The DOI matches its Crossref record; 22 of the 22 references it cites were found in a registry or an index.
Control of Synaptic Strength by Glial TNFα
Abstract
Activity-dependent modulation of synaptic efficacy in the brain contributes to neural circuit development and experience-dependent plasticity. Although glia are affected by activity and ensheathe synapses, their influence on synaptic strength has largely been ignored. Here, we show that a protein produced by glia, tumor necrosis factor alpha (TNFalpha), enhances synaptic efficacy by increasing surface expression of AMPA receptors. Preventing the actions of endogenous TNFalpha has the opposite effects. Thus, the continual presence of TNFalpha is required for preservation of synaptic strength at excitatory synapses. Through its effects on AMPA receptor trafficking, TNFalpha may play roles in synaptic plasticity and modulating responses to neural injury.
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
“This model is based on the observations that TNFa levels are elevated by prolonged (48 h) activity blockade, acute application of TNFa (or conditioned media from activity-blocked cultures) increases mEPSC amplitude, and scaling up in response to prolonged activity blockade is prevented by blocking TNFa signaling (Beattie et al. 2002;Stellwagen et al. 2005;Stellwagen and Malenka 2006).”
From Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function (2012) · cites this paper as Beattie et al. 2002
In the citing paper
“This model is based on the observations that TNFa levels are elevated by prolonged (48 h) activity blockade, acute application of TNFa (or conditioned media from activity-blocked cultures) increases mEPSC amplitude, and scaling up in response to prolonged activity blockade is prevented by blocking TNFa signaling (Beattie et al. 2002;Stellwagen et al. 2005;Stellwagen and Malenka 2006).”
From Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function (2012) · cites this paper as Beattie et al. 2002
In the citing paper
“This model is based on the observations that TNFa levels are elevated by prolonged (48 h) activity blockade, acute application of TNFa (or conditioned media from activity-blocked cultures) increases mEPSC amplitude, and scaling up in response to prolonged activity blockade is prevented by blocking TNFa signaling (Beattie et al. 2002;Stellwagen et al. 2005;Stellwagen and Malenka 2006).”
From Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function (2012) · cites this paper as Beattie et al. 2002
Citations
Cites
CNS synaptogenesis promoted by glia-derived cholesterol
Mauch, D. H., Nägler, K., Schumacher, S., Göritz, C., Müller, E.-C., Otto, A., & Pfrieger, F. W. (2001) · Science · doi:10.1126/science.294.5545.1354 · Cited by 1,711
Glia: listening and talking to the synapse
Haydon, P. G. (2001) · Nature reviews. Neuroscience · doi:10.1038/35058528 · Cited by 1,454
Short-Term Synaptic Plasticity
Zucker, R. S. (1989) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.12.030189.000305 · Cited by 1,450
Control of Synapse Number by Glia
Ullian, E. M., Sapperstein, S. K., Christopherson, K. S., & Barres, B. A. (2001) · Science · doi:10.1126/science.291.5504.657 · Cited by 1,380
Cytokines and acute neurodegeneration
Allan, S. M., & Rothwell, N. J. (2001) · Nature reviews. Neuroscience · doi:10.1038/35094583 · Cited by 1,145
Bezzi, P., Domercq, M., Brambilla, L., Galli, R., Schols, D., De Clercq, E., Vescovi, A., Bagetta, G., Kollias, G., Meldolesi, J., et al. (2001) · Nature Neuroscience · doi:10.1038/89490 · Cited by 1,102
Three-Dimensional Relationships between Hippocampal Synapses and Astrocytes
Ventura, R. E., & Harris, K. M. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-16-06897.1999 · Cited by 907
Synaptic Efficacy Enhanced by Glial Cells in Vitro
Pfrieger, F. W., & Barres, B. A. (1997) · Science · doi:10.1126/science.277.5332.1684 · Cited by 793
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
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
Self-citation
Research works printed but not linked: 2
- Supplementary material is available on Science Online at www.sciencemag.org/cgi/content/full/295/5563/2282/DC1
- M. Noble M. Mayer-Proschel in Culturing Nerve Cells G. Banker K. Goslin Eds. (MIT Press Cambridge MA ed. 2 1998) pp. 526–529.
Cited by
Sorted by citations
Items 601–700 of 1,001
Schwann Cell-Derived Factors Modulate Synaptic Activities at Developing Neuromuscular Synapses
Cao, G., & Ko, C. P. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.1329-07.2007 · Cited by 42
Stone, T. W., & Williams, R. O. (2023) · Journal of Neurochemistry · doi:10.1111/jnc.16015 · Cited by 45
Wang, X., Lippi, G., Carlson, D. M., & Berg, D. K. (2013) · Journal of Neurochemistry · doi:10.1111/jnc.12436 · Cited by 43
Rossi, S., Motta, C., Musella, A., & Centonze, D. (2014) · Neuropharmacology · doi:10.1016/j.neuropharm.2014.09.022 · Cited by 42
Emerging role of microglial kinin B1 receptor in diabetic pain neuropathy
Talbot, S., & Couture, R. (2011) · Experimental Neurology · doi:10.1016/j.expneurol.2011.11.032 · Cited by 43
Lotrich, F. E., Ferrell, R. E., Rabinovitz, M., & Pollock, B. G. (2010) · Clinical Neuropharmacology · doi:10.1097/wnf.0b013e3181de8966 · Cited by 42
Westfall, S., Iqbal, U. H., Sebastian-Valverde, M., & Pasinetti, G. M. (2019) · Progress in molecular biology and translational science · doi:10.1016/bs.pmbts.2019.06.013 · Cited by 42
Astrocytic Ephrin-B1 Controls Excitatory-Inhibitory Balance in Developing Hippocampus
Nguyen, A. Q., Sutley-Koury, S. N., Koeppen, J., Mina, K., Woodruff, S., Hanna, S., Vengala, A., Hickmott, P. W., Obenaus, A., & Ethell, I. M. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.0413-20.2020 · Cited by 41
An emerging role for microglia in stress‐effects on memory
Sanguino‐Gómez, J., Buurstede, J. C., Abiega, O., Fitzsimons, C. P., Lucassen, P. J., Eggen, B. J. L., Lesuis, S. L., Meijer, O. C., & Krugers, H. J. (2021) · European Journal of Neuroscience · doi:10.1111/ejn.15188 · Cited by 43
A cellular star atlas: using astrocytes from human pluripotent stem cells for disease studies
Krencik, R., & Ullian, E. M. (2013) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2013.00025 · Cited by 40
Is human malarial coma caused, or merely deepened, by sequestration?
Clark, I. A., & Alleva, L. M. (2009) · Trends in Parasitology · doi:10.1016/j.pt.2009.04.003 · Cited by 43
Gehlot, P., Kumar, S., Vyas, V. K., Choudhary, B. S., Sharma, M., & Malik, R. (2022) · Bioorganic & Medicinal Chemistry · doi:10.1016/j.bmc.2022.117047 · Cited by 40
Ignatowski, T. A., Spengler, R. N., Dhandapani, K. M., Folkersma, H., Butterworth, R. F., & Tobinick, E. L. (2014) · CNS Drugs · doi:10.1007/s40263-014-0174-2 · Cited by 41
Human astrocytes are distinct contributors to the complexity of synaptic function
Krencik, R., van Asperen, J. V., & Ullian, E. M. (2016) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2016.08.012 · Cited by 43
Wigerblad, G., Huie, J. R., Yin, H. Z., Leinders, M., Pritchard, R. A., Koehrn, F. J., Xiao, W. H., Bennett, G. J., Huganir, R. L., Ferguson, A. R., et al. (2017) · Experimental Neurology · doi:10.1016/j.expneurol.2017.04.004 · Cited by 40
Emerging themes in GABAergic synapse development
Kuzirian, M. S., & Paradis, S. (2011) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2011.07.002 · Cited by 40
Turovskaya, M. V., Turovsky, E. A., Зинченко, В. П., Levin, S. G., & Godukhin, O. V. (2012) · Neuroscience Letters · doi:10.1016/j.neulet.2012.03.084 · Cited by 40
Carriba, P., Jiménez, S., Navarro, V., Moreno‐González, I., Barneda‐Zahonero, B., Moubarak, R. S., López‐Soriano, J., Gutiérrez, A., Vitórica, J., & Comella, J. X. (2015) · Cell Death and Disease · doi:10.1038/cddis.2015.6 · Cited by 40
Spinal Astrogliosis in Pain Models: Cause and Effects
Hald, A. (2009) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-009-9390-6 · Cited by 44
Role of neuroinflammation in morphine tolerance: Effect of tumor necrosis factor-α
Shen, C., Tsai, R.-Y., & Wong, C. (2012) · Acta anaesthesiologica Taiwanica · doi:10.1016/j.aat.2012.12.004 · Cited by 39
Targeting tumour necrosis factor-α in hypoxia and synaptic signalling
O'Connor, J. J. (2013) · Irish Journal of Medical Science (1971 -) · doi:10.1007/s11845-013-0911-4 · Cited by 37
Vitamin D3 for the Treatment of Epilepsy: Basic Mechanisms, Animal Models, and Clinical Trials
Pendo, K., & DeGiorgio, C. M. (2016) · Frontiers in Neurology · doi:10.3389/fneur.2016.00218 · Cited by 39
Epilepsy and vitamin D: a comprehensive review of current knowledge
Yazdi, S. A. M., Abbasi, M., & Yazdi, S. M. M. (2016) · Reviews in the Neurosciences · doi:10.1515/revneuro-2016-0044 · Cited by 39
Matrix Metalloproteinases, Neural Extracellular Matrix, and Central Nervous System Pathology
Luca, C. D., & Papa, M. (2017) · Progress in molecular biology and translational science · doi:10.1016/bs.pmbts.2017.04.002 · Cited by 39
More than a sidekick: glia and homeostatic synaptic plasticity
Turrigiano, G. G. (2006) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2006.08.002 · Cited by 39
Instrumental Learning Within the Rat Spinal Cord: Localization of the Essential Neural Circuit.
Liu, G. T., Ferguson, A. R., Crown, E. D., Bopp, A. C., Miranda, R. C., & Grau, J. W. (2005) · Behavioral Neuroscience · doi:10.1037/0735-7044.119.2.538 · Cited by 39
Rho kinase inhibitor fasudil reduces l‐DOPA‐induced dyskinesia in a rat model of Parkinson's disease
Lopez‐Lopez, A., Labandeira, C. M., Labandeira‐Garcia, J. L., & Muñoz, A. (2020) · British Journal of Pharmacology · doi:10.1111/bph.15275 · Cited by 40
Understanding neuron-glia crosstalk and biological clocks in insomnia
Carvalhas-Almeida, C., Serra, J., Moita, J. J., Cavadas, C., & Álvaro, A. R. (2023) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2023.105100 · Cited by 41
McGrath, A. G., & Briand, L. A. (2019) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2019.09.007 · Cited by 39
Singh, A., Jones, O. D., Mockett, B. G., Ohline, S. M., & Abraham, W. C. (2019) · Journal of Neuroscience · doi:10.1523/jneurosci.1492-19.2019 · Cited by 40
Wijayatunge, R., Chen, L., Cha, Y. M., Zannas, A. S., Frank, C. L., & West, A. E. (2014) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2014.06.008 · Cited by 37
A Comparative Perspective on Wnt/β-Catenin Signalling in Cell Fate Determination
Garcin, C. L., & Habib, S. J. (2017) · Results and problems in cell differentiation · doi:10.1007/978-3-319-53150-2_15 · Cited by 40
Kim, S. M., McIlwraith, E. K., Chalmers, J. A., & Belsham, D. D. (2018) · Neuroendocrinology · doi:10.1159/000494759 · Cited by 37
Cytokines, synaptic plasticity and network dynamics: a matter of balance
Bellingacci, L., Canonichesi, J., Mancini, A., Parnetti, L., & Filippo, M. D. (2023) · Neural Regeneration Research · doi:10.4103/1673-5374.371344 · Cited by 41
Maternal Overnutrition Programs Central Inflammation and Addiction-Like Behavior in Offspring
Montalvo-Martínez, L., Maldonado‐Ruiz, R., Cárdenas‐Tueme, M., Reséndez‐Pérez, D., & Camacho‐Morales, A. (2018) · BioMed Research International · doi:10.1155/2018/8061389 · Cited by 42
Repurposing Immunomodulatory Imide Drugs (IMiDs) in Neuropsychiatric and Neurodegenerative Disorders
Jung, Y. J., Tweedie, D., Scerba, M. T., Kim, D. S., Palmas, M. F., Pisanu, A., Carta, A. R., & Greig, N. H. (2021) · Frontiers in Neuroscience · doi:10.3389/fnins.2021.656921 · Cited by 37
Minematsu, T., Nakagami, G., Yamamoto, Y., Kanazawa, T., Huang, L., Koyanagi, H., Sasaki, S., Uchida, G., Fujita, H., Haga, N., et al. (2013) · Wound Repair and Regeneration · doi:10.1111/wrr.12017 · Cited by 37
Tumor Necrosis Factor Potentiates Central Vagal Afferent Signaling by Modulating Ryanodine Channels
Rogers, R. C., Meter, M. J. V., & Hermann, G. E. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.3530-06.2006 · Cited by 37
Su, Z.-Z., Kang, D., Chen, Y., Pekarskaya, O., Chao, W., Volsky, D. J., & Fisher, P. B. (2003) · Journal of NeuroVirology · doi:10.1080/13550280390201263 · Cited by 37
Bertoglio, D., Verhaeghe, J. A. J., Santermans, E., Amhaoul, H., Jonckers, E., Wyffels, L., der Linden, A. V., Hens, N., Staelens, S. G., & Dedeurwaerdere, S. (2016) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2016.12.015 · Cited by 36
Zhang, Y., Xu, H., Zhang, F., Shao, F., Ellenbroek, B. A., Wang, J., & Wang, W. (2019) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2019.02.010 · Cited by 34
Microorganisms in the Placenta: Links to Early-Life Inflammation and Neurodevelopment in Children
Tomlinson, M. S., Lü, K., Stewart, J. R., Marsit, C. J., O’Shea, T. M., & Fry, R. C. (2019) · Clinical Microbiology Reviews · doi:10.1128/cmr.00103-18 · Cited by 38
Mironets, E., Fischer, R., Bracchi-Ricard, V. C., Saltos, T. M., Truglio, T. S., O’Reilly, M. L., Swanson, K. A., Bethea, J. R., & Tom, V. J. (2019) · Journal of Neuroscience · doi:10.1523/jneurosci.2417-19.2019 · Cited by 37
Extracellular Metalloproteinases in the Plasticity of Excitatory and Inhibitory Synapses
Wiera, G., & Mozrzymas, J. W. (2021) · Cells · doi:10.3390/cells10082055 · Cited by 36
Davis, C. J., & Krueger, J. M. (2012) · Sleep Medicine Clinics · doi:10.1016/j.jsmc.2012.06.006 · Cited by 36
The Glial Cells Respond to Spinal Cord Injury
Wang, R., Zhou, R., Chen, Z., Gao, S., & Zhou, F. (2022) · Frontiers in Neurology · doi:10.3389/fneur.2022.844497 · Cited by 35
Wall, A. M., Mukandala, G., Greig, N. H., & O'Connor, J. J. (2015) · Journal of Neuroscience Research · doi:10.1002/jnr.23540 · Cited by 35
Gao, F., Liu, Z., Ren, W., & Jiang, W. (2014) · Neuropsychiatric Disease and Treatment · doi:10.2147/ndt.s65695 · Cited by 36
Tumor Necrosis Factor Alpha Enhances Glutamatergic Transmission onto Spinal Motoneurons
Han, P., & Whelan, P. J. (2009) · Journal of Neurotrauma · doi:10.1089/neu.2009.1016 · Cited by 36
Cytokine Signalling at the Microglial Penta-Partite Synapse
Aramideh, J. A., Vidal-Itriago, A., Morsch, M., & Graeber, M. B. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222413186 · Cited by 35
CX3CL1 Pathway as a Molecular Target for Treatment Strategies in Alzheimer’s Disease
Bivona, G., Iemmolo, M., & Ghersi, G. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24098230 · Cited by 35
Microglia modulate TNFα ‐mediated synaptic plasticity
Kleidonas, D., Kirsch, M., Andrieux, G., Pfeifer, D., Boerries, M., & Vlachos, A. (2023) · Glia · doi:10.1002/glia.24383 · Cited by 37
Davidson, J. O., Green, C. R., Nicholson, L. F. B., Bennet, L., & Gunn, A. J. (2012) · International Journal of Molecular Sciences · doi:10.3390/ijms13056303 · Cited by 35
Bañuelos‐Cabrera, I., Valle-Dorado, M. G., Aldana, B. I., Orozco-Suárez, S. A., & Rocha, L. (2014) · Archives of Medical Research · doi:10.1016/j.arcmed.2014.11.010 · Cited by 36
Ferguson, A. R., Huie, J. R., Crown, E. D., & Grau, J. W. (2012) · Frontiers in Physiology · doi:10.3389/fphys.2012.00396 · Cited by 35
Hasni, D. S. M., Lim, S. M., Chin, A., Tan, M. P., Poi, P. J. H., Kamaruzzaman, S. B., Majeed, A. B. A., & Ramasamy, K. (2016) · Geriatrics and gerontology international/Geriatrics & gerontology international · doi:10.1111/ggi.12783 · Cited by 35
Regulation of microglia by neuromodulators: Modulations in major and minor modes
Albertini, G., Etienne, F., & Roumier, A. (2020) · Neuroscience Letters · doi:10.1016/j.neulet.2020.135000 · Cited by 35
Wegrzyn, D., Freund, N., Faissner, A., & Juckel, G. (2021) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2021.637549 · Cited by 37
Neuro-Immune Cross-Talk in the Striatum: From Basal Ganglia Physiology to Circuit Dysfunction
Mancini, A., Ghiglieri, V., Parnetti, L., Calabresi, P., & Filippo, M. D. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.644294 · Cited by 38
Movers and shakers: Microglial dynamics and modulation of neural networks
Whitelaw, B. S., Stoessel, M. B., & Majewska, A. K. (2022) · Glia · doi:10.1002/glia.24323 · Cited by 34
Ye, P., Price, W. A., Kassiotis, G., Kollias, G. A., & D’Ercole, A. J. (2002) · Journal of Neuroscience Research · doi:10.1002/jnr.10512 · Cited by 35
Neuroprotective effect of TNFα against the β-amyloid neurotoxicity mediated by CDK5 kinase
Orellana, D. I., Quintanilla, R. A., & Maccioni, R. B. (2006) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2006.10.010 · Cited by 36
Liguz‐Lecznar, M., Zakrzewska, R., & Kossut, M. M. (2015) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2015.06.015 · Cited by 34
Kwon, M., Lee, J.-K., Park, S.-H., Sim, Y., Jung, J., Won, M., Kim, S., & Suh, H. (2010) · Korean Journal of Physiology and Pharmacology · doi:10.4196/kjpp.2010.14.5.257 · Cited by 34
(Putative) sex differences in neuroimmune modulation of memory
Tronson, N. C., & Collette, K. M. (2016) · Journal of Neuroscience Research · doi:10.1002/jnr.23921 · Cited by 36
Woods, C., Marques-Lopes, J., Contoreggi, N. H., Milner, T. A., Pickel, V. M., Wang, G., & Glass, M. J. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.2360-19.2020 · Cited by 34
Sathler, M. F., Khatri, L., Roberts, J. P., Schmidt, I. G., Zaytseva, A., Kubrusly, R. C. C., Ziff, E. B., & Kim, S. (2021) · Journal of Cell Science · doi:10.1242/jcs.257972 · Cited by 38
Tobinick, E. L. (2012) · Current Alzheimer Research · doi:10.2174/156720512799015073 · Cited by 34
Jiang, E., Chapp, A. D., Fan, Y., Larson, R. A., Hahka, T. M., Huber, M. J., Yan, J., Chen, Q., & Shan, Z. J. (2018) · Frontiers in Physiology · doi:10.3389/fphys.2018.00104 · Cited by 34
Yao, P., Wang, S.-K., Chen, S., Xin, W., Liu, X., & Zang, Y. (2019) · Neurobiology of Disease · doi:10.1016/j.nbd.2019.04.012 · Cited by 33
Galea, L. A. M., Roes, M., Dimech, C. J., Chow, C., Mahmoud, R., Lieblich, S. E., & Duarte‐Guterman, P. (2018) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2018.06.030 · Cited by 33
Ellagic Acid Inhibits Neuroinflammation and Cognitive Impairment Induced by Lipopolysaccharides
Dornelles, G. L., de Oliveira, J. S., de Almeida, E. J. R., Mello, C. B. E., Rodrigues, B. R. E., da Silva, C. B., Petry, L. D. S., Pillat, M. M., Palma, T. V., & de Andrade, C. M. (2020) · Neurochemical Research · doi:10.1007/s11064-020-03105-z · Cited by 34
Challenges in researching the immune pathways between early life adversity and psychopathology
Reid, B. M., & Danese, A. (2020) · Development and Psychopathology · doi:10.1017/s0954579420001157 · Cited by 37
TNF-α and Microglial Hormetic Involvement in Neurological Health & Migraine
Kraig, R. P., Mitchell, H. M., Christie-Pope, B. C., Kunkler, P. E., White, D. M., Tang, Y., & Langan, G. P. (2010) · Dose-Response · doi:10.2203/dose-response.09-056.kraig · Cited by 34
Addiction: A dysregulation of satiety and inflammatory processes
Harricharan, R., Abboussi, O., & Daniels, W. M. U. (2017) · Progress in brain research · doi:10.1016/bs.pbr.2017.07.012 · Cited by 35
Viral Triggers and Inflammatory Mechanisms in Pediatric Epilepsy
Bartolini, L., Libbey, J. E., Ravizza, T., Fujinami, R. S., Jacobson, S., & Gaillard, W. D. (2018) · Molecular Neurobiology · doi:10.1007/s12035-018-1215-5 · Cited by 34
Discovering novel phenotype-selective neurotrophic factors to treat neurodegenerative diseases
Petrova, P. S., Raibekas, A. A., Pevsner, J., Vigo, N. T., Anafi, M., Moore, M. K., Peaire, A. E., Shridhar, V., Smith, D. I., Kelly, J., et al. (2004) · Progress in brain research · doi:10.1016/s0079-6123(03)46012-3 · Cited by 33
Shi, Z., Chen, Y., Lu, C., Dong, L.-M., Lv, J.-W., Tuo, Q.-H., Qin, L., Cheng, S.-W., Bu, L.-L., Lin, N., et al. (2018) · Pharmacological Research · doi:10.1016/j.phrs.2018.09.002 · Cited by 32
Normal aging of offspring mice of mothers with induced inflammation during pregnancy
Golan, H., Stilman, M., Lev, V., & Huleihel, M. (2006) · Neuroscience · doi:10.1016/j.neuroscience.2006.05.045 · Cited by 32
Mahaman, Y. A. R., Huang, F., Salissou, M. T. M., Yacouba, M. B. M., Wang, J., Liu, R., Zhang, B., Li, H., Zhu, F., & Wang, X. (2023) · Neurotherapeutics · doi:10.1007/s13311-023-01356-6 · Cited by 34
Verkhratsky, A., & Butt, A. M. (2023) · Elsevier eBooks · doi:10.1016/b978-0-12-821565-4.00008-0 · Cited by 31
Rodríguez, M. J., Martínez‐Sánchez, M., Bernal, F., & Mahy, N. (2004) · Journal of Neuroscience Research · doi:10.1002/jnr.20177 · Cited by 32
Glial involvement in trigeminal central sensitization
Xie, Y. (2008) · Acta Pharmacologica Sinica · doi:10.1111/j.1745-7254.2008.00801.x · Cited by 32
A Common Language: How Neuroimmunological Cross Talk Regulates Adult Hippocampal Neurogenesis
Leiter, O., Kempermann, G., & Walker, T. L. (2016) · Stem Cells International · doi:10.1155/2016/1681590 · Cited by 32
Brown, E. V., Falnikar, A., Heinsinger, N. M., Cheng, L., Andrews, C. E., DeMarco, M., & Lepore, A. C. (2021) · Experimental Neurology · doi:10.1016/j.expneurol.2021.113757 · Cited by 32
Synapse Dysfunctions in Multiple Sclerosis
Schwarz, K., & Schmitz, F. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24021639 · Cited by 36
Blond, S., Mertens, P., David, R., Manuel Roulaud, B., & Rigoard, P. (2015) · Neurochirurgie · doi:10.1016/j.neuchi.2014.11.001 · Cited by 32
Xu, J., Molinas, A., Mukerjee, S., Morgan, D. A., Rahmouni, K., Zsombok, A., & Lazartigues, E. D. (2019) · Hypertension · doi:10.1161/hypertensionaha.119.12832 · Cited by 31
Long-chain polyunsaturated fatty acids in memory formation and consolidation:
Das, U. N. (2003) · Nutrition · doi:10.1016/s0899-9007(03)00174-6 · Cited by 32
De, A., Krueger, J. M., & Simasko, S. M. (2005) · Brain Research · doi:10.1016/j.brainres.2005.06.044 · Cited by 32
Diwakarla, S., Nylander, E., Grönbladh, A., Vanga, S. R., Shamsudin, Y., Gutiérrez‐de‐Terán, H., Sävmarker, J., Ng, L., Pham, V., Lundbäck, T., et al. (2016) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.6b00146 · Cited by 31
Stenfors, C. U. D., Jónsdóttir, I. H., Hanson, L. L. M., & Theorell, T. (2017) · Journal of Psychosomatic Research · doi:10.1016/j.jpsychores.2017.03.010 · Cited by 32
Mashhadizadeh, S., Farbood, Y., Dianat, M., Khodadadi, A., & Sarkaki, A. (2017) · Europe PMC (PubMed Central) · doi:10.22038/ijbms.2017.8581 · Cited by 31
The role of glia in Parkinson's disease: Emerging concepts and therapeutic applications
Kuter, K. Z., Cenci, M. A., & Carta, A. R. (2020) · Progress in brain research · doi:10.1016/bs.pbr.2020.02.004 · Cited by 31
Multiple sclerosis: Inflammation, autoimmunity and plasticity
Bassi, M. S., Iezzi, E., & Centonze, D. (2022) · Handbook of clinical neurology · doi:10.1016/b978-0-12-819410-2.00024-2 · Cited by 34
Neural–immune interactions in disorders of sleep-wakefulness organization
Bentivoglio, M., & Kristensson, K. (2007) · Trends in Neurosciences · doi:10.1016/j.tins.2007.09.004 · Cited by 31
Shen, C., Tsai, R., Tai, Y.-H., Lin, S., Chien, C., & Wong, C. (2011) · Anesthesia & Analgesia · doi:10.1213/ane.0b013e318217f7eb · Cited by 31
Zhang, K., Li, Y.-J., Feng, D., Zhang, P., Wang, Y., Li, X., Liu, S., Wu, Y., & Zhao, M. (2017) · Scientific Reports · doi:10.1038/srep43594 · Cited by 32
Cytokines in CNS Inflammation and Disease
Tansey, M. G., & Wyss‐Coray, T. (2007) · Springer eBooks · doi:10.1007/978-0-387-73894-9_5 · Cited by 32
Caspases orchestrate microglia instrumental functions
Shen, X., Venero, J. L., Joseph, B., & Burguillos, M. Á. (2018) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2018.09.007 · Cited by 31
Metadata
- Authors
- Beattie, E. C., Stellwagen, D., Morishita, W., Bresnahan, J. C., Ha, B. K., Von Zastrow, M., Beattie, M. S., & Malenka, R. C.
- Affiliations
- Stanford Medicine (US)
- The Ohio State University Wexner Medical Center (US)
- Departments of Psychiatry and Cellular and Molecular Pharmacology, University of California, San Francisco, CA 94143, USA.
- Corresponding author
- Beattie, Michael S.
- Malenka, Robert C.
- Venue
- Science
- Published
- 2002-03-22
- Volume
- 295
- Issue
- 5563
- Pages
- 2282-2285
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- OpenAlex
- W1548862642
- Cited by
- 1,344
- References
- 22
- Citations by year
- 2026: 36 · 2025: 33 · 2024: 47 · 2023: 58 · 2022: 57 · 2021: 82 · 2020: 65 · 2019: 56 · 2018: 59 · 2017: 67 · 2016: 58 · 2015: 61 · 2014: 64 · 2013: 73 · 2012: 73
- FWCI
- 14.84
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Science (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institute of Mental Health (MH 063394)
- National Institute on Drug Abuse (DA 00439)
- National Institute of Neurological Disorders and Stroke (NS38079, R01NS031193, R01NS038079, NS 31193)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetics and Neurodevelopmental Disorders
- Keywords
- synaptic efficacy, AMPA receptor trafficking, synaptic plasticity, excitatory synapses, nerve injury
- MeSH terms
- Animals, Astrocytes, Cells, Cultured, Gene Expression Regulation, Hippocampus, Synaptic Transmission, Neuronal Plasticity, Neurons, Synapses, Tumor Necrosis Factor-alpha, Antigens, CD, Culture Media, Conditioned, Rats, Sprague-Dawley, Receptors, AMPA, Receptors, Tumor Necrosis Factor, Receptors, Tumor Necrosis Factor, Type 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.
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