The DOI matches its Crossref record; 178 of the 178 references it cites were found in a registry or an index.
The identity and function of microglia in neurodegeneration
Abstract
The predominant type of immune cell in the brain is the microglia, a type of tissue-resident macrophage. In a variety of neurodegenerative settings, microglia alter their transcriptional profile, morphology and function in similar ways; thus, these activated cells have been called 'degeneration- or disease-associated microglia' (DAM). These activated microglia can perform different functions and exert both positive effects and negative effects in different mouse disease models. In humans, mutations in genes expressed in microglia are linked to various neurodegenerative diseases. Here we provide an overview of the common microglial response to neurodegeneration and key contributing pathways; delineate the multifaceted functions of activated microglia spanning various diseases; and discuss insights from the study of human disease-associated genes. We argue that strong evidence from both mouse models and human genetics causally links the function of activated microglia to neurodegeneration.
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“The DAM phenotype has been proposed to represent a universal and intrinsic microglial response program to CNS disease, since it appears to be retained across a number of neurodegenerative and non-neurodegenerative diseases [74, 291]”
From Microglia and monocytes in inflammatory CNS disease: integrating phenotype and function (2022) · cites this paper as [291]
In the citing paper
“DAM-expressed factors, such as apolipoprotein, colony-stimulating factor 1 (CSF1) and secreted phosphoprotein 1, act as autocrine ligands on DAM-expressed receptors, together sustaining and perpetuating the neurodegenerative phenotype [291]”
From Microglia and monocytes in inflammatory CNS disease: integrating phenotype and function (2022) · cites this paper as [291]
In the citing paper
“complement activation, which is important for microglial phagocytosis, can exacerbate synaptic loss [152, 284, 291] and contribute to memory loss and cognitive decline [75]”
From Microglia and monocytes in inflammatory CNS disease: integrating phenotype and function (2022) · cites this paper as [291]
In the citing paper
“Microglia are classified into two subtypes: classically activated (M1) cells, which secrete proinflammatory cytokines, and alternatively activated (M2) cells, which promote tissue regeneration and repair [9–12].”
From Neuron secrete exosomes containing miR-9-5p to promote polarization of M1 microglia in depression (2022) · cites this paper as [11]
In the citing paper
“Microgliosis is a known feature of AD [reviewed in (92, 93)]”
From The Transcriptional Landscape of Microglial Genes in Aging and Neurodegenerative Disease (2019) · cites this paper as [92]
Citations
Cites
1 retracted
Microglia-dependent synapse loss in type I interferon-mediated lupus
Bialas, A. R., Presumey, J., Das, A., van der Poel, C. E., Lapchak, P. H., Mesin, L., Victora, G., Tsokos, G. C., Mawrin, C., Herbst, R., et al. (2017) · Nature · doi:10.1038/nature22821 · Cited by 197
RetractedMACDONALD, M. (1993) · Cell · doi:10.1016/0092-8674(93)90585-e · Cited by 8,366
Mutation in the α-Synuclein Gene Identified in Families with Parkinson's Disease
Polymeropoulos, M. H., Lavedan, C., Leroy, E., Ide, S. E., Dehejia, A., Dutra, A., Pike, B., Root, H., Rubenstein, J., Boyer, R., et al. (1997) · Science · doi:10.1126/science.276.5321.2045 · Cited by 8,240
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
Rosen, D. R., Siddique, T., Patterson, D., Figlewicz, D. A., Sapp, P., Hentati, A., Donaldson, D., Goto, J., O'Regan, J. P., Deng, H.-X., et al. (1993) · Nature · doi:10.1038/362059a0 · Cited by 7,062
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
Self-citationFate Mapping Analysis Reveals That Adult Microglia Derive from Primitive Macrophages
Ginhoux, F., Greter, M., Leboeuf, M., Nandi, S., See, P., Gokhan, S., Mehler, M. F., Conway, S. J., Ng, L. G., Stanley, E. R., et al. (2010) · Science · doi:10.1126/science.1194637 · Cited by 5,175
DeJesus-Hernandez, M., Mackenzie, I. R., Boeve, B. F., Boxer, A. L., Baker, M., Rutherford, N. J., Nicholson, A. M., Finch, N. A., Flynn, H., Adamson, J., et al. (2011) · Neuron · doi:10.1016/j.neuron.2011.09.011 · Cited by 4,936
A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD
Renton, A. E., Majounie, E., Waite, A., Simón-Sánchez, J., Rollinson, S., Gibbs, J. R., Schymick, J. C., Laaksovirta, H., van Swieten, J. C., Myllykangas, L., et al. (2011) · Neuron · doi:10.1016/j.neuron.2011.09.010 · Cited by 4,409
Meta-Analysis of 74,046 Individuals Identifies 11 New Susceptibility Loci for Alzheimer’s Disease
(EADI), E. A. D. I., Lambert, J.-C., (GERAD), G. A. E. R. I. A. D., Alzheimer's Disease Genetic Consortium (ADGC), (CHARGE), C. F. H. A. A. R. I. G. E., Ibrahim-Verbaas, C. A., Harold, D., Naj, A. C., Sims, R., Bellenguez, C., et al. (2013) · Nature Genetics · doi:10.1038/ng.2802 · Cited by 4,336
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Items 101–200 of 308
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Illés, P., Rubini, P., Huang, L., & Tang, Y. (2019) · Expert Opinion on Therapeutic Targets · doi:10.1080/14728222.2019.1575811 · Cited by 50
Esteban, S. R. D. M., Benito‐Cuesta, I., Irastorza, I. T., Martínez-Relimpio, A. M., Arnanz, M. A., Ruiz‐Pérez, G., Korn, C., Raposo, C., Sarott, R. C., Westphal, M. V., et al. (2022) · Frontiers in Pharmacology · doi:10.3389/fphar.2022.841766 · Cited by 48
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Chi, Y., Jiang, H., Yin, Y., Zhou, X., Shao, Y., Li, Y., & Rao, J. (2025) · MedComm · doi:10.1002/mco2.70256 · Cited by 54
Long-Term Microgliosis Driven by Acute Systemic Inflammation
Trzeciak, A. J., Lerman, Y. V., Kim, T., Kim, M. R., Mai, N., Halterman, M. W., & Kim, M. (2019) · The Journal of Immunology · doi:10.4049/jimmunol.1900317 · Cited by 44
Samuels, J. D., Moore, K. A., Ennerfelt, H. E., Johnson, A. M., Walsh, A. E., Price, R. J., & Lukens, J. R. (2023) · Alzheimer's & Dementia · doi:10.1002/alz.13089 · Cited by 46
Mu, X., Liu, J., Wang, H., Yuan, L., Wang, C., Li, Y., & Qiu, J. Y. (2022) · Environmental Science & Technology · doi:10.1021/acs.est.2c01531 · Cited by 46
Turner, T. J., Brun, P., Gruber, R. C., & Ofengeim, D. (2024) · Drugs in R&D · doi:10.1007/s40268-024-00468-4 · Cited by 46
Dysfunction of the neurovascular unit in diabetes-related neurodegeneration
Yan, C., Zhou, Y., Chen, Q., Luo, Y., Zhang, J. H., Huang, H., & Shao, A. (2020) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2020.110656 · Cited by 47
Wang, B., Ma, Y., Li, S., Yao, H., Gu, M.-N., Liu, Y., Xue, Y., Ding, J., Ma, C., Yang, S., et al. (2023) · Acta Pharmaceutica Sinica B · doi:10.1016/j.apsb.2023.04.008 · Cited by 45
ATM-deficiency-induced microglial activation promotes neurodegeneration in ataxia-telangiectasia
Lai, J. F., Demirbas, D., Kim, J., Jeffries, A. M., Tolles, A. K., Park, J., Chittenden, T. W., Buckley, P. G., Yu, T. W., Lodato, M. A., et al. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.113622 · Cited by 46
Kovács, G. G. (2019) · Current Opinion in Neurology · doi:10.1097/wco.0000000000000664 · Cited by 45
microRNA-132 regulates gene expression programs involved in microglial homeostasis
Walgrave, H., Penning, A., Tosoni, G., Snoeck, S., Davie, K., Davis, E., Wolfs, L., Sierksma, A., Mars, M., Bu, T., et al. (2023) · iScience · doi:10.1016/j.isci.2023.106829 · Cited by 41
Gas6 Inhibits Toll-Like Receptor-Mediated Inflammatory Pathways in Mouse Microglia via Axl and Mer
Gilchrist, S. E., Goudarzi, S., & Hafizi, S. (2020) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2020.576650 · Cited by 46
Melbourne, J. K., Thompson, K. R., Peng, H., & Nixon, K. (2019) · Progress in molecular biology and translational science · doi:10.1016/bs.pmbts.2019.06.011 · Cited by 40
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van Olst, L., Coenen, L., Nieuwland, J. M., Rodriguez-Mogeda, C., de Wit, N. M., Kamermans, A., Middeldorp, J., & de Vries, H. E. (2022) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2022.114398 · Cited by 45
Afsar, A., Castro, M. D. C. C., Soladogun, A. S., & Li, Z. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24087258 · Cited by 45
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Abellanas, M. A., Purnapatre, M., Burgaletto, C., & Schwartz, M. (2025) · Nature Neuroscience · doi:10.1038/s41593-024-01847-5 · Cited by 40
Schlecht, A., Zhang, P., Wolf, J., Thien, A., Rosmus, D.-D., Boneva, S., Schlunck, G., Lange, C., & Wieghofer, P. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.618598 · Cited by 42
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Ganz, T., Fainstein, N., & Ben-Hur, T. (2022) · Molecular Neurodegeneration · doi:10.1186/s13024-022-00559-3 · Cited by 39
Wang, J., Gao, S., Fu, S., Li, Y., Su, L., Li, X., Wu, G., Jiang, J., Zhao, Z., Yang, C., et al. (2024) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2024.12.019 · Cited by 40
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Islam, S., Noorani, A. A., Sun, Y., Michikawa, M., & Zou, K. (2025) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2025.1535280 · Cited by 43
Blood-brain barrier and innate immunity in the pathogenesis of Alzheimer's disease
Šimić, G., Španić, E., Horvat, L. L., & Hof, P. R. (2019) · Progress in molecular biology and translational science · doi:10.1016/bs.pmbts.2019.06.003 · Cited by 40
Chen, Y.-N., Sha, H., Wang, Y., Zhou, Q., Bhuiyan, P., Li, N., Qian, Y., & Dong, H. (2020) · Journal of Neuroinflammation · doi:10.1186/s12974-020-01886-2 · Cited by 40
Tóth, K., Lénárt, N., Berki, P., Fekete, R., Szabadits, E., Pósfai, B., Cserép, C., Alatshan, A., Benkő, S., Kiss, D. K., et al. (2022) · PLoS Biology · doi:10.1371/journal.pbio.3001526 · Cited by 40
Lee, H.-L., Jung, K.-M., Fotio, Y., Squire, E., Palese, F., Lin, L., Torrens, A., Ahmed, F., Mabou Tagne, A., Ramirez, J., et al. (2022) · Biological Psychiatry · doi:10.1016/j.biopsych.2022.04.017 · Cited by 38
Expression of HIV-1 Intron-Containing RNA in Microglia Induces Inflammatory Responses
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Huang, Y., Guimarães, T. R., Todd, N., Ferguson, C., Weiss, K. M., Stauffer, F., McDermott, B., Hurtle, B. T., Saito, T., Saido, T. C., et al. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2204828119 · Cited by 37
Lee, J., Villarreal, O. D., Chen, X., Zandee, S., Young, Y. K., Torok, C., Lamarche-Vane, N., Prat, A., Rivest, S., Gosselin, D., et al. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.108560 · Cited by 38
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Hu, Y., Yao, Y., Qi, H., Yang, J., Zhang, C., Zhang, A., Liu, X., Zhang, C., Gan, G., & Zhu, X. (2023) · Pharmacological Research · doi:10.1016/j.phrs.2023.106881 · Cited by 36
TMEM59 interacts with TREM2 and modulates TREM2-dependent microglial activities
Liu, Z., Ning, J., Zheng, X., Meng, J., Han, L., Zheng, H., Zhong, L., Chen, X., Zhang, X., Luo, H., et al. (2020) · Cell Death and Disease · doi:10.1038/s41419-020-02874-3 · Cited by 35
Microglia in Alzheimer’s Disease: An Unprecedented Opportunity as Prospective Drug Target
Kulkarni, B., Martins, N. A., & Kumar, D. (2022) · Molecular Neurobiology · doi:10.1007/s12035-021-02661-x · Cited by 38
Manchanda, S., Galán-Acosta, L., Abelein, A., Tambaro, S., Chen, G., Nilsson, P., & Johansson, J. (2022) · Molecular Therapy · doi:10.1016/j.ymthe.2022.08.010 · Cited by 34
Heinz, R., & Schneider, U. C. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232012618 · Cited by 33
Plastira, I., Joshi, L., Bernhart, E. M., Schoene, J., Specker, E., Nazaré, M., & Sattler, W. (2019) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2019.00531 · Cited by 32
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Qureshi, Y. H., Berman, D. E., Marsh, S. E., Klein, R. L., Patel, V. M., Simoes, S., Kannan, S., Petsko, G. A., Stevens, B., & Small, S. A. (2022) · Cell Reports · doi:10.1016/j.celrep.2021.110262 · Cited by 31
Sabzali, M., Eidi, A., Khaksari, M., & Khastar, H. (2022) · Neurotoxicity Research · doi:10.1007/s12640-022-00499-2 · Cited by 31
Dave, B. P., Shah, Y. B., Maheshwari, K. G., Mansuri, M. K. A., Prajapati, B., Postwala, H. I., & Chorawala, M. R. (2023) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-023-01408-7 · Cited by 33
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Goldshtein, H., Muhire, A., Légaré, V. P., Pushett, A., Rotkopf, R., Shefner, J. M., Peterson, R. T., Armstrong, G. A. B., & Russek‐Blum, N. (2020) · Annals of Clinical and Translational Neurology · doi:10.1002/acn3.51174 · Cited by 30
Icariin: A Potential Neuroprotective Agent in Alzheimer’s Disease and Parkinson’s Disease
Khezri, M. R., & Ghasemnejad‐Berenji, M. (2022) · Neurochemical Research · doi:10.1007/s11064-022-03667-0 · Cited by 30
Modulation of Microglial Function by ATP-Gated P2X7 Receptors: Studies in Rat, Mice and Human
Tewari, M., Michalski, S. A., & Egan, T. M. (2024) · Cells · doi:10.3390/cells13020161 · Cited by 36
Modeling Cell-Cell Interactions in Parkinson’s Disease Using Human Stem Cell-Based Models
Simmnacher, K., Lanfer, J., Rizo, T., Kaindl, J., & Winner, B. (2020) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2019.00571 · Cited by 32
Mold, M. J., O’Farrell, A., Morris, B., & Exley, C. (2020) · Journal of Alzheimer s Disease · doi:10.3233/jad-200838 · Cited by 31
Boreland, A. J., Stillitano, A. C., Lin, H., Abbo, Y., Hart, R. P., Jiang, P., Pang, Z. P., & Rabson, A. B. (2024) · iScience · doi:10.1016/j.isci.2024.109628 · Cited by 30
The emerging role of disease-associated microglia in Parkinson’s disease
Samant, R. R., Standaert, D. G., & Harms, A. S. (2024) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2024.1476461 · Cited by 32
He, J., Fu, Y., Ge, L., Dai, J., Fang, Y., Li, Y., Gu, X., Tao, Z., Zou, T., Li, M., et al. (2022) · Theranostics · doi:10.7150/thno.67954 · Cited by 30
Targeting mitophagy for depression amelioration: a novel therapeutic strategy
Xu, W., Gao, W.-P., Guo, Y., Feng, X., Di, L., Fang, S., Fan, L., He, Y., Zhou, Y., Xie, X., et al. (2023) · Frontiers in Neuroscience · doi:10.3389/fnins.2023.1235241 · Cited by 30
Microglia depletion leads to increased susceptibility to ocular hypertension-dependent glaucoma
Diemler, C. A., MacLean, M., Heuer, S. E., Hewes, A. A., Marola, O. J., Libby, R. T., & Howell, G. R. (2024) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2024.1396443 · Cited by 26
Neurodegenerative phagocytes mediate synaptic stripping in Neuro-HIV
Liberto, G. D., Égervári, K., Kreutzfeldt, M., Schürch, C. M., Hewer, E., Wagner, I., Pasquier, R. D., & Merkler, D. (2022) · Brain · doi:10.1093/brain/awac102 · Cited by 28
Gattlen, C., Deftu, A., Tonello, R., Ling, Y., Berta, T., Ristoiu, V., & Suter, M. R. (2020) · Glia · doi:10.1002/glia.23831 · Cited by 26
Davies, C. L., Patir, A., & McColl, B. W. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.01048 · Cited by 24
Liu, F., Tao, X., Pang, G., Wu, D., Hu, Y., Xue, S., Liu, J., Li, B., Zhou, L., Liu, Q., et al. (2020) · Frontiers in Pharmacology · doi:10.3389/fphar.2019.01569 · Cited by 25
Cytokine changes in cerebrospinal fluid and plasma after emergency orthopaedic surgery
Fertleman, M. B., Pereira, C., Dani, M., Harris, B. H. L., Giovannantonio, M. D., & Taylor-Robinson, S. D. (2022) · Scientific Reports · doi:10.1038/s41598-022-06034-9 · Cited by 25
Microglial Endocannabinoid Signalling in AD
Scipioni, L., Ciaramellano, F., Carnicelli, V., Leuti, A., Lizzi, A. R., Dominicis, N. D., Oddi, S., & Maccarrone, M. (2022) · Cells · doi:10.3390/cells11071237 · Cited by 26
Nicotinic acetylcholine receptors: Key targets for attenuating neurodegenerative diseases
Bye, L. J., Finol‐Urdaneta, R. K., Tae, H., & Adams, D. J. (2023) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2023.106387 · Cited by 28
Microglia in Alzheimer’s Disease
Süß, P., & Schlachetzki, J. C. M. (2020) · Current Alzheimer Research · doi:10.2174/1567205017666200212155234 · Cited by 26
In vivo imaging in mouse spinal cord reveals that microglia prevent degeneration of injured axons
Wu, W., He, Y., Chen, Y., Fu, Y., He, S., Liu, K., & Qu, J. Y. (2024) · Nature Communications · doi:10.1038/s41467-024-53218-0 · Cited by 25
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Vecchia, S. D., Ogi, A., Licitra, R., Abramo, F., Nardi, G., Mero, S., Landi, S., Battini, R., Sicca, F., Ratto, G. M., et al. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23126874 · Cited by 23
FAM69C functions as a kinase for eIF2α and promotes stress granule assembly
Wu, Z., Mei, F., Gan, Y., Liu, A., Hu, J., Jin, Y., & Yin, Y. (2023) · EMBO Reports · doi:10.15252/embr.202255641 · Cited by 28
Barbalace, M. C., Freschi, M., Rinaldi, I., Mazzara, E., Maraldi, T., Malaguti, M., Prata, C., Maggi, F., Petrelli, R., Hrelia, S., et al. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms242316601 · Cited by 24
Tanaka, M., & Vécsei, L. (2024) · Journal of Neural Transmission · doi:10.1007/s00702-024-02812-z · Cited by 23
Pauls, E., Bayod, S., Mateo, L., Alcalde, V., Juan-Blanco, T., Sánchez‐Soto, M., Saido, T. C., Saito, T., Berenguer, A., Attolini, C. S., et al. (2021) · Genome Medicine · doi:10.1186/s13073-021-00983-y · Cited by 23
Apigenin Regulates Activation of Microglia and Counteracts Retinal Degeneration
Chumsakul, O., Wakayama, K., Tsuhako, A., Baba, Y., Takai, Y., Kurose, T., Honma, Y., & Watanabe, S. (2020) · Journal of Ocular Pharmacology and Therapeutics · doi:10.1089/jop.2019.0163 · Cited by 22
Jonavičė, U., Romenskaja-Avgul, D., Kriaučiūnaitė, K., Jarmalavičiūtė, A., Pajarskienė, J., Kašėta, V., Tunaitis, V., Malm, T., Giniatullin, R. A., & Pivoriūnas, A. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222010970 · Cited by 20
Wang, S., Wu, L., Xie, Y., Ge, S., Wu, Y., Chen, L., Yi, L., Yang, J., Duan, F., & Huang, L. (2024) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2024.118412 · Cited by 20
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Zammit, N. W., McDowell, J., Warren, J. A., Muskovic, W., Gamble, J., Shi, Y., Kaczorowski, D. C., Chan, C., Powell, J. E., Ormandy, C. J., et al. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.811525 · Cited by 21
Li, D., Xu, J., Qin, Y., Cai, N., Cheng, Y., & Wang, H. (2020) · International Immunopharmacology · doi:10.1016/j.intimp.2020.107176 · Cited by 20
Lin, J., Shao, X., Shi, T., Wang, H., Zhang, P., Zhou, Y., Liu, N., He, Y., Fang, D., Shi, Y., et al. (2026) · Nature Aging · doi:10.1038/s43587-026-01075-5 · Cited by 20
Analysis of ALS-related proteins during herpes simplex virus-2 latent infection
Cabrera, J. R., Rodríguez‐Izquierdo, I., Jiménez, J. L., & Muñoz‐Fernández, M. Á. (2020) · Journal of Neuroinflammation · doi:10.1186/s12974-020-02044-4 · Cited by 19
Schmal, Z., Hammer, B., Müller, A., & Rübe, C. E. (2021) · International Journal of Radiation Oncology*Biology*Physics · doi:10.1016/j.ijrobp.2021.07.007 · Cited by 20
Chellappan, R., Guha, A., Si, Y., Kwan, T., Nabors, B., Filippova, N., Yang, X., Myneni, A. S., Meesala, S., Harms, A. S., et al. (2021) · Glia · doi:10.1002/glia.24094 · Cited by 20
The Dual Nature of Microglia in Alzheimer’s Disease: A Microglia-Neuron Crosstalk Perspective
Xie, Z., Meng, J., Wu, Z., Nakanishi, H., Hayashi, Y., Kong, W., Lan, F., Narengaowa, Yang, Q., Qing, H., et al. (2023) · The Neuroscientist · doi:10.1177/10738584211070273 · Cited by 19
Li, H., Wei, J., Zhang, Z., Li, J., Ma, Y., Zhang, P., & Lin, J. (2023) · Stem Cell Research & Therapy · doi:10.1186/s13287-023-03330-7 · Cited by 19
Peng, Z., Luchtman, D. W., Wang, X., Zhang, Y., & Song, C. (2019) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2019.01.024 · Cited by 19
Navarro, E., Norden, D. M., Trojanowski, P. J., Godbout, J. P., & López, M. G. (2021) · Molecules · doi:10.3390/molecules26082107 · Cited by 20
Sánchez‐Ruiz de Gordoa, J., Erro, M. E., Vicuña‐Urriza, J., Zelaya, M. V., Tellechea, P., Acha, B., Zueco, S., Urdánoz‐Casado, A., Roldán, M., Blanco‐Luquin, I., et al. (2020) · Movement Disorders · doi:10.1002/mds.27992 · Cited by 18
Jin, Z., Lu, Y., Tang, H., & Cui, H. (2025) · Alzheimer s & Dementia · doi:10.1002/alz.70472 · Cited by 24
Ni, R. (2021) · Pharmaceuticals · doi:10.3390/ph14111179 · Cited by 18
Sirkis, D. W., Solsberg, C. W., Johnson, T. P., Bonham, L. W., Sturm, V. E., Lee, S. E., Rankin, K. P., Rosen, H. J., Boxer, A. L., Seeley, W. W., et al. (2023) · Genome Medicine · doi:10.1186/s13073-023-01205-3 · Cited by 19
Bobotis, B. C., Halvorson, T., Carrier, M., & Tremblay, M. (2024) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2024.1317125 · Cited by 22
An in vitro model for studying CNS white matter: functional properties and experimental approaches
Bijland, S., Thomson, G., Euston, M., Michail, K., Thümmler, K., Mücklisch, S., Crawford, C. L., Barnett, S. C., McLaughlin, M., Anderson, T. J., et al. (2019) · F1000Research · doi:10.12688/f1000research.16802.1 · Cited by 17
Cong, L., Dai, S., Shi, R., He, X., Wang, Y., He, B., Sun, X., Du, H., Liu, C., & Teng, Z. (2021) · Glia · doi:10.1002/glia.23966 · Cited by 18
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Sirkis, D. W., Bonham, L. W., & Yokoyama, J. S. (2021) · The Application of Clinical Genetics · doi:10.2147/tacg.s245029 · Cited by 21
Zajac, D. J., Simpson, J., Zhang, E., Parikh, I., & Estus, S. (2023) · Genes · doi:10.3390/genes14030763 · Cited by 18
Bianchin, M. M., & Snow, Z. (2022) · Neuroscience · doi:10.1016/j.neuroscience.2022.06.032 · Cited by 17
Schmal, Z., & Rübe, C. E. (2022) · Cancers · doi:10.3390/cancers14225477 · Cited by 17
Kodali, M., Madhu, L. N., Somayaji, Y., Attaluri, S., Huard, C., Panda, P. K., Shankar, G., Rao, S., Shuai, B., Gonzalez, J. J., et al. (2024) · Aging Cell · doi:10.1111/acel.14398 · Cited by 18
SIRPα deficiency accelerates the pathologic process in models of Parkinson disease
Wang, J., Ding, X., Wu, X., Liu, J., Zhou, R., Wei, P., Zhang, Q., Zhang, C., Zen, K., & Li, L. (2019) · Glia · doi:10.1002/glia.23689 · Cited by 20
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Sexton, C. E., Bitan, G., Bowles, K. R., Bryś, M., Buée, L., Maina, M. B., Clelland, C. D., Cohen, A. D., Crary, J. F., Dage, J. L., et al. (2024) · Alzheimer s & Dementia · doi:10.1002/alz.13533 · Cited by 16
Oxidative Effects in Early Stages of Embryo Development Due to Alcohol Consumption
González, D., Márquez, A., & Casimiro, I. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25074100 · Cited by 18
Han, J., Zhu, K., Zhou, K., Hakim, R., Sankavaram, S. R., Blomgren, K., Lund, H., Zhang, X., & Harris, R. A. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21186824 · Cited by 16
Xiao, H., Song, B., Li, Q., Shao, Y., Zhang, Y.-B., Chang, X., & Zhou, Z. (2021) · Toxicology Letters · doi:10.1016/j.toxlet.2021.11.017 · Cited by 16
Pérez-Martín, E., Pérez-Revuelta, L., Barahona-López, C., Pérez-Boyero, D., Alonso, J. R., Díaz, D., & Weruaga, E. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24119691 · Cited by 16
Kecheliev, V., Spinelli, F., Herde, A. M., Haider, A., Mu, L., Klohs, J., Ametamey, S. M., & Ni, R. (2022) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2022.1018610 · Cited by 15
Immunological signatures in frontotemporal lobar degeneration
Sirkis, D. W., Bonham, L. W., Karch, C. M., & Yokoyama, J. S. (2019) · Current Opinion in Neurology · doi:10.1097/wco.0000000000000665 · Cited by 14
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Nie, W., Yue, Y., & Hu, J. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1590909 · Cited by 15
Zhao, Z., Yu, X., Yang, X., Zhang, J., Zhang, D., Sun, N., & Fan, Z. (2020) · International Ophthalmology · doi:10.1007/s10792-020-01519-w · Cited by 14
Boyd, M. M., Litscher, S. J., Seitz, L. L., Messing, A., Hagemann, T. L., & Collier, L. S. (2021) · Journal of Neuroinflammation · doi:10.1186/s12974-021-02118-x · Cited by 14
Metadata
- Authors
- Song, W. M., & Colonna, M.
- Affiliations
- Washington University in St. Louis (US)
- Corresponding author
- Colonna, Marco
- Venue
- Nature Immunology
- Published
- 2018-09-24
- Volume
- 19
- Issue
- 10
- Pages
- 1048-1058
- ISSN
- 1529-2908 (ISSN-L)
- 1529-2916
- OpenAlex
- W2891888347
- Semantic Scholar
- 56fd070c6693804f7ada07ce3ee33529dfa55dbf
- Cited by
- 308
- References
- 178
- Citations by year
- 2026: 21 · 2025: 28 · 2024: 37 · 2023: 49 · 2022: 53 · 2021: 42 · 2020: 42 · 2019: 33 · 2018: 3
- FWCI
- 2.84
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature Immunology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Life Sciences › Neuroscience › Neurology › Neurological Disease Mechanisms and Treatments
- Health Sciences › Medicine › Clinical Neurology › Multiple Sclerosis Research Studies
- Keywords
- microglia, neurodegeneration, disease-associated microglia, microglial activation, tissue-resident macrophages, microglial morphology, neurodegenerative disease models, microglial function
- MeSH terms
- Animals, Humans, Microglia, Neurodegenerative Diseases
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