The DOI matches its Crossref record; 24 of the 24 references it cites were found in a registry or an index.
Opposite effects of fear conditioning and extinction on dendritic spine remodelling.
Abstract
It is generally believed that fear extinction is a form of new learning that inhibits rather than erases previously acquired fear memories. Although this view has gained much support from behavioural and electrophysiological studies, the hypothesis that extinction causes the partial erasure of fear memories remains viable. Using transcranial two-photon microscopy, we investigated how neural circuits are modified by fear learning and extinction by examining the formation and elimination of postsynaptic dendritic spines of layer-V pyramidal neurons in the mouse frontal association cortex. Here we show that fear conditioning by pairing an auditory cue with a footshock increases the rate of spine elimination. By contrast, fear extinction by repeated presentation of the same auditory cue without a footshock increases the rate of spine formation. The degrees of spine remodelling induced by fear conditioning and extinction strongly correlate with the expression and extinction of conditioned fear responses, respectively. Notably, spine elimination and formation induced by fear conditioning and extinction occur on the same dendritic branches in a cue- and location-specific manner: cue-specific extinction causes formation of dendritic spines within a distance of two micrometres from spines that were eliminated after fear conditioning. Furthermore, reconditioning preferentially induces elimination of dendritic spines that were formed after extinction. Thus, within vastly complex neuronal networks, fear conditioning, extinction and reconditioning lead to opposing changes at the level of individual synapses. These findings also suggest that fear memory traces are partially erased after extinction.
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
“For example, a fear conditioning paradigm that pairs auditory cues with foot shocks has demonstrated opposite effects in auditory and frontal cortex.”
From Spatiotemporal dynamics of dendritic spines in the living brain (2014) · cites this paper as Lai et al., 2012
In the citing paper
“Similar spatial selectivity of spine dynamics has been observed in the fear conditioning paradigm: a spine eliminated during fear conditioning is usually replaced by a spine in its vicinity (within 2 μm) during fear extinction (Lai et al., 2012).”
From Spatiotemporal dynamics of dendritic spines in the living brain (2014) · cites this paper as Lai et al., 2012
Citations
Cites
Two-photon laser scanning fluorescence microscopy
Denk, W., Strickler, J. H., & Webb, W. W. (1990) · Science · doi:10.1126/science.2321027 · Cited by 9,488
LeDoux, J. E. (2000) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.23.1.155 · Cited by 8,444
Neurons in medial prefrontal cortex signal memory for fear extinction
Milad, M. R., & Quirk, G. J. (2002) · Nature · doi:10.1038/nature01138 · Cited by 1,836
Context and Behavioral Processes in Extinction: Table 1.
Bouton, M. E. (2004) · Learning & Memory · doi:10.1101/lm.78804 · Cited by 1,808
Neural Mechanisms of Extinction Learning and Retrieval
Quirk, G. J., & Mueller, D. (2008) · Neuropsychopharmacology · doi:10.1038/sj.npp.1301555 · Cited by 1,645
Myers, K. M., & Davis, M. (2007) · Molecular Psychiatry · doi:10.1038/sj.mp.4001939 · Cited by 1,277
Long-term dendritic spine stability in the adult cortex
Grutzendler, J., Kasthuri, N., & Gan, W.-B. (2002) · Nature · doi:10.1038/nature01276 · Cited by 1,198
Self-citationStably maintained dendritic spines are associated with lifelong memories
Yang, G., Pan, F., & Gan, W.-B. (2009) · Nature · doi:10.1038/nature08577 · Cited by 1,182
Self-citationSwitching on and off fear by distinct neuronal circuits
Herry, C., Ciocchi, S., Senn, V., Demmou, L., Müller, C., & Lüthi, A. (2008) · Nature · doi:10.1038/nature07166 · Cited by 950
Evidence for a Role of Dendritic Filopodia in Synaptogenesis and Spine Formation
Ziv, N. E., & Smith, S. J. (1996) · Neuron · doi:10.1016/s0896-6273(00)80283-4 · Cited by 882
Cited by
Sorted by citations
Microglia promote learning-dependent synapse formation through brain-derived neurotrophic factor
Parkhurst, C. N., Yang, G., Ninan, I., Savas, J. N., Yates, J. R., Lafaille, J. J., Hempstead, B. L., Littman, D. R., & Gan, W.-B. (2013) · Cell · doi:10.1016/j.cell.2013.11.030 · Cited by 2,599
Self-citationBalancing Plasticity/Stability Across Brain Development
Takesian, A. E., & Hensch, T. K. (2013) · Progress in Brain Research · doi:10.1016/b978-0-444-63327-9.00001-1 · Cited by 667
Memory Engram Cells Have Come of Age
Tonegawa, S., Liu, X., Ramirez, S., & Redondo, R. L. (2015) · Neuron · doi:10.1016/j.neuron.2015.08.002 · Cited by 661
Structural plasticity upon learning: regulation and functions
Caroni, P., Donato, F., & Muller, D. (2012) · Nature Reviews Neuroscience · doi:10.1038/nrn3258 · Cited by 491
Dendritic Spines: The Locus of Structural and Functional Plasticity
Sala, C., & Segal, M. (2014) · Physiological Reviews · doi:10.1152/physrev.00012.2013 · Cited by 491
The microbiota regulate neuronal function and fear extinction learning
Chu, C., Murdock, M. H., Jing, D., Won, T. H., Chung, H., Kressel, A. M., Tsaava, T., Addorisio, M. E., Putzel, G. G., Zhou, L., et al. (2019) · Nature · doi:10.1038/s41586-019-1644-y · Cited by 421
Altered fear learning across development in both mouse and human
Pattwell, S. S., Duhoux, S., Hartley, C. A., Johnson, D. C., Jing, D., Elliott, M. D., Ruberry, E. J., Powers, A., Mehta, N., Yang, R. R., et al. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1206834109 · Cited by 404
Structural Components of Synaptic Plasticity and Memory ConsolidationPreprint
Bailey, C. H., Kandel, E. R., & Harris, K. M. (2015) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a021758 · Cited by 419
What is memory? The present state of the engram
Poo, M.-M., Pignatelli, M., Ryan, T. J., Tonegawa, S., Bonhoeffer, T., Martin, K. C., Rudenko, A., Tsai, L., Tsien, R. W., Fishell, G., et al. (2016) · BMC Biology · doi:10.1186/s12915-016-0261-6 · Cited by 409
The Impact of Studying Brain Plasticity
Mateos‐Aparicio, P., & Moreno, A. R. (2019) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2019.00066 · Cited by 465
Nogo limits neural plasticity and recovery from injury
Schwab, M. E., & Strittmatter, S. M. (2014) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2014.02.011 · Cited by 379
Is plasticity of synapses the mechanism of long-term memory storage?
Abraham, W. C., Jones, O. D., & Glanzman, D. L. (2019) · npj Science of Learning · doi:10.1038/s41539-019-0048-y · Cited by 398
Epigenetic Priming of Memory Updating during Reconsolidation to Attenuate Remote Fear Memories
Gräff, J., Joseph, N. F., Horn, M. E., Samiei, A., Meng, J., Seo, J., Rei, D., Bero, A. W., Phan, T. X., Wagner, F., et al. (2014) · Cell · doi:10.1016/j.cell.2013.12.020 · Cited by 357
Circadian glucocorticoid oscillations promote learning-dependent synapse formation and maintenance.
Liston, C., Cichon, J. M., Jeanneteau, F., Jia, Z., Chao, M. V., & Gan, W.-B. (2013) · Nature Neuroscience · doi:10.1038/nn.3387 · Cited by 358
Self-citationImmediate Early Genes, Memory and Psychiatric Disorders: Focus on c-Fos, Egr1 and Arc
Gallo, F. T., Katche, C., Morici, J. F., Medina, J. H., & Weisstaub, N. (2018) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2018.00079 · Cited by 363
Synaptic plasticity in depression: Molecular, cellular and functional correlates
Marsden, W. N. (2012) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2012.12.012 · Cited by 323
Tsai, N.-P., Wilkerson, J. R., Guo, W., Maksimova, M. A., DeMartino, G. N., Cowan, C. W., & Huber, K. M. (2012) · Cell · doi:10.1016/j.cell.2012.11.040 · Cited by 316
Synaptic tagging during memory allocation
Rogerson, T., Cai, D. J., Frank, A. C., Sano, Y., Shobe, J. L., López‐Aranda, M. F., & Silva, A. J. (2014) · Nature reviews. Neuroscience · doi:10.1038/nrn3667 · Cited by 317
Dendritic spines: from structure to in vivo function
Rochefort, N. L., & Konnerth, A. (2012) · The EMBO Reports · doi:10.1038/embor.2012.102 · Cited by 299
Blockade of Estrogen by Hormonal Contraceptives Impairs Fear Extinction in Female Rats and Women
Graham, B. M., & Milad, M. R. (2013) · Biological Psychiatry · doi:10.1016/j.biopsych.2012.09.018 · Cited by 281
Exploring the Role of Neuroplasticity in Development, Aging, and Neurodegeneration
Marzola, P., Melzer, T., Pavesi, E., Gil-Mohapel, J., & Brocardo, P. S. (2023) · Brain Sciences · doi:10.3390/brainsci13121610 · Cited by 281
Secondary Motor Cortex: Where ‘Sensory’ Meets ‘Motor’ in the Rodent Frontal Cortex
Barthas, F., & Kwan, A. C. (2016) · Trends in Neurosciences · doi:10.1016/j.tins.2016.11.006 · Cited by 277
Rescue of fragile X syndrome phenotypes in Fmr1 KO mice by the small-molecule PAK inhibitor FRAX486
Dolan, B. M., Duron, S. G., Campbell, D. A., Vollrath, B., Rao, B. S. S., Ko, H.-Y., Lin, G. G., Govindarajan, A., Choi, S.-Y., & Tonegawa, S. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1219383110 · Cited by 260
Dendritic spines: Revisiting the physiological role
Chidambaram, S. B., Rathipriya, A. G., Bolla, S. R., Bhat, A., Ray, B., Mahalakshmi, A. M., Manivasagam, T., Thenmozhi, A. J., Essa, M. M., Guillemin, G. J., et al. (2019) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2019.01.005 · Cited by 266
The Corticohippocampal Circuit, Synaptic Plasticity, and MemoryPreprint
Basu, J., & Siegelbaum, S. A. (2015) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a021733 · Cited by 269
Functional and structural underpinnings of neuronal assembly formation in learning
Holtmaat, A., & Caroni, P. (2016) · Nature Neuroscience · doi:10.1038/nn.4418 · Cited by 239
Dendritic Spine Plasticity: Function and Mechanisms
Runge, K., Cardoso, C., & de Chevigny, A. (2020) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2020.00036 · Cited by 248
Circuit Mechanisms of Sensorimotor Learning
Makino, H., Hwang, E. J., Hedrick, N. G., & Komiyama, T. (2016) · Neuron · doi:10.1016/j.neuron.2016.10.029 · Cited by 228
“The reduction in population responses may be a common feature of learning-driven changes in population coding (see also the motor skill learning section below), which could reduce overlaps between representations in space and time and facilitate decoding by downstream areas (Laurent, 2002).”
Schmid, L., Mittag, M., Poll, S., Steffen, J., Wagner, J., Geis, H., Schwarz, I., Schmidt, B., Schwarz, M. K., Remy, S., et al. (2016) · Neuron · doi:10.1016/j.neuron.2016.08.034 · Cited by 219
Morris, G. P., Clark, I. A., Zinn, R., & Vissel, B. (2013) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2013.07.002 · Cited by 236
Biochemical Computation for Spine Structural Plasticity
Nishiyama, J., & Yasuda, R. (2015) · Neuron · doi:10.1016/j.neuron.2015.05.043 · Cited by 199
Selective synaptic remodeling of amygdalocortical connections associated with fear memory
Yang, Y., Liu, D., Huang, W., Deng, J., Sun, Y.-G., Zuo, Y., & Poo, M. (2016) · Nature Neuroscience · doi:10.1038/nn.4370 · Cited by 191
GABA promotes the competitive selection of dendritic spines by controlling local Ca2+ signaling
Hayama, T., Noguchi, J., Watanabe, S., Takahashi, N., Hayashi-Takagi, A., Ellis-Davies, G. C. R., Matsuzaki, M., & Kasai, H. (2013) · Nature Neuroscience · doi:10.1038/nn.3496 · Cited by 193
Fear Extinction Causes Target-Specific Remodeling of Perisomatic Inhibitory Synapses
Trouche, S. G., Sasaki, J. M., Tu, T., & Reijmers, L. G. J. E. (2013) · Neuron · doi:10.1016/j.neuron.2013.07.047 · Cited by 192
Hotspots of dendritic spine turnover facilitate clustered spine addition and learning and memory
Frank, A. C., Huang, S., Zhou, M., Gdalyahu, A., Kastellakis, G., Silva, T. K., Lu, E. D., Wen, X., Poirazi, P., Trachtenberg, J. T., et al. (2018) · Nature Communications · doi:10.1038/s41467-017-02751-2 · Cited by 187
Depletion of Perineuronal Nets in the Amygdala to Enhance the Erasure of Drug Memories
Xue, Y.-X., Xue, L.-F., Liu, J.-F., He, J., Deng, J.-H., Sun, S.-C., Han, H.-B., Luo, Y.-X., Xu, L.-Z., Wu, P., et al. (2014) · The Journal of Neuroscience · doi:10.1523/jneurosci.5390-13.2014 · Cited by 176
Exercise training improves motor skill learning via selective activation of mTOR
Chen, K., Zheng, Y., Wei, J., Ouyang, H., Huang, X., Zhang, F., Lai, C. S. W., Ren, C., So, K., & Zhang, L. (2019) · Science Advances · doi:10.1126/sciadv.aaw1888 · Cited by 168
Self-citationBian, W.-J., Miao, W., He, S., Qiu, Z., & Yu, X. (2015) · Cell · doi:10.1016/j.cell.2015.07.018 · Cited by 166
AMPA receptors as drug targets in neurological disease—advantages, caveats, and future outlook
Chang, P. K. ‐., Verbich, D., & McKinney, R. A. (2012) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2012.08165.x · Cited by 155
Sex-Specific Neuroanatomical Correlates of Fear Expression in Prefrontal-Amygdala Circuits
Gruene, T. M., Roberts, E., Thomas, V., Ronzio, A., & Shansky, R. M. (2014) · Biological Psychiatry · doi:10.1016/j.biopsych.2014.11.014 · Cited by 169
Inhibitory connectivity defines the realm of excitatory plasticity
Mongillo, G., Rumpel, S., & Loewenstein, Y. (2018) · Nature Neuroscience · doi:10.1038/s41593-018-0226-x · Cited by 148
BDNF signaling during the lifetime of dendritic spines
Zagrebelsky, M., Tacke, C., & Korte, M. (2020) · Cell and Tissue Research · doi:10.1007/s00441-020-03226-5 · Cited by 147
Pathophysiological Bases of Comorbidity: Traumatic Brain Injury and Post-Traumatic Stress Disorder
Kaplan, G. B., Leite‐Morris, K. A., Wang, L., Rumbika, K. K., Heinrichs, S. C., Zeng, X., Wu, L., Arena, D. T., & Teng, Y. D. (2017) · Journal of Neurotrauma · doi:10.1089/neu.2016.4953 · Cited by 148
Long-term depression triggers the selective elimination of weakly integrated synapses
Wiegert, J. S., & Oertner, T. G. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1315926110 · Cited by 139
REM sleep promotes experience-dependent dendritic spine elimination in the mouse cortex
Zhou, Y., Lai, C. S. W., Bai, Y., Li, W., Zhao, R., Yang, G., Frank, M. G., & Gan, W. (2020) · Nature Communications · doi:10.1038/s41467-020-18592-5 · Cited by 139
Self-citationJarome, T. J., & Helmstetter, F. J. (2013) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2013.03.009 · Cited by 140
Keifer Jr, O. P., Hurt, R. C., Gutman, D. A., Keilholz, S. D., Gourley, S. L., & Ressler, K. J. (2015) · Nature Communications · doi:10.1038/ncomms8582 · Cited by 132
Phoumthipphavong, V., Barthas, F., Hassett, S., & Kwan, A. C. (2016) · eneuro · doi:10.1523/eneuro.0133-15.2016 · Cited by 132
CX3CR1+ monocytes modulate learning and learning-dependent dendritic spine remodeling via TNF-α
Garré, J. M., Silva, H. M., Lafaille, J. J., & Yang, G. (2017) · Nature Medicine · doi:10.1038/nm.4340 · Cited by 132
An Unconditioned Stimulus Retrieval Extinction Procedure to Prevent the Return of Fear Memory
Liu, J., Zhao, L., Xue, Y.-X., Shi, J., Suo, L., Luo, Y., Chai, B.-S., Yang, C., Fang, Q., Zhang, Y., et al. (2014) · Biological Psychiatry · doi:10.1016/j.biopsych.2014.03.027 · Cited by 137
Synaptic retinoic acid signaling and homeostatic synaptic plasticity
Chen, L., Lau, A. G., & Sarti, F. (2012) · Neuropharmacology · doi:10.1016/j.neuropharm.2012.12.004 · Cited by 134
Dynamics of dendritic spines in the mouse auditory cortex during memory formation and memory recall.
Moczulska, K. E., Tinter-Thiede, J., Peter, M., Ushakova, L., Wernle, T., Bathellier, B., & Rumpel, S. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1312508110 · Cited by 127
Dendritic spines: Morphological building blocks of memory
Segal, M. (2016) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2016.06.007 · Cited by 131
Maiti, P., Manna, J., Ilavazhagan, G., Rossignol, J., & Dunbar, G. L. (2015) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2015.09.020 · Cited by 128
Activity-regulated trafficking of the palmitoyl-acyl transferase DHHC5
Brigidi, G. S., Santyr, B. G., Shimell, J. J., Jovellar, D. B., & Bamji, S. X. (2015) · Nature Communications · doi:10.1038/ncomms9200 · Cited by 125
Lattal, K. M., & Wood, M. A. (2013) · Nature Neuroscience · doi:10.1038/nn.3302 · Cited by 121
The Pattern of Cortical Dysfunction in a Mouse Model of a Schizophrenia-Related Microdeletion
Fénelon, K., Xu, B., Lai, C. S., Mukai, J., Markx, S., Stark, K. L., Hsu, P.-K., Gan, W.-B., Fischbach, G. D., MacDermott, A. B., et al. (2013) · The Journal of Neuroscience · doi:10.1523/jneurosci.1611-13.2013 · Cited by 116
Self-citationPsychological and neural mechanisms of experimental extinction: A selective review
Delamater, A. R., & Westbrook, R. F. (2013) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2013.09.016 · Cited by 120
Intrinsic volatility of synaptic connections — a challenge to the synaptic trace theory of memory
Mongillo, G., Rumpel, S., & Loewenstein, Y. (2017) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2017.06.006 · Cited by 119
Location-dependent synaptic plasticity rules by dendritic spine cooperativity
Weber, J. P., Andrásfalvy, B. K., Polito, M., Magó, Á., Ujfalussy, B. B., & Makara, J. K. (2016) · Nature Communications · doi:10.1038/ncomms11380 · Cited by 114
Anatomical Plasticity of Adult Brain Is Titrated by Nogo Receptor 1
Akbik, F. V., Bhagat, S. M., Patel, P. R., Cafferty, W. B. J., & Strittmatter, S. M. (2013) · Neuron · doi:10.1016/j.neuron.2012.12.027 · Cited by 115
van Balkom, T. D., van den Heuvel, O. A., Berendse, H. W., van der Werf, Y. D., & Vriend, C. (2020) · Neuropsychology Review · doi:10.1007/s11065-020-09440-w · Cited by 122
Jung, C. K. E., & Herms, J. W. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhs317 · Cited by 112
The Role of Actin Cytoskeleton in Dendritic Spines in the Maintenance of Long-Term Memory
Basu, S., & Lamprecht, R. (2018) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2018.00143 · Cited by 117
Synaptic correlates of associative fear memory in the lateral amygdala
Choi, D. I., Kim, J., Lee, H., Kim, J., Sung, Y., Choi, J. E., Venkat, S. J., Park, P., Jung, H., & Kaang, B. (2021) · Neuron · doi:10.1016/j.neuron.2021.07.003 · Cited by 106
Estradiol and Progesterone have Opposing Roles in the Regulation of Fear Extinction in Female Rats
Graham, B. M., & Daher, M. (2015) · Neuropsychopharmacology · doi:10.1038/npp.2015.202 · Cited by 106
Paradoxical somatodendritic decoupling supports cortical plasticity during REM sleep
Aime, M., Calcini, N., Borsa, M., Campelo, T., Rusterholz, T., Sattin, A., Fellin, T., & Adamantidis, A. (2022) · Science · doi:10.1126/science.abk2734 · Cited by 106
Zimmermann, K. S., Richardson, R., & Baker, K. (2019) · Brain Sciences · doi:10.3390/brainsci9030065 · Cited by 111
Dendritic Spine Elimination: Molecular Mechanisms and Implications
Stein, I. S., & Zito, K. (2018) · The Neuroscientist · doi:10.1177/1073858418769644 · Cited by 110
The role of intracellular calcium stores in synaptic plasticity and memory consolidation
Baker, K., Edwards, T. M., & Rickard, N. S. (2013) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2013.04.011 · Cited by 99
Molecular mechanisms of dendrite morphogenesis
Arikkath, J. (2012) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2012.00061 · Cited by 113
Elimination of Dendritic Spines with Long-Term Memory Is Specific to Active Circuits
Sanders, J. D., Cowansage, K. K., Baumgärtel, K., & Mayford, M. R. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.1131-12.2012 · Cited by 101
Activity Shapes Neural Circuit Form and Function: A Historical Perspective
Pan, Y., & Monje, M. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.0740-19.2019 · Cited by 98
Long-TermIn VivoImaging of Dendritic Spines in the Hippocampus Reveals Structural Plasticity
Gu, L., Poll, S., Schmid, L., Nebeling, F. C., Chamoun, M., Steffen, J., Wagner, J., & Fuhrmann, M. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.1464-14.2014 · Cited by 105
Extracellular matrix control of dendritic spine and synapse structure and plasticity in adulthood
Levy, A. D., Omar, M. H., & Koleske, A. J. (2014) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2014.00116 · Cited by 102
Harnessing plasticity to understand learning and treat disease
Kilgard, M. P. (2012) · Trends in Neurosciences · doi:10.1016/j.tins.2012.09.002 · Cited by 93
p300/CBP-Associated Factor Selectively Regulates the Extinction of Conditioned Fear
Wei, W., Coelho, C. M., Li, X., Marek, R., Yan, S., Anderson, S., Meyers, D., Mukherjee, C., Sbardella, G., Castellano, S., et al. (2012) · The Journal of Neuroscience · doi:10.1523/jneurosci.0178-12.2012 · Cited by 93
Nakayama, D., Iwata, H., Teshirogi, C., Ikegaya, Y., Matsuki, N., & Nomura, H. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.2525-14.2015 · Cited by 95
Gdalyahu, A., Lázaro, M. T., Peñagarikano, O., Golshani, P., Trachtenberg, J. T., & Gescwind, D. H. (2015) · PLoS ONE · doi:10.1371/journal.pone.0125633 · Cited by 96
Farrell, M. R., Holland, F. H., Shansky, R. M., & Brenhouse, H. C. (2016) · Behavioural Brain Research · doi:10.1016/j.bbr.2016.05.009 · Cited by 95
Biophysics of Biochemical Signaling in Dendritic Spines: Implications in Synaptic Plasticity
Yasuda, R. (2017) · Biophysical Journal · doi:10.1016/j.bpj.2017.07.029 · Cited by 85
New learning and unlearning: strangers or accomplices in threat memory attenuation?
Clem, R. L., & Schiller, D. (2016) · Trends in Neurosciences · doi:10.1016/j.tins.2016.03.003 · Cited by 90
Hall, B. S., Moda, R. N., & Liston, C. M. (2014) · Neurobiology of Stress · doi:10.1016/j.ynstr.2014.10.008 · Cited by 94
Molecular signature of rapid estrogen regulation of synaptic connectivity and cognition
Sellers, K. J., Raval, P., & Srivastava, D. P. (2014) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2014.08.001 · Cited by 94
Shi, D., Huang, Y., Lai, C. S. W., Dong, C. M., Ho, L. C., Li, X., Wu, E. X., Li, Q., Wang, X., Chen, Y., et al. (2019) · Molecular Neurobiology · doi:10.1007/s12035-019-1474-9 · Cited by 89
Self-citationSpatiotemporal dynamics of dendritic spines in the living brain
Chen, C.-C., Lu, J., & Zuo, Y. (2014) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2014.00028 · Cited by 88
Maroun, M., Ioannides, P. J., Bergman, K. L., Kavushansky, A., Holmes, A., & Wellman, C. L. (2013) · European Journal of Neuroscience · doi:10.1111/ejn.12259 · Cited by 86
Synapse rearrangements upon learning: from divergent–sparse connectivity to dedicated sub-circuits
Caroni, P., Chowdhury, A., & Lahr, M. (2014) · Trends in Neurosciences · doi:10.1016/j.tins.2014.08.011 · Cited by 85
Nabel, E. M., & Morishita, H. (2013) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2013.00146 · Cited by 85
Lai, C. S. W., Adler, A., & Gan, W. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1801504115 · Cited by 89
Self-citationKong, C., Pilger, C., Hachmeister, H., Wei, X., Cheung, T. H., Lai, C. S. W., Lee, N. P. Y., Tsia, K. K., Wong, K. K. Y., & Huser, T. R. (2020) · Light Science & Applications · doi:10.1038/s41377-020-0259-2 · Cited by 87
Self-citationvan den Oever, M. C., Rotaru, D. C., Heinsbroek, J. A., Gouwenberg, Y., Deisseroth, K. A., Stuber, G. D., Mansvelder, H. D., & Smit, A. B. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.2412-13.2013 · Cited by 85
Ng, L. H. L., Huang, Y., Han, L., Chang, R. C.-C., Chan, Y. S., & Lai, C. S. W. (2018) · Translational Psychiatry · doi:10.1038/s41398-018-0321-5 · Cited by 82
Self-citationCohen, M. M., Tottenham, N., & Casey, B. J. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2013.01.023 · Cited by 89
Optical inactivation of synaptic AMPA receptors erases fear memory
Takemoto, K., Iwanari, H., Tada, H., Suyama, K., Sano, A., Nagai, T., Hamakubo, T., & Takahashi, T. (2016) · Nature Biotechnology · doi:10.1038/nbt.3710 · Cited by 83
A metaplasticity view of the interaction between homeostatic and Hebbian plasticity
Yee, A. X., Hsu, Y., & Chen, L. (2017) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2016.0155 · Cited by 85
A Upf3b-mutant mouse model with behavioral and neurogenesis defects
Huang, L., Shum, E. Y., Jones, S. H., Lou, C.-H., Chousal, J. N., Kim, H. Y., Roberts, A. J., Jolly, L. A., Espinoza, J. L., Skarbrevik, D., et al. (2017) · Molecular Psychiatry · doi:10.1038/mp.2017.173 · Cited by 79
Shen, H., Gipson, C. D., Huits, M., & Kalivas, P. W. (2013) · Neuropsychopharmacology · doi:10.1038/npp.2013.318 · Cited by 81
Rule learning enhances structural plasticity of long-range axons in frontal cortex
Johnson, C. M., Peckler, H., Tai, L.-H., & Wilbrecht, L. (2016) · Nature Communications · doi:10.1038/ncomms10785 · Cited by 79
Chen, K., Zhang, L., Tan, M., Lai, C. S. W., Li, A., Ren, C., & So, K. (2017) · Translational Psychiatry · doi:10.1038/tp.2017.41 · Cited by 79
Self-citation
Metadata
- Authors
- Lai, C. S. W., Franke, T. F., & Gan, W.-B.
- Affiliations
- New York University (US)
- NYU Langone Health (US)
- Corresponding author
- Gan, Wen-Biao
- Venue
- Nature
- Published
- 2012-02-19
- Volume
- 483
- Issue
- 7387
- Pages
- 87-91
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- OpenAlex
- W1980452424
- Cited by
- 392
- References
- 24
- Citations by year
- 2026: 13 · 2025: 15 · 2024: 16 · 2023: 20 · 2022: 16 · 2021: 26 · 2020: 26 · 2019: 28 · 2018: 27 · 2017: 36 · 2016: 38 · 2015: 35 · 2014: 30 · 2013: 42 · 2012: 23
- FWCI
- 21.02
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- The HKU Scholars Hub (University of Hong Kong) (submittedVersion)
- Funders
- National Institute of Neurological Disorders and Stroke (R01NS047325, NS047325)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurobiology and Insect Physiology Research
- Keywords
- fear conditioning, fear extinction, spine formation, fear memory, reconditioning, layer 5 pyramidal neurons, frontal association cortex, synaptic plasticity
- MeSH terms
- Acoustic Stimulation, Animals, Conditioning, Classical, Cues, Electric Stimulation, Extinction, Psychological, Extremities, Fear, Frontal Lobe, Male, Mice, Inbred C57BL, Mice, Transgenic, Models, Neurological, Neuronal Plasticity, Pyramidal Cells, Dendritic Spines, Mice
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