The DOI matches its Crossref record; 128 of the 129 references it cites were found in a registry or an index.
Cellular Specificity of NF-κB Function in the Nervous System
Open accessAbstract
Nuclear Factor Kappa B (NF-κB) is a ubiquitously expressed transcription factor with key functions in a wide array of biological systems. While the role of NF-κB in processes, such as host immunity and oncogenesis has been more clearly defined, an understanding of the basic functions of NF-κB in the nervous system has lagged behind. The vast cell-type heterogeneity within the central nervous system (CNS) and the interplay between cell-type specific roles of NF-κB contributes to the complexity of understanding NF-κB functions in the brain. In this review, we will focus on the emerging understanding of cell-autonomous regulation of NF-κB signaling as well as the non-cell-autonomous functional impacts of NF-κB activation in the mammalian nervous system. We will focus on recent work which is unlocking the pleiotropic roles of NF-κB in neurons and glial cells (including astrocytes and microglia). Normal physiology as well as disorders of the CNS in which NF-κB signaling has been implicated will be discussed with reference to the lens of cell-type specific responses.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
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
“Activation of NFκB by inflammatory stimuli is mediated by phosphorylation and ubiquitin-mediated degradation of IκB which disinhibits NFκB, allowing for nuclear translocation to target genes and activation of transcription [140].”
From ROS Generation in Microglia: Understanding Oxidative Stress and Inflammation in Neurodegenerative Disease (2020) · cites this paper as [140]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
A Unique Microglia Type Associated with Restricting Development of Alzheimer’s Disease
Keren-Shaul, H., Spinrad, A., Weiner, A., Matcovitch-Natan, O., Dvir-Szternfeld, R., Ulland, T. K., David, E., Baruch, K., Lara-Astaiso, D., Toth, B., et al. (2017) · Cell · doi:10.1016/j.cell.2017.05.018 · Cited by 5,493
Dauer, W., & Przedborski, S. (2003) · Neuron · doi:10.1016/s0896-6273(03)00568-3 · Cited by 5,469
Shared Principles in NF-κB Signaling
Hayden, M. S., & Ghosh, S. (2008) · Cell · doi:10.1016/j.cell.2008.01.020 · Cited by 4,954
Microglia-mediated neurotoxicity: uncovering the molecular mechanisms
Block, M. L., Zecca, L., & Hong, J.-S. (2007) · Nature Reviews Neuroscience · doi:10.1038/nrn2038 · Cited by 4,110
Complement and microglia mediate early synapse loss in Alzheimer mouse models
Hong, S., Beja-Glasser, V. F., Nfonoyim, B. M., Frouin, A., Li, S., Ramakrishnan, S., Merry, K. M., Shi, Q., Rosenthal, A., Barres, B. A., et al. (2016) · Science · doi:10.1126/science.aad8373 · Cited by 3,343 · cited 1×
“Since microglia are active participants in the formation, remodeling, and elimination of synapses, this research may also shed light on the mechanisms which underlie synapse loss in AD (93, 94).”
BackgroundTREM2 Variants in Alzheimer's Disease
Guerreiro, R., Wojtas, A., Bras, J., Carrasquillo, M., Rogaeva, E., Majounie, E., Cruchaga, C., Sassi, C., Kauwe, J. S. K., Younkin, S., et al. (2013) · New England Journal of Medicine · doi:10.1056/nejmoa1211851 · Cited by 3,020
Wang, C.-Y., Mayo, M., Korneluk, R., Goeddel, D., & Baldwin, A. (1998) · Science · doi:10.1126/science.281.5383.1680 · Cited by 2,950
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
Suppression of TNF-α-Induced Apoptosis by NF-κB
Antwerp, D. J. V., Martin, S. J., Kafri, T., Green, D. R., & Verma, I. M. (1996) · Science · doi:10.1126/science.274.5288.787 · Cited by 2,581
Molecular Architecture of the Mouse Nervous System
Zeisel, A., Hochgerner, H., Lönnerberg, P., Johnsson, A., Memic, F., van der Zwan, J., Häring, M., Braun, E., Borm, L. E., La Manno, G., et al. (2018) · Cell · doi:10.1016/j.cell.2018.06.021 · Cited by 2,552
The Cellular Phase of Alzheimer’s Disease
De Strooper, B., & Karran, E. (2016) · Cell · doi:10.1016/j.cell.2015.12.056 · Cited by 1,990
30 Years of NF-κB: A Blossoming of Relevance to Human Pathobiology
Zhang, Q., Lenardo, M. J., & Baltimore, D. (2017) · Cell · doi:10.1016/j.cell.2016.12.012 · Cited by 1,979
Drosophila pink1 is required for mitochondrial function and interacts genetically with parkin
Clark, I. E., Dodson, M. W., Jiang, C., Cao, J. H., Huh, J. R., Seol, J. H., Yoo, S. J., Hay, B. A., & Guo, M. (2006) · Nature · doi:10.1038/nature04779 · Cited by 1,788
Mitochondrial dysfunction in Drosophila PINK1 mutants is complemented by parkin
Park, J., Lee, S. B., Lee, S., Kim, Y., Song, S., Kim, S., Bae, E., Kim, J., Shong, M., Kim, J.-M., et al. (2006) · Nature · doi:10.1038/nature04788 · Cited by 1,705
NF-κB, the first quarter-century: remarkable progress and outstanding questions
Hayden, M. S., & Ghosh, S. (2012) · Genes & Development · doi:10.1101/gad.183434.111 · Cited by 1,693
Bates, G. P., Dorsey, R., Gusella, J. F., Hayden, M. R., Kay, C., Leavitt, B. R., Nance, M., Ross, C. A., Scahill, R. I., Wetzel, R., et al. (2015) · Nature Reviews Disease Primers · doi:10.1038/nrdp.2015.5 · Cited by 1,641
Mutations of optineurin in amyotrophic lateral sclerosis
Maruyama, H., Morino, H., Ito, H., Izumi, Y., Kato, H., Watanabe, Y., Kinoshita, Y., Kamada, M., Nodera, H., Suzuki, H., et al. (2010) · Nature · doi:10.1038/nature08971 · Cited by 1,265
TREM2 Maintains Microglial Metabolic Fitness in Alzheimer’s Disease
Ulland, T. K., Song, W. M., Huang, S. C.-C., Ulrich, J. D., Sergushichev, A., Beatty, W. L., Loboda, A. A., Zhou, Y., Cairns, N. J., Kambal, A., et al. (2017) · Cell · doi:10.1016/j.cell.2017.07.023 · Cited by 1,263 · cited 1×
“Findings of this study are inline with a second recent report, from different investigators, which showed that TREM2 intracellular signaling functions to maintain the metabolic fitness and phagocytic responses of microglia operating to defend the brain in AD (91, 92).”
ResultGauthier, L. R., Charrin, B. C., Borrell-Pagès, M., Dompierre, J. P., Rangone, H., Cordelières, F. P., De Mey, J., MacDonald, M. E., Leßmann, V., Humbert, S., et al. (2004) · Cell · doi:10.1016/j.cell.2004.06.018 · Cited by 1,178
NF-kappaB Signaling Pathways in Neurological Inflammation: A Mini Review
Shih, R., Wang, C.-Y., & Yang, C. (2015) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2015.00077 · Cited by 935
Yang, Y., Gehrke, S., Imai, Y., Huang, Z., Ouyang, Y., Wang, J.-W., Yang, L., Beal, M. F., Vogel, H., & Lu, B. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0602493103 · Cited by 798
The Rel/NF-κB Family Directly Activates Expression of the Apoptosis Inhibitor Bcl-x L
Chen, C., Edelstein, L. C., & Gélinas, C. (2000) · Molecular and Cellular Biology · doi:10.1128/mcb.20.8.2687-2695.2000 · Cited by 760
Zong, W.-X., Edelstein, L., Chen, C.-L., Bash, J., & Gélinas, C. (1999) · Genes & Development · doi:10.1101/gad.13.4.382 · Cited by 738
NF-κB functions in synaptic signaling and behavior
Meffert, M. K., Chang, J. M., Wiltgen, B. J., Fanselow, M. S., & Baltimore, D. (2003) · Nature Neuroscience · doi:10.1038/nn1110 · Cited by 691
Self-citationHunot, S., Brugg, B., Ricard, D., Michel, P. P., Muriel, M., Ruberg, M., Faucheux, B. A., Agid, Y., & Hirsch, É. C. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.14.7531 · Cited by 678
Microglia contact induces synapse formation in developing somatosensory cortex
Miyamoto, A., Wake, H., Ishikawa, A. W., Eto, K., Shibata, K., Murakoshi, H., Koizumi, S., Moorhouse, A. J., Yoshimura, Y., & Nabekura, J. (2016) · Nature Communications · doi:10.1038/ncomms12540 · Cited by 649
Microglia Induce Motor Neuron Death via the Classical NF-κB Pathway in Amyotrophic Lateral Sclerosis
Frakes, A. E., Ferraiuolo, L., Haidet-Phillips, A. M., Schmelzer, L., Braun, L., Miranda, C. J., Ladner, K. J., Bevan, A. K., Foust, K. D., Godbout, J. P., et al. (2014) · Neuron · doi:10.1016/j.neuron.2014.01.013 · Cited by 638
Brambilla, R., Bracchi-Ricard, V. C., Hu, W.-H., Frydel, B. R., Bramwell, A., Karmally, S., Green, E. J., & Bethea, J. R. (2005) · The Journal of Experimental Medicine · doi:10.1084/jem.20041918 · Cited by 607
Wang, C.-Y., Guttridge, D. C., Mayo, M. W., & Baldwin, A. S. (1999) · Molecular and Cellular Biology · doi:10.1128/mcb.19.9.5923 · Cited by 594
Tamatani, M., Ho, Y., Matsuzaki, H., Ogawa, S., Okado, H., Miyake, S., Mizuno, T., & Tohyama, M. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.13.8531 · Cited by 549
Mutant huntingtin impairs axonal trafficking in mammalian neurons in vivo and in vitro
Trushina, E., Dyer, R. B., Badger, J. D., Ure, D., Eide, L., Tran, D. D., Vrieze, B. T., Legendre-Guillemin, V., McPherson, P. S., Mandavilli, B. S., et al. (2004) · Molecular and Cellular Biology · doi:10.1128/mcb.24.18.8195-8209.2004 · Cited by 520
Srinivasan, R., Lu, T.-Y., Chai, H., Xu, J., Huang, B. S., Golshani, P., Coppola, G., & Khakh, B. S. (2016) · Neuron · doi:10.1016/j.neuron.2016.11.030 · Cited by 443
Ghosh, A., Roy, A., Liu, X., Kordower, J. H., Mufson, E. J., Hartley, D. M., Ghosh, S., Mosley, R. L., Gendelman, H. E., & Pahan, K. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0704908104 · Cited by 438
TREM2 variants: new keys to decipher Alzheimer disease pathogenesis
Colonna, M., & Wang, Y. (2016) · Nature Reviews Neuroscience · doi:10.1038/nrn.2016.7 · Cited by 418
Grumont, R. J., Rourke, I. J., & Gerondakis, S. (1999) · Genes & Development · doi:10.1101/gad.13.4.400 · Cited by 403
Swarup, V., Phaneuf, D., Dupré, N., Petri, S., Strong, M. J., Križ, J., & Julien, J. (2011) · The Journal of Experimental Medicine · doi:10.1084/jem.20111313 · Cited by 346
Huntingtin facilitates dynein/dynactin-mediated vesicle transport
Caviston, J. P., Ross, J. L., Antony, S. M., Tokito, M. K., & Holzbaur, E. L. F. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0610628104 · Cited by 334
Genes associated with Alzheimer's disease: an overview and current status
Giri, M., Lü, Y., & Zhang, M. (2016) · Clinical Interventions in Aging · doi:10.2147/cia.s105769 · Cited by 311
Constitutive Nuclear Factor-κB Activity Is Required for Central Neuron Survival
Bhakar, A. L., Tannis, L.-L., Zeindler, C., Russo, M. P., Jobin, C., Park, D. S., MacPherson, S., & Barker, P. A. (2002) · The Journal of Neuroscience · doi:10.1523/jneurosci.22-19-08466.2002 · Cited by 310
Kaltschmidt, C., Kaltschmidt, B., & Baeuerle, P. A. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.21.9618 · Cited by 303
Physiological functions for brain NF-κB
Meffert, M. K., & Baltimore, D. (2004) · Trends in Neurosciences · doi:10.1016/j.tins.2004.11.002 · Cited by 298
Self-citationSynaptic activation of NF-kappa B by glutamate in cerebellar granule neurons in vitro.
Guerrini, L., Blasi, F., & Denis‐Donini, S. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.20.9077 · Cited by 287
From Calcium to NF-κB Signaling Pathways in Neurons
Lilienbaum, A., & Israël, A. (2003) · Molecular and Cellular Biology · doi:10.1128/mcb.23.8.2680-2698.2003 · Cited by 254
Hsiao, H., Chen, Y., Chen, H., Tu, P., & Chern, Y. (2013) · Human Molecular Genetics · doi:10.1093/hmg/ddt036 · Cited by 242
The IκB Kinase Regulates Chromatin Structure during Reconsolidation of Conditioned Fear Memories
Lubin, F. D., & Sweatt, J. D. (2007) · Neuron · doi:10.1016/j.neuron.2007.07.039 · Cited by 241
Kaltschmidt, B., Ndiaye‐Lobry, D., Körte, M., Pothion, S., Arbibe, L., Prüllage, M., Pfeiffer, J., Lindecke, A., Staiger, V., Israël, A., et al. (2006) · Molecular and Cellular Biology · doi:10.1128/mcb.26.8.2936-2946.2006 · Cited by 230
NF-κB activity in transgenic mice: developmental regulation and tissue specificity
Schmidt‐Ullrich, R., Mémet, S., Lilienbaum, A., Feuillard, J., Raphaël, M., & Israël, A. (1996) · Development · doi:10.1242/dev.122.7.2117 · Cited by 227
A20 critically controls microglia activation and inhibits inflammasome-dependent neuroinflammation
Voet, S., Mc Guire, C., Hagemeyer, N., Martens, A., Schroeder, A., Wieghofer, P., Daems, C., Staszewski, O., Vande Walle, L., Jordao, M. J. C., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-04376-5 · Cited by 227
Khoshnan, A., Ko, J., Watkin, E. E., Paige, L. A., Reinhart, P. H., & Patterson, P. H. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.2675-04.2004 · Cited by 223
Brain synapses contain inducible forms of the transcription factor NF-κB
Kaltschmidt, C., Kaltschmidt, B., & Baeuerle, P. A. (1993) · Mechanisms of Development · doi:10.1016/0925-4773(93)90031-r · Cited by 221
Rojo, A. I., Salinas, M., Martı́n, D., Perona, R., & Cuadrado, A. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.2111-04.2004 · Cited by 216
Gene expression of the transcription factor NF-κ B in hippocampus: regulation by synaptic activity
Meberg, P. J., Kinney, W. R., Valcourt, E. G., & Routtenberg, A. (1996) · Molecular Brain Research · doi:10.1016/0169-328x(95)00229-l · Cited by 215
Sha, D., Chin, L., & Li, L. (2009) · Human Molecular Genetics · doi:10.1093/hmg/ddp501 · Cited by 187
Ling, H., Gray, C. B. B., Zambon, A. C., Grimm, M. F., Gu, Y., Dalton, N. D., Purcell, N. H., Peterson, K. L., & Brown, J. H. (2013) · Circulation Research · doi:10.1161/circresaha.112.276915 · Cited by 184
Takano, H., & Gusella, J. F. (2002) · BMC Neuroscience · doi:10.1186/1471-2202-3-15 · Cited by 179
Levenson, J. M., Choi, S., Lee, S.-Y., Cao, Y. A., Ahn, H. J., Worley, K. C., Pizzi, M., Liou, H.-C., & Sweatt, J. D. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.5646-03.2004 · Cited by 175
Parkin Mediates Neuroprotection through Activation of IκB Kinase/Nuclear Factor-κB Signaling
Henn, I. H., Bouman, L., Schlehe, J. S., Schlierf, A., Schramm, J. E., Wegener, E., Nakaso, K., Culmsee, C., Berninger, B., Krappmann, D., et al. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.5537-06.2007 · Cited by 173
A Requirement for Nuclear Factor-κB in Developmental and Plasticity-Associated Synaptogenesis
Boersma, M. C. H., Dresselhaus, E. C., De Biase, L. M., Mihalas, A. B., Bergles, D. E., & Meffert, M. K. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.2456-10.2011 · Cited by 168
Self-citationFridmacher, V., Kaltschmidt, B., Goudeau, B., Ndiaye, D., Rossi, F. M., Pfeiffer, J., Kaltschmidt, C., Israël, A., & Mémet, S. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-28-09403.2003 · Cited by 167
NF‐κB activation in astrocytes drives a stage‐specific beneficial neuroimmunological response in ALS
Alami, N. O., Schurr, C., Heuvel, F. O., Tang, L., Li, Q., Tasdogan, A., Kimbara, A., Nettekoven, M. H., Ottaviani, G., Raposo, C., et al. (2018) · The EMBO Journal · doi:10.15252/embj.201798697 · Cited by 164
Zhang, Y., Reichel, J. M., Han, C., Zuniga-Hertz, J. P., & Cai, D. (2017) · Cell Metabolism · doi:10.1016/j.cmet.2017.04.002 · Cited by 162
Neuronal Gene Targets of NF-κB and Their Dysregulation in Alzheimer's Disease
Snow, W. M., & Albensi, B. C. (2016) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2016.00118 · Cited by 161
Role of microglial IKKβ in kainic acid-induced hippocampal neuronal cell death
Cho, I., Hong, J., Suh, E. C., Kim, J. H., Lee, H., Lee, J. E., Lee, S., Kim, C., Kim, D. W., Jo, E., et al. (2008) · Brain · doi:10.1093/brain/awn230 · Cited by 156
Ahn, H. J., Hernandez, C. M., Levenson, J. M., Lubin, F. D., Liou, H.-C., & Sweatt, J. D. (2008) · Learning & Memory · doi:10.1101/lm.866408 · Cited by 149
Carrasco, D. R., Ryseck, R.-P., & Bravo, R. (1993) · Development · doi:10.1242/dev.118.4.1221 · Cited by 148
Simmons, L. J., Surles-Zeigler, M. C., Li, Y., Ford, G. D., Newman, G. W., & Ford, B. D. (2016) · Journal of Neuroinflammation · doi:10.1186/s12974-016-0703-7 · Cited by 144
Schmeißer, M. J., Baumann, B., Johannsen, S., Vindedal, G. F., Jensen, V., Hvalby, Ø., Sprengel, R., Seither, J., Maqbool, A., Magnutzki, A., et al. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.0111-12.2012 · Cited by 137
REGISTRY Investigators of the European Huntington's Disease Network, Bečanović, K., Nørremølle, A., Neal, S. J., Kay, C., Collins, J. A., Arenillas, D., Lilja, T., Gaudenzi, G., Manoharan, S., et al. (2015) · Nature Neuroscience · doi:10.1038/nn.4014 · Cited by 135
Yabe, T., Wilson, D., & Schwartz, J. P. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m107831200 · Cited by 134
Brambilla, R., Hurtado, A., Persaud, T., Esham, K., Pearse, D. D., Oudega, M., & Bethea, J. R. (2009) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2009.06190.x · Cited by 131
Jones, S. V., & Kounatidis, I. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.01805 · Cited by 131
Chami, L., Buggia-Prévot, V., Duplan, E., Delprete, D., Chami, M., Peyron, J., & Checler, F. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.333054 · Cited by 123
NF-KappaB in Long-Term Memory and Structural Plasticity in the Adult Mammalian Brain
Kaltschmidt, B., & Kaltschmidt, C. (2015) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2015.00069 · Cited by 121
Regulation of Nuclear Factor κB in the Hippocampus by Group I Metabotropic Glutamate Receptors
O’Riordan, K. J., Huang, I.-C., Pizzi, M., Spano, P., Boroni, F., Egli, R. E., Desai, P., Fitch, O., Malone, L. M., Ahn, H. J., et al. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.4527-05.2006 · Cited by 113
NF-κB/Rel Regulates Inhibitory and Excitatory Neuronal Function and Synaptic Plasticity
O'Mahony, A., Raber, J., Montano, M., Foehr, E., Han, V., Lu, S.-M., Kwon, H., LeFevour, A., Chakraborty-Sett, S., & Greene, W. C. (2006) · Molecular and Cellular Biology · doi:10.1128/mcb.00510-06 · Cited by 110
Mikenberg, I., Widera, D., Kaus, A., Kaltschmidt, B., & Kaltschmidt, C. (2007) · PLoS ONE · doi:10.1371/journal.pone.0000589 · Cited by 107
Hughes, K. A., Edin, S., Antonsson, Å., & Grundström, T. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m106125200 · Cited by 107
Kassed, C. A., Willing, A. E., Garbuzova-Davis, S., Sanberg, P. R., & Pennypacker, K. R. (2002) · Experimental Neurology · doi:10.1006/exnr.2002.7967 · Cited by 103
Microglia: Phagocytosing to Clear, Sculpt, and Eliminate
Hong, S. Y., & Stevens, B. (2016) · Developmental Cell · doi:10.1016/j.devcel.2016.07.006 · Cited by 102
Pizzi, M., Sarnico, I., Boroni, F., Benarese, M., Steimberg, N., Mazzoleni, G., Dietz, G. P. H., Bähr, M., Liou, H.-C., & Spano, P. (2005) · Cell Death and Differentiation · doi:10.1038/sj.cdd.4401598 · Cited by 100
Kassed, C. A., & Herkenham, M. A. (2004) · Behavioural Brain Research · doi:10.1016/j.bbr.2004.03.026 · Cited by 99
Marcora, E. M., & Kennedy, M. B. (2010) · Human Molecular Genetics · doi:10.1093/hmg/ddq358 · Cited by 99
Brambilla, R., Dvoriantchikova, G., Barakat, D. J., Ivanov, D., Bethea, J. R., & Shestopalov, V. I. (2012) · Journal of Neuroinflammation · doi:10.1186/1742-2094-9-213 · Cited by 98
Ghosh, M., Yang, Y., Rothstein, J. D., & Robinson, M. B. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.0302-11.2011 · Cited by 97
Tanji, K., Kamitani, T., Mori, F., Kakita, A., Takahashi, H., & Wakabayashi, K. (2010) · Neurobiology of Disease · doi:10.1016/j.nbd.2010.01.007 · Cited by 97
Shrum, C. K., DeFrancisco, D., & Meffert, M. K. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0806677106 · Cited by 95
Self-citationNuclear Factor Kappa B Signaling Initiates Early Differentiation of Neural Stem Cells
Zhang, Y., Liu, J., Yao, S., Li, F., Xin, L., Lai, M., Bracchi-Ricard, V. C., Xu, H., Yen, W., Meng, W., et al. (2011) · Stem Cells · doi:10.1002/stem.1006 · Cited by 91
Late-onset Parkinsonism in NF B/c-Rel-deficient mice
Baiguera, C., Alghisi, M., Pinna, A., Bellucci, A., Luca, M. A. D., Frau, L., Morelli, M., Ingrassia, R., Benarese, M., Porrini, V., et al. (2012) · Brain · doi:10.1093/brain/aws193 · Cited by 86
Wang, H., Li, Y., Ryder, J. W., Hole, J. T., Ebert, P. J., Airey, D. C., Qian, H.-R., Logsdon, B., Fisher, A., Ahmed, Z., et al. (2018) · Molecular Neurodegeneration · doi:10.1186/s13024-018-0296-y · Cited by 83
Bellucci, A., Bubacco, L., Longhena, F., Parrella, E., Faustini, G., Porrini, V., Bono, F., Missale, C., & Pizzi, M. (2020) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2020.00068 · Cited by 82
Cherry, E. M., Lee, D. W., Jung, J.-U., & Sitcheran, R. (2015) · Molecular Cancer · doi:10.1186/s12943-014-0273-1 · Cited by 78
IKK2/NF‐κB signaling protects neurons after traumatic brain injury
Mettang, M., Reichel, S. N., Lattke, M., Palmer, A., Abaei, A., Rasche, V., Huber-Lang, M. S., Baumann, B., & Wirth, T. (2017) · The FASEB Journal · doi:10.1096/fj.201700826r · Cited by 78
Neidl, R., Schneider‐Anthony, A., Bousiges, O., Majchrzak, M. J., Barbelivien, A., de Vasconcelos, A. P., Dorgans, K., Doussau, F., Loeffler, J., Cassel, J., et al. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.3239-15.2016 · Cited by 77
Lahiri, D. K. (2004) · Journal of Molecular Neuroscience · doi:10.1385/jmn:23:3:225 · Cited by 71
TRIM9-Mediated Resolution of Neuroinflammation Confers Neuroprotection upon Ischemic Stroke in Mice
Zeng, J., Wang, Y., Luo, Z., Chang, L.-C., Yoo, J., Yan, H., Choi, Y., Xie, X., Deverman, B. E., Gradinaru, V., et al. (2019) · Cell Reports · doi:10.1016/j.celrep.2018.12.055 · Cited by 65
Divergent Neuroinflammatory Regulation of Microglial TREM Expression and Involvement of NF-κB
Owens, R., Grabert, K., Davies, C. L., Alfieri, A., Antel, J. P., Healy, L. M., & McColl, B. W. (2017) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2017.00056 · Cited by 62
Astroglial nuclear factor‐κB regulates learning and memory and synaptic plasticity in female mice
Bracchi-Ricard, V. C., Brambilla, R., Levenson, J. M., Hu, W., Bramwell, A., Sweatt, J. D., Green, E. J., & Bethea, J. R. (2007) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2007.04993.x · Cited by 59
NF-κB p50 subunit knockout impairs late LTP and alters long term memory in the mouse hippocampus
Oikawa, K., Odero, G. L., Platt, E., Neuendorff, M., Hatherell, A., Bernstein, M. J., & Albensi, B. C. (2012) · BMC Neuroscience · doi:10.1186/1471-2202-13-45 · Cited by 55
Kainate receptors activate NF-κB via MAP kinase in striatal neurones
Cruise, L., Ho, L. K., Veitch, K., Fuller, G. W., & MORRIS, B. J. (2000) · Neuroreport · doi:10.1097/00001756-200002070-00034 · Cited by 47
Kyrargyri, V., Vega‐Flores, G., Gruart, A., Delgado-Garcia, J. M., & Probert, L. (2014) · Glia · doi:10.1002/glia.22756 · Cited by 44
Glutamate-Dependent Activation of NF-κB During Mouse Cerebellum Development
Guerrini, L., Molteni, A., Wirth, T. C., Kistler, B., & Blasi, F. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-16-06057.1997 · Cited by 42
CaMKIIδ interacts directly with IKKβ and modulates NF-κB signalling in adult cardiac fibroblasts
Martin, T. P., McCluskey, C., Cunningham, M., Beattie, J., Paul, A., & Currie, S. (2018) · Cellular Signalling · doi:10.1016/j.cellsig.2018.07.008 · Cited by 39
Targeting of NF-κB to Dendritic Spines Is Required for Synaptic Signaling and Spine Development
Dresselhaus, E. C., Boersma, M. C. H., & Meffert, M. K. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.2663-16.2018 · Cited by 34
Self-citationSynaptically Localized Transcriptional Regulators in Memory Formation
Uchida, S., & Shumyatsky, G. P. (2017) · Neuroscience · doi:10.1016/j.neuroscience.2017.07.023 · Cited by 33
Kiebala, M., Polesskaya, O., Yao, Z., Perry, S. W., & Maggirwar, S. B. (2010) · PLoS ONE · doi:10.1371/journal.pone.0011875 · Cited by 32
NF-κB transcription factor role in consolidation and reconsolidation of persistent memories
de la Fuente, V., Federman, N., Zalcman, G., Salles, A., Freudenthal, R., & Romano, A. G. (2015) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2015.00050 · Cited by 31
Mincheva-Tasheva, S., Garcerá, A., Gou-Fàbregas, M., Encinas, M., Dolcet, X., & Soler, R. M. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.0206-11.2011 · Cited by 31
Ramis, M. R., Sarubbo, F., Tejada, S., Jiménez-García, M., Esteban, S., Miralles, A., & Moranta, D. (2020) · Nutrients · doi:10.3390/nu12020326 · Cited by 31
Glutamate-Induced NFκB Activation in the Retina
Fan, W., & Cooper, N. G. F. (2009) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.08-2555 · Cited by 29
Du, Y.-S., Chen, X., Wei, X.-L., Bales, K., Berg, D., Paul, S., Farlow, M., Maloney, B., Ge, Y.-W., & Lahiri, D. (2005) · Molecular Brain Research · doi:10.1016/j.molbrainres.2005.02.001 · Cited by 28
Essential Role for Epidermal Growth Factor Receptor in Glutamate Receptor Signaling to NF-κB
Sitcheran, R., Comb, W. C., Cogswell, P. C., & Baldwin, A. S. (2008) · Molecular and Cellular Biology · doi:10.1128/mcb.00578-08 · Cited by 28
Sun, J., Huang, P., Liang, J., Li, J., Shen, M., She, X., Feng, Y., Luo, X., Liu, T., & Sun, X. (2017) · Cell Death and Disease · doi:10.1038/cddis.2017.502 · Cited by 28
RelB controls adaptive responses of astrocytes during sterile inflammation
Gupta, A. S., Waters, M. R., Biswas, D. D., Brown, L. N., Surace, M. J., Floros, C., Siebenlist, U. K., & Kordula, T. (2019) · Glia · doi:10.1002/glia.23619 · Cited by 28
Mihalas, A. B., Araki, Y., Huganir, R. L., & Meffert, M. K. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.2131-13.2013 · Cited by 27
Self-citationArivazhagan, L., Ruiz, H. H., Wilson, R. A., Manigrasso, M. B., Gugger, P. F., Fisher, E. A. A., Moore, K. J., Ramasamy, R., & Schmidt, A. M. (2020) · Circulation Research · doi:10.1161/circresaha.120.315900 · Cited by 25
Deng, F., Cai, L., Zhou, B., Zhou, Z., & Xu, G. (2020) · 3 Biotech · doi:10.1007/s13205-020-02190-9 · Cited by 24
Tanaka, Y., Sabharwal, L., Ota, M., Nakagawa, I., Jiang, J., Arima, Y., Ogura, H., Okochi, M., Ishii, M., Kamimura, D., et al. (2018) · The Journal of Immunology · doi:10.4049/jimmunol.1701446 · Cited by 22
Caccamo, D., Campisi, A., Marini, H. R., Adamo, E. B., Volti, G. L., Squadrito, F., & Ientile, R. (2005) · Experimental Neurology · doi:10.1016/j.expneurol.2005.01.014 · Cited by 21
Xiao, X., Putatunda, R., Zhang, Y., Soni, P. V., Li, F., Zhang, T., Xin, M., Luo, J. J., Bethea, J. R., Cheng, Y. Z., et al. (2018) · Journal of Neuroinflammation · doi:10.1186/s12974-018-1074-z · Cited by 20
Li, Y.-K., Li, C., Sun, L., Chu, G., Li, J., Chen, F., Li, G., & Zhao, Y. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2013.06.030 · Cited by 19
Salles, A., Boccia, M. M., Blake, M. G., Corbi, N., Passananti, C., Baratti, C. M., Romano, A. G., & Freudenthal, R. (2015) · Neuroscience · doi:10.1016/j.neuroscience.2015.01.063 · Cited by 17
Sancho‐Balsells, A., Brito, V., Fernández, B., Pardo, M., Straccia, M., Ginés, S., Alberch, J., Hernández, I., Arranz, B., Canals, J. M., et al. (2020) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2020.00093 · Cited by 14
TREM2: Keeping Microglia Fit during Good Times and Bad
Hong, S. Y., & Stevens, B. (2017) · Cell Metabolism · doi:10.1016/j.cmet.2017.09.010 · Cited by 13
NF-κB regulates neuronal ankyrin-G via a negative feedback loop
König, H., Schwamborn, R., Andresen, S., Kinsella, S. M., Watters, O., Fenner, B. J., & Prehn, J. H. M. (2017) · Scientific Reports · doi:10.1038/srep42006 · Cited by 10
Widera, D., Klenke, C., Nair, D. K., Heidbreder, M., Malkusch, S., Sibarita, J., Choquet, D., Kaltschmidt, B., Heilemann, M., & Kaltschmidt, C. (2016) · Neurophotonics · doi:10.1117/1.nph.3.4.041804 · Cited by 9
IKK Kinase Assay for Assessment of Canonical NF-κB Activation in Neurons
Mihalas, A. B., & Meffert, M. K. (2015) · Methods in molecular biology · doi:10.1007/978-1-4939-2422-6_5 · Cited by 8
Self-citationThe NF-κB Family in Learning and Memory
Shrum, C. K., & Meffert, M. K. (2008) · Elsevier eBooks · doi:10.1016/b978-012370509-9.00031-0 · Cited by 5
Self-citationKumar, A., & Thakur, M. K. (2016) · Neuroscience Letters · doi:10.1016/j.neulet.2016.05.013 · Cited by 5
Cited by
Sorted by citations
Simpson, D. S. A., & Oliver, P. L. (2020) · Antioxidants · doi:10.3390/antiox9080743 · Cited by 1,044
The Nuclear Factor Kappa B (NF-kB) signaling in cancer development and immune diseases
Zinatizadeh, M. R., Schock, B. C., Chalbatani, G. M., Zarandi, P. K., Jalali, S. A., & Miri, S. R. (2020) · Genes & Diseases · doi:10.1016/j.gendis.2020.06.005 · Cited by 568
Microglial NF-κB drives tau spreading and toxicity in a mouse model of tauopathy
Wang, C., Fan, L., Khawaja, R. R., Liu, B., Zhan, L., Kodama, L., Chin, M., Li, Y., Le, D., Zhou, Y., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-29552-6 · Cited by 333
Singh, S., & Singh, T. G. (2020) · Current Neuropharmacology · doi:10.2174/1570159x18666200207120949 · Cited by 307
Pouyan, A., Ghorbanlo, M., Eslami, M., Jahanshahi, M., Ziaei, E., Salami, A., Mokhtari, K., Shahpasand, K., Farahani, N., Meybodi, T. E., et al. (2025) · Molecular Cancer · doi:10.1186/s12943-025-02267-0 · Cited by 338
Metadata
- Authors
- Dresselhaus, E. C., & Meffert, M. K.
- Affiliations
- Johns Hopkins University (US)
- Corresponding author
- Meffert, Mollie K.
- Venue
- Frontiers in Immunology
- Publisher
- Frontiers Media SA
- Published
- 2019-05-09
- Volume
- 10
- Pages
- 1043-1043
- ISSN
- 1664-3224 (ISSN-L)
- PMC
- PMC6520659
- OpenAlex
- W2944682402
- Cited by
- 345
- References
- 129
- Citations by year
- 2026: 37 · 2025: 46 · 2024: 54 · 2023: 48 · 2022: 54 · 2021: 58 · 2020: 45 · 2019: 2
- FWCI
- 3.88
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Frontiers in Immunology (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- National Institutes of Health
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › NF-κB Signaling Pathways
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Keywords
- NF-κB, nervous system, cell type specificity, central nervous system, neurons, glial cells, astrocytes, microglia, cell-autonomous signaling, non-cell-autonomous signaling, central nervous system disorders, neuroinflammation
- MeSH terms
- Animals, Central Nervous System, Humans, Nervous System, Neuroglia, Neurons, Organ Specificity, Signal Transduction, NF-kappa B, Microglia
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