structure, function, and allosteric modulation of NMDA receptors
Hansen, K. B., Yi, F., Perszyk, R. E., Furukawa, H., Wollmuth, L. P., Gibb, A. J., & Traynelis, S. F. (2018) · The Journal of General Physiology · doi:10.1085/jgp.201812032 · Cited by 612
Gao, R., & Penzes, P. (2015) · Current Molecular Medicine · doi:10.2174/1566524015666150303003028 · Cited by 516
“NMDAR phosphorylation by PKA, in turn, can affect the receptor’s release from the endoplasmic reticulum onto the surface [316].”
BackgroundN-Methyl-d-aspartate (NMDA) receptor function and excitotoxicity in Huntington's disease
FAN, M., & Raymond, L. A. (2006) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2006.11.003 · Cited by 410
Regulation of NMDA receptors by phosphorylation
Chen, B.-S., & Roche, K. W. (2007) · Neuropharmacology · doi:10.1016/j.neuropharm.2007.05.018 · Cited by 386
Homeostatic 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
Self-citationThe COPI system: Molecular mechanisms and function
Beck, R., Ravet, M., Wieland, F., & Cassel, D. (2009) · FEBS Letters · doi:10.1016/j.febslet.2009.07.032 · Cited by 305
The NMDA receptor as a target for cognitive enhancement
Collingridge, G. L., Volianskis, A., Bannister, N. J., France, G., Hanna, L., Mercier, M., Tidball, P., Fang, G., Irvine, M. W., Costa, B. M., et al. (2012) · Neuropharmacology · doi:10.1016/j.neuropharm.2012.06.051 · Cited by 255
NMDA hypofunction as a convergence point for progression and symptoms of schizophrenia
Snyder, M. A., & Gao, W. (2013) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2013.00031 · Cited by 254
Michelsen, K., Yuan, H., & Schwappach, B. (2005) · The EMBO Reports · doi:10.1038/sj.embor.7400480 · Cited by 235
Dual Palmitoylation of NR2 Subunits Regulates NMDA Receptor Trafficking
Hayashi, T., Thomas, G. M., & Huganir, R. L. (2009) · Neuron · doi:10.1016/j.neuron.2009.08.017 · Cited by 220
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Lee, H. (2006) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2006.06.003 · Cited by 222
Naylor, D. E., Liu, H., Niquet, J., & Wasterlain, C. G. (2013) · Neurobiology of Disease · doi:10.1016/j.nbd.2012.12.015 · Cited by 220
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Hansen, K. B., Yi, F., Perszyk, R. E., Menniti, F. S., & Traynelis, S. F. (2017) · Methods in molecular biology · doi:10.1007/978-1-4939-7321-7_1 · Cited by 216
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Gladding, C. M., & Raymond, L. A. (2011) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2011.05.001 · Cited by 214
Srinivasan, R., Pantoja, R., Moss, F. J., Mackey, E. D. W., Son, C. D., Miwa, J., & Lester, H. A. (2011) · Journal of General Physiology · doi:10.1085/jgp.201010532 · Cited by 169
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Harris, G. C., Wimmer, M. E., Byrne, R., & Aston‐Jones, G. (2004) · Neuroscience · doi:10.1016/j.neuroscience.2004.09.018 · Cited by 145
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Ramírez, O. A., & Couve, A. (2011) · Trends in Cell Biology · doi:10.1016/j.tcb.2010.12.003 · Cited by 149
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Newpher, T. M., & Ehlers, M. D. (2009) · Trends in Cell Biology · doi:10.1016/j.tcb.2009.02.004 · Cited by 140
Self-citationBrenner, G. J., Ji, R., Shaffer, S., & Woolf, C. J. (2004) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2004.03506.x · Cited by 132
Besshoh, S., Bawa, D., Teves, L. M., Wallace, M. C., & Gurd, J. W. (2005) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2004.03009.x · Cited by 128
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Yang, Z.-J., Torbey, M., Li, X., Bernardy, J., Golden, W. C., Martin, L. J., & Koehler, R. C. (2007) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/sj.jcbfm.9600440 · Cited by 127
Endocytosis and Degradative Sorting of NMDA Receptors by Conserved Membrane-Proximal Signals
Scott, D. B., Michailidis, I. E., Mu, Y., Logothetis, D. E., & Ehlers, M. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.0780-04.2004 · Cited by 130
Self-citationSNAP-25 is a target of protein kinase C phosphorylation critical to NMDA receptor trafficking
Lau, C. G., Takayasu, Y., Rodenas-Ruano, A., Paternain, A. V., Lerma, J., Bennett, M. V. L., & Zukin, R. S. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.4933-08.2010 · Cited by 120
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Hughes, H., & Stephens, D. J. (2007) · Histochemistry and Cell Biology · doi:10.1007/s00418-007-0363-x · Cited by 121
Murphy, J. A., Stein, I. S., Lau, C. G., Peixoto, R. T., Aman, T. K., Kaneko, N., Aromolaran, K. A., Saulnier, J. L., Popescu, G., Sabatini, B. L., et al. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.4538-13.2014 · Cited by 118
Basselin, M., Chang, L., Bell, J. M., & Rapoport, S. I. (2005) · Neuropsychopharmacology · doi:10.1038/sj.npp.1300920 · Cited by 114
Pérez‐Otaño, I., & Ehlers, M. (2004) · Neurosignals · doi:10.1159/000077524 · Cited by 118
Self-citationPostmortem Brain: An Underutilized Substrate for Studying Severe Mental Illness
McCullumsmith, R. E., Hammond, J. H., Shan, D., & Meador‐Woodruff, J. H. (2013) · Neuropsychopharmacology · doi:10.1038/npp.2013.239 · Cited by 115
Rondón, L. J., Privat, A. M., Daulhac, L., Davin, N., Mazur, A., Fialip, J., Eschalier, A., & Courteix, C. (2010) · The Journal of Physiology · doi:10.1113/jphysiol.2010.197004 · Cited by 107
Palmer, K. J., Konkel, J. E., & Stephens, D. J. (2005) · Journal of Cell Science · doi:10.1242/jcs.02496 · Cited by 99
Mouri, A., Noda, Y., Noda, A., Nakamura, T., Tokura, T., Yura, Y., Nitta, A., Furukawa, H., & Nabeshima, T. (2007) · Molecular Pharmacology · doi:10.1124/mol.106.032961 · Cited by 96
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Hallaq, H., Yang, Z., VISWANATHAN, P., Fukuda, K., SHEN, W., WANG, D., Wells, K. S., ZHOU, J., YI, J., & Murray, K. J. (2006) · Cardiovascular Research · doi:10.1016/j.cardiores.2006.08.007 · Cited by 95
Tang, B., Ji, Y.-P., & Traub, R. (2008) · Pain · doi:10.1016/j.pain.2007.10.017 · Cited by 90
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Kjærgaard, M., & Kragelund, B. B. (2017) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-017-2562-5 · Cited by 93
Coultrap, S. J., Nixon, K. M., Alvestad, R. M., Valenzuela, C. F., & Browning, M. D. (2005) · Molecular Brain Research · doi:10.1016/j.molbrainres.2004.12.005 · Cited by 86
Katano, T., Furue, H., Okuda‐Ashitaka, E., Tagaya, M., Watanabe, M., Yoshimura, M., & Ito, S. (2008) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2008.06293.x · Cited by 85
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Horak, M., & Wenthold, R. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m807050200 · Cited by 83
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Suvarna, N. U., Borgland, S. L., Wang, J., Phamluong, K., Auberson, Y. P., Bonci, A., & Dorit Ron, A. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m504120200 · Cited by 83
Li, Q., Yue, N., Liu, S., Wang, Z., Mi, W., Jiang, J., Wu, G.-C., Yu, J. M., & Wang, Y.-Q. (2014) · Evidence-based Complementary and Alternative Medicine · doi:10.1155/2014/158987 · Cited by 79
Shikano, S., Coblitz, B., Wu, M., & Li, M. (2006) · Trends in Cell Biology · doi:10.1016/j.tcb.2006.05.006 · Cited by 79
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Smith, A. J., Daut, J., & Schwappach, B. (2011) · Physiology · doi:10.1152/physiol.00042.2010 · Cited by 75
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Jouvenceau, A., Hédou, G., Potier, B., Kollen, M., Dutar, P., & Mansuy, I. (2006) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2006.04938.x · Cited by 79
Tillo, S., Xiong, W.-H., Takahashi, M., Miao, S., Andrade, A. L., Fortin, D. A., Yang, G., Qin, M., Smoody, B. F., Stork, P. A., et al. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.03.070 · Cited by 72
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Yang, Z.-J., Carter, E. L., Torbey, M., Martin, L. J., & Koehler, R. C. (2009) · Experimental Neurology · doi:10.1016/j.expneurol.2009.10.019 · Cited by 63
Yoo, D. S., Fang, L., Mason, A., Kim, B. Y., & Welling, P. A. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m504836200 · Cited by 59
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Li, Y., Liu, G., Hu, J., Gao, W., & Huang, Y. (2010) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2010.06720.x · Cited by 59
Sarantis, K., Matsokis, N. A., & Angelatou, F. (2009) · Neuroscience · doi:10.1016/j.neuroscience.2009.07.056 · Cited by 58
Caudle, R. M., Perez, F. M., Valle-Pinero, A. Y. D., & Iadarola, M. J. (2005) · Molecular Pain · doi:10.1186/1744-8069-1-25 · Cited by 54
Jeffrey, R., Ch’ng, T. H., O’Dell, T. J., & Martin, K. C. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.3314-09.2009 · Cited by 53
O'Connell, A. D., Leng, Q., Dong, K., MacGregor, G. G., Giebisch, G., & Hébert, S. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0504332102 · Cited by 53
Lontay, B., Kiss, A., Virág, L., & Tar, K. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21124282 · Cited by 55
Stepanchick, A. N., McKenna, J., McGovern, O. L., Huang, Y. S., & Breitwieser, G. E. (2010) · Cellular Physiology and Biochemistry · doi:10.1159/000320560 · Cited by 52
Tian, S.-L., Wang, X., & Ding, G. (2008) · Life Sciences · doi:10.1016/j.lfs.2008.06.027 · Cited by 51
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Wang, Y., Rao, W., Zhang, C., Zhang, C., Liu, M.-D., Han, F., Yao, L.-B., Han, H., Luo, P., Su, N., et al. (2015) · Cell Death and Disease · doi:10.1038/cddis.2015.216 · Cited by 49
Nasu‐Nishimura, Y., Jaffe, H., Isaac, J. T. R., & Roche, K. W. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.081141 · Cited by 50
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Will, R. G., Hull, E. M., & Dominguez, J. M. (2014) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2014.02.005 · Cited by 50
Chatelain, F. C., Bichet, D., Feliciangeli, S. F., Larroque, M. M., Braud, V. M., Douguet, D., & Lesage, F. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.503318 · Cited by 49
Magnesium enhances opioid-induced analgesia – What we have learnt in the past decades?
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Niimura, M., Moussa, R. A.-G., Bissoon, N., Ikeda-Douglas, C. J., Milgram, N. W., & Gurd, J. W. (2005) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2005.02977.x · Cited by 49
Li, B., Devidze, N., Barengolts, D., Prostak, N., Sphicas, E., Apicella, A. J., Malinow, R., & Emamian, E. S. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.2109-09.2009 · Cited by 48
Xu, H., Bae, M. H., Tovar‐y‐Romo, L. B., Patel, N. P., Bandaru, V. V. R., Pomerantz, D. J., Steiner, J. P., & Haughey, N. J. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.4072-11.2011 · Cited by 51
Garraway, S. M., Xu, Q., & Inturrisi, C. E. (2009) · Journal of Pain · doi:10.1016/j.jpain.2008.09.013 · Cited by 47
Sarantis, K., Antoniou, K., Matsokis, N. A., & Angelatou, F. (2011) · Neurochemistry International · doi:10.1016/j.neuint.2011.10.018 · Cited by 46
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Zhang, L., Foster, K., Li, Q., & Martens, J. R. (2007) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00480.2006 · Cited by 46
Clapp, P., Gibson, E. S., Dell’Acqua, M. L., & Hoffman, P. L. (2009) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.109.158741 · Cited by 45
Okamoto, Y., & Shikano, S. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.199695 · Cited by 43
King, J. E., Eugenin, E. A., Hazleton, J. E., Morgello, S., & Berman, J. W. (2010) · American Journal Of Pathology · doi:10.2353/ajpath.2010.090642 · Cited by 43
Liu, C., Li, Q., Su, Y., & Bao, L. (2009) · Traffic · doi:10.1111/j.1600-0854.2009.01027.x · Cited by 42
Li, D., Zhu, L.-H., Pachuau, J., Lee, H., & Pan, H. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.4295-13.2014 · Cited by 42
MLC1 trafficking and membrane expression in astrocytes: Role of caveolin-1 and phosphorylation
Lanciotti, A., Brignone, M. S., Camerini, S., Serafini, B., Macchia, G., Raggi, C., Molinari, P., Crescenzi, M., Musumeci, M., Sargiacomo, M., et al. (2009) · Neurobiology of Disease · doi:10.1016/j.nbd.2009.11.008 · Cited by 41
Marchetti, C., Tafi, E., Middei, S., Rubinacci, M. A., Restivo, L., Ammassari‐Teule, M., & Marie, H. (2009) · Biological Psychiatry · doi:10.1016/j.biopsych.2009.09.017 · Cited by 42
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Petralia, R. S., Wenthold, R. J., & Al‐Hallaq, R. A. (2008) · Frontiers in neuroscience · doi:10.1201/9781420044157.ch8 · Cited by 45
Choi, S., Moon, J.-Y., Roh, D., Yoon, S. Y., Kwon, S. G., Choi, H., Kang, S.-Y., Han, H., Beitz, A. J., & Lee, J. (2016) · Journal of Pain · doi:10.1016/j.jpain.2016.12.002 · Cited by 40
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Bejarano, E., Cabrera, M., Vega, L., Hidalgo, J., & Velasco, A. (2006) · Journal of Cell Science · doi:10.1242/jcs.03146 · Cited by 40
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Cao, J., Yang, X. Z., Liu, Y., Suo, Z., Shi, L., Zheng, C., Yang, H., Li, S., & Hu, X. (2011) · Neuropharmacology · doi:10.1016/j.neuropharm.2011.01.034 · Cited by 39
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Vingtdeux, V., Chang, E. H., Frattini, S. A., Zhao, H., Chandakkar, P., Adrien, L. R., Strohl, J. J., Gibson, E. L., Ohmoto, M., Matsumoto, I., et al. (2016) · Scientific Reports · doi:10.1038/srep24250 · Cited by 38
The role of cyclin-dependent kinase 5 in neuropathic pain
Gómez, K., Vallecillo, T., Moutal, A., Perez‐Miller, S., Delgado‐Lezama, R., Felix, R., & Khanna, R. (2020) · Pain · doi:10.1097/j.pain.0000000000002027 · Cited by 35
Yang, Z.-J., Ni, X., Carter, E. L., Kibler, K. K., Martin, L. J., & Koehler, R. C. (2011) · Neurobiology of Disease · doi:10.1016/j.nbd.2011.04.018 · Cited by 37
Dendritic trafficking for neuronal growth and plasticity
Ehlers, M. (2013) · Biochemical Society Transactions · doi:10.1042/bst20130081 · Cited by 37
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Metadata
- Authors
- Scott, D. B., Blanpied, T. A., & Ehlers, M. D.
- Affiliations
- Duke Medical Center (US)
- Duke University (US)
- Corresponding author
- Ehlers, Michael D.
- Venue
- Neuropharmacology
- Publisher
- Elsevier BV
- Published
- 2003-11
- Volume
- 45
- Issue
- 6
- Pages
- 755-767
- ISSN
- 0028-3908 (ISSN-L)
- OpenAlex
- W2052488789
- Cited by
- 186
- References
- 62
- Citations by year
- 2025: 2 · 2024: 3 · 2023: 2 · 2022: 7 · 2021: 5 · 2020: 5 · 2019: 3 · 2018: 7 · 2017: 8 · 2016: 6 · 2015: 6 · 2014: 7 · 2013: 9 · 2012: 6
- FWCI
- 4.04
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Neuropharmacology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institute on Alcohol Abuse and Alcoholism (F31 AA13220, F31AA013220)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Receptor Mechanisms and Signaling
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular transport and secretion
- Keywords
- NMDA receptor, NR1 subunit, endoplasmic reticulum retention, protein kinase A, protein kinase C, phosphorylation, receptor trafficking, ER export, quality control, G protein-coupled receptors, ion channels
- MeSH terms
- Amino Acid Sequence, Animals, Arginine, Cell Membrane, Chlorocebus aethiops, Endoplasmic Reticulum, Humans, Molecular Sequence Data, Neurons, Phosphorylation, Protein Kinase C, Receptors, N-Methyl-D-Aspartate, Cyclic AMP-Dependent Protein Kinases, COS Cells, Amino Acid Motifs, Rats
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