TGFβ produced by IL‐10 redirected astrocytes attenuates microglial activation
Open accessAbstract
While there clearly is an intimate relationship between astrocytes and microglia, few studies have examined these potentially dynamic interactions. In this study, cytokine‐mediated communication between microglia and astrocytes under inflammatory conditions was investigated. We have previously shown that activated microglia produce Interleukin (IL)‐10, a regulatory cytokine that plays an important role in resolving neuroinflammation. Nonetheless, the mechanism by which IL‐10 attenuates pro‐inflammatory cytokine expression in the brain is unclear. Here, we show that IL‐10 redirected astrocytes regulate the activation of microglia in a transforming growth factor (TGF)‐β dependent manner. In support of this concept, astrocytes in the brain maintained higher IL‐10 receptor (IL‐10R1) expression and primary astrocytes in culture were markedly more sensitive to the anti‐inflammatory effects of IL‐10 compared with microglia. Moreover, studies using primary cultures and an astrocyte‐microglia coculture system revealed that astrocytes mediated the anti‐inflammatory effects of IL‐10 on microglia through the production of TGFβ. For instance, only when astrocytes were present did IL‐10 stimulation reduce the expression of IL‐1β and increase expression of anti‐inflammatory mediators fractalkine receptor (CX 3 CR1) and interleukin 4 receptor‐α (IL‐4Rα) in microglia. Importantly, these IL‐10‐astrocyte dependent effects on microglia were blocked by a TGFβ inhibitor. Furthermore, inhibition of TGFβ signaling in the brain resulted in prolonged sickness behavior and amplified pro‐inflammatory cytokine expression in mice challenged with lipopolysaccharide. Taken together, IL‐10 stimulated the production of TGFβ by astrocytes, which in turn, attenuated microglial activation. Overall, these findings provide novel insight into the mechanisms by which astrocytes modulate microglia under inflammatory conditions. GLIA 2014;62:881–895
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
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?
Microglial IL-10 binds to astrocytes that modulate microglial inflammatory signaling in a transforming growth factor (TGF)-β-dependent manner.
“A recent study showed that microglial IL-10 binds to astrocytes that modulate microglial inflammatory signaling in a transforming growth factor (TGF)-β-dependent manner (Norden et al, 2014).”
From Microglia Priming with Aging and Stress (2017) · cites this paper as Norden et al, 2014
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
The mouse brain in stereotaxic coordinates
Konsman, J. (2003) · Psychoneuroendocrinology · doi:10.1016/s0306-4530(03)00088-x · Cited by 16,796 · see citing works
From inflammation to sickness and depression: when the immune system subjugates the brain
Dantzer, R., O'Connor, J. C., Freund, G. G., Johnson, R. W., & Kelley, K. W. (2008) · Nature Reviews Neuroscience · doi:10.1038/nrn2297 · Cited by 7,395 · see citing works
Interleukin-10 and the Interleukin-10 Receptor
Moore, K. W., de Waal Malefyt, R., Coffman, R. L., & O'Garra, A. (2001) · Annual Review of Immunology · doi:10.1146/annurev.immunol.19.1.683 · Cited by 6,737 · see citing works
Resting microglial cells are highly dynamic surveillants of brain parenchyma in vivo
Nimmerjahn, A., Kirchhoff, F., & Helmchen, F. (2005) · Science · doi:10.1126/science.1110647 · Cited by 5,827 · see citing works
ATP mediates rapid microglial response to local brain injury in vivo
Davalos, D., Grutzendler, J., Yang, G., Kim, J. V., Zuo, Y., Jung, S., Littman, D. R., Dustin, M. L., & Gan, W.-B. (2005) · Nature Neuroscience · doi:10.1038/nn1472 · Cited by 3,913 · see citing works
Identification of a unique TGF-β–dependent molecular and functional signature in microglia
Butovsky, O., Jedrychowski, M. P., Moore, C. S., Cialic, R., Lanser, A. J., Gabriely, G., Koeglsperger, T., Dake, B., Wu, P. M., Doykan, C. E., et al. (2014) · Nature Neuroscience · doi:10.1038/nn.3599 · Cited by 2,543 · see citing works
Genomic analysis of reactive astrogliosis
Zamanian, J. L., Xu, L., Foo, L. C., Nouri, N., Zhou, L., Giffard, R. G., & Barres, B. A. (2012) · The Journal of Neuroscience · doi:10.1523/jneurosci.6221-11.2012 · Cited by 2,404 · see citing works
Inman, G. J., Nicolás, F. J., Callahan, J. F., Harling, J. D., Gaster, L. M., Reith, A. D., Laping, N. J., & Hill, C. S. (2002) · Molecular Pharmacology · doi:10.1124/mol.62.1.65 · Cited by 1,636 · see citing works
Astrocyte activation and reactive gliosis
Pekny, M., & Nilsson, M. (2005) · Glia · doi:10.1002/glia.20207 · Cited by 1,611 · see citing works
Astrocytes are active players in cerebral innate immunity
Farina, C., Aloisi, F., & Meinl, E. (2007) · Trends in Immunology · doi:10.1016/j.it.2007.01.005 · Cited by 1,304 · see citing works
Godbout, J. P., Chen, J., Abraham, J., Richwine, A. F., Berg, B. M., Kelley, K. W., & Johnson, R. W. (2005) · The FASEB Journal · doi:10.1096/fj.05-3776fje · Cited by 813 · see citing works
Self-citationReview: microglia of the aged brain: primed to be activated and resistant to regulation
Norden, D. M., & Godbout, J. P. (2013) · Neuropathology and Applied Neurobiology · doi:10.1111/j.1365-2990.2012.01306.x · Cited by 792 · see citing works
Self-citationMicroglia and neurodegeneration: The role of systemic inflammation
Cunningham, C. (2013) · Glia · doi:10.1002/glia.22350 · Cited by 769 · see citing works
Microglia derived from aging mice exhibit an altered inflammatory profile
Sierra, A., Gottfried‐Blackmore, A. C., McEwen, B. S., & Bulloch, K. (2007) · Glia · doi:10.1002/glia.20468 · Cited by 688 · see citing works
Henry, C. J., Huang, Y., Wynne, A. M., & Godbout, J. P. (2009) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2008.09.002 · Cited by 565 · see citing works
Self-citationDifferential activation of astrocytes by innate and adaptive immune stimuli
Carpentier, P. A., Begolka, W. S., Olson, J. K., Elhofy, A., Karpus, W. J., & Miller, S. D. (2004) · Glia · doi:10.1002/glia.20117 · Cited by 359 · see citing works
Peripheral infection and aging interact to impair hippocampal memory consolidation
Barrientos, R. M., Higgins, E. A., Biedenkapp, J. C., Sprunger, D. B., Wright-Hardesty, K. J., Watkins, L. R., Rudy, J. W., & Maier, S. F. (2006) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2005.03.010 · Cited by 330 · see citing works
Transforming growth factor-beta suppresses activation and proliferation of microglia in vitro.
Suzumura, A., Sawada, M., Yamamoto, H., & Marunouchi, T. (1993) · The Journal of Immunology · doi:10.4049/jimmunol.151.4.2150 · Cited by 305 · see citing works
Liu, W., Tang, Y., & Feng, J. (2011) · Life Sciences · doi:10.1016/j.lfs.2011.05.011 · Cited by 303 · cited 2× · see citing works
“neuroinflammation (Farina et al., 2007; Liu et al., 2011; Pekny and Nilsson, 2005).”
Godbout, J. P., Moreau, M., Lestage, J., Chen, J., Sparkman, N. L., Connor, J. O., Castanon, N., Kelley, K. W., Dantzer, R., & Johnson, R. W. (2008) · Neuropsychopharmacology · doi:10.1038/sj.npp.1301649 · Cited by 299 · see citing works
Self-citationToll‐like receptor 3 on adult human astrocytes triggers production of neuroprotective mediators
Bsibsi, M., Persoon-Deen, C., Verwer, R. W. H., Meeuwsen, S., Ravid, R., & van Noort, J. M. (2006) · Glia · doi:10.1002/glia.20328 · Cited by 296 · see citing works
Wohleb, E. S., Fenn, A. M., Pacenta, A. M., Powell, N. D., Sheridan, J. F., & Godbout, J. P. (2012) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2012.02.003 · Cited by 275 · see citing works
Self-citationMin, K.-J., Yang, M.-S., Kim, S.-U., Jou, I., & Joe, E. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.3696-05.2006 · Cited by 269 · see citing works
Protracted downregulation of CX3CR1 on microglia of aged mice after lipopolysaccharide challenge
Wynne, A. M., Henry, C. J., Huang, Y., Cleland, A., & Godbout, J. P. (2010) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2010.05.011 · Cited by 224 · see citing works
Self-citationHuang, Y., Henry, C. J., Dantzer, R., Johnson, R. W., & Godbout, J. P. (2007) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2007.04.012 · Cited by 218 · see citing works
Self-citationAngiotensin II sustains brain inflammation in mice via TGF-β
Lanz, T. V., Ding, Z., Ho, P. P.-K., Luo, J., Agrawal, A., Srinagesh, H. K., Axtell, R. C., Zhang, H., Platten, M., Wyss‐Coray, T., et al. (2010) · Journal of Clinical Investigation · doi:10.1172/jci41709 · Cited by 200 · see citing works
Corona, A. W., Huang, Y., O’Connor, J. C., Dantzer, R., Kelley, K. W., Popovich, P. G., & Godbout, J. P. (2010) · Journal of Neuroinflammation · doi:10.1186/1742-2094-7-93 · Cited by 200 · see citing works
Self-citationFenn, A. M., Henry, C. J., Huang, Y., Dugan, A., & Godbout, J. P. (2012) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2011.10.003 · Cited by 198 · see citing works
Self-citationLedeboer, A., Brevé, J. J. P., Wierinckx, A., Jagt, S. V. D., Bristow, A. F., Leysen, J. E., Tilders, F. J. H., & van Dam, A. (2002) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2002.02200.x · Cited by 190 · see citing works
Central Nervous System Expression of IL-10 Inhibits Autoimmune Encephalomyelitis
Cua, D. J., Hutchins, B., LaFace, D., Stohlman, S. A., & Coffman, R. L. (2001) · The Journal of Immunology · doi:10.4049/jimmunol.166.1.602 · Cited by 182 · see citing works
Central injection of IL-10 antagonizes the behavioural effects of lipopolysaccharide in rats
Bluthé, R.-M., Castanon, N., Pousset, F., Bristow, A., Ball, C., Lestage, J., Michaud, B., KELLEY, K. W., & Dantzer, R. (1999) · Psychoneuroendocrinology · doi:10.1016/s0306-4530(98)00077-8 · Cited by 179 · see citing works
Interleukin-1β Induces a Reactive Astroglial Phenotype via Deactivation of the Rho GTPase–Rock Axis
John, G. R., Chen, L., Rivieccio, M. A., Melendez‐Vasquez, C. V., Hartley, A., & Brosnan, C. F. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.4789-03.2004 · Cited by 172 · see citing works
Cotrina, M. L., & Nedergaard, M. (2001) · Journal of Neuroscience Research · doi:10.1002/jnr.10121 · Cited by 162 · see citing works
Lynch, A. M., Walsh, C., Delaney, A., Nolan, Y. M., Campbell, V. A., & Lynch, M. A. (2004) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2003.02157.x · Cited by 145 · see citing works
Neuroprotection by IL-10-producing MOG CD4+ T cells following ischemic stroke.
Frenkel, D., Huang, Z., Maron, R., Koldzic, D. N., Moskowitz, M., & Weiner, H. (2005) · Journal of Neurological Sciences · doi:10.1016/j.jns.2005.03.022 · Cited by 141 · see citing works
Interleukin-10 inhibits endotoxin-induced pro-inflammatory cytokines in microglial cell cultures
Kremlev, S. G., & Palmer, C. (2005) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2005.01.010 · Cited by 128 · see citing works
Donnelly, D. J., Gensel, J. C., Ankeny, D. P., van Rooijen, N., & Popovich, P. G. (2009) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2009.04.010 · Cited by 128 · see citing works
Li, Q., Wei, S., Zhang, D., Hu, X., Xu, Z., Wilson, B. C., Benna, J. E., Hong, J., & Flood, P. M. (2008) · The Journal of Immunology · doi:10.4049/jimmunol.181.1.660 · Cited by 128 · see citing works
Luo, J., Ho, P. P.-K., Buckwalter, M. S., Hsu, T., Lee, L. Y., Zhang, H., Kim, D., Kim, S., Gambhir, S. S., Steinman, L., et al. (2007) · Journal of Clinical Investigation · doi:10.1172/jci31763 · Cited by 115 · see citing works
Cognitive deficits in interleukin-10-deficient mice after peripheral injection of lipopolysaccharide
Richwine, A. F., Sparkman, N. L., Dilger, R. N., Buchanan, J. B., & Johnson, R. W. (2009) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2009.02.020 · Cited by 111 · see citing works
Aging sensitizes rapidly isolated hippocampal microglia to LPS ex vivo
Frank, M. G., Barrientos, R. M., Watkins, L. R., & Maier, S. F. (2010) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2010.05.022 · Cited by 109 · see citing works
Puig, I. P.-D., Miró‐Mur, F., Salas-Perdomo, A., Bonfill‐Teixidor, E., Ferrer-Ferrer, M., Márquez‐Kisinousky, L., & Planas, A. M. (2013) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.2013.155 · Cited by 101 · see citing works
Microglia and Astrocyte Activation by Toll‐Like Receptor Ligands: Modulation by PPAR‐γ Agonists
Gurley, C. M., Nichols, J. R., Liu, S., Phulwani, N. K., Esen, N., & Kielian, T. (2008) · PPAR Research · doi:10.1155/2008/453120 · Cited by 84 · see citing works
α-Tocopherol attenuates lipopolysaccharide-induced sickness behavior in mice
Berg, B. M., Godbout, J. P., Kelley, K. W., & Johnson, R. W. (2003) · Brain Behavior and Immunity · doi:10.1016/s0889-1591(03)00113-2 · Cited by 83 · see citing works
Self-citationOrellana, J. A., Montero, T. D., & Rommy von Bernhardi, M. (2013) · Glia · doi:10.1002/glia.22573 · Cited by 82 · see citing works
Characterization of Adult Rat Astrocyte Cultures
de Souza, D. G., Bellaver, B., Souza, D. O., & Quincozes‐Santos, A. (2013) · PLoS ONE · doi:10.1371/journal.pone.0060282 · Cited by 82 · see citing works
Central inhibition of interleukin-1β ameliorates sickness behavior in aged mice
Abraham, J., & Johnson, R. W. (2009) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2008.12.008 · Cited by 80 · see citing works
TGF-β1 protects against Aβ-neurotoxicity via the phosphatidylinositol-3-kinase pathway
Caraci, F., Battaglia, G., Busceti, C., Biagioni, F., Mastroiacovo, F., Bosco, P., Drago, F., Nicoletti, F., Sortino, M. A., & Copani, A. (2008) · Neurobiology of Disease · doi:10.1016/j.nbd.2008.01.007 · Cited by 79 · see citing works
IL-10 within the CNS is necessary for CD4+ T cells to mediate neuroprotection
Xin, J., Wainwright, D. A., Mesnard, N. A., Serpe, C. J., Sanders, V. M., & Jones, K. J. (2010) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2010.08.004 · Cited by 78 · see citing works
TLR2 Expression in Astrocytes Is Induced by TNF-α- and NF-κB-Dependent Pathways
Phulwani, N. K., Esen, N., Syed, M., & Kielian, T. (2008) · The Journal of Immunology · doi:10.4049/jimmunol.181.6.3841 · Cited by 73 · see citing works
Ishii, H., Tanabe, S., Ueno, M., Kubo, T., Kayama, H., Serada, S., Fujimoto, M., Takeda, K., Naka, T., & Yamashita, T. (2013) · Cell Death and Disease · doi:10.1038/cddis.2013.234 · Cited by 64 · see citing works
Ramírez, G., Toro, R., Döbeli, H., & von Bernhardi, R. (2005) · Neurobiology of Disease · doi:10.1016/j.nbd.2005.01.007 · Cited by 60 · see citing works
Central Interleukin‐1 Receptors as Mediators of Sicknessa
Kelley, K. W., Hutchison, K. A., French, R. A., Bluthé, R.-M., Parnet, P., Johnson, R. W., & Dantzer, R. (1997) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1997.tb48395.x · Cited by 29 · see citing works
Wei, S. H.-Y., Ming‐Lum, A., Liu, Y., Wallach, D., Ong, C. J., Chung, S. W., Moore, K. W., & Mui, A. (2006) · Journal of Interferon & Cytokine Research · doi:10.1089/jir.2006.26.281 · Cited by 20 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
Neuroinflammation: The Devil Is in the Details
DiSabato, D. J., Quan, N., & Godbout, J. P. (2016) · Journal of Neurochemistry · doi:10.1111/jnc.13607 · Cited by 1,640 · see citing works
Self-citationMicroglia in neurodegenerative diseases: mechanism and potential therapeutic targets
Gao, C., Jiang, J., Tan, Y., & Chen, S. (2023) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-023-01588-0 · Cited by 1,616 · see citing works
Astrocyte barriers to neurotoxic inflammation
Sofroniew, M. V. (2015) · Nature Reviews Neuroscience · doi:10.1038/nrn3898 · Cited by 1,202 · see citing works
Biology and therapeutic potential of interleukin-10
Saraiva, M., Vieira, P., & O’Garra, A. (2019) · The Journal of Experimental Medicine · doi:10.1084/jem.20190418 · Cited by 1,123 · see citing works
Astrocyte Crosstalk in CNS Inflammation
Linnerbauer, M., Wheeler, M. A., & Quintana, F. J. (2020) · Neuron · doi:10.1016/j.neuron.2020.08.012 · Cited by 989 · see citing works
Norden, D. M., Trojanowski, P. J., Villanueva, E., Navarro, E., & Godbout, J. P. (2015) · Glia · doi:10.1002/glia.22930 · Cited by 596 · see citing works
Self-citationInteraction of Microglia and Astrocytes in the Neurovascular Unit
Liu, L., Liu, J., Bao, J.-S., Bai, Q.-Q., & Wang, G. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.01024 · Cited by 591 · see citing works
Microglia-Astrocyte Crosstalk: An Intimate Molecular Conversation
Jha, M. K., Jo, M., Kim, J.-H., & Suk, K. (2019) · The Neuroscientist · doi:10.1177/1073858418783959 · Cited by 579 · see citing works
Neuroinflammation in the central nervous system: Symphony of glial cells
Yang, Q., & Zhou, J. (2018) · Glia · doi:10.1002/glia.23571 · Cited by 520 · see citing works
Balancing the immune response in the brain: IL-10 and its regulation
Lobo‐Silva, D., Carriche, G. M., Castro, A. G., Roque, S., & Saraiva, M. (2016) · Journal of Neuroinflammation · doi:10.1186/s12974-016-0763-8 · Cited by 427 · see citing works
Norden, D. M., Muccigrosso, M. M., & Godbout, J. P. (2015) · Neuropharmacology · doi:10.1016/j.neuropharm.2014.10.028 · Cited by 413 · see citing works
Self-citationImmune Cells in the BBB Disruption After Acute Ischemic Stroke: Targets for Immune Therapy?
Qiu, Y., Zhang, C., Chen, A., Wang, H.-L., Zhou, Y., Li, Y., & Hu, B. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.678744 · Cited by 405 · see citing works
Microglia Priming with Aging and Stress
Niraula, A., Sheridan, J. F., & Godbout, J. P. (2017) · Neuropsychopharmacology · doi:10.1038/npp.2016.185 · Cited by 398 · see citing works
Self-citationLively, S. S., & Schlichter, L. C. (2018) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2018.00215 · Cited by 384 · see citing works
Preterm birth and sustained inflammation: consequences for the neonate
Humberg, A., Fortmann, M. I., Siller, B., Kopp, M., Herting, E., Göpel, W., & Härtel, C. (2020) · Seminars in Immunopathology · doi:10.1007/s00281-020-00803-2 · Cited by 312 · see citing works
A1/A2 astrocytes in central nervous system injuries and diseases: Angels or devils?
Fan, Y., & Huo, J. (2021) · Neurochemistry International · doi:10.1016/j.neuint.2021.105080 · Cited by 310 · see citing works
IL4-driven microglia modulate stress resilience through BDNF-dependent neurogenesis
Zhang, J., Rong, P., Zhang, L., He, H., Zhou, T., Fan, Y., Mo, L., Zhao, Q., Han, Y., Li, S., et al. (2021) · Science Advances · doi:10.1126/sciadv.abb9888 · Cited by 287 · see citing works
TGF-β1 modulates microglial phenotype and promotes recovery after intracerebral hemorrhage
Taylor, R. A., Chang, C.-F., Goods, B. A., Hammond, M. D., Grory, B. M., Ai, Y., Steinschneider, A. F., Renfroe, S. C., Askenase, M. H., McCullough, L. D., et al. (2016) · Journal of Clinical Investigation · doi:10.1172/jci88647 · Cited by 277 · see citing works
Priming Microglia for Innate Immune Memory in the Brain
Neher, J. J., & Cunningham, C. M. (2019) · Trends in Immunology · doi:10.1016/j.it.2019.02.001 · Cited by 255 · see citing works
Modulation of learning and memory by cytokines: Signaling mechanisms and long term consequences
Donzis, E. J., & Tronson, N. C. (2014) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2014.08.008 · Cited by 254 · see citing works
Palmer, A. L., & Ousman, S. S. (2018) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2018.00337 · Cited by 246 · see citing works
Role of Interleukin-10 in Acute Brain Injuries
Garcia, J. M., Stillings, S. A., Leclerc, J. L., Phillips, H., Edwards, N. J., Robicsek, S. A., Hoh, B. L., Blackburn, S., & Doré, S. (2017) · Frontiers in Neurology · doi:10.3389/fneur.2017.00244 · Cited by 247 · see citing works
Glial Cells Shape Pathology and Repair After Spinal Cord Injury
Gaudet, A. D., & Fonken, L. K. (2018) · Neurotherapeutics · doi:10.1007/s13311-018-0630-7 · Cited by 232 · see citing works
Protective Functions of Reactive Astrocytes Following Central Nervous System Insult
Linnerbauer, M., & Rothhammer, V. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.573256 · Cited by 221 · see citing works
The Interleukin-10 Family of Cytokines and Their Role in the CNS
Burmeister, A. R., & Marriott, I. (2018) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2018.00458 · Cited by 208 · see citing works
Fenn, A. M., Hall, J. C. E., Gensel, J. C., Popovich, P. G., & Godbout, J. P. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.1146-14.2014 · Cited by 207 · see citing works
Self-citationMicroglial immune checkpoint mechanisms
Deczkowska, A., Amit, I., & Schwartz, M. (2018) · Nature Neuroscience · doi:10.1038/s41593-018-0145-x · Cited by 185 · see citing works
Silencing of TGFβ signalling in microglia results in impaired homeostasis
Zöller, T., Schneider, A., Kleimeyer, C., Masuda, T., Potru, P. S., Pfeifer, D., Blank, T., Prinz, M., & Spittau, B. (2018) · Nature Communications · doi:10.1038/s41467-018-06224-y · Cited by 189 · see citing works
Zăgrean, A., Hermann, D. M., Opriș, I. C., Zăgrean, L., & Popa‐Wagner, A. (2018) · Frontiers in Neuroscience · doi:10.3389/fnins.2018.00811 · Cited by 170 · see citing works
Tezel, G. (2021) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2021.100998 · Cited by 172 · see citing works
Astrocytes and the TGF-β1 Pathway in the Healthy and Diseased Brain: a Double-Edged Sword
Diniz, L. P., Matias, I. C. P., Siqueira, M., Stipursky, J., & Gomes, F. C. A. (2018) · Molecular Neurobiology · doi:10.1007/s12035-018-1396-y · Cited by 163 · see citing works
Witcher, K. G., Bray, C. E., Dziabis, J. E., McKim, D. B., Benner, B. N., Rowe, R. K., Kokiko‐Cochran, O. N., Popovich, P. G., Lifshitz, J., Eiferman, D. S., et al. (2018) · Glia · doi:10.1002/glia.23523 · Cited by 153 · see citing works
Self-citationMuccigrosso, M. M., Ford, J., Benner, B., Moussa, D., Burnsides, C., Fenn, A. M., Popovich, P. G., Lifshitz, J., Walker, F. R., Eiferman, D. S., et al. (2016) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2016.01.009 · Cited by 146 · see citing works
Self-citationRegulation of Innate and Adaptive Immunity by TGFβ
Kelly, A., Houston, S. A., Sherwood, E., Casulli, J., & Travis, M. A. (2017) · Advances in immunology · doi:10.1016/bs.ai.2017.01.001 · Cited by 142 · see citing works
Microglial activation states and their implications for Alzheimer's Disease
Valiukas, Z., Tangalakis, K., Apostolopoulos, V., & Feehan, J. (2025) · The Journal of Prevention of Alzheimer s Disease · doi:10.1016/j.tjpad.2024.100013 · Cited by 155 · see citing works
O’Neil, S. M., Witcher, K. G., McKim, D. B., & Godbout, J. P. (2018) · Acta Neuropathologica Communications · doi:10.1186/s40478-018-0636-8 · Cited by 138 · see citing works
Self-citationSphingosine-1-phosphate receptor 1 activation in astrocytes contributes to neuropathic pain
Chen, Z., Doyle, T. M., Luongo, L., Largent‐Milnes, T. M., Giancotti, L. A., Kolar, G. R., Squillace, S., Boccella, S., Walker, J. K., Pendleton, A. L., et al. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1820466116 · Cited by 127 · see citing works
Inyang, K. E., Szabo-Pardi, T. A., Winchester, E. W., McDougal, T. A., Dussor, G. O., Burton, M. D., & Price, T. J. (2018) · Pharmacological Research · doi:10.1016/j.phrs.2018.10.027 · Cited by 129 · see citing works
Long, Y., Li, X., Deng, J., Ye, Q., Li, D., Ma, Y., Wu, Y., Hu, Y., He, X.-F., Wen, J., et al. (2023) · Ageing Research Reviews · doi:10.1016/j.arr.2023.102160 · Cited by 127 · see citing works
Clark, D. P. Q., Perreau, V. M., Shultz, S. R., Brady, R. D., Lei, E., Dixit, S., Taylor, J. M., Beart, P. M., & Boon, W. C. (2019) · Neurochemical Research · doi:10.1007/s11064-019-02721-8 · Cited by 127 · see citing works
Prolonged inflammation leads to ongoing damage after spinal cord injury
Kwiecień, J. M., Dąbrowski, W., Dąbrowska‐Bouta, B., Sułkowski, G., Oakden, W., Kwiecien-Delaney, C. J., Yaron, J. R., Zhang, L., Schutz, L. N., Marzec‐Kotarska, B., et al. (2020) · PLoS ONE · doi:10.1371/journal.pone.0226584 · Cited by 126 · see citing works
Functional immune cell–astrocyte interactions
Sanmarco, L. M., Polonio, C. M., Wheeler, M. A., & Quintana, F. J. (2021) · The Journal of Experimental Medicine · doi:10.1084/jem.20202715 · Cited by 126 · see citing works
Lipid metabolism in astrocytic structure and function
Lee, J. A., Hall, B., Allsop, J., Alqarni, R., & Allen, S. P. (2021) · Seminars in Cell & Developmental Biology · doi:10.1016/j.semcdb.2020.07.017 · Cited by 116 · see citing works
Loss of IL-10 Promotes Differentiation of Microglia to a M1 Phenotype
Laffer, B., Bauer, D., Wasmuth, S., Busch, M., Jalilvand, T. V., Thanos, S., Meyer zu Hörste, G., Loser, K., Langmann, T., Heiligenhaus, A., et al. (2019) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2019.00430 · Cited by 120 · see citing works
de Bartolomeis, A., Barone, A., Vellucci, L., Mazza, B., Austin, M. C., Iasevoli, F., & Ciccarelli, M. (2022) · Molecular Neurobiology · doi:10.1007/s12035-022-02976-3 · Cited by 113 · see citing works
Models and mechanisms for hippocampal dysfunction in obesity and diabetes
Stranahan, A. M. (2015) · Neuroscience · doi:10.1016/j.neuroscience.2015.04.045 · Cited by 101 · see citing works
Neuroinflammation in preterm babies and autism spectrum disorders
Bokobza, C., Steenwinckel, J. V., Mani, S., Mezger, V., Fleiss, B., & Gressèns, P. (2018) · Pediatric Research · doi:10.1038/s41390-018-0208-4 · Cited by 103 · see citing works
Sawicki, C. M., McKim, D. B., Wohleb, E. S., Jarrett, B. L., Reader, B. F., Norden, D. M., Godbout, J. P., & Sheridan, J. F. (2015) · Neuroscience · doi:10.1016/j.neuroscience.2014.10.004 · Cited by 101 · see citing works
Self-citationKim, S. M., & Son, Y. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22168800 · Cited by 101 · see citing works
The psychoneuroimmunology of pregnancy
Sherer, M. L., Posillico, C. K., & Schwarz, J. M. (2017) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2017.10.006 · Cited by 93 · see citing works
Stress and aging act through common mechanisms to elicit neuroinflammatory priming
Fonken, L. K., Frank, M. G., Gaudet, A. D., & Maier, S. F. (2018) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2018.07.012 · Cited by 94 · see citing works
Glaucoma: from pathogenic mechanisms to retinal glial cell response to damage
Fernández‐Albarral, J. A., Ramirez, A. I., de Hoz, R., Matamoros, J. A., Salobrar‐García, E., Elvira‐Hurtado, L., López‐Cuenca, I., Sánchez-Puebla, L., Salazar, J. J., & Ramirez, J. M. (2024) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2024.1354569 · Cited by 99 · see citing works
Menzel, L., Kleber, L., Friedrich, C., Hummel, R., Dangel, L., Winter, J., Schmitz, K., Tegeder, I., & Schäfer, M. K. E. (2016) · Glia · doi:10.1002/glia.23091 · Cited by 92 · see citing works
Gullotta, G. S., Costantino, G., Sortino, M. A., & Spampinato, S. F. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24119144 · Cited by 90 · see citing works
Eryptosis as a marker of Parkinson's disease
Pretorius, E., Swanepoel, A. C., Buys, A. V., Vermeulen, N., Duim, W., & Kell, D. B. (2014) · Aging · doi:10.18632/aging.100695 · Cited by 91 · see citing works
The Microbiota–Gut–Brain Axis and Neurological Disorders: A Comprehensive Review
Nakhal, M. M., Yassin, L. K., Alyaqoubi, R., Saeed, S., Alderei, A., Alhammadi, A., Alshehhi, M., Almehairbi, A., Houqani, S. A., BaniYas, S., et al. (2024) · Life · doi:10.3390/life14101234 · Cited by 134 · see citing works
The involvement of astrocytes in early‐life adversity induced programming of the brain
Abbink, M. R., van Deijk, A. F., Heine, V. M., Verheijen, M. H. G., & Kőrösi, A. (2019) · Glia · doi:10.1002/glia.23625 · Cited by 92 · see citing works
Sun, L., Shen, R., Agnihotri, S. K., Chen, Y., Huang, Z., & Büeler, H. (2018) · Scientific Reports · doi:10.1038/s41598-017-18786-w · Cited by 87 · see citing works
Hadjihambi, A., Konstantinou, C., Klohs, J., Monsorno, K., Guennec, A. D. L., Donnelly, C., Cox, I. J., Kusumbe, A. P., Hosford, P. S., Soffientini, U., et al. (2022) · Journal of Hepatology · doi:10.1016/j.jhep.2022.08.008 · Cited by 87 · see citing works
Steliga, A., Kowiański, P., Czuba, E., Waśkow, M., Moryś, J., & Lietzau, G. (2019) · Translational Stroke Research · doi:10.1007/s12975-019-00744-5 · Cited by 87 · see citing works
Impaired regulatory T cell control of astroglial overdrive and microglial pruning in schizophrenia
Zuelli, F. M. D. G. C., & Deakin, J. F. W. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2021.03.004 · Cited by 85 · see citing works
The cytokine network in the pathogenesis of major depressive disorder. Close to translation?
Petralia, M. C., Mazzon, E., Fagone, P., Basile, M. S., Lenzo, V., Quattropani, M. C. A., Nuovo, S. D., Bendtzen, K., & Nicoletti, F. (2020) · Autoimmunity Reviews · doi:10.1016/j.autrev.2020.102504 · Cited by 86 · see citing works
Zhang, Z., Bassam, B., Thomas, A. G., Williams, M., Liu, J., Nance, E., Rojas, C., Slusher, B. S., & Kannan, S. (2016) · Neurobiology of Disease · doi:10.1016/j.nbd.2016.06.010 · Cited by 84 · see citing works
Recent insights on astrocyte mechanisms in CNS homeostasis, pathology, and repair
Hart, C. G., & Karimi‐Abdolrezaee, S. (2021) · Journal of Neuroscience Research · doi:10.1002/jnr.24922 · Cited by 85 · see citing works
Sepsis-associated encephalopathy: From pathophysiology to clinical management
Hong, Y., Chen, P., Gao, J., Lin, Y., Chen, L., & Shang, X. (2023) · International Immunopharmacology · doi:10.1016/j.intimp.2023.110800 · Cited by 89 · see citing works
Neuroimmune crosstalk in chronic neuroinflammation: microglial interactions and immune modulation
Müller, L., & Benedetto, S. D. (2025) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2025.1575022 · Cited by 90 · see citing works
Neuroinflammatory responses of microglia in central nervous system trauma
Shields, D. C., Haque, A., & Banik, N. L. (2020) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1177/0271678x20965786 · Cited by 82 · see citing works
Navarro, E., González‐Lafuente, L., Pérez-Liébana, I., Buendía, I., López-Bernardo, E., Sánchez‐Ramos, C., Priéto, I., Cuadrado, A., Satrústegui, J., Cadenas, S., et al. (2016) · Antioxidants and Redox Signaling · doi:10.1089/ars.2016.6698 · Cited by 84 · see citing works
Xie, L., Zhang, N., Zhang, Q., Li, C., Sandhu, A. F., Williams, G., III, Lin, S.-R., Lv, P., Liu, Y., Wu, Q., et al. (2020) · Aging · doi:10.18632/aging.103663 · Cited by 80 · see citing works
Alizadeh, A., Dyck, S. M., Kataria, H., Shahriary, G. M., Nguyen, D. H., Santhosh, K. T., & Karimi‐Abdolrezaee, S. (2017) · Glia · doi:10.1002/glia.23150 · Cited by 78 · see citing works
Inflammation in the pathogenesis of depression: a disorder of neuroimmune origin
Corrigan, M., O’Rourke, A. M., Moran, B., Fletcher, J. M., & Harkin, A. (2023) · Neuronal Signaling · doi:10.1042/ns20220054 · Cited by 77 · see citing works
Role of Microglial Activation in the Pathophysiology of Bacterial Meningitis
Barichello, T., Generoso, J. S., Simões, L. R., Goularte, J. A., Petronilho, F. C., Saigal, P., Badawy, M., & Quevedo, J. (2015) · Molecular Neurobiology · doi:10.1007/s12035-015-9107-4 · Cited by 76 · see citing works
Bray, C. E., Witcher, K. G., Adekunle-Adegbite, D., Ouviña, M., Witzel, M., Hans, E., Tapp, Z. M., Packer, J. M., Goodman, E. J., Zhao, F., et al. (2022) · Journal of Neuroscience · doi:10.1523/jneurosci.1910-21.2022 · Cited by 76 · see citing works
Self-citationSignaling pathways regulating neuron–glia interaction and their implications in Alzheimer's disease
Lian, H., & Zheng, H. (2015) · Journal of Neurochemistry · doi:10.1111/jnc.13424 · Cited by 75 · see citing works
Zhang, L., Lei, Z., Guo, Z., Pei, Z., Chen, Y., Zhang, F., Cai, A., Mok, G., Lee, G., Swaminathan, V., et al. (2020) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2020.594170 · Cited by 86 · see citing works
Matisz, C. E., & Gruber, A. J. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2021.12.020 · Cited by 70 · see citing works
Neuro-immune dysfunction during brain aging: new insights in microglial cell regulation
Matt, S. M., & Johnson, R. W. (2015) · Current Opinion in Pharmacology · doi:10.1016/j.coph.2015.10.009 · Cited by 73 · see citing works
Norden, D. M., Trojanowski, P. J., Walker, F. R., & Godbout, J. P. (2016) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2016.04.014 · Cited by 73 · see citing works
Self-citationPang, Q.-M., Chen, S., Xu, Q.-J., Zhang, M., Liang, D.-F., Fu, S.-P., Jiang, Y. P., Liu, Z.-L., Zhang, Q., & Zhang, T. (2022) · International Immunopharmacology · doi:10.1016/j.intimp.2022.108754 · Cited by 70 · see citing works
Microglia depletion fails to abrogate inflammation-induced sickness in mice and rats
Vichaya, E. G., Malik, S., Sominsky, L., Ford, B. G., Spencer, S. J., & Dantzer, R. (2020) · Journal of Neuroinflammation · doi:10.1186/s12974-020-01832-2 · Cited by 68 · see citing works
Stigger, F. S., Zago Marcolino, M. A., Portela, K. M., & Plentz, R. D. M. (2019) · The Journals of Gerontology: Series A · doi:10.1093/gerona/gly173 · Cited by 68 · see citing works
Mamun, A. A., Chauhan, A., Yu, H., Xu, Y., Sharmeen, R., & Liu, F. (2017) · European Journal of Neuroscience · doi:10.1111/ejn.13778 · Cited by 66 · see citing works
Neuroimmune Response in Ischemic Preconditioning
McDonough, A., & Weinstein, J. R. (2016) · Neurotherapeutics · doi:10.1007/s13311-016-0465-z · Cited by 62 · see citing works
Mirza, R., & Sharma, B. (2019) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2019.108758 · Cited by 60 · see citing works
Affective Immunology: The Crosstalk Between Microglia and Astrocytes Plays Key Role?
Yang, L., Zhou, Y., Jia, H., Qi, Y., Tu, S., & Shao, A. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.01818 · Cited by 64 · see citing works
Xie, L., Wu, Q., Li, K., Khan, M. A. S., Zhang, A., Sinha, B., Li, S., Chang, S. L., Brody, D. L., Grinstaff, M. W., et al. (2024) · Aging and Disease · doi:10.14336/ad.2024.0134 · Cited by 63 · see citing works
Crosstalk of Astrocytes and Other Cells during Ischemic Stroke
He, T., Yang, G., & Zhang, Z. (2022) · Life · doi:10.3390/life12060910 · Cited by 62 · see citing works
Dugan, A. M., Parrott, J. M., Redus, L., Hensler, J. G., & O’Connor, J. C. (2015) · The International Journal of Neuropsychopharmacology · doi:10.1093/ijnp/pyv089 · Cited by 61 · see citing works
Self-citationAlmolda, B., de Labra, C., Barrera, I., Gruart, A., Delgado-Garcia, J. M., Villacampa, N., Vilella, A., Hofer, M. J., Hidalgo, J., Campbell, I. L., et al. (2014) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2014.10.015 · Cited by 58 · see citing works
Gliotoxicity and Glioprotection: the Dual Role of Glial Cells
Quincozes‐Santos, A., Santos, C. L., Almeida, R. R. D. S., da Silva, A., Thomaz, N. K., Costa, N. L. F., Weber, F. B., Schmitz, I., Medeiros, L. S., Medeiros, L., et al. (2021) · Molecular Neurobiology · doi:10.1007/s12035-021-02574-9 · Cited by 57 · see citing works
Microglia as therapeutic target in central nervous system disorders
Fatoba, O., Itokazu, T., & Yamashita, T. (2020) · Journal of Pharmacological Sciences · doi:10.1016/j.jphs.2020.07.004 · Cited by 56 · see citing works
Role of cytokines and reactive oxygen species in brain aging
MohanKumar, S. M. J., Murugan, A., Palaniyappan, A., & MohanKumar, P. S. (2023) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2023.111855 · Cited by 58 · see citing works
Mirza, R., & Sharma, B. (2018) · Life Sciences · doi:10.1016/j.lfs.2018.10.045 · Cited by 55 · see citing works
Mirza, R., & Sharma, B. (2019) · International Journal of Developmental Neuroscience · doi:10.1016/j.ijdevneu.2019.05.006 · Cited by 56 · see citing works
Sheng, L., Stewart, T., Yang, D., Thorland, E., Soltys, D., Aro, P., Khrisat, T., Xie, Z., Li, N., Liu, Z., et al. (2020) · Acta Neuropathologica Communications · doi:10.1186/s40478-020-00983-w · Cited by 56 · see citing works
Liu, R., Xu, N., Wei, Y., & Ji, C. (2020) · Evidence-based Complementary and Alternative Medicine · doi:10.1155/2020/8163052 · Cited by 55 · see citing works
O’Neil, S. M., Hans, E., Jiang, S., Wangler, L. M., & Godbout, J. P. (2022) · Glia · doi:10.1002/glia.24147 · Cited by 56 · see citing works
Self-citationNeuroinflammation and Post-Stroke Depression: Focus on the Microglia and Astrocytes
Lu, W., & Wen, J. (2024) · Aging and Disease · doi:10.14336/ad.2024.0214-1 · Cited by 63 · see citing works
The role of glial autophagy in Alzheimer’s disease
Litwiniuk, A., Juszczak, G. R., Stankiewicz, A. M., & Urbańska, K. (2023) · Molecular Psychiatry · doi:10.1038/s41380-023-02242-5 · Cited by 54 · see citing works
Chen, X., Wang, X., Cui, Z., Luo, Q., Jiang, Z., Huang, Y., Jiang, J., Qiu, J., Li, Y., Yu, K., et al. (2023) · International Journal of Biological Sciences · doi:10.7150/ijbs.79784 · Cited by 53 · see citing works
- Authors
- Norden, D. M., Fenn, A. M., Dugan, A., & Godbout, J. P.
- Affiliations
- The Ohio State University (US)
- Corresponding author
- Godbout, Jonathan P.
- ORCID
- Godbout, Jonathan P.
- Venue
- Glia
- Publisher
- Wiley
- Published
- 2014-02-25
- Volume
- 62
- Issue
- 6
- Pages
- 881-895
- ISSN
- 0894-1491 (ISSN-L)
- 1098-1136
- PMC
- PMC4061706
- OpenAlex
- W1568207206
- Cited by
- 332
- References
- 54
- Citations by year
- 2026: 28 · 2025: 38 · 2024: 33 · 2023: 48 · 2022: 23 · 2021: 29 · 2020: 29 · 2019: 23 · 2018: 28 · 2017: 11 · 2016: 17 · 2015: 16 · 2014: 9
- FWCI
- 9.20
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Glia (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- Howard Hughes Medical Institute
- National Institute on Aging (R01AG033028)
- Topics
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Life Sciences › Neuroscience › Biological Psychiatry › Tryptophan and brain disorders
- Health Sciences › Medicine › Neurology › Traumatic Brain Injury and Neurovascular Disturbances
- Keywords
- IL-10, TGF-beta, astrocytes, microglial activation, astrocyte-microglia interaction, neuroinflammation, IL-10 receptor, IL-1β, CX3CR1, IL-4 receptor alpha, sickness behavior, lipopolysaccharide, anti-inflammatory signaling
- MeSH terms
- Animals, Animals, Newborn, Astrocytes, Cells, Cultured, Mice, Inbred BALB C, Transforming Growth Factor beta, Interleukin-10, Microglia, Coculture Techniques, 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