The DOI matches its Crossref record; 205 of the 205 references it cites were found in a registry or an index.
The contribution of astrocytes to the neuroinflammatory response in multiple sclerosis and experimental autoimmune encephalomyelitis
Open accessAbstract
Neuroinflammation is the coordinated response of the central nervous system (CNS) to threats to its integrity posed by a variety of conditions, including autoimmunity, pathogens and trauma. Activated astrocytes, in concert with other cellular elements of the CNS and immune system, are important players in the modulation of the neuroinflammatory response. During neurological disease, they produce and respond to cellular signals that often lead to dichotomous processes, which can promote further damage or contribute to repair. This occurs also in multiple sclerosis (MS), where astrocytes are now recognized as key components of its immunopathology. Evidence supporting this role has emerged not only from studies in MS patients, but also from animal models, among which the experimental autoimmune encephalomyelitis (EAE) model has proved especially instrumental. Based on this premise, the purpose of the present review is to summarize the current knowledge of astrocyte behavior in MS and EAE. Following a brief description of the pathological characteristics of the two diseases and the main functional roles of astrocytes in CNS physiology, we will delve into the specific responses of this cell population, analyzing MS and EAE in parallel. We will define the temporal and anatomical profile of astroglial activation, then focus on key processes they participate in. These include: (1) production and response to soluble mediators (e.g., cytokines and chemokines), (2) regulation of oxidative stress, and (3) maintenance of BBB integrity and function. Finally, we will review the state of the art on the available methods to measure astroglial activation in vivo in MS patients, and how this could be exploited to optimize diagnosis, prognosis and treatment decisions. Ultimately, we believe that integrating the knowledge obtained from studies in MS and EAE may help not only better understand the pathophysiology of MS, but also uncover new signals to be targeted for therapeutic intervention.
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
“MS-associated genes were highly expressed in glioblastoma, consistent with the emerging view that astrocyte-mediated neuroinflammation is a key contributor to the MS pathogenesis39.”
From A computational tool (H-MAGMA) for improved prediction of brain-disorder risk genes by incorporating brain chromatin interaction profiles (2020) · cites this paper as [39]
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
Neurotoxic reactive astrocytes are induced by activated microglia
Liddelow, S. A., Guttenplan, K. A., Clarke, L. E., Bennett, F. C., Bohlen, C. J., Schirmer, L., Bennett, M. L., Münch, A. E., Chung, W.-S., Peterson, T. C., et al. (2017) · Nature · doi:10.1038/nature21029 · Cited by 7,971
Astrocyte-endothelial interactions at the blood-brain barrier
Abbott, N. J., Rönnbäck, L., & Hansson, E. (2006) · Nature Reviews Neuroscience · doi:10.1038/nrn1824 · Cited by 5,595
Astrocytes: Biology and pathology
Sofroniew, M. V., & Vinters, H. V. (2010) · Acta Neuropathologica · doi:10.1007/s00401-009-0619-8 · Cited by 5,196
The pro- and anti-inflammatory properties of the cytokine interleukin-6
Scheller, J., Chalaris, A., Schmidt-Arras, D., & Rose-John, S. (2011) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2011.01.034 · Cited by 3,212
NF-κB, inflammation, immunity and cancer: coming of age
Taniguchi, K., & Karin, M. (2018) · Nature Reviews Immunology · doi:10.1038/nri.2017.142 · Cited by 2,679
Molecular dissection of reactive astrogliosis and glial scar formation
Sofroniew, M. V. (2009) · Trends in Neurosciences · doi:10.1016/j.tins.2009.08.002 · Cited by 2,594
Tripartite synapses: glia, the unacknowledged partner
Araque, A., Parpura, V., Sanzgiri, R. P., & Haydon, P. G. (1999) · Trends in Neurosciences · doi:10.1016/s0166-2236(98)01349-6 · Cited by 2,529
Astrocyte scar formation aids central nervous system axon regeneration
Anderson, M. A., Burda, J. E., Ren, Y., Ao, Y., O’Shea, T. M., Kawaguchi, R., Coppola, G., Khakh, B. S., Deming, T. J., & Sofroniew, M. V. (2016) · Nature · doi:10.1038/nature17623 · Cited by 1,851
Cortical demyelination and diffuse white matter injury in multiple sclerosis
Kutzelnigg, A., Lucchinetti, C. F., Stadelmann, C., Brück, W., Rauschka, H., Bergmann, M., Schmidbauer, M., Parisi, J. E., & Lassmann, H. (2005) · Brain · doi:10.1093/brain/awh641 · Cited by 1,836
Multiple sclerosis--the plaque and its pathogenesis.
Frohman, E., Racke, M., & Raine, C. (2006) · New England Journal of Medicine · doi:10.1056/nejmra052130 · Cited by 1,793
Cited by
Sorted by citations
Items 201–246 of 246
Prasad, M., Pulukuri, S. V., Sampani, K., Yarala, R. R., Mittal, R., Xia, W., Stein, T. D., Aytan, N., Chen, X., Ness, S. D., et al. (2026) · Journal of Alzheimer s Disease · doi:10.1177/13872877261452676 · Cited by 1
Li, M., Sun, P., Zhou, X., Yang, X., & Li, W. (2026) · Nutritional Neuroscience · doi:10.1080/1028415x.2026.2686736 · Cited by 1
Interleukin-6 trans-signalling as a selectively targetable driver of neurodegeneration
Risby-Jones, G., Lee, J. D., & Fung, J. N. (2026) · Trends in Neurosciences · doi:10.1016/j.tins.2026.07.002 · Cited by 1
Samtleben, S., Mina, L., Yap, M. C., Branton, W. G., Yousuf, M. S., Tenorio, G., Ballanyi, K., Giuliani, F., Kerr, B. J., Power, C., et al. (2022) · European Journal of Neuroscience · doi:10.1111/ejn.15817 · Cited by 1
Neuroprotective effect of Vesatolimod in an experimental autoimmune encephalomyelitis mice model
Jiang, X., Song, Y., Fang, J., Yang, X., Mu, S., & Zhang, J. (2023) · International Immunopharmacology · doi:10.1016/j.intimp.2023.109717 · Cited by 1
Astrocyte Activation and Drug Target in Pathophysiology of Multiple Sclerosis
Bisht, P., Rathore, C., Rathee, A., & Kabra, A. (2024) · Methods in molecular biology · doi:10.1007/978-1-0716-3662-6_30 · Cited by 1
Madsen, P. M., Desu, H. L., Vaccari, J. P. D. R., Florimon, Y., Ellman, D. G., Keane, R. W., Clausen, B. H., Lambertsen, K. L., & Brambilla, R. (2021) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2021.04.017 · Cited by 1
Self-citationThe effects of long-term sucrose consumption on olfactory neurogenesis and neuroinflammation
Keys, C. (2023) · Queensland University of Technology · doi:10.5204/thesis.eprints.244721 · Cited by 1
Yousuf, M. S. (2020) · ERA: Education and Research Archive (University of Alberta) · doi:10.7939/r3-2wwz-x005
Kk, K., Allahbadia, G., & Singh, M. (2020) · SunText Review of BioTechnology · doi:10.51737/2766-5097.2020.004
Light of the stars: calcium signals light up astrocytes in the presence of autoreactive CD4+ T cells
Pristov, J. B., & Nikolic, L. M. (2021) · Neural Regeneration Research · doi:10.4103/1673-5374.313036
Astrocytes in the pathogenesis of multiple sclerosis
Takarada‐Iemata, M., & Hori, O. (2021) · Folia Pharmacologica Japonica · doi:10.1254/fpj.21030
Thorburn, K. C. (2021) · ERA: Education and Research Archive (University of Alberta) · doi:10.7939/r3-vk71-pt78
Mechanisms of brain protection against autoimmune inflammation
Волков, А. Ю., Melnikov, M., & Boyko, A. N. (2021) · Neurology neuropsychiatry Psychosomatics · doi:10.14412/2074-2711-2021-1s-4-9
Tiwari, V. K., & Singh, A. P. (2020) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.737515832.793574153
Tunley, S. (2024) · Open Access Victoria University of Wellington | Te Herenga Waka (Figshare) · doi:10.26686/wgtn.25201913
The Emerging Applications of Machine Learning in the Diagnosis of Multiple Sclerosis
Sharma, A., Sharma, N., Arora, A., & Pal, R. (2024) · Studies in computational intelligence · doi:10.1007/978-981-99-9029-0_6
Correale, J. D., & Marrodán, M. (2024) · Springer eBooks · doi:10.1007/978-3-031-24297-7_10-1
Astrocyte Reprogramming by Th17 Cells in Autoimmune Neuroinflammation: Mechanisms and Implications
Milne, S. M. (2024) · The Research Repository @ WVU (West Virginia University) · doi:10.33915/etd.12577
Correale, J. D., & Marrodán, M. (2024) · Springer eBooks · doi:10.1007/978-3-031-60006-7_10
Gao, Y., Shi, Z., Zhang, S., Wu, Z., Zhou, T., Zhou, P., Chu, W., & Wang, X. (2025) · Acta Biochimica et Biophysica Sinica · doi:10.3724/abbs.2025131
Liu, X., Zhou, F., Wang, W., Chen, G., Zhang, Q., Lv, R., Zhao, Z., Li, X., Yu, Q., Meves, J. M., et al. (2021) · Figshare · doi:10.6084/m9.figshare.14570713
Liu, X., Zhou, F., Wang, W., Chen, G., Zhang, Q., Lv, R., Zhao, Z., Li, X., Yu, Q., Meves, J. M., et al. (2021) · Figshare · doi:10.6084/m9.figshare.14570716
GFAP and the genetic code of astrocyte activation in Alzheimer’s disease
Upadhyay, R., Srinivasan, T. B., Umapriya, R., Chandrapragasam, V., & Sevanan, M. (2026) · International review of neurobiology · doi:10.1016/bs.irn.2026.01.007
The effect of astrocyte depletion and repopulation approaches in pathological condition of CNS
Tahmasebi, F., Safarian, A., Asl, E. R., Vahidinia, Z., & Barati, S. (2026) · Acta Neurologica Belgica · doi:10.1007/s13760-026-03005-z
Matanaq, H. R., Mohammadzadeh, A., Sheykhsaran, E., Abbasi, A., Jafari-Sales, A., Rasizadeh, R., & Baghi, H. B. (2026) · Future Virology · doi:10.1080/17460794.2026.2635310 · Cited by 1
Kariminejad-Farsangi, H., Kariminejad-Farsangi, H., Sharifi, M., Azh, S., Nasab, Z. G., Dehghan-Kuroki, M., & Joushi, S. (2026) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-026-01715-9
Zhong, X., Zhang, H., Xie, J., Gao, Y., Wang, H., Peng, Y., Yi, F., & Chen, J. (2026) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2026.1683599
Mechanisms of autophagy–lysosome pathway impairment in Alzheimer's disease
Lü, K., Lu, Y., Tang, R., Dong, X., Zhuang, P., Gao, Y., Cheng, M., Wang, Y., & Wang, Y. (2026) · Journal of Alzheimer s Disease · doi:10.1177/13872877261460879
Astrocytes in Multiple Sclerosis: Getting to the Core
Tinkey, R. A., Smith, B. C., & Williams, J. L. (2026) · International Journal of Molecular Sciences · doi:10.3390/ijms27146520
Araújo-Andrade, L., Nogueira, P., Mota, B., Lima, N., Silva, A., Pereira, P. A., Madeira, M. D., & Cardoso, A. (2026) · Antibiotics · doi:10.3390/antibiotics15080728
Milosevic, A., Janjic, M. M., Dimitrijevic, D., & Bjelobaba, I. M. (2026) · Biomedicines · doi:10.3390/biomedicines14081796
Hu, S., Xiao, X., Cheng, X., Huang, Y., Cui, T., Shen, S., Cui, C., Xiao, L., Tan, H., Qiu, W., et al. (2026) · CNS Neuroscience & Therapeutics · doi:10.1002/cns.71091
Park, J., Cheon, S. Y., & Guo, F. (2026) · Glia · doi:10.1002/glia.70211 · Cited by 1
Li, Y., Jiang, W., Zhong, F., & Dong, M. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1895546
Immune cells and nanotechnology: Innovations in therapy
Naomi, R., Balan, S. S., Zubairi, S. I., Halim, S., David, P. R., & Rajikan, R. (2026) · Elsevier eBooks · doi:10.1016/b978-0-443-44631-3.00008-1
Apigenin as a Potential Modulator of Neuroinflammation in Multiple Sclerosis: A Review
de Santana, M. R., Silva, N. N., de Oliveira, J. V. R., Victor, M. M., Butt, A. M., & Costa, S. L. (2026) · Biology · doi:10.3390/biology15171545
Kalaitzaki, V., Oldrati, P., Ferreira, F. M., Katsoulas, A., Ali, A., Baselgia, L., Liu, B., Fang, J., Sankowski, R., Matsushita, M., et al. (2026) · Science Advances · doi:10.1126/sciadv.aeg6770
Hyun, D., 명준형, Park, J.-W., Leow, W. L., Cho, Y., Lee, H., Lee, H., Lee, J., Kim, B.-J., & Hong, S. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1899823
Schumacher, M., & Ghoumari, A. M. (2026) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2026.101293
Metadata
- Authors
- Brambilla, R.
- Affiliations
- University of Miami (US)
- Corresponding author
- Brambilla, Roberta
- ORCID
- Brambilla, Roberta
- Venue
- Acta Neuropathologica
- Published
- 2019-03-07
- Volume
- 137
- Issue
- 5
- Pages
- 757-783
- ISSN
- 0001-6322 (ISSN-L)
- 1432-0533
- PMC
- PMC6483860
- OpenAlex
- W2921019730
- Cited by
- 246
- References
- 205
- Citations by year
- 2026: 26 · 2025: 22 · 2024: 34 · 2023: 30 · 2022: 32 · 2021: 50 · 2020: 34 · 2019: 17
- FWCI
- 4.95
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- Locations
- Acta Neuropathologica (publishedVersion)
- University of Southern Denmark Research Portal (University of Southern Denmark) (publishedVersion, other-oa)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institute of Neurological Disorders and Stroke (1R01NS094522-01)
- National Multiple Sclerosis Society (NMSS PP-1804-30716)
- Fondazione Italiana Sclerosi Multipla (FISM 2015/R/7)
- Topics
- Health Sciences › Medicine › Clinical Neurology › Multiple Sclerosis Research Studies
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Health Sciences › Medicine › Clinical Neurology › Spinal Cord Injury Research
- Keywords
- astrocytes, neuroinflammation, multiple sclerosis, experimental autoimmune encephalomyelitis, astroglial activation, cytokines, chemokines, oxidative stress, blood-brain barrier integrity, autoimmunity
- MeSH terms
- Animals, Astrocytes, Encephalomyelitis, Autoimmune, Experimental, Humans, Inflammation, Multiple Sclerosis
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