The DOI matches its Crossref record; 125 of the 127 references it cites were found in a registry or an index.
Integration of biochemical signalling in spines
Abstract
Short-term and long-term changes in the strength of synapses in neural networks underlie working memory and long-term memory storage in the brain. These changes are regulated by many biochemical signalling pathways in the postsynaptic spines of excitatory synapses. Recent findings about the roles and regulation of the small GTPases Ras, Rap and Rac in spines provide new insights into the coordination and cooperation of different pathways to effect synaptic plasticity. Here, we present an initial working representation of the interactions of five signalling cascades that are usually studied individually. We discuss their integrated function in the regulation of postsynaptic plasticity.
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“Calcium ions in dendritic spines have an important function in activating signaling cascades that underlie and regulate synaptic plasticity (Kennedy et al., 2005).”
From Barriers in the brain: resolving dendritic spine morphology and compartmentalization (2014) · cites this paper as Kennedy et al., 2005
In the citing paper
“The precise crosstalk and integration is however not completely understood (Kennedy et al., 2005).”
From Barriers in the brain: resolving dendritic spine morphology and compartmentalization (2014) · cites this paper as Kennedy et al., 2005
In the citing paper
“This broad action of SynGAP on dendritic spine signaling arises from its central location in the NMDAR complex (Kennedy et al., 2005) and its endowment with a promiscuous GAP domain that can regulate a variety of small G-proteins (Krapivinsky et al., 2004; Pena et al., 2008).”
From Pathogenic SYNGAP1 Mutations Impair Cognitive Development by Disrupting Maturation of Dendritic Spine Synapses (2012) · cites this paper as Kennedy et al., 2005
Citations
Cites
Alzheimer's Disease Is a Synaptic Failure
Selkoe, D. J. (2002) · Science · doi:10.1126/science.1074069 · Cited by 4,420
Cellular survival: a play in three Akts
Datta, S. R., Brunet, A., & Greenberg, M. E. (1999) · Genes & Development · doi:10.1101/gad.13.22.2905 · Cited by 4,216
Regulation of Synaptic Efficacy by Coincidence of Postsynaptic APs and EPSPs
Markram, H., Lübke, J., Frotscher, M., & Sakmann, B. (1997) · Science · doi:10.1126/science.275.5297.213 · Cited by 3,832
Kyriakis, J. M., & Avruch, J. (2001) · Physiological Reviews · doi:10.1152/physrev.2001.81.2.807 · Cited by 3,400
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
Trk Receptors: Roles in Neuronal Signal Transduction
Huang, E. J., & Reichardt, L. F. (2003) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.72.121801.161629 · Cited by 2,537 · cited 1×
“TrkB is activated in spines and dendrites by brain-derived neurotrophic factor (BDNF) that is released from neighbouring neuron”
BackgroundGlutamate, nitric oxide and cell-cell signalling in the nervous system
Garthwaite, J. (1991) · Trends in Neurosciences · doi:10.1016/0166-2236(91)90022-m · Cited by 2,401
Signaling Through Scaffold, Anchoring, and Adaptor Proteins
Pawson, T., & Scott, J. D. (1997) · Science · doi:10.1126/science.278.5346.2075 · Cited by 2,256
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
Neurotrophins as synaptic modulators
Poo, M.-M. (2001) · Nature Reviews Neuroscience · doi:10.1038/35049004 · Cited by 1,775
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- Klee, C. B. in Calmodulin Vol. 5 (eds Cohen, P. & Klee, C. B.) 35–56 (Elsevier, Amsterdam, 1988).
- Stiles, J. R., Bartol, T. M., Salpeter, M. M., Salpeter, E. & Sejnowski, T. J. in Synapses (eds Cowan, W. M., Stevens, C. F. & Sudhof, T. C.) 681–731 (Johns Hopkins Univ. Press, Baltimore, USA, 2001).
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Sorted by citations
Items 101–200 of 286
Antunes, G., & Schutter, E. D. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.5976-11.2012 · Cited by 64
de Ven, T. V., VanDongen, H. M. A., & VanDongen, A. M. J. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.2450-05.2005 · Cited by 66
Borroto‐Escuela, D. O., Hinz, S., Navarro, G., Franco, R., Müller, C. E., & Fuxé, K. (2018) · Frontiers in Neuroscience · doi:10.3389/fnins.2018.00043 · Cited by 69
Intrinsic and extrinsic determinants of ion channel localization in neurons
Hedstrom, K. L., & Rasband, M. (2006) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2006.04001.x · Cited by 67
The microtubule cytoskeleton at the synapse
Parato, J., & Bartolini, F. (2021) · Neuroscience Letters · doi:10.1016/j.neulet.2021.135850 · Cited by 67
Zeng, Y.-Q., Zhang, J., Zhu, Y.-G., Zhang, J., Shen, H., Lu, J.-P., Pan, X.-D., Lin, N., Dai, X.-M., Zhou, M., et al. (2015) · Journal of Neurochemistry · doi:10.1111/jnc.13056 · Cited by 55
Barriers in the brain: resolving dendritic spine morphology and compartmentalization
Adrian, M., Kusters, R., Wierenga, C. J., Storm, C., Hoogenraad, C. C., & Kapitein, L. C. (2014) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2014.00142 · Cited by 62
“Calcium ions in dendritic spines have an important function in activating signaling cascades that underlie and regulate synaptic plasticity (Kennedy et al., 2005).”
Nakazawa, T., Kuriu, T., Tezuka, T., Umemori, H., Okabe, S., & Yamamoto, T. (2008) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2008.05335.x · Cited by 63
Opioid-induced structural and functional plasticity of medium-spiny neurons in the nucleus accumbens
Thompson, B. L., Oscar‐Berman, M., & Kaplan, G. B. (2020) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2020.10.015 · Cited by 64
Nicholson, D. A., & Geinisman, Y. (2008) · The Journal of Comparative Neurology · doi:10.1002/cne.21896 · Cited by 57
Dong, H., Murphy, K. M., Meng, L., Montalvo‐Ortiz, J. L., Zeng, Z., Kolber, B. J., Zhang, S., Muglia, L. J., & Csernansky, J. G. (2012) · Journal of Alzheimer s Disease · doi:10.3233/jad-2011-111328 · Cited by 62
Interactions between drebrin and Ras regulate dendritic spine plasticity
Biou, V., Brinkhaus, H., Malenka, R. C., & Matus, A. I. (2008) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2008.06269.x · Cited by 61
Seguella, L., Pesce, M., Capuano, R., Casano, F., Pesce, M., Corpetti, C., Vincenzi, M., Maftei, D., Lattanzi, R., Re, A., et al. (2021) · Journal of Neuroinflammation · doi:10.1186/s12974-021-02164-5 · Cited by 62
Nagura, H., Ishikawa, Y., Kobayashi, K., Takao, K., Tanaka, T., Nishikawa, K., Tamura, H., Shiosaka, S., Suzuki, H., Miyakawa, T., et al. (2012) · Molecular Brain · doi:10.1186/1756-6606-5-43 · Cited by 58
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Ewald, R. C., & Cline, H. T. (2008) · Frontiers in neuroscience · doi:10.1201/9781420044157.ch1 · Cited by 59
Zhong, Y., Zhu, Y., He, T., Li, W., Li, Q., & Miao, Y. (2018) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2018.3933 · Cited by 55
Li, S., Tian, X., Hartley, D. M., & Feig, L. A. (2006) · Current Biology · doi:10.1016/j.cub.2006.10.028 · Cited by 52
Smalla, K., Mikhaylova, M., Sahin, J., Hg, B., Bogerts, B., Schmitt, A., van der Schors, R. C., Smit, A. B., Li, K. W., Gundelfinger, E. D., et al. (2008) · Molecular Psychiatry · doi:10.1038/mp.2008.60 · Cited by 51
Lee, H. W., Choi, J., Shin, H., Kim, K., Yang, J., Na, M., Choi, S. Y., Kang, G. B., Eom, S. H., Kim, H., et al. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.3112-08.2008 · Cited by 55
Inhibition and Termination of Physiological Responses by GTPase Activating Proteins
Ligeti, E., Welti, S., & Scheffzek, K. (2012) · Physiological Reviews · doi:10.1152/physrev.00045.2010 · Cited by 61
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Dougherty, D. A. (2008) · The Journal of Organic Chemistry · doi:10.1021/jo8001722 · Cited by 50
Zou, G.-J., Chen, Z.-R., Wang, X., Cui, Y.-H., Li, F., Li, C.-Q., Wang, L.-F., & Huang, F. (2024) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2024.176759 · Cited by 51
Shank Proteins Differentially Regulate Synaptic Transmission
Shi, R., Redman, P. T., Ghose, D., Hwang, H., Liu, Y., Ren, X., Ding, L. J., Liu, M., Jones, K. J., & Xu, W. (2017) · eNeuro · doi:10.1523/eneuro.0163-15.2017 · Cited by 50
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Intensiometric biosensors visualize the activity of multiple small GTPases in vivo
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Iida, J., Ishizaki, H., Tanaka, M., Kawata, A., Sumita, K., Ohgake, S., Sato, Y., Yorifuji, H., Nukina, N., Ohashi, K., et al. (2007) · Molecular and Cellular Biology · doi:10.1128/mcb.01901-06 · Cited by 48
Korkotian, E., & Segal, M. (2006) · Cell Calcium · doi:10.1016/j.ceca.2006.08.008 · Cited by 43
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Guerrini, I., Thomson, A. D., & Gurling, H. (2006) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2006.06.022 · Cited by 35
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Ding, Z., Wu, P., Luo, Y., Shi, H., Shen, H., Wang, S., & Lü, L. (2013) · Psychopharmacology · doi:10.1007/s00213-013-3050-8 · Cited by 35
Treviño, S., Vázquez‐Roque, R. A., López‐López, G., Perez‐Cruz, C., Morán, C., Handal‐Silva, A., Vergara, E. G., Flores, G., Guevara, J., & Díaz, A. (2017) · Journal of Chemical Neuroanatomy · doi:10.1016/j.jchemneu.2017.02.007 · Cited by 34
Kurisaki, A., Inoue, I., Kurisaki, K., Yamakawa, N., Tsuchida, K., & Sugino, H. (2008) · Neuroscience · doi:10.1016/j.neuroscience.2007.12.012 · Cited by 33
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Baucum, A. J., Jalan‐Sakrikar, N., Jiao, Y., Gustin, R. M., Carmody, L., Tabb, D. L., Ham, A. L., & Colbran, R. J. (2010) · Molecular & Cellular Proteomics · doi:10.1074/mcp.m900387-mcp200 · Cited by 33
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Yasuda, R. (2012) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a005611 · Cited by 33
Mattingly, R. R. (2013) · ISRN Oncology · doi:10.1155/2013/536529 · Cited by 33
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Rathour, R. K., & Narayanan, R. (2012) · Journal of Neurophysiology · doi:10.1152/jn.00846.2011 · Cited by 29
Gao, Q., Yao, W., Wang, J., Yang, T., Liu, C., Tao, Y., Chen, Y., Liu, X., & Ma, L. (2015) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2015.00065 · Cited by 29
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Han, K. A., & Ko, J. (2023) · Experimental & Molecular Medicine · doi:10.1038/s12276-023-01004-1 · Cited by 31
Djagaeva, I., & Doronkin, S. (2009) · PLoS ONE · doi:10.1371/journal.pone.0007598 · Cited by 28
Actin and Diseases of the Nervous System
Bernstein, B. W., Maloney, M. T., & Bamburg, J. R. (2010) · Advances in neurobiology · doi:10.1007/978-1-4419-7368-9_11 · Cited by 31
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Terstege, D. J., & Epp, J. R. (2022) · Biology · doi:10.3390/biology12010034 · Cited by 23
Varshavsky, A. J. (2012) · Protein Science · doi:10.1002/pro.2148 · Cited by 25
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Walkup, W. G., Sweredoski, M. J., Graham, R. L., Hess, S. Y., & Kennedy, M. B. (2018) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2018.07.087 · Cited by 22
Self-citationAntunes, G., Roque, A. C., & de Souza, F. M. S. (2016) · Scientific Reports · doi:10.1038/srep23730 · Cited by 22
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Jacobs, S., Wei, W., Wang, D., & Tsien, J. Z. (2015) · Learning & Memory · doi:10.1101/lm.038521.115 · Cited by 22
Ashhad, S., Johnston, D., & Narayanan, R. (2014) · Journal of Neurophysiology · doi:10.1152/jn.00833.2014 · Cited by 23
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He, Z., Song, H., Liu, T., Ma, J., Xing, Z., Yin, Y.-Y., Liu, L., Zhang, Y.-N., Zhao, Y., Yu, H., et al. (2019) · Cerebral Cortex · doi:10.1093/cercor/bhz036 · Cited by 20
de Bartolomeis, A., Avagliano, C., Vellucci, L., D’Ambrosio, L., Manchia, M., D’Urso, G., Buonaguro, E. F., & Iasevoli, F. (2019) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2019.08.019 · Cited by 19
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Self-citationOuyang, Y., Yang, X., Hu, X. Y., Altay, E. E., Zeng, L., Lee, J., & Wong, M. (2007) · Brain Research · doi:10.1016/j.brainres.2007.01.077 · Cited by 21
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Jacobs, S., Cui, Z., Feng, R., Wang, H., Wang, D., & Tsien, J. Z. (2014) · PLoS ONE · doi:10.1371/journal.pone.0111865 · Cited by 20
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Wu, P., Ding, Z., Meng, S., Shen, H., Sun, S.-C., Luo, Y., Liu, J., Lü, L., Zhu, W., & Shi, J. (2014) · Psychopharmacology · doi:10.1007/s00213-014-3462-0 · Cited by 19
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Keifer, J., Zheng, Z., & Zhu, D. (2007) · Journal of Neurophysiology · doi:10.1152/jn.01154.2006 · Cited by 19
Iijima, K., Abe, H., Okazawa, M., Moriyoshi, K., & Nakanishi, S. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0805574105 · Cited by 18
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Michalski, P. J., & Loew, L. M. (2012) · Physical Biology · doi:10.1088/1478-3975/9/3/036010 · Cited by 19
Kähne, T., Richter, S., Kolodziej, A., Smalla, K., Pielot, R., Engler, A., Ohl, F. W., Dieterich, D. C., Seidenbecher, C. I., Tischmeyer, W., et al. (2016) · Journal of Neurochemistry · doi:10.1111/jnc.13636 · Cited by 16
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Bai, Y., Qiu, S., Li, Y., Li, Y., Zhong, W., Shi, M., Zhu, X., Jiang, H., Yu, Y., Cheng, Y., et al. (2018) · IUBMB Life · doi:10.1002/iub.1876 · Cited by 17
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Walkup, W. G., & Kennedy, M. B. (2014) · Protein Expression and Purification · doi:10.1016/j.pep.2014.02.015 · Cited by 13
Self-citationThe ROR2 tyrosine kinase receptor regulates dendritic spine morphogenesis in hippocampal neurons
Alfaro, I. E., Varela‐Nallar, L., Varas‐Godoy, M., & Inestrosa, N. C. (2015) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2015.05.002 · Cited by 15
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Chang, D., Hammer, C., Holweg, C. T. J., Selvaraj, S. K., Rathore, N., McCarthy, M. I., Yaspan, B. L., & Choy, D. F. (2022) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2022.10.019 · Cited by 13
Johnson, T., Bartol, T., B, T. J. S. A., & Mjolsness, E. (2015) · Physical Biology · doi:10.1088/1478-3975/12/4/045005 · Cited by 13
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Metadata
- Authors
- Kennedy, M. B., Beale, H. C., Carlisle, H. J., & Washburn, L. R.
- Affiliations
- California Institute of Technology (US)
- Corresponding author
- Kennedy, Mary B.
- Venue
- Nature Reviews Neuroscience
- Published
- 2005-06-01
- Volume
- 6
- Issue
- 6
- Pages
- 423-434
- ISSN
- 1471-003X (ISSN-L)
- 1471-0048
- OpenAlex
- W2005797241
- Cited by
- 286
- References
- 127
- Citations by year
- 2025: 3 · 2024: 7 · 2023: 4 · 2022: 5 · 2021: 7 · 2020: 9 · 2019: 11 · 2018: 12 · 2017: 6 · 2016: 10 · 2015: 10 · 2014: 14 · 2013: 14 · 2012: 38
- FWCI
- 2.35
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Nature reviews. Neuroscience (publishedVersion)
- PubMed (publishedVersion)
- CaltechAUTHORS (California Institute of Technology) (submittedVersion)
- Funders
- John Douglas French Alzheimer's Foundation
- National Institutes of Health
- National Institute on Drug Abuse (R01DA030749)
- National Institute of Neurological Disorders and Stroke (P01NS044306)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Kinase Regulation and GTPase Signaling
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Keywords
- postsynaptic spines, synaptic plasticity, Ras, rap, Rac, small GTPases, excitatory synapses, working memory, long-term memory, signaling pathways
- MeSH terms
- Animals, Humans, Neuronal Plasticity, Synapses, Signal Transduction, Calcium Signaling, Dendritic Spines
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