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Synaptic scaling mediated by glial TNF-α
Abstract
Two general forms of synaptic plasticity that operate on different timescales are thought to contribute to the activity-dependent refinement of neural circuitry during development: (1) long-term potentiation (LTP) and long-term depression (LTD), which involve rapid adjustments in the strengths of individual synapses in response to specific patterns of correlated synaptic activity, and (2) homeostatic synaptic scaling, which entails uniform adjustments in the strength of all synapses on a cell in response to prolonged changes in the cell's electrical activity. Without homeostatic synaptic scaling, neural networks can become unstable and perform suboptimally. Although much is known about the mechanisms underlying LTP and LTD, little is known about the mechanisms responsible for synaptic scaling except that such scaling is due, at least in part, to alterations in receptor content at synapses. Here we show that synaptic scaling in response to prolonged blockade of activity is mediated by the pro-inflammatory cytokine tumour-necrosis factor-alpha (TNF-alpha). Using mixtures of wild-type and TNF-alpha-deficient neurons and glia, we also show that glia are the source of the TNF-alpha that is required for this form of synaptic scaling. We suggest that by modulating TNF-alpha levels, glia actively participate in the homeostatic activity-dependent regulation of synaptic connectivity.
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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 Stellwagen and Malenka 2006
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 Stellwagen and Malenka 2006
In the citing paper
“It was recently proposed that prolonged activity blockade (with TTX) increases glial release of TNFa, which then acts on neurons to enhance AMPAR insertion and scale up mEPSC amplitude (Stellwagen and Malenka 2006).”
From Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function (2012) · cites this paper as Stellwagen and Malenka 2006
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 Stellwagen and Malenka 2006
In the citing paper
“Interestingly, the TNFa involved in scaling up synaptic strengths in response to TTX originates from glia rather than neurons, because wild-type neurons grown on TNFa 2/2 glia did not scale up synaptic strengths in response to 48 h of TTX treatment, whereas TNFa 2/2 neurons grown on wild-type glia did (Stellwagen and Malenka 2006).”
From Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function (2012) · cites this paper as Stellwagen and Malenka 2006
In the citing paper
“Inconsistent with the above model is the observation that scaling is a gradual and cumulative process evident after as little as 4-6 h of activity blockade (Sutton et al. 2006;Ibata et al. 2008), whereas TNFa-dependent scaling was only observed after prolonged activity block (48 h) (Stellwagen and Malenka 2006).”
From Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function (2012) · cites this paper as Stellwagen and Malenka 2006
In the citing paper
“Interestingly, the delayed potentiation in visual cortex following lid suture requires TNFa and Arc signaling (Kaneko et al. 2008;McCurry et al. 2011) as does synaptic scaling in vitro (Shepherd et al. 2006;Stellwagen and Malenka 2006;Steinmetz and Turrigiano 2010); however, both these manipulations likely affect many forms of plasticity, so it still remains to be seen if synaptic scaling”
From Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function (2012) · cites this paper as Stellwagen and Malenka 2006
Citations
Cites
Malenka, R. C., & Bear, M. F. (2004) · Neuron · doi:10.1016/j.neuron.2004.09.012 · Cited by 3,968
Self-citationA simple method for organotypic cultures of nervous tissue
Stoppini, L., Buchs, P., & Muller, D. (1991) · Journal of Neuroscience Methods · doi:10.1016/0165-0270(91)90128-m · Cited by 3,096
Homeostatic plasticity in the developing nervous system
Turrigiano, G. G., & Nelson, S. B. (2004) · Nature Reviews Neuroscience · doi:10.1038/nrn1327 · Cited by 2,485
Synaptic plasticity: taming the beast
Abbott, L. F., & Nelson, S. B. (2000) · Nature Neuroscience · doi:10.1038/81453 · Cited by 2,263
Activity-dependent scaling of quantal amplitude in neocortical neurons
Turrigiano, G. G., Leslie, K. R., Desai, N. S., Rutherford, L. C., & Nelson, S. B. (1998) · Nature · doi:10.1038/36103 · Cited by 2,226
Thrombospondins are astrocyte-secreted proteins that promote CNS synaptogenesis
Christopherson, K. S., Ullian, E. M., Stokes, C. C. A., Mullowney, C. E., Hell, J. W., Agah, A., Lawler, J., Mosher, D. F., Bornstein, P., & Barres, B. A. (2005) · Cell · doi:10.1016/j.cell.2004.12.020 · Cited by 1,688
Hayashi, Y., Shi, S.-H., Esteban, J. A., Piccini, A., Poncer, J.-C., & Malinow, R. (2000) · Science · doi:10.1126/science.287.5461.2262 · Cited by 1,524
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
Control of Synaptic Strength by Glial TNFα
Beattie, E. C., Stellwagen, D., Morishita, W., Bresnahan, J. C., Ha, B. K., Von Zastrow, M., Beattie, M. S., & Malenka, R. C. (2002) · Science · doi:10.1126/science.1067859 · Cited by 1,344
Self-citationRapid Spine Delivery and Redistribution of AMPA Receptors After Synaptic NMDA Receptor Activation
Shi, S.-H., Hayashi, Y., Petralia, R. S., Zaman, S. H., Wenthold, R. J., Svoboda, K., & Malinow, R. (1999) · Science · doi:10.1126/science.284.5421.1811 · Cited by 1,276
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Lalo, U., Koh, W., Lee, C. J., & Pankratov, Y. (2021) · Neuropharmacology · doi:10.1016/j.neuropharm.2021.108758 · Cited by 87
AMPA‐receptor trafficking and injury‐induced cell death
Beattie, M. S., Ferguson, A. R., & Bresnahan, J. C. (2010) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2010.07343.x · Cited by 87
Aquaporin-4 water channels and synaptic plasticity in the hippocampus
Scharfman, H. E., & Binder, D. K. (2013) · Neurochemistry International · doi:10.1016/j.neuint.2013.05.003 · Cited by 87
Spreading Depression Sends Microglia on Lévy Flights
Grinberg, Y. Y., MILTON, J. G., & Kraig, R. P. (2011) · PLoS ONE · doi:10.1371/journal.pone.0019294 · Cited by 87
Almonte, A. G., & Sweatt, J. D. (2011) · Brain Research · doi:10.1016/j.brainres.2011.06.042 · Cited by 87
Homeostatic mechanisms regulate distinct aspects of cortical circuit dynamics
Wu, Y. K., Hengen, K. B., Turrigiano, G. G., & Gjorgjieva, J. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1918368117 · Cited by 86
Ikeda, H., Tsuda, M., Inoue, K., & Murase, K. (2007) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2007.05386.x · Cited by 86
AMPAR trafficking in synapse maturation and plasticity
Bassani, S., Folci, A., Zapata, J., & Passafaro, M. (2013) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-013-1309-1 · Cited by 86
The transition from acute to chronic pain: understanding how different biological systems interact
Mifflin, K. A., & Kerr, B. J. (2013) · Canadian Journal of Anesthesia/Journal canadien d anesthésie · doi:10.1007/s12630-013-0087-4 · Cited by 85
Balosso, S., Ravizza, T., Pierucci, M., Calcagno, E., Invernizzi, R. W., Giovanni, G. D., Esposito, E., & Vezzani, A. (2009) · Neuroscience · doi:10.1016/j.neuroscience.2009.03.005 · Cited by 85
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
Bachstetter, A. D., Bodnar, C., & Morganti, J. M. (2018) · Neural Regeneration Research · doi:10.4103/1673-5374.238604 · Cited by 85
Clark, I. A., & Vissel, B. (2015) · British Journal of Pharmacology · doi:10.1111/bph.13181 · Cited by 84
Jara, J. H., Singh, B. B., Floden, A. M., & Combs, C. K. (2006) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2006.04330.x · Cited by 84
The dual role of TNF-α and its receptors in seizures
Balosso, S., Ravizza, T., Aronica, E., & Vezzani, A. (2013) · Experimental Neurology · doi:10.1016/j.expneurol.2013.05.010 · Cited by 84
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Gordleeva, S., Tsybina, Y., Krivonosov, M., Ivanchenko, M., Zaikin, A. A., Kazantsev, V., & Gorban, A. N. (2021) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2021.631485 · Cited by 83
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Davis, C. J., Bohnet, S. G., Meyerson, J. M., & Krueger, J. M. (2007) · Neuroscience Letters · doi:10.1016/j.neulet.2007.06.005 · Cited by 83
Li, K., Li, L., Cui, B., Gai, Z., Li, Q., Wang, S., Yan, J., Lin, B., Tian, L., Liu, H., et al. (2017) · Toxicological Sciences · doi:10.1093/toxsci/kfx240 · Cited by 82
Das, U. N. (2013) · Nutrition · doi:10.1016/j.nut.2013.01.012 · Cited by 82
York, E. M., Zhang, J., Choi, H. B., & MacVicar, B. A. (2020) · Glia · doi:10.1002/glia.23913 · Cited by 81
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Bozzi, Y., Dunleavy, M., & Henshall, D. C. (2011) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2011.00045 · Cited by 81
Buehler, M. R. (2011) · Medical Hypotheses · doi:10.1016/j.mehy.2011.02.038 · Cited by 81
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Clark, I. A., & Vissel, B. (2017) · Seminars in Immunopathology · doi:10.1007/s00281-017-0628-y · Cited by 81
Taj, S. H., Blon, D. L., Hoornaert, C., Daans, J., Quarta, A., Praet, J., der Linden, A. V., Ponsaerts, P., & Hoehn, M. (2018) · Journal of Neuroinflammation · doi:10.1186/s12974-018-1212-7 · Cited by 80
Manzoor, N. F., Gao, Y., Licari, F. G., & Kaltenbach, J. A. (2012) · Hearing Research · doi:10.1016/j.heares.2012.04.003 · Cited by 80
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Xavier, A. L. R., Menezes, J. R. L., Goldman, S. A., & Nedergaard, M. (2014) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2013.0593 · Cited by 80
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Carta, A. R., Mulas, G., Bortolanza, M., Duarte, T. T., Pillai, E., Fisone, G., Raisman‐Vozari, R., & Bel, E. A. D. (2016) · European Journal of Neuroscience · doi:10.1111/ejn.13482 · Cited by 80
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Westermann, J., Lange, T., Textor, J. C., & Jan Born, A. (2015) · Trends in Neurosciences · doi:10.1016/j.tins.2015.07.007 · Cited by 79
Iizumi, T., Takahashi, S., Mashima, K., Minami, K., Izawa, Y., Abe, T., Hishiki, T., Suematsu, M., Kajimura, M., & Suzuki, N. (2016) · Journal of Neuroinflammation · doi:10.1186/s12974-016-0564-0 · Cited by 79
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Corrigan, M., O’Rourke, A. M., Moran, B., Fletcher, J. M., & Harkin, A. (2023) · Neuronal Signaling · doi:10.1042/ns20220054 · Cited by 81
Rossi, S., Furlan, R., Chiara, V. D., Muzio, L., Musella, A., Motta, C., Studer, V., Cavasinni, F., Bernardi, G., Martino, G., et al. (2011) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2011.03.017 · Cited by 78
Whiting, B. A., Moiseff, A., & Rubio, M. E. (2009) · Neuroscience · doi:10.1016/j.neuroscience.2009.07.049 · Cited by 78
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Church, J. S., Bannish, J. A. M., Adrian, L. A., Martinez, K. R., Henshaw, A., & Schwartzer, J. J. (2023) · Frontiers in Neuroscience · doi:10.3389/fnins.2023.1134080 · Cited by 76
Cumiskey, D., Butler, M. P., Moynagh, P. N., & O'Connor, J. J. (2007) · Brain Research · doi:10.1016/j.brainres.2006.12.019 · Cited by 76
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Pistono, C., Bister, N., Stanová, I., & Malm, T. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.623771 · Cited by 75
Grochowska, K. M., Yuanxiang, P., Bär, J., Raman, R., Brugal, G. N., Sahu, G., Schweizer, M., Bikbaev, A. F., Schilling, S., Demuth, H., et al. (2017) · EMBO Reports · doi:10.15252/embr.201643519 · Cited by 75
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Guillamón-Vivancos, T., Gómez‐Pinedo, U., & Matías‐Guiu, J. (2015) · Neurología (English Edition) · doi:10.1016/j.nrleng.2014.12.005 · Cited by 75
Vargas, J. R., Takahashi, D. K., Thomson, K. E., & Wilcox, K. S. (2013) · Journal of Neuropathology & Experimental Neurology · doi:10.1097/nen.0b013e3182a4b266 · Cited by 75
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Carmen, J., Rothstein, J. D., & Kerr, D. A. (2009) · Brain Research · doi:10.1016/j.brainres.2009.01.040 · Cited by 73
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Uzunova, G., Hollander, E., & Shepherd, J. D. (2014) · Current Neuropharmacology · doi:10.2174/1570159x113116660046 · Cited by 73
Mackay, M. C. (2015) · Immunologic Research · doi:10.1007/s12026-015-8716-3 · Cited by 73
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Nimmervoll, B. V., White, R., Yang, J., An, S., Henn, C., Sun, J., & Luhmann, H. J. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhs156 · Cited by 71
Pouget, J. G., Gonçalves, V. F., Spain, S. L., Finucane, H. K., Raychaudhuri, S., Kennedy, J. L., & Knight, J. (2016) · Schizophrenia Bulletin · doi:10.1093/schbul/sbw059 · Cited by 71
Prowse, N. A., & Hayley, S. P. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2021.09.018 · Cited by 72
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Hegazy, H. G., Ali, E. H. A., & Elgoly, A. H. M. (2014) · Cytokine · doi:10.1016/j.cyto.2014.10.027 · Cited by 70
Lindskog, M., Li, L., Groth, R. D., Poburko, D., Thiagarajan, T. C., Han, X., & Tsien, R. W. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1016399107 · Cited by 70
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Whitt, J. L., Petrus, E., & Lee, H. (2013) · Neuropharmacology · doi:10.1016/j.neuropharm.2013.02.016 · Cited by 70
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Mishima, T., Nagai, T., Yahagi, K., Akther, S., Oe, Y., Monai, H., Kohsaka, S., & Hirase, H. (2019) · eNeuro · doi:10.1523/eneuro.0204-19.2019 · Cited by 70
Yahfoufi, N., Matar, C., & Ismail, N. (2020) · The Journals of Gerontology Series A · doi:10.1093/gerona/glaa006 · Cited by 70
Diamond, B., Huerta, P. T., Tracey, K., & Volpe, B. T. (2011) · BioEssays · doi:10.1002/bies.201100042 · Cited by 69
Bradesi, S., Svensson, C. I., Steinauer, J., Pothoulakis, C., Yaksh, T. L., & Mayer, E. A. (2009) · Gastroenterology · doi:10.1053/j.gastro.2008.12.044 · Cited by 69
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Youn, D., Wang, H., & Jeong, S. (2008) · Journal of Neuroscience Research · doi:10.1002/jnr.21726 · Cited by 69
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Metadata
- Authors
- Stellwagen, D., & Malenka, R. C.
- Affiliations
- Stanford Medicine (US)
- Corresponding author
- Malenka, Robert C.
- Venue
- Nature
- Published
- 2006-04-01
- Volume
- 440
- Issue
- 7087
- Pages
- 1054-1059
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- OpenAlex
- W1542136448
- Cited by
- 1,715
- References
- 31
- Citations by year
- 2026: 73 · 2025: 66 · 2024: 72 · 2023: 70 · 2022: 102 · 2021: 102 · 2020: 117 · 2019: 80 · 2018: 87 · 2017: 94 · 2016: 80 · 2015: 92 · 2014: 92 · 2013: 104 · 2012: 103
- FWCI
- 27.28
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- Funders
- National Institutes of Health
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Keywords
- synaptic scaling, homeostatic plasticity, TNF-α, neuron-glia interactions, long-term potentiation, long-term depression, neural network stability
- MeSH terms
- Animals, Hippocampus, Nerve Net, Neuroglia, Neurons, Synapses, Tetrodotoxin, Tumor Necrosis Factor-alpha, Signal Transduction, Rats, Sprague-Dawley, Long-Term Potentiation, Receptors, AMPA, Receptors, Tumor Necrosis Factor, Excitatory Postsynaptic Potentials, Long-Term Synaptic Depression, Mice, Rats
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