TGFβ produced by IL‐10 redirected astrocytes attenuates microglial activation

The mouse brain in stereotaxic coordinates

Konsman, J. (2003) · Psychoneuroendocrinology · doi:10.1016/s0306-4530(03)00088-x · Cited by 16,796

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

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

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

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

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

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

SB-431542 Is a Potent and Specific Inhibitor of Transforming Growth Factor-β Superfamily Type I Activin Receptor-Like Kinase (ALK) Receptors ALK4, ALK5, and ALK7

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

Astrocyte activation and reactive gliosis

Pekny, M., & Nilsson, M. (2005) · Glia · doi:10.1002/glia.20207 · Cited by 1,611

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

Reversing Glial Scar Back To Neural Tissue Through NeuroD1-Mediated Astrocyte-To-Neuron ConversionPreprint

Zhang, L., Lei, Z., Guo, Z., Pei, Z., Chen, Y.-C., Zhang, F., Cai, A., Mok, Y.-K., Lee, G., Swaminnathan, V., et al. (2018) · bioRxiv · doi:10.1101/261438 · Cited by 18

Neuron-glia crosstalk and inflammatory mediators in migraine pathophysiology

Song, Y., Zhao, S., Peng, P., Zhang, C., Liu, Y., Chen, Y., Luo, Y., Li, B., & Liu, L. (2024) · Neuroscience · doi:10.1016/j.neuroscience.2024.10.006 · Cited by 22

Astrocyte–microglia crosstalk in subarachnoid hemorrhage: mechanisms and treatments

Yu, K., Wang, D., & Yu, W. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1547858 · Cited by 15

Molecular mechanisms of microglia- and astrocyte-driven neurorestoration triggered by application of electromagnetic fields

Isaković, J., Gorup, D., & Mitrečić, D. (2019) · Croatian Medical Journal · doi:10.3325/cmj.2019.60.127 · Cited by 14

Emerging Roles of Microglia in Blood-Brain Barrier Integrity in Aging and Neurodegeneration

Zhang, S., Meng, R., Jiang, M., Qing, H., & Ni, J. (2023) · Current Neuropharmacology · doi:10.2174/1570159x21666230203103910 · Cited by 16

Astrocytes in Spinal Cord Injury: Current Opportunities and Prospects for Directional Polarization

Bilalova, A., Tutova, O. N., Mukhamedshina, Y. O., & Rizvanov, A. A. (2024) · Frontiers in Bioscience-Landmark · doi:10.31083/j.fbl2903094 · Cited by 15

Refining the interactions between microglia and astrocytes in Alzheimer’s disease pathology

Chen, J., Xu, S., Wang, L., Liu, X., Liu, G., Tan, Q., Li, W., Zhang, S., & Du, Y. (2025) · Neuroscience · doi:10.1016/j.neuroscience.2025.03.033 · Cited by 17

The p38alpha mitogen-activated protein kinase limits the CNS proinflammatory cytokine response to systemic lipopolysaccharide, potentially through an IL-10 dependent mechanism

Bachstetter, A. D., Xing, B., & Eldik, L. J. V. (2014) · Journal of Neuroinflammation · doi:10.1186/s12974-014-0175-6 · Cited by 15

The histamine-4 receptor antagonist JNJ7777120 prevents immune abnormalities by inhibiting RORγt/T-bet transcription factor signaling pathways in BTBR T+ Itpr3tf/J mice exposed to gamma rays

Ahmad, S. F., Nadeem, A., Ansari, M. A., Bakheet, S. A., Al‐Mazroua, H. A., Khan, M. R., Alasmari, A. F., Alanazi, W. A., Sobeai, H. M. A., & Attia, S. M. (2019) · Molecular Immunology · doi:10.1016/j.molimm.2019.09.007 · Cited by 15

Plasma concentrations of anti-inflammatory cytokine TGF-β are associated with hippocampal structure related to explicit memory performance in older adults

Raschick, M., Richter, A., Fischer, L., Knopf, L., Schult, A., Yakupov, R., Behnisch, G., Guttek, K., Düzel, E., Dunay, I. R., et al. (2023) · Journal of Neural Transmission · doi:10.1007/s00702-023-02638-1 · Cited by 14

Neuroprotective astroglial response to neural damage and its relevance to affective disorders

Miguel-Hidalgo, J. J. (2023) · Exploration of Neuroprotective Therapy · doi:10.37349/ent.2023.00054 · Cited by 14

Nanomaterials as therapeutic agents to modulate astrocyte-mediated inflammation in spinal cord injury

Luo, W., Li, Y., Xiang, C., Aizawa, T., Niu, R., Wang, Y., Zhao, J., Liu, Z., Li, C., Liu, W., et al. (2023) · Materials Today Bio · doi:10.1016/j.mtbio.2023.100888 · Cited by 15

Neurosteroid [3α,5α]-3-hydroxy-pregnan-20-one enhances IL-10 production via endosomal TRIF-dependent TLR4 signaling pathway

Balan, I. S., Grusca, A., O’Buckley, T. K., & Morrow, A. L. (2023) · Frontiers in Endocrinology · doi:10.3389/fendo.2023.1299420 · Cited by 14

Impacts of PI3K/protein kinase B pathway activation in reactive astrocytes: from detrimental effects to protective functions

Pérez-Núñez, R., González, M. F., Avalos, A. M., & Leyton, L. (2024) · Neural Regeneration Research · doi:10.4103/nrr.nrr-d-23-01756 · Cited by 17

Cellular Model of Endotoxin Tolerance in Astrocytes: Role of Interleukin 10 and Oxylipins

Chistyakov, D. V., Astakhova, A. A., Azbukina, N. V., Goriainov, S. V., Chistyakov, V. V., & Sergeeva, M. G. (2019) · Cells · doi:10.3390/cells8121553 · Cited by 15

Apolipoprotein E knockout induced inflammatory responses related to microglia in neonatal mice brain via astrocytes.

(2015) · PubMed Central · Cited by 14

MicroRNA-mediated regulation of reactive astrocytes in central nervous system diseases

Fan, Y., Huang, H., Shao, J., & Huang, W. (2023) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2022.1061343 · Cited by 13

Microglia trigger the structural plasticity of GABAergic neurons in the hippocampal CA1 region of a lipopolysaccharide-induced neuroinflammation model

Chen, J., Wang, T., Zhou, Y., Hong, Y., Zhang, S., Zhou, Z., Jiang, A., & Liu, D. (2023) · Experimental Neurology · doi:10.1016/j.expneurol.2023.114565 · Cited by 13

Characterization of Astrocytes in the Minocycline-Administered Mouse Photothrombotic Ischemic Stroke Model

Kondo, M., Okazaki, H., Nakayama, K., Hohjoh, H., Nakagawa, K., Segi‐Nishida, E., & Hasegawa, H. (2022) · Neurochemical Research · doi:10.1007/s11064-022-03703-z · Cited by 13

Microglia-Astrocyte Crosstalk in Post-Stroke Neuroinflammation: Mechanisms and Therapeutic Strategies

Shang, T., Kuang, B., Shang, Y., & Zou, W. (2025) · Current Neuropharmacology · doi:10.2174/011570159x350639250403072430 · Cited by 12

Enhancing axonal myelination in seniors: A review exploring the potential impact cannabis has on myelination in the aged brain

Murray, C. J., Vecchiarelli, H. A., & Tremblay, M. (2023) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2023.1119552 · Cited by 12

Antidepressant Effects of Ginsenoside Rc on L-Alpha-Aminoadipic Acid-Induced Astrocytic Ablation and Neuroinflammation in Mice

Kwon, D.-H., Kim, Y., & Cho, S. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25179673 · Cited by 12

Acupressure attenuates fibromyalgia central sensitization via MAPK phosphorylation-mediated neuroinflammation regulation

Liu, K., Lin, Y., Rao, T., Huang, Y., Kan, Y., & Liao, J. (2025) · Journal of Orthopaedic Surgery and Research · doi:10.1186/s13018-025-05986-8 · Cited by 11

Should We Consider Neurodegeneration by Itself or in a Triangulation with Neuroinflammation and Demyelination? The Example of Multiple Sclerosis and Beyond

Perdaens, O., & Pesch, V. V. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms252312637 · Cited by 12

The relationships between neuroglial alterations and neuronal changes in Alzheimer’s disease, and the related controversies I: Gliopathogenesis and glioprotection

Toledano‐Díaz, A., Álvarez, M., & Tolédano, A. (2022) · Journal of Central Nervous System Disease · doi:10.1177/11795735221128703 · Cited by 11

Secretory products of DPSC mitigate inflammatory effects in microglial cells by targeting MAPK pathway

Howlader, M. S. I., Prateeksha, P., Hansda, S., Naidu, P., Das, M., Barthels, D., & Das, H. (2023) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2023.115971 · Cited by 10

IL ‐10 and Cdc42 modulate astrocyte‐mediated microglia activation in methamphetamine‐induced neuroinflammation

Silva, A. I., Socodato, R., Pinto, C., Terceiro, A. F., Canedo, T., Relvas, J. B., Saraiva, M., & Summavielle, T. (2024) · Glia · doi:10.1002/glia.24542 · Cited by 11

Myelin oligodendrocyte glycoprotein reactive Th17 cells drive Janus Kinase 1 dependent transcriptional reprogramming in astrocytes and alter cell surface cytokine receptor profiles during experimental autoimmune encephalomyelitis

Milne, S. M., Lahiri, A., Sanchez, C. L., Marshall, M. J., Jahan, I., & Meares, G. P. (2024) · Scientific Reports · doi:10.1038/s41598-024-63877-0 · Cited by 10

Do Periodontal Pathogens or Associated Virulence Factors Have a Deleterious Effect on the Blood-Brain Barrier, Contributing to Alzheimer’s Disease?

Kouki, M. A., Pritchard, A. B., Alder, J. E., & Crean, S. (2021) · Journal of Alzheimer s Disease · doi:10.3233/jad-215103 · Cited by 14

Retinoid X receptor activation promotes photoreceptor survival and modulates the inflammatory response in a mouse model of retinitis pigmentosa

Volonté, Y., Ayala-Peña, V. B., Vallese-Maurizi, H., Garelli, A., Rotstein, N. P., Politi, L. E., & German, O. L. (2021) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2021.119098 · Cited by 10

CSF1R blockade slows progression of cerebral hemorrhage by reducing microglial proliferation and increasing infiltration of CD8 + CD122+ T cells into the brain

Cheng, F., Wang, C., Yan, B., Yin, Z., Liu, Y., Zhang, L., Li, M., Liao, P., Gao, H., Jia, Z., et al. (2024) · International Immunopharmacology · doi:10.1016/j.intimp.2024.112071 · Cited by 9

Microglia-Astroglia-Neuron network following stroke: Novel insight into extracellular vesicles communication

Wan, H., Cui, Y., Zeng, Y., Hu, J., Li, M., & Xiao, Z. (2025) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2025.111537 · Cited by 9

Metabolic and inflammatory roles of glial cells in neurodegenerative and cerebrovascular diseases

OGUNLEYE, F. A., Zhou, Y., Yan, L., Abhulimen, P. O., Xu, Y., Lai, M. K. P., Okunowo, W. O., Sethi, G., Fang, C., & Ma, Y. (2026) · Ageing Research Reviews · doi:10.1016/j.arr.2026.103120 · Cited by 11

Clinical Ageing

Surugiu, R., Burdusel, D., Ruscu, M.-A., Cercel, A., Hermann, D. M., Fernández‐Cadenas, I., & Popa‐Wagner, A. (2023) · Sub-cellular biochemistry/Subcellular biochemistry · doi:10.1007/978-3-031-26576-1_16 · Cited by 9

Transforming Growth Factor β1 Ameliorates Microglial Activation in Perioperative Neurocognitive Disorders

Lin, D., Sun, Y., Wang, Y., Yang, D., Shui, M., Wang, Y., Xue, Z., Huang, X. D., Zhang, Y., Wu, A., et al. (2023) · Neurochemical Research · doi:10.1007/s11064-023-03994-w · Cited by 9

ALS iPSC-derived microglia and motor neurons respond to astrocyte-targeted IL-10 and CCL2 modulation

Allison, R. L., & Ebert, A. D. (2023) · Human Molecular Genetics · doi:10.1093/hmg/ddad209 · Cited by 9

Mesenchymal Stem Cells Combined With Electroacupuncture Treatment Regulate the Subpopulation of Macrophages and Astrocytes to Facilitate Axonal Regeneration in Transected Spinal Cord

Zhang, R., Wang, J., Deng, Q., Xiao, X., Zeng, X., Lai, B., Li, G., Ma, Y., Ruan, J., Han, I., et al. (2023) · Neurospine · doi:10.14245/ns.2346824.412 · Cited by 9

Non-neuronal crosstalk promotes an inflammatory response in nodose ganglia cultures after exposure to byproducts from gram positive, high-fat-diet-associated gut bacteria

Cawthon, C. R., Kirkland, R. A., Pandya, S., Brinson, N. A., & Serre, C. B. D. L. (2020) · Physiology & Behavior · doi:10.1016/j.physbeh.2020.113124 · Cited by 9

Different Activation of IL-10 in the Hippocampus and Prefrontal Cortex During Neurodegeneration Caused by Trimethyltin Chloride

Kamaltdinova, E. R., Pershina, E. V., Mikheeva, I. B., Bugaev-Makarovskiy, N. A., & Arkhipov, V. I. (2020) · Journal of Molecular Neuroscience · doi:10.1007/s12031-020-01682-w · Cited by 9

Correction to: Neuroimmune Response in Ischemic Preconditioning

McDonough, A., & Weinstein, J. R. (2017) · Neurotherapeutics · doi:10.1007/s13311-017-0580-5 · Cited by 9

Targeting glial fibrillary acidic protein in glaucoma: a monoclonal antibody approach to modulate glial reactivity and neuroinflammation for neuroprotection

Guan, C., Zhang, L., Fomo, K. N., Yang, J., Pfeiffer, N., & Grus, F. H. (2025) · Journal of Neuroinflammation · doi:10.1186/s12974-025-03482-8 · Cited by 12

2-carba-cyclic phosphatidic acid modulates astrocyte-to-microglia communication and influences microglial polarization towards an anti-inflammatory phenotype

Takei, R., Nakashima, M., Gotoh, M., Endo, M., Hashimoto, K., Miyamoto, Y., & Murakami‐Murofushi, K. (2023) · Neuroscience Letters · doi:10.1016/j.neulet.2023.137063 · Cited by 8

Dopaminergic agonist pramipexole improves memory and increases IL-10 production in LPS-challenged rats.

Mihaylova, A., Doncheva, N., Zlatanova, H., Delev, D. P., Ivanovska, M., Koeva, Y. A., Murdjeva, M., & Kostadinov, I. (2021) · PubMed · doi:10.22038/ijbms.2021.50439.11488 · Cited by 8

The Dual Role of Microglia in Multiple Sclerosis and its Implications for Diagnostics and Repair

Goulart, M. T., Queiroz, D. T. U., & Ribeiro, F. M. (2025) · Current Neuropharmacology · doi:10.2174/011570159x352356241126044933 · Cited by 8

Astrocytes in maintaining neuronal health and brain function: interplay of aging, diet, and environment

Dembitskaya, Y., & Popov, A. (2025) · Metabolic Brain Disease · doi:10.1007/s11011-025-01706-7 · Cited by 8

Role of transforming growth factorβ in neurovascular unit during cerebral small vessel disease

Li, Y., Cai, Y., Xie, K., Hu, F., Li, J., Li, C., Zhang, R., & Zhong, Z. (2025) · Fluids and Barriers of the CNS · doi:10.1186/s12987-025-00713-1 · Cited by 7

Role of glycolysis-mediated histone lactylation in microglial activation and progression of neurodegenerative diseases

Wang, S., Wang, J., Hu, Z., Wu, L., & Huang, L. (2026) · Experimental Neurology · doi:10.1016/j.expneurol.2026.115663 · Cited by 7

Astrocytes and microglia in multiple sclerosis and neuromyelitis optica

Zhang, L., Verkhratsky, A., & Shi, F. (2025) · Handbook of clinical neurology · doi:10.1016/b978-0-443-19102-2.00001-6 · Cited by 7

The effect of dehydroepiandrosterone on inflammatory response of astroglial cells

Buyanova, S., Chistyakov, D. V., Astakhova, A. A., & Sergeeva, M. G. (2017) · Biochemistry (Moscow) Supplement Series A Membrane and Cell Biology · doi:10.1134/s199074781704002x · Cited by 7

GABAB receptor activation alters astrocyte phenotype changes induced by trimethyltin via ERK signaling in the dentate gyrus of mice

Hwang, Y., Park, J. H., Kim, H., & Shin, E. (2023) · Life Sciences · doi:10.1016/j.lfs.2023.121529 · Cited by 7

Narrating the psychoneuroimmunomodulatory properties of serotonin 5-HT2A receptor psychedelics from a transdiagnostic perspective

Thuery, G., Sheridan, C., Iusan, P., Brar, G., Ledden, K., Freyne, A., Kelly, J. R., & Harkin, A. (2025) · Acta Neuropsychiatrica · doi:10.1017/neu.2025.10030 · Cited by 7

Pulmonary accumulation and immune modulation by intravenously administered environmentally relevant microplastics in mice

Lee, Y., Kim, H.-K., Kim, H.-K., Sung, S., Sung, S.-E., Kang, K.-K., Kim, D., Lee, S., & Lee, S. (2025) · Journal of Hazardous Materials · doi:10.1016/j.jhazmat.2025.140311 · Cited by 6

Targeting glial-orchestrated neuroinflammation in migraine pathophysiology

Lu, W., Zhang, Y., Shi, C., Tao, Y., Li, S., Sun, Y., Ji, F., Chen, G., Snutch, T., & Tao, J. (2026) · The Journal of Headache and Pain · doi:10.1186/s10194-026-02272-8 · Cited by 8

Investigation of the Immunomodulatory and Neuroprotective Properties of Nigella sativa Oil in Experimental Systemic and Neuroinflammation

Mihaylova, A., Doncheva, N., Vlasheva, M., Katsarova, M. N., Gardjeva, P. A., Dimitrova, S. Z., & Kostadinov, I. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26052235 · Cited by 8

The glia‐immune network: Astrocytes and oligodendrocytes as microglial co‐ordinators in health and disease

Mitchener, V. F. T., Thackray, M. J., & Arancibia‐Cárcamo, I. L. (2025) · The Journal of Physiology · doi:10.1113/jp287015 · Cited by 8

Morphofunctional Changes in Brain and Peripheral Blood in Adult and Aged Wistar Rats with AlCl3-Induced Neurodegeneration

Sentyabreva, A. V., Miroshnichenko, E. A., Melnikova, E. A., Цветков, И. С., & Kosyreva, A. M. (2023) · Biomedicines · doi:10.3390/biomedicines11092336 · Cited by 7

Study on the Polarization of Astrocytes in the Optic Nerve Head of Rats Under High Intraocular Pressure: In Vitro

Ma, B., Ren, J., & Qian, X. (2025) · Bioengineering · doi:10.3390/bioengineering12020104 · Cited by 6

Shielding Effect of Ryanodine Receptor Modulator in Rat Model of Autism

Kumar, H., Kulkarni, G. T., Diwan, V., & Sharma, B. (2021) · Basic and Clinical Neuroscience Journal · doi:10.32598/bcn.2021.2966.1 · Cited by 5

The impact of early life stress and immune challenge on behavior and glia cells alteration in late adolescent rats

Réus, G. Z., Giridharan, V. V., de Moura, A. B., Borba, L. A., Botelho, M. E. M., Behenck, J. P., Generoso, J. S., Selvaraj, S., Bhatti, G. S., Barichello, T., et al. (2021) · International Journal of Developmental Neuroscience · doi:10.1002/jdn.10108 · Cited by 5

AjTGFβ alleviates V. splendidus-induced inflammation through SMADs pathway in Apostichopus japonicus

Zhang, Z., wenwen, Y., Guanghui, H., Cheng-hua, L., & Lv, Z. (2023) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2023.108593 · Cited by 4

Chronic Inflammation Offers Hints About Viable Therapeutic Targets for Preeclampsia and Potentially Related Offspring Sequelae

Prasad, J. D., Steenwinckel, J. V., Gunn, A. J., Bennet, L., Korzeniewski, S. J., Gressèns, P., & Dean, J. M. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms252312999 · Cited by 5

IL-1ra and CCL5, but not IL-10, are promising targets for treating SMA astrocyte-driven pathology

Allison, R. L., Mangione, C. C., Suneja, M., Gawrys, J. E., Melvin, B. M., Belous, N., LaCroix, M., Harmelink, M. M., Burnett, B. G., & Ebert, A. D. (2024) · Molecular Therapy · doi:10.1016/j.ymthe.2024.12.016 · Cited by 4

Adolescent Alcohol and the Spectrum of Cognitive Dysfunction in Aging

Deak, T., Burzynski, H. E., Nunes, P. T., Day, S. M., & Savage, L. M. (2025) · Advances in experimental medicine and biology · doi:10.1007/978-3-031-81908-7_12 · Cited by 3

Synthesis, characterization and biological evaluation of poly [LA-co-(Glc-alt-Lys)] for nerve regeneration scaffold

Yin, Y., Yi, J., Xie, L., Yan, Q., Dai, H., & Li, S. (2014) · Frontiers of Materials Science · doi:10.1007/s11706-014-0239-7 · Cited by 4

Analysis of Why Alzheimer’s Dementia Never Spontaneously Reverses, Suggests the Basis for Curative Treatment

Fessel, J. (2023) · Journal of Clinical Medicine · doi:10.3390/jcm12144873 · Cited by 5

Microglial TRPV1 in epilepsy: Is it druggable for new antiepileptic treatment?

HU, J., Mo, J., & Cheng, X. (2023) · Biocell · doi:10.32604/biocell.2023.029409 · Cited by 3

A cutting-edge strategy for spinal cord injury treatment: resident cellular transdifferentiation

Fang, Y.-M., Chen, W.-C., Zheng, W.-J., Yang, Y.-S., Zhang, Y., Chen, X.-L., Pei, M.-Q., Lin, S., & He, H. (2023) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2023.1237641 · Cited by 3

Maternal Immune Activation and Neuropsychiatric Disorders: The Intricate Puzzle of Autism Spectrum Disorder

Fontes‐Dutra, M., Rabelo, B. F., Santos‐Terra, J., Deckmann, I., Schwingel, G. B., & Gottfried, C. (2020) · Progress in inflammation research · doi:10.1007/978-3-030-39335-9_11 · Cited by 3

High concentrations of fructose cause brain damage in mice

Cargnin‐Carvalho, A., da Silva, M. R., Costa, A. B., Engel, N. A., de Farias, B. X., Bressan, J. B., Backes, K. M., de Souza, F., da Rosa, N., de Oliveira, A. N., et al. (2023) · Biochemistry and Cell Biology · doi:10.1139/bcb-2022-0088 · Cited by 2

Immunomodulation of microglia/macrophages and neutrophils as immunotherapeutic targets in ischemic stroke: A narrative review

Ekingen, E., & Dinç, R. (2025) · Brain Circulation · doi:10.4103/bc.bc_41_25 · Cited by 2

Regulatory B cells in the central nervous system: From immune regulation to neuroprotection

Stanaszek, L., & Janowski, M. (2026) · Neuroprotection/Neuroprotection (Chichester, England. Print) · doi:10.1002/nep3.70027 · Cited by 2

Migraine: Epidemiology, Risk Factors, Pathophysiology, and Treatment

Lu, W., Zhang, Y., Shi, C., Tao, Y., Li, S., Sun, Y., Ji, F., Jiang, D., Snutch, T. P., & Tao, J. (2026) · MedComm · doi:10.1002/mco2.70933 · Cited by 2

Revisiting Functional Heterogeneity of Microglia and Astroglia

Kotova, M. M., Apukhtin, K. V., Nikitin, S. V., & Kalueff, A. V. (2024) · Journal of Evolutionary Biochemistry and Physiology · doi:10.1134/s0022093024060036 · Cited by 2

The Role of Immune Cells in the Brain during Physiological and Pathological Conditions

Franklin, T., Wohleb, E. S., & Duman, R. S. (2015) · Psychiatric Annals · doi:10.3928/00485713-20150501-05 · Cited by 2

Does physical exercise influence in the development of neuroeschistosomiasis?

de Carvalho, T. P. V., Peixoto, C. A., de Paiva, I. H. R., Loyo, R. M., do Nascimento, W. R. C., Vasconcelos, L. R. S., Gomes, E. C. D. S., & Barbosa, C. S. (2019) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2019.07.029 · Cited by 2

Targeting glial PD-1/PD-L1 restores microglial homeostasis and attenuates neuronal hyperactivity in an Alzheimer’s disease modelPreprint

Park, T., Chang, L., Chung, S. W., Lee, S., Bae, S., Condello, C., Kim, Y. H., Lee, J., Kim, H.-J., Kwon, H.-K., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.09.13.612389 · Cited by 2

Role of astrocytes in neuroinflammation (review)

Mordovina, A. I., Rudenko, Е. Е., & Демура, Т. А. (2023) · Saratov Journal of Medical Scientific Research · doi:10.15275/ssmj1901089 · Cited by 1

Research Trends and Evolution of Astrocytes in Depression and Antidepressant Treatment: A Bibliometric Analysis

Pan, S., Li, Z., Zhou, J., Shang, X., Gu, T., Sun, X.-M., & Zhu, Z. (2025) · Current Neuropharmacology · doi:10.2174/011570159x353752250227113751 · Cited by 1

Impact of Psychological Stress and Spontaneous Tumour Regression on the Hippocampal Proteome in a Mouse Model of Breast Cancer

Mampay, M., Alhity, G., Rolle, S. O., Alzboon, W., Stewart, N. A., Flint, M. S., & Sheridan, G. K. (2025) · Journal of Neurochemistry · doi:10.1111/jnc.70052 · Cited by 1

Molecular mechanism linking sleep disturbances to neurodegenaration

Keikhaei, N., Tahergourabi, S. H. A., Hekmatnezhad, H., Baniaghil, M. A., Hassanpoor, P., & Asgharihajimahalleh, S. (2025) · Journal of Current Biomedical Reports · doi:10.61882/jcbior.6.2.322 · Cited by 1

Unveiling core acupoints in acupuncture treatment for primary depressive disorder: integrating data mining and network acupuncture-based analysis

Siyu, L. I. U., Xinnan, L. U. O., Jiayun, X. I. E., Miqun, Z. H. O. U., Xiaona, H. U., & Song, S. L. (2025) · Digital Chinese Medicine · doi:10.1016/j.dcmed.2025.12.006 · Cited by 2

Insights into Astrogliosis, Inflammation Processes, and Emerging Treatments by Exosome Therapy and Low-Level Laser Therapy for Spinal Cord Injury: A Systematic Review

Mosleh, H., Bahrami, M., Tahmasebinia, F., Abdi, S., Khajavi, M., Jalali, M., Tasa, D., Abbaszadeh, H., & Keramatinia, A. (2025) · Journal of lasers in medical sciences · doi:10.34172/jlms.2025.68 · Cited by 2

Research progress on biomarkers of traumatic brain injury

Shen, X., Cheng, S., Chen, S., Wang, M., Li, T., Xu, W., Zhang, Y., Yuan, P., & Shi, L. (2026) · Animal Models and Experimental Medicine · doi:10.1002/ame2.70173 · Cited by 1

Insights gained from single-cell sequencing analysis of ischemic stroke

梅艳琴, Guan, T., Fu, L., Kong, J., & Lv, Y. (2026) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2026.1784660 · Cited by 1

HMC3 revealed: how much do these “Microglia” really tell us?

Buccarello, L., Privitera, A., Partsinevelos, K., Serwa, K., Carota, G., Pietro, L. D., Cardaci, V., Mangione, R., Sibbitts, J., Lazzarino, G., et al. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1778798 · Cited by 2

Neuroinflammation in glaucoma: a myriad of cellular pathways and players

MacLean, M., Lydon, S. D., Gomes, C., Pizzi, E. M., Diemler, C. A., Yablonski, S. E. R., Howell, G. R., Meyer, J. S., & Libby, R. T. (2026) · Mammalian Genome · doi:10.1007/s00335-026-10253-0 · Cited by 1

Neuroglia in Infectious Brain Diseases

Skar, G. L. (2015) · Colloquium Series on Neuroglia in Biology and Medicine From Physiology to Disease · doi:10.4199/c00125ed1v01y201503ngl005 · Cited by 1

Reactive Astrocytes in Cerebral Ischemic Reperfusion Injury

Mishra, A., Nayak, R., & Sun, D. (2018) · Springer series in translational stroke research · doi:10.1007/978-3-319-90194-7_6 · Cited by 1

Crosstalk of Highly Purified Microglia and Astrocytes in the Frame of Toll-like Receptor (TLR)2/1 Activation

Zelenka, L., Jarek, M., Pägelow, D., Geffers, R., van Vorst, K., & Fulde, M. (2023) · Neuroscience · doi:10.1016/j.neuroscience.2023.05.001 · Cited by 1

Nimodipine attenuates neuroinflammation and delayed apoptotic neuronal death induced by trimethyltin in the dentate gyrus of mice

Hwang, Y., Park, J. H., Kim, H., & Shin, E. (2024) · Journal of Molecular Histology · doi:10.1007/s10735-024-10226-0 · Cited by 1

Contribution of protein-derived bioactive molecules (cytokines and chemokines) in neuroinflammation, resolution, and neuroprotection

Farooqui, A. A. (2021) · Elsevier eBooks · doi:10.1016/b978-0-323-88460-0.00001-1 · Cited by 1

Neuroinflammation in Aging

Fenn, A. M., Norden, D. M., & Godbout, J. P. (2015) · Wiley eBooks · doi:10.1002/9781118732748.ch6 · Cited by 1

Infection-Specific Reprogramming of Microglia Reveals Distinct Virulence Pathways Linking Periodontal Pathogens to Alzheimer’s DiseasePreprint

Kamińska, M., Dudzinska, N. A. M., Klapper, A., Geißler, S., Taudte, N., Greiser, S., Potempa, J., Cynis, H., & Mydel, P. M. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.06.06.658266 · Cited by 1

Neuroinflammation: Peripheral and Neurogenic Underlying Processes

Rodriguez-Ramirez, J., Adalid-Peralta, L. V., Fragoso, G., Rosas, G., Meneses, G., Fleury, A., Sciutto, E., & Gardenas, G. (2015) · Journal of Contemporary Immunology · doi:10.7726/jci.2015.1002

The role of microglia in methamphetamine exposure

Canedo, T. (2014) · Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT) · doi:10.34626/0rv0-m465

Glia in Neuroimmunology

Suzumura, A. (2016) · Springer eBooks · doi:10.1007/978-4-431-55594-0_2

Novel role for Gas6 as a positive regulator of myelination

Goudarzi, S. (2016)

ВЛИЯНИЕ ДЕГИДРОЭПИАНДРОСТЕРОНА НА ВОСПАЛИТЕЛЬНЫЙ ОТВЕТ АСТРОГЛИАЛЬНЫХ КЛЕТОК, "Биологические мембраны: Журнал мембранной и клеточной биологии"

Buyanova, S., Чистяков, Д. В., Астахова, А. А., & Сергеева, М. Г. (2017) · Биологические мембраны Журнал мембранной и клеточной биологии · doi:10.7868/s0233475517050036

The Role of Interleukin-10 in CD4+ T Cell-Mediated Neuroprotection after Facial Nerve Injury

Runge, E. M. (2019) · IUScholarWorks (Indiana University) · doi:10.7912/c2/2118

Toward a Wholly Organic, Immunomodulatory Neuroelectronic Interface

Crawford, L. (2021) · ResearchWorks at the University of Washington (University of Washington)

132. The role of astrocytes in IL-10 mediated regulation of inflammation within the CNS

Norden, D. M., Fenn, A. M., & Godbout, J. P. (2013) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2013.07.144 · Cited by 1

Age-related impairments in the dynamic regulation of active microglia by astrocytes

Norden, D. M., Trojanowski, P. T., Walker, F. R., & Godbout, J. P. (2015) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2015.06.076 · Cited by 2

Attenuation of Astroglial Reactivity by Interleukin-10

Balasingam, V., & Yong, V. W. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-09-02945.1996 · Cited by 186

Astrocyte‐targeted IL‐10 production decreases proliferation and induces a downregulation of activated microglia/macrophages after PPT

Recasens, M., Shrivastava, K., Almolda, B., González, B., & Castellano, B. (2018) · Glia · doi:10.1002/glia.23573 · Cited by 39

Insensitivity of astrocytes to interleukin 10 signaling following peripheral immune challenge results in prolonged microglial activation in the aged brain

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