The DOI matches its Crossref record; 148 of the 148 references it cites were found in a registry or an index.
The pro-remyelination properties of microglia in the central nervous system
Open accessAbstract
Microglia are resident macrophages of the CNS that are involved in its development, homeostasis and response to infection and damage. Microglial activation is a common feature of neurological disorders, and although in some instances this activation can be damaging, protective and regenerative functions of microglia have been revealed. The most prominent example of the regenerative functions is a role for microglia in supporting regeneration of myelin after injury, a process that is critical for axonal health and relevant to numerous disorders in which loss of myelin integrity is a prevalent feature, such as multiple sclerosis, Alzheimer disease and motor neuron disease. Although drugs that are intended to promote remyelination are entering clinical trials, the mechanisms by which remyelination is controlled and how microglia are involved are not completely understood. In this Review, we discuss work that has identified novel regulators of microglial activation - including molecular drivers, population heterogeneity and turnover - that might influence their pro-remyelination capacity. We also discuss therapeutic targeting of microglia as a potential approach to promoting remyelination.
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?
The check wasn’t confident either way, so it gives no verdict — never disputed.
In the citing paper
“Efficient clearance of myelin debris after demyelination can favorably impact OPC recruitment and differentiation into remyelinating oligodendrocytes [29].”
From TREM2 activation on microglia promotes myelin debris clearance and remyelination in a model of multiple sclerosis (2020) · cites this paper as [29]
Experimental — accuracy not yet measuredThe check wasn’t confident either way, so it gives no verdict — never disputed.
In the citing paper
“Microglia activation and myelin debris clearance are critical steps for successful remyelination [29].”
From TREM2 activation on microglia promotes myelin debris clearance and remyelination in a model of multiple sclerosis (2020) · cites this paper as [29]
Experimental — accuracy not yet measuredThe check wasn’t confident either way, so it gives no verdict — never disputed.
In the citing paper
“Microglia drive a critical response to demyelination by clearing myelin debris and enabling newly formed oligodendrocytes to remyelinate denuded axons (8).”
From Peroxisomal integrity in demyelination-associated microglia enables cellular debris clearance and myelin renewal in mice (2026) · cites this paper as [8]
Experimental — accuracy not yet measuredThe check wasn’t confident either way, so it gives no verdict — never disputed.
In the citing paper
“Long-term demyelination occurs post-SCI, with lipid-containing myelin debris being absorbed and processed by inflammatory cells, including microglia—a process crucial for paving the way for regenerative reactions and inflammation resolution [9–11].”
From miR-223 accelerates lipid droplets clearance in microglia following spinal cord injury by upregulating ABCA1 (2024) · cites this paper as [11]
Experimental — accuracy not yet measured
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
Macrophage activation and polarization: nomenclature and experimental guidelines
Murray, P. J., Allen, J. E., Biswas, S. K., Fisher, E. A., Gilroy, D. W., Goerdt, S., Gordon, S., Hamilton, J. A., Ivashkiv, L. B., Lawrence, T., et al. (2014) · Immunity · doi:10.1016/j.immuni.2014.06.008 · Cited by 6,337
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
Microglia Sculpt Postnatal Neural Circuits in an Activity and Complement-Dependent Manner
Schafer, D. P., Lehrman, E. K., Kautzman, A. G., Koyama, R., Mardinly, A. R., Yamasaki, R., Ransohoff, R. M., Greenberg, M. E., Barres, B. A., & Stevens, B. (2012) · Neuron · doi:10.1016/j.neuron.2012.03.026 · Cited by 4,089
Krasemann, S., Madore, C., Cialic, R., Baufeld, C., Calcagno, N., El Fatimy, R., Beckers, L., O’Loughlin, E., Xu, Y., Fanek, Z., et al. (2017) · Immunity · doi:10.1016/j.immuni.2017.08.008 · Cited by 2,979
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
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
Hammond, T. R., Dufort, C., Dissing-Olesen, L., Giera, S., Young, A., Wysoker, A., Walker, A. J., Segel, M., Nemesh, J., Saunders, A., et al. (2018) · doi:10.1101/406140 · Cited by 2,225
Transcriptome-Based Network Analysis Reveals a Spectrum Model of Human Macrophage Activation
Xue, J., Schmidt, S. V., Sander, J., Draffehn, A., Krebs, W., Quester, I., De Nardo, D., Gohel, T. D., Emde, M., Schmidleithner, L., et al. (2014) · Immunity · doi:10.1016/j.immuni.2014.01.006 · Cited by 2,210
Heterogeneity in the distribution and morphology of microglia in the normal adult mouse brain
Lawson, L. J., Perry, V. H., Dri, P., & Gordon, S. (1990) · Neuroscience · doi:10.1016/0306-4522(90)90229-w · Cited by 2,045
Elmore, M. R. P., Najafi, A. R., Koike, M. A., Dagher, N. N., Spangenberg, E. E., Rice, R. A., Kitazawa, M., Matusow, B., Nguyen, H., West, B. L., et al. (2014) · Neuron · doi:10.1016/j.neuron.2014.02.040 · Cited by 1,968
Cited by
Sorted by citations
Microglia: Immune and non-immune functions
Borst, K., Dumas, A. A., & Prinz, M. (2021) · Immunity · doi:10.1016/j.immuni.2021.09.014 · Cited by 804
Cignarella, F., Filipello, F., Bollman, B., Cantoni, C., Locca, A., Mikesell, R., Manis, M., Ibrahim, A., Deng, L., Benitez, B. A., et al. (2020) · Acta Neuropathologica · doi:10.1007/s00401-020-02193-z · Cited by 392
Remyelination in multiple sclerosis: From basic science to clinical translation
Lubetzki, C., Zalc, B., Williams, A., Stadelmann, C., & Stankoff, B. (2020) · The Lancet Neurology · doi:10.1016/s1474-4422(20)30140-x · Cited by 350
Single-cell RNA-seq reveals the transcriptional landscape in ischemic stroke
Zheng, K., Lin, L., Jiang, W., Chen, L., Zhang, X., Zhang, Q., Ren, Y., & Hao, J. (2021) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1177/0271678x211026770 · Cited by 308
Microglia and the aging brain: are senescent microglia the key to neurodegeneration?
Angelova, D. M., & Brown, D. R. (2019) · Journal of Neurochemistry · doi:10.1111/jnc.14860 · Cited by 262
Cellular senescence and Alzheimer disease: the egg and the chicken scenario
Saez-Atienzar, S., & Masliah, E. (2020) · Nature Reviews Neuroscience · doi:10.1038/s41583-020-0325-z · Cited by 257
Cellular immunology of relapsing multiple sclerosis: interactions, checks, and balances
Bar‐Or, A., & Li, R. (2021) · The Lancet Neurology · doi:10.1016/s1474-4422(21)00063-6 · Cited by 261
He, W., Kapate, N., Shields, C. W., & Mitragotri, S. (2019) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2019.12.001 · Cited by 243
Transcriptional and epigenetic decoding of the microglial aging process
Li, X., Li, Y., Jin, Y., Zhang, Y., Wu, J., Xu, Z., Huang, Y., Cai, L., Gao, S., Liu, T., et al. (2023) · Nature Aging · doi:10.1038/s43587-023-00479-x · Cited by 234
Bruton tyrosine kinase inhibitors for multiple sclerosis
Krämer, J., Bar-Or, A., Turner, T. J., & Wiendl, H. (2023) · Nature Reviews Neurology · doi:10.1038/s41582-023-00800-7 · Cited by 206
Neuroinflammation — a common thread in neurological disorders
Gilhus, N. E., & Deuschl, G. (2019) · Nature Reviews Neurology · doi:10.1038/s41582-019-0227-8 · Cited by 198
TREM2-dependent lipid droplet biogenesis in phagocytes is required for remyelination
Gouna, G., Klose, C., Bosch-Queralt, M., Liu, L., Gokce, O., Schifferer, M., Cantuti-Castelvetri, L., & Simons, M. (2021) · Journal of Experimental Medicine · doi:10.1084/jem.20210227 · Cited by 186
The extracellular matrix as modifier of neuroinflammation and remyelination in multiple sclerosis
Ghorbani, S., & Yong, V. W. (2021) · Brain · doi:10.1093/brain/awab059 · Cited by 191
Microglia in multiple sclerosis: protectors turn destroyers
Yong, V. W. (2022) · Neuron · doi:10.1016/j.neuron.2022.06.023 · Cited by 185
Microglia regulation of central nervous system myelin health and regeneration
Kent, S. A., & Miron, V. E. (2024) · Nature Reviews Immunology · doi:10.1038/s41577-023-00907-4 · Cited by 183
Self-citationAstrocyte-oligodendrocyte interaction regulates central nervous system regeneration
Molina-Gonzalez, I., Holloway, R. K., Jiwaji, Z., Dando, O., Kent, S. A., Emelianova, K., Lloyd, A. F., Forbes, L. H., Mahmood, A., Skripuletz, T., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-39046-8 · Cited by 176
Self-citationCNS remyelination and inflammation: From basic mechanisms to therapeutic opportunities
Franklin, R. J. M., & Simons, M. (2022) · Neuron · doi:10.1016/j.neuron.2022.09.023 · Cited by 184
Han, J., Chiţu, V., Stanley, E. R., Wszołek, Z. K., Karrenbauer, V. D., & Harris, R. A. (2022) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-022-04225-1 · Cited by 169
Microglia and lipids: how metabolism controls brain innate immunity
Chausse, B., Kakimoto, P. A., & Kann, O. (2021) · Seminars in Cell & Developmental Biology · doi:10.1016/j.semcdb.2020.08.001 · Cited by 181
Cunha, M. I., Su, M., Cantuti-Castelvetri, L., Müller, S. A., Schifferer, M., Djannatian, M., Alexopoulos, I., van der Meer, F., Winkler, A., van Ham, T. J., et al. (2020) · Journal of Experimental Medicine · doi:10.1084/jem.20191390 · Cited by 160
Kamma, E., Lasisi, W. O., Libner, C. D., Ng, H. S., & Plemel, J. R. (2022) · Journal of Neuroinflammation · doi:10.1186/s12974-022-02408-y · Cited by 157
TNF Production and Release from Microglia via Extracellular Vesicles: Impact on Brain Functions
Raffaele, S., Lombardi, M., Verderio, C., & Fumagalli, M. (2020) · Cells · doi:10.3390/cells9102145 · Cited by 147
Robust Myelination of Regenerated Axons Induced by Combined Manipulations of GPR17 and Microglia
Wang, J., He, X., Meng, H., Li, Y., Dmitriev, P., Tian, F., Page, J. C., Lu, Q. R., & He, Z. (2020) · Neuron · doi:10.1016/j.neuron.2020.09.016 · Cited by 139
Protective Microglial Subset in Development, Aging, and Disease: Lessons From Transcriptomic Studies
Benmamar-Badel, A., Owens, T., & Wlodarczyk, A. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.00430 · Cited by 124
Lesion stage-dependent causes for impaired remyelination in MS
Heß, K., Starost, L. J., Kieran, N. W., Thomas, C., Vincenten, M. C. J., Antel, J. P., Martino, G., Huitinga, I., Healy, L. M., & Kuhlmann, T. (2020) · Acta Neuropathologica · doi:10.1007/s00401-020-02189-9 · Cited by 144
Shen, K., Reichelt, M., Kyauk, R. V., Ngu, H., Shen, Y.-A. A., Foreman, O., Modrusan, Z., Friedman, B. A., Sheng, M., & Yuen, T. J. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.108835 · Cited by 138
Zhao, L., Li, Z., Vong, J. S. L., Chen, X., Lai, H. M., Yan, L. Y. C., Huang, J., Sy, S. K. H., Tian, X. Y., Huang, Y., et al. (2020) · Nature Communications · doi:10.1038/s41467-020-18249-3 · Cited by 125
White matter aging and its impact on brain function
Groh, J., & Simons, M. (2025) · Neuron · doi:10.1016/j.neuron.2024.10.019 · Cited by 124
Ronzano, R., Roux, T., Thétiot, M., Aigrot, M., Richard, L., Lejeune, F., Mazuir, E., Vallat, J., Lubetzki, C., & Desmazières, A. (2021) · Nature Communications · doi:10.1038/s41467-021-25486-7 · Cited by 122
Inflammation in multiple sclerosis: consequences for remyelination and disease progression
Klotz, L., Antel, J. P., & Kuhlmann, T. (2023) · Nature Reviews Neurology · doi:10.1038/s41582-023-00801-6 · Cited by 125
Remyelination and ageing: Reversing the ravages of time
Neumann, B., Segel, M., Chalut, K. J., & Franklin, R. J. M. (2019) · Multiple Sclerosis Journal · doi:10.1177/1352458519884006 · Cited by 114
Oligodendrocytes and Microglia: Key Players in Myelin Development, Damage and Repair
Kalafatakis, I., & Karagogeos, D. (2021) · Biomolecules · doi:10.3390/biom11071058 · Cited by 126
Raffaele, S., Gelosa, P., Bonfanti, E., Lombardi, M., Castiglioni, L., Cimino, M., Sironi, L., Abbracchio, M. P., Verderio, C., & Fumagalli, M. (2020) · Molecular Therapy · doi:10.1016/j.ymthe.2020.12.009 · Cited by 109
Oligodendrocytes in the aging brain
Sams, E. C. (2021) · Neuronal Signaling · doi:10.1042/ns20210008 · Cited by 113
The roles of microglia and astrocytes in myelin phagocytosis in the central nervous system
Xu, T., Liu, C., Deng, S., Gan, L., Zhang, Z., Yang, G., Tian, H., & Tang, Y. (2022) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1177/0271678x221137762 · Cited by 110
Lipoprotein Lipase Regulates Microglial Lipid Droplet Accumulation
Loving, B. A., Tang, M., Neal, M. C., Gorkhali, S., Murphy, R., Eckel, R. H., & Bruce, K. D. (2021) · Cells · doi:10.3390/cells10020198 · Cited by 105
“Similarly, microglial “clearance” of myelin derived lipids is required for optimal remyelination following demyelination events [11,15].”
BackgroundInfluentialThe white matter is a pro-differentiative niche for glioblastoma
Brooks, L. J., Clements, M., Burden, J. J., Kocher, D., Richards, L., Devesa, S. C., Zakka, L., Woodberry, M., Ellis, M. J., Jaunmuktane, Z., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-22225-w · Cited by 106
Heterogeneity of microglia and their differential roles in white matter pathology
Lee, J. C. L., Hamanaka, G., Lo, E. H., & Arai, K. (2019) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.13266 · Cited by 105
White matter microglia heterogeneity in the CNS
Amor, S., McNamara, N. B., Gerrits, E., Marzin, M. C., Kooistra, S. M., Miron, V. E., & Nutma, E. (2022) · Acta Neuropathologica · doi:10.1007/s00401-021-02389-x · Cited by 89
Self-citationMyelination-independent functions of oligodendrocyte precursor cells in health and disease
Xiao, Y. C., & Czopka, T. (2023) · Nature Neuroscience · doi:10.1038/s41593-023-01423-3 · Cited by 97
Diet-dependent regulation of TGFβ impairs reparative innate immune responses after demyelination
Bosch-Queralt, M., Cantuti-Castelvetri, L., Damkou, A., Schifferer, M., Schlepckow, K., Alexopoulos, I., Lütjohann, D., Klose, C., Vaculčiaková, L., Masuda, T., et al. (2021) · Nature Metabolism · doi:10.1038/s42255-021-00341-7 · Cited by 88
Hou, J., Zhou, Y., Cai, Z., Terekhova, M., Swain, A., Andhey, P. S., Guimaraes, R. M., Ulezko Antonova, A., Qiu, T., Sviben, S., et al. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.112293 · Cited by 85
Raffaele, S., Boccazzi, M., & Fumagalli, M. (2021) · Cells · doi:10.3390/cells10030565 · Cited by 90
Bruton’s Tyrosine Kinase Inhibition Promotes Myelin Repair
Martin, E., Aigrot, M., Grenningloh, R., Stankoff, B., Lubetzki, C., Boschert, U., & Zalc, B. (2019) · Brain Plasticity · doi:10.3233/bpl-200100 · Cited by 83
Microglia as Therapeutic Target for Radiation-Induced Brain Injury
Liu, Q., Yan, H., Duan, M., Yang, Q., Ren, B., & Tang, F. R. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23158286 · Cited by 84
Wang, N., Wang, M., Jeevaratnam, S., Rosenberg, C., Ikezu, T. C., Shue, F., Doss, S. V., Alnobani, A., Martens, Y. A., Wren, M., et al. (2022) · Molecular Neurodegeneration · doi:10.1186/s13024-022-00577-1 · Cited by 82
Diversity and Function of Glial Cell Types in Multiple Sclerosis
Schirmer, L., Schafer, D. P., Bartels, T., Rowitch, D. H., & Calabresi, P. A. (2021) · Trends in Immunology · doi:10.1016/j.it.2021.01.005 · Cited by 78
Positron emission tomography in multiple sclerosis - straight to the target
Bodini, B., Tonietto, M., Airas, L., & Stankoff, B. (2021) · Nature Reviews Neurology · doi:10.1038/s41582-021-00537-1 · Cited by 74
Wittekindt, M., Kaddatz, H., Joost, S., Staffeld, A., Bitar, Y., Kipp, M., & Frintrop, L. (2022) · Cells · doi:10.3390/cells11111723 · Cited by 74
Mangale, V., Syage, A. R., Ekiz, H. A., Skinner, D. D., Cheng, Y., Stone, C. L., Brown, R. M., O'Connell, R. M., Green, K. N., & Lane, T. E. (2020) · Glia · doi:10.1002/glia.23844 · Cited by 71
Psenicka, M. W., Smith, B. C., Tinkey, R. A., & Williams, J. L. (2021) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2021.654284 · Cited by 73
Hamzaoui, M., Garcia, J., Boffa, G., Lazzarotto, A., Absinta, M., Ricigliano, V. A. G., Soulier, T., Tonietto, M., Gervais, P., Bissery, A., et al. (2023) · Annals of Neurology · doi:10.1002/ana.26657 · Cited by 69
Dimovasili, C., Fair, A. E., Garza, I., Batterman, K. V., Mortazavi, F., Moore, T. L., & Rosene, D. L. (2022) · GeroScience · doi:10.1007/s11357-022-00621-4 · Cited by 74
Androvic, P., Schifferer, M., Perez Anderson, K., Cantuti-Castelvetri, L., Jiang, H., Ji, H., Liu, L., Gouna, G., Berghoff, S. A., Besson-Girard, S., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-39447-9 · Cited by 67
Quan, L., Uyeda, A., & Muramatsu, R. (2022) · Inflammation and Regeneration · doi:10.1186/s41232-022-00193-y · Cited by 75
Tackling the glial scar in spinal cord regeneration: new discoveries and future directions
Shafqat, A., Albalkhi, I., Magableh, H. M., Saleh, T., AlKattan, K. M., & Yaqinuddin, A. (2023) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2023.1180825 · Cited by 71
Retinal and brain microglia in multiple sclerosis and neurodegeneration
Choi, S., Guo, L., & Cordeiro, M. F. (2021) · Cells · doi:10.3390/cells10061507 · Cited by 63
Microglial Function and Regulation during Development, Homeostasis and Alzheimer’s Disease
Casali, B. T., & Reed-Geaghan, E. G. (2021) · Cells · doi:10.3390/cells10040957 · Cited by 70
Microglia Pyroptosis: A Candidate Target for Neurological Diseases Treatment
Wu, X., Wan, T., Gao, X., Fu, M., Duan, Y., Shen, X., & Guo, W. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2022.922331 · Cited by 64
Regulation and signaling of the GPR17 receptor in oligodendroglial cells
Lecca, D., Raffaele, S., Abbracchio, M. P., & Fumagalli, M. (2020) · Glia · doi:10.1002/glia.23807 · Cited by 57
Zhao, X., Sun, J., Li, X., She, L., Li, L., Tang, H., Zeng, Y., Chen, F., Han, X., Ye, S., et al. (2023) · International Journal of Biological Sciences · doi:10.7150/ijbs.81900 · Cited by 65
Tiwari, V., Prajapati, B., Asare, Y., Damkou, A., Ji, H., Liu, L., Naser, N., Gouna, G., Leszczyńska, K. B., Mieczkowski, J., et al. (2024) · Immunity · doi:10.1016/j.immuni.2024.07.001 · Cited by 58
Understanding microglial diversity and implications for neuronal function in health and disease
Schepper, S. D., Crowley, G., & Hong, S. Y. (2020) · Developmental Neurobiology · doi:10.1002/dneu.22777 · Cited by 54
TREM2 ‐dependent microglial function is essential for remyelination and subsequent neuroprotection
Wang, Y., Kyauk, R. V., Shen, Y. A., Xie, L., Reichelt, M., Lin, H., Jiang, Z., Ngu, H., Shen, K., Greene, J. J., et al. (2023) · Glia · doi:10.1002/glia.24335 · Cited by 54
Microglial innate memory and epigenetic reprogramming in neurological disorders
Martins-Ferreira, R., Leal, B., Costa, P., & Ballestar, E. (2020) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2020.101971 · Cited by 55
Sun, Y., Wei, K., Liao, X., Wang, J., Gao, L., & Pang, B. (2025) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2025.5580 · Cited by 63
Tau induces inflammasome activation and microgliosis through acetylating NLRP3
Zhang, L., Gai, Y., Liu, Y., Meng, D., Zeng, Y., Luo, Y., Zhang, H., Wang, Z., Yang, M., Li, Y., et al. (2024) · Clinical and Translational Medicine · doi:10.1002/ctm2.1623 · Cited by 52
The multiple faces of extracellular vesicles released by microglia: Where are we 10 years after?
Gabrielli, M., Raffaele, S., Fumagalli, M., & Verderio, C. (2022) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2022.984690 · Cited by 55
Current Understanding on the Role of Lipids in Macrophages and Associated Diseases
Florance, I., & Seenivasan, R. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms24010589 · Cited by 51
The role of the complement system in Multiple Sclerosis: A review
Saez-Calveras, N., & Stüve, O. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.970486 · Cited by 51
Wang, J., Xu, L., Lin, W., Yao, Y., Li, H., Shen, G., Cao, X., He, N., Chen, J., Hu, J., et al. (2022) · Cell Death and Disease · doi:10.1038/s41419-022-04864-z · Cited by 53
Central Nervous System Macrophages in Health and Disease
Hove, H. V., Feo, D. D., Greter, M., & Becher, B. (2025) · Annual Review of Immunology · doi:10.1146/annurev-immunol-082423-041334 · Cited by 53
Towards a definition of microglia heterogeneity
Healy, L. M., Zia, S., & Plemel, J. R. (2022) · Communications Biology · doi:10.1038/s42003-022-04081-6 · Cited by 50
Scalabrino, G. (2020) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-020-00989-x · Cited by 49
Soluble TREM2 triggers microglial dysfunction in neuromyelitis optica spectrum disorders
Qin, C., Chen, M., Dong, M., Yang, S., Zhang, H., You, Y., Zhou, L., Chu, Y., Tang, Y., Pang, X., et al. (2023) · Brain · doi:10.1093/brain/awad321 · Cited by 54
New insight on microglia activation in neurodegenerative diseases and therapeutics
Xu, Y., Gao, W., Sun, Y., & Wu, M. (2023) · Frontiers in Neuroscience · doi:10.3389/fnins.2023.1308345 · Cited by 50
Incontro, S., Musella, M. L., Sammari, M., Scala, C. D., Fantini, J., & Debanne, D. (2024) · Physiological Reviews · doi:10.1152/physrev.00004.2024 · Cited by 51
White matter and neurological disorders
Bae, H., Kim, T. K., Suk, H. Y., Jung, S., & Jo, D. (2020) · Archives of Pharmacal Research · doi:10.1007/s12272-020-01270-x · Cited by 47
Li, S., Bi, G., Han, S., & Huang, R. (2022) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2021.744942 · Cited by 45
Microglia in developing white matter and perinatal brain injury
McNamara, N. B., & Miron, V. E. (2019) · Neuroscience Letters · doi:10.1016/j.neulet.2019.134539 · Cited by 46
Self-citationHanhai, Z., Qin, B. Y., Zhou, S., Jingbo, L., Guo, Y., Cai, L., Shenglong, C., Zhou, H., Huaijun, C., Jianfeng, Z., et al. (2021) · Aging · doi:10.18632/aging.202993 · Cited by 45
Monitoring phagocytic uptake of amyloid β into glial cell lysosomes in real time
Prakash, P., Jethava, K. P., Korte, N., Izquierdo, P., Favuzzi, E., Rose, I. V. L., Guttenplan, K. A., Manchanda, P., Dutta, S., Rochet, J.-C., et al. (2021) · Chemical Science · doi:10.1039/d1sc03486c · Cited by 45
Chronic oligodendrocyte injury in central nervous system pathologies
Molina-González, I., Miron, V. E., & Antel, J. P. (2022) · Communications Biology · doi:10.1038/s42003-022-04248-1 · Cited by 48
Self-citationSpecies differences in immune‐mediated CNS tissue injury and repair: A (neuro)inflammatory topic
Healy, L. M., Yaqubi, M., Ludwin, S. K., & Antel, J. P. (2019) · Glia · doi:10.1002/glia.23746 · Cited by 41
The Role of MicroRNAs in Repair Processes in Multiple Sclerosis
Duffy, C. P., & McCoy, C. E. (2020) · Cells · doi:10.3390/cells9071711 · Cited by 42
Life and death of microglia: Mechanisms governing microglial states and fates
Matsudaira, T., & Prinz, M. (2022) · Immunology Letters · doi:10.1016/j.imlet.2022.04.001 · Cited by 47
Li, Z., Chen, X., Vong, J. S. L., Zhao, L., Huang, J., Yan, L. Y. C., Ip, B., Wing, Y. K., Lai, H.-M., Mok, V. C. T., et al. (2021) · Communications Biology · doi:10.1038/s42003-021-02208-9 · Cited by 42
Neurodegeneration in Multiple Sclerosis: The Role of Nrf2-Dependent Pathways
Maldonado, P. P., Guevara, C., Olesen, M. A., Orellana, J. A., Quintanilla, R. A., & Ortíz, F. C. (2022) · Antioxidants · doi:10.3390/antiox11061146 · Cited by 44
Myelin Repair: From Animal Models to Humans
Cayre, M., Falque, M., Mercier, O., Magalon, K., & Durbec, P. (2021) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2021.604865 · Cited by 44
Investigating Microglia in Health and Disease: Challenges and Opportunities
Miron, V. E., & Priller, J. (2020) · Trends in Immunology · doi:10.1016/j.it.2020.07.002 · Cited by 43
Self-citationLi, W., He, T., Shi, R., Song, Y., Wang, L., Zhang, Z., Tang, Y., Yang, G., & Wang, Y. (2021) · Aging and Disease · doi:10.14336/ad.2021.0416 · Cited by 42
Neuroinflammation in Friedreich’s Ataxia
Apolloni, S., Milani, M., & D’Ambrosi, N. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23116297 · Cited by 40
Go, V., Sarıkaya, D., Zhou, Y., Bowley, B. G. E., Pessina, M. A., Rosene, D. L., Zhang, Z. G., Chopp, M., Finklestein, S. P., Medalla, M., et al. (2020) · Experimental Neurology · doi:10.1016/j.expneurol.2020.113540 · Cited by 43
Mishra, M. K., Rawji, K. S., Keough, M. B., Kappen, J., Dowlatabadi, R., Vogel, H. J., Chopra, S., Distéfano‐Gagné, F., Dufour, A., Gosselin, D., et al. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.1948-20.2021 · Cited by 44
Remyelination in the central nervous system
Franklin, R. J. M., Bodini, B., & Goldman, S. A. (2024) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a041371 · Cited by 40
Wang, Y., Sun, J., Zhu, K., Wang, D., Zhao, X., Zhang, H., Wu, S., Wang, J., & Wang, J. (2023) · Journal of Neuroinflammation · doi:10.1186/s12974-023-02764-3 · Cited by 41
Maimaiti, M., Li, C., Cheng, M., Zhong, Z., Hu, J., Yang, L., Zhang, L., Hong, Z., Song, J., Pan, M., et al. (2024) · Med · doi:10.1016/j.medj.2024.03.018 · Cited by 41
Multifaceted Involvement of Microglia in Gray Matter Pathology in Multiple Sclerosis
Tsouki, F., & Williams, A. (2021) · Stem Cells · doi:10.1002/stem.3374 · Cited by 39
(Re)building the nervous system: A review of neuron–glia interactions from development to disease
Demmings, M. D., Chagas, L. D. S., Traetta, M. E., Rodrigues, R. S., Acutain, M. F., Barykin, E. P., Datusalia, A. K., German‐Castelan, L., Mattera, V. S., Mazengenya, P., et al. (2024) · Journal of Neurochemistry · doi:10.1111/jnc.16258 · Cited by 44
Raffaele, S., & Fumagalli, M. (2022) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2022.950819 · Cited by 40
Metadata
- Authors
- Lloyd, A. F., & Miron, V. E.
- Affiliations
- Multiple Sclerosis Society (GB)
- Venue
- Nature Reviews Neurology
- Published
- 2019-06-29
- Volume
- 15
- Issue
- 8
- Pages
- 447-458
- ISSN
- 1759-4758 (ISSN-L)
- 1759-4766
- OpenAlex
- W2954946400
- Cited by
- 381
- References
- 148
- Citations by year
- 2026: 47 · 2025: 48 · 2024: 59 · 2023: 65 · 2022: 57 · 2021: 57 · 2020: 37 · 2019: 11
- FWCI
- 4.27
- Type
- journal article
- Language
- en
- Open access
- Licence
- Locations
- Nature Reviews Neurology (publishedVersion)
- PubMed (publishedVersion)
- Edinburgh Research Explorer (University of Edinburgh) (submittedVersion, other-oa)
- Funders
- Action Medical Research
- Medical Research Council (MR/M020827/1, MR/N022556/1)
- Topics
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Health Sciences › Medicine › Clinical Neurology › Multiple Sclerosis Research Studies
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Keywords
- microglia, remyelination, microglial activation, demyelinating disease, multiple sclerosis, microglial heterogeneity
- MeSH terms
- Remyelination, Aging, Animals, Central Nervous System, Demyelinating Diseases, Homeostasis, Humans, Macrophage Activation, 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