The DOI matches its Crossref record; 55 of the 55 references it cites were found in a registry or an index.
Heterogeneity in the distribution and morphology of microglia in the normal adult mouse brain
Abstract
We have examined the distribution of microglia in the normal adult mouse brain using immunocytochemical detection of the macrophage specific plasma membrane glycoprotein F4/80. We were interested to learn whether the distribution of microglia in the adult brain is related to regional variation in the magnitude of cell death during development and resulting monocyte recruitment, or whether the adult distribution is influenced by other local microenvironmental cues. We further investigated the possibility that microglia are sensitive to their microenvironment by studying their morphology in different brain regions. Microglia are present in large numbers in all major divisions of the brain but are not uniformly distributed. There is a more than five-fold variation in the density of immunostained microglial processes between different regions. More microglia are found in gray matter than white. Particularly, densely populated areas include the hippocampus, olfactory telencephalon, basal ganglia and substantia nigra. In comparison, the less densely populated areas include fibre tracts, cerebellum and much of the brainstem. The cerebral cortex, thalamus and hypothalamus have average cell densities. There was no simple relationship between the amount of developmental cell death and the adult distribution of microglia. An estimate of the total number of microglia in the adult mouse brain, 3.5 x 10(6), is comparable to that found in the liver on a weight for weight basis. However, microglia possess up to twice the surface area of membrane of Kupffer cells, the large resident macrophages of the liver. The proportion of cells that were microglia varied from 5% in the cortex and corpus callosum, to 12% in the substantia nigra. Microglia vary in morphology depending on their location. They were broadly classified into three categories. Compact cells are rounded cells, sometimes with one or two short thick limbs, bearing short processes ("bristles"). They resemble Kupffer cells of the liver and are found exclusively in sites lacking a blood-brain barrier. Longitudinally branched cells are found in fibre tracts and possess several long processes which are usually aligned parallel to, or more occasionally perpendicular to, the longitudinal axis of the nerve fibres. Radially branched cells are found throughout the neuropil. They can be extremely elaborate and there is wide variation in the length and complexity of branching of the processes. There was no evidence of monocyte-like cells in the adult CNS. The systematic variation in microglial morphology provides further evidence that these cells are sensitive to their microenvironment.
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In the citing paper
“Microglia constitute 5–12% of CNS cells, depending on the region9.”
From Microglia in neurodegeneration (2018) · cites this paper as [9]
In the citing paper
“Microglia form a network spanning the CNS9.”
From Microglia in neurodegeneration (2018) · cites this paper as [9]
In the citing paper
“Only NAc displayed microglial density (380 ± 7 cells/mm2) comparable to that in cortex and hippocampus (Lawson et al., 1990).”
From Local cues establish and maintain region-specific phenotypes of basal ganglia microglia (2017) · cites this paper as Lawson et al., 1990
In the citing paper
“previous immunohistochemical studies of microglia did not distinguish between SNc/SNr (Lawson et al., 1990; Sharaf et al., 2013; Yang et al., 2013)”
From Local cues establish and maintain region-specific phenotypes of basal ganglia microglia (2017) · cites this paper as Lawson et al., 1990
Citations
Cites
The Rat Brain in Stereotaxic Coordinates
Paxinos, G., & Watson, C. (1983) · Elsevier eBooks · doi:10.1016/c2009-0-63235-9 · Cited by 28,585
Estimation of nuclear population from microtome sections
Abercrombie, M. (1946) · The Anatomical Record · doi:10.1002/ar.1090940210 · Cited by 4,363
PERIODATE-LYSINE-PARAFORMALDEHYDE FIXATIVE A NEW FIXATIVE FOR IMMUNOELECTRON MICROSCOPY
McLean, I. W., & Nakane, P. K. (1974) · Journal of Histochemistry & Cytochemistry · doi:10.1177/22.12.1077 · Cited by 3,789
F4/80, a monoclonal antibody directed specifically against the mouse macrophage
Austyn, J. M., & Gordon, S. (1981) · European Journal of Immunology · doi:10.1002/eji.1830111013 · Cited by 1,580
Self-citationPerivascular microglial cells of the CNS are bone marrow-derived and present antigen in vivo
Hickey, W. F., & Kimura, H. (1988) · Science · doi:10.1126/science.3276004 · Cited by 1,466
Unkeless, J. C. (1979) · The Journal of Experimental Medicine · doi:10.1084/jem.150.3.580 · Cited by 1,271
Mac‐1: a macrophage differentiation antigen identified by monoclonal antibody
Springer, T. A., Galfré, G., Secher, D. S., & Milstein, C. (1979) · European Journal of Immunology · doi:10.1002/eji.1830090410 · Cited by 1,108
Cytology & cellular pathology of the nervous system
Penfield, W. G. (1965) · Medical Entomology and Zoology · Cited by 1,035
Functional plasticity of microglia: A review
Streit, W. J., Graeber, M. B., & Kreutzberg, G. W. (1988) · Glia · doi:10.1002/glia.440010502 · Cited by 937
Perry, V. H., Hume, D. A., & Gordon, S. (1985) · Neuroscience · doi:10.1016/0306-4522(85)90215-5 · Cited by 902
Self-citation
Research works printed but not linked: 3
- Colello, 1987, Relationship of axonal growth cones to macrophage like cells in the eye stalk of embryonic mouse, J. Anat., 152, 264
- Fujita, 1976, Origin of brain macrophages and the nature of the microglia, Prog. Neuropath., 3, 1
- Perry, 1985, Macrophages, microglia and cell death in the developing mouse brain, Pontificiae Academiae Scientiarum Scripta Varia, 59, 281
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Baaklini, C. S., Rawji, K. S., Duncan, G. J., Ho, M. F. S., & Plemel, J. R. (2019) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2019.00225 · Cited by 88
Su, S.-H., Xu, W., Li, M., Zhang, L., Wu, Y., Yu, F., & Hai, J. (2014) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2014.01.009 · Cited by 86
TNF-α from hippocampal microglia induces working memory deficits by acute stress in mice
Ohgidani, M., Kato, T. A., Sagata, N., Hayakawa, K., Shimokawa, N., Sato‐Kasai, M., & Kanba, S. (2015) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2015.08.022 · Cited by 79
Unique role for dentate gyrus microglia in neuroblast survival and in VEGF‐induced activation
Kreisel, T., Wolf, B., Keshet, E., & Licht, T. (2018) · Glia · doi:10.1002/glia.23505 · Cited by 86
Lowery, R. L., Tremblay, M., Hopkins, B. E., & Majewska, A. K. (2017) · Glia · doi:10.1002/glia.23192 · Cited by 86
Glia-Driven Neuroinflammation and Systemic Inflammation in Alzheimer’s Disease
Hashioka, S., Wu, Z., & Klegeris, A. (2021) · Current Neuropharmacology · doi:10.2174/1570159x18666201111104509 · Cited by 78
Modeling ischemic stroke in a triculture neurovascular unit on-a-chip
Wevers, N. R., Nair, A. L., Fowke, T. M., Pontier, M., Kasi, D. G., Spijkers, X. M., Hallard, C., Rabussier, G., van Vught, R., Vulto, P., et al. (2021) · Fluids and Barriers of the CNS · doi:10.1186/s12987-021-00294-9 · Cited by 78
Microbiome Gut-Brain-Axis: Impact on Brain Development and Mental Health
Ramadan, Y. N., Alqifari, S. F., Alshehri, K., Alhowiti, A., Mirghani, H. O., Alrasheed, T., Aljohani, F., Alghamdi, A. M., & Hetta, H. F. (2025) · Molecular Neurobiology · doi:10.1007/s12035-025-04846-0 · Cited by 100
Classical and unconventional pathways of vesicular release in microglia
Prada, I., Furlan, R., Matteoli, M., & Verderio, C. (2013) · Glia · doi:10.1002/glia.22497 · Cited by 86
Repeated Iron–Soot Exposure and Nose-to-brain Transport of Inhaled Ultrafine Particles
Hopkins, L. E., Laing, E. A., Peake, J. L., Uyeminami, D. L., Mack, S. M., Li, X., Smiley‐Jewell, S. M., & Pinkerton, K. E. (2017) · Toxicologic Pathology · doi:10.1177/0192623317729222 · Cited by 79
Fetal Alcohol Spectrum Disorders and Neuroimmune Changes
Drew, P. D., & Kane, C. J. M. (2014) · International review of neurobiology · doi:10.1016/b978-0-12-801284-0.00003-8 · Cited by 82
Burns, J. C., Cotleur, B., Walther, D. M., Bajrami, B., Rubino, S. J., Wei, R., Franchimont, N., Cotman, S. L., Ransohoff, R. M., & Mingueneau, M. (2020) · eLife · doi:10.7554/elife.57495 · Cited by 82
Neuroprotective effects of natural compounds on LPS-induced inflammatory responses in microglia.
An, J., Chen, B., Kang, X., Zhang, R., Guo, Y., Zhao, J., & Yang, H. (2020) · PubMed Central · Cited by 79
Age-related changes in glial cells of dopamine midbrain subregions in rhesus monkeys
Kanaan, N. M., Kordower, J. H., & Collier, T. J. (2008) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2008.07.006 · Cited by 78
Heterogeneous induction of microglia M2a phenotype by central administration of interleukin-4
Pepe, G., Calderazzi, G., Maglie, M. D., Villa, A. M., & Vegeto, E. (2014) · Journal of Neuroinflammation · doi:10.1186/s12974-014-0211-6 · Cited by 78
The mysterious origins of microglia
Ginhoux, F., & Garel, S. (2018) · Nature Neuroscience · doi:10.1038/s41593-018-0176-3 · Cited by 78
Mathews, S., Woods, A. B., Katano, I., Makarov, E., Thomas, M. B., Gendelman, H. E., Poluektova, L. Y., Ito, M., & Gorantla, S. (2019) · Molecular Neurodegeneration · doi:10.1186/s13024-019-0311-y · Cited by 79
Entry, dispersion and differentiation of microglia in the developing central nervous system
Navascués, J., Calvente, R., Marín‐Teva, J. L., & Cuadros, M. Á. (2000) · Anais da Academia Brasileira de Ciências · doi:10.1590/s0001-37652000000100013 · Cited by 78
Rossi, C., Cusimano, M., Zambito, M., Finardi, A., Capotondo, A., Garcia-Manteiga, J. M., Comi, G., Furlan, R., Martino, G., & Muzio, L. (2018) · Cell Death & Disease · doi:10.1038/s41419-018-0288-4 · Cited by 77
González Ibanez, F., Picard, K., Bordeleau, M., Sharma, K., Bisht, K., & Tremblay, M.-È. (2019) · Journal of Visualized Experiments · doi:10.3791/60510 · Cited by 77
Redox Signaling, Neuroinflammation, and Neurodegeneration
Aguilera, G., Colín-González, A. L., Rangel‐López, E., Chavarría, A., & Santamaría, A. (2017) · Antioxidants and Redox Signaling · doi:10.1089/ars.2017.7099 · Cited by 81
Picard, K., St‐Pierre, M., Vecchiarelli, H. A., Bordeleau, M., & Tremblay, M. (2021) · Neurochemistry International · doi:10.1016/j.neuint.2021.104987 · Cited by 79
Vulnerability of the Hippocampus to Insults: Links to Blood–Brain Barrier Dysfunction
Davidson, T. L., & Stevenson, R. J. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25041991 · Cited by 80
Cohen, P. E., Zhu, L., Nishimura, K., & Pollard, J. W. (2002) · Endocrinology · doi:10.1210/endo.143.4.8754 · Cited by 76
Hernangómez, M., Carrillo-Salinas, F. J., Mecha, M., Correa, F., Mestre, L., Loría, F., Feliú, A., Docagne, F., & Guaza, C. (2014) · Current Pharmaceutical Design · doi:10.2174/1381612820666140130202911 · Cited by 77
Ashbrook, D. G., Hing, B. W. Q., Michalovicz, L. T., Kelly, K. A., Miller, J. V., de Vega, W. C., Miller, D. B., Broderick, G., O'Callaghan, J. P., & McGowan, P. O. (2018) · Journal of Neuroinflammation · doi:10.1186/s12974-018-1113-9 · Cited by 80
Microglial cells in neurodegenerative disorders.
Wojtera, M., Sikorska, B., Sobów, T., & Liberski, P. P. (2005) · PubMed · Cited by 78
How microbiota shape microglial phenotypes and epigenetics
Erny, D., & Prinz, M. (2020) · Glia · doi:10.1002/glia.23822 · Cited by 80
IL-1/IL-1ra balance in the brain revisited – Evidence from transgenic mouse models
Spulber, S. D., Bartfai, T., & Schultzberg, M. (2009) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2009.02.015 · Cited by 83
Fine-tuning the central nervous system: microglial modelling of cells and synapses
Xavier, A. L. R., Menezes, J. R. L., Goldman, S. A., & Nedergaard, M. (2014) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2013.0593 · Cited by 80
l ‐DOPA‐induced dyskinesia and neuroinflammation: do microglia and astrocytes play a role?
Carta, A. R., Mulas, G., Bortolanza, M., Duarte, T. T., Pillai, E., Fisone, G., Raisman‐Vozari, R., & Bel, E. A. D. (2016) · European Journal of Neuroscience · doi:10.1111/ejn.13482 · Cited by 80
Beier, E. E., Neal, M. P., Alam, G., Edler, M. K., Wu, L., & Richardson, J. R. (2017) · Neurobiology of Disease · doi:10.1016/j.nbd.2017.08.009 · Cited by 78
Reid, D. M., Perry, V. H., Andersson, P.-B., & Gordon, S. (1993) · Neuroscience · doi:10.1016/0306-4522(93)90353-h · Cited by 76
Self-citationDiversity and function of brain-associated macrophages
Mildenberger, W., Stifter, S. A., & Greter, M. (2022) · Current Opinion in Immunology · doi:10.1016/j.coi.2022.102181 · Cited by 81
Divecha, Y. A., Rampes, S., Tromp, S., Boyanova, S., Fleckney, A. L., Fidanboylu, M., & Thomas, S. A. (2025) · Pharmacological Reviews · doi:10.1016/j.pharmr.2025.100052 · Cited by 83
Histamine production by cultured microglial cells of the mouse
Katoh, Y., Niimi, M., Yamamoto, Y., Kawamura, T., Morimoto-Ishizuka, T., Sawada, M., Takemori, H., & Yamatodani, A. (2001) · Neuroscience Letters · doi:10.1016/s0304-3940(01)01835-3 · Cited by 75
Ubink, R., Halasz, N. A., Zhang, X., Dagerlind, Å., & Hökfelt, T. G. M. (1994) · Neuroscience · doi:10.1016/0306-4522(94)90499-5 · Cited by 75
Rod microglia and their role in neurological diseases
Holloway, O. G., Canty, A. J., King, A. E., & Ziebell, J. M. (2019) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2019.02.005 · Cited by 76
Microglia dynamics in sleep/wake states and in response to sleep loss
Deurveilher, S., Golovin, T., Hall, S., & Semba, K. (2020) · Neurochemistry International · doi:10.1016/j.neuint.2020.104944 · Cited by 75
PARK7/DJ-1 in microglia: implications in Parkinson’s disease and relevance as a therapeutic target
Mogensen, F. L., Scafidi, A., Poli, A., & Michelucci, A. (2023) · Journal of Neuroinflammation · doi:10.1186/s12974-023-02776-z · Cited by 80
Microglial diversity in neuropathic pain
Tsuda, M., Masuda, T., & Kohno, K. (2023) · Trends in Neurosciences · doi:10.1016/j.tins.2023.05.001 · Cited by 81
Microglia and Central Nervous System Immunity
Kaur, G., Han, S. J., Yang, I., & Crane, C. A. (2009) · Neurosurgery Clinics of North America · doi:10.1016/j.nec.2009.08.009 · Cited by 73
Hou, Y., Wu, C. F., Yang, J., He, X., Bi, X. L., Yu, L., & Guo, T. (2006) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2006.05.006 · Cited by 74
McPherson, C. A., Aoyama, M., & Harry, G. J. (2010) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2010.09.003 · Cited by 75
Role of nitric oxide in the brain during lipopolysaccharide‐evoked systemic inflammation
Czapski, G. A., Cąkała, M., Chalimoniuk, M., Gajkowska, B., & Strosznajder, J. B. (2007) · Journal of Neuroscience Research · doi:10.1002/jnr.21294 · Cited by 74
Jones, M., Lebonville, C. L., Paniccia, J. E., Balentine, M. E., Reissner, K. J., & Lysle, D. T. (2017) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2017.09.016 · Cited by 74
Alzarea, S., & Rahman, S. (2019) · Behavioural Brain Research · doi:10.1016/j.bbr.2019.03.019 · Cited by 75
Regulation of microglia polarization after cerebral ischemia
Wang, H., Li, J., Zhang, H., Wang, M., Xiao, L., Wang, Y., & Cheng, Q. (2023) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2023.1182621 · Cited by 81
Manganese chloride stimulates rat microglia to release hydrogen peroxide
Zhang, P., Hatter, A., & Liu, B. (2007) · Toxicology Letters · doi:10.1016/j.toxlet.2007.06.013 · Cited by 73
Cortese, G. P., & Bürger, C. (2016) · Behavioural Brain Research · doi:10.1016/j.bbr.2016.08.027 · Cited by 77
Torres, A., Vidal, P. P., & de Waele, C. (1999) · Neuroscience · doi:10.1016/s0306-4522(99)00078-0 · Cited by 73
Masrori, P., Beckers, J., Gossye, H., & Damme, P. V. (2022) · Molecular Neurodegeneration · doi:10.1186/s13024-022-00525-z · Cited by 80
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Shui, X., Chen, J., Fu, Z., Zhu, H., Tao, H., & Li, Z. (2024) · Journal of Inflammation Research · doi:10.2147/jir.s461795 · Cited by 80
CD200–CD200R Regulation of Microglia Activation in the Pathogenesis of Parkinson’s Disease
Wang, X., Ye, M., Zhang, Y., & Chen, S. (2007) · Journal of Neuroimmune Pharmacology · doi:10.1007/s11481-007-9075-1 · Cited by 71
He, Q. W., Yu, W., Wu, J., Chen, C., Lou, Z., Zhang, Q., Zhao, J., Wang, J., & Xiao, B. (2013) · PLoS ONE · doi:10.1371/journal.pone.0078418 · Cited by 72
Modeling neuro-immune interactions during Zika virus infection
Mesci, P., Macia, Á., LaRock, C. N., Tejwani, L., Fernandes, I. R., Suarez, N. A., Zanotto, P. M. D. A., Beltrão-Braga, P. C. B., Nizet, V., & Muotri, A. R. (2017) · Human Molecular Genetics · doi:10.1093/hmg/ddx382 · Cited by 71
Macrophage Membrane Molecules: Markers of Tissue Differentiation and Heterogeneity
Martínez‐Pomares, L., Platt, N., Mcknight, A. J., da Silva, R. P., & Gordon, S. (1996) · Immunobiology · doi:10.1016/s0171-2985(96)80012-x · Cited by 72
Self-citationCharacterisation of two new monoclonal antibodies directed against rat microglia
Gehrmann, J., & Kreutzberg, G. W. (1991) · The Journal of Comparative Neurology · doi:10.1002/cne.903130302 · Cited by 72
Nitric oxide-mediated tumoricidal activity of murine microglial cells
Brantley, E. C., Guo, L., Zhang, C., Lin, Q., Yokoi, K., Langley, R. R., Kruzel, E., Maya, M., Kim, S. W., Kim, S.-J., et al. (2010) · Translational Oncology · doi:10.1593/tlo.10208 · Cited by 71
Shi, L., Rocha, M., Zhang, W., Jiang, M., Li, S., Ye, Q., Hassan, S. H., Liu, L., Adair, M. N., Xu, J., et al. (2020) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1177/0271678x20925655 · Cited by 71
Neuroinflammation and Glial Phenotypic Changes in Alpha-Synucleinopathies
Refolo, V., & Stefanova, N. (2019) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2019.00263 · Cited by 72
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Yu, F., Huang, T., Ran, Y., Li, D., Ye, L., Tian, G., Xi, J., & Liu, Z. (2021) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2021.727899 · Cited by 74
Microglial Activation and Oxidative Stress in PM2.5-Induced Neurodegenerative Disorders
Song, J., Han, K., Wang, Y., Qu, R., Liu, Y., Wang, S., Wang, Y., An, Z., Li, J., Wu, H., et al. (2022) · Antioxidants · doi:10.3390/antiox11081482 · Cited by 79
Bedolla, A., Wegman, E., Weed, M., Stevens, M. K., Ware, K., Paranjpe, A., Alkhimovitch, A., Ifergan, I., Таранов, А., Peter, J. D., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-49596-0 · Cited by 85
Chertoff, M., Paolo, N. D., Schöneberg, A., Depino, A. M., Ferrari, C. C., Wurst, W., Pfizenmaier, K., Eisel, U. L. M., & Pitossi, F. J. (2010) · Experimental Neurology · doi:10.1016/j.expneurol.2010.11.010 · Cited by 73
Microglia: a sensor to threats in the nervous system?
Gehrmann, J. (1996) · Research in Virology · doi:10.1016/0923-2516(96)80220-2 · Cited by 71
Macrophages in tissues and in vitro
Gordon, S., Fraser, I. P., Nath, D., Hughes, D. A., & Clarke, S. (1992) · Current Opinion in Immunology · doi:10.1016/0952-7915(92)90119-y · Cited by 75
Self-citationClinical implications of the involvement of tPA in neuronal cell death
Tsirka, S. E. (1997) · Journal of Molecular Medicine · doi:10.1007/s001090050119 · Cited by 71
Microglia Diversity in Health and Multiple Sclerosis
Zia, S., Rawji, K. S., Michaels, N. J., Burr, M. K., Kerr, B. J., Healy, L. M., & Plemel, J. R. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.588021 · Cited by 70
Universal autofocus for quantitative volumetric microscopy of whole mouse brains
Silvestri, L., Müllenbroich, M. C., Costantini, I., Giovanna, A. P. D., Mazzamuto, G., Franceschini, A., Kutra, D., Kreshuk, A., Checcucci, C., Toresano, L. O., et al. (2021) · Nature Methods · doi:10.1038/s41592-021-01208-1 · Cited by 72
Boas, S. M., Joyce, K. L., & Cowell, R. M. (2021) · Antioxidants · doi:10.3390/antiox11010008 · Cited by 70
Pharmacological effects of cannabidiol by transient receptor potential channels
Etemad, L., Karimi, G., Alavi, M. S., & Roohbakhsh, A. (2022) · Life Sciences · doi:10.1016/j.lfs.2022.120582 · Cited by 73
Peña‐Altamira, E., Prati, F., Massenzio, F., Virgili, M., Contestabile, A., Bolognesi, M. L., & Monti, B. (2015) · Expert Opinion on Therapeutic Targets · doi:10.1517/14728222.2016.1121237 · Cited by 70
Wang, J.-W., Chen, S.-D., Zhang, X.-L., & Jonas, J. B. (2016) · Journal of Glaucoma · doi:10.1097/ijg.0000000000000200 · Cited by 69
Characterization of human monocyte‐derived microglia‐like cells
Leone, C., Le Pavec, G., Même, W., Porcheray, F., Samah, B., Dormont, D., & Gras, G. (2006) · Glia · doi:10.1002/glia.20372 · Cited by 70
Sex differences in the inflammatory response to stroke
Tariq, M. B., Lee, J., & McCullough, L. D. (2022) · Seminars in Immunopathology · doi:10.1007/s00281-022-00969-x · Cited by 72
Neuroinflammation: Microglial Activation During Sepsis
Michels, M., Danielski, L. G., Dal‐Pizzol, F., & Petronilho, F. C. (2014) · Current Neurovascular Research · doi:10.2174/1567202611666140520122744 · Cited by 70
Microglia in Cell Culture and in Transplantation Therapy for Central Nervous System Disease
Dobrenis, K. (1998) · Methods · doi:10.1006/meth.1998.0688 · Cited by 68
Ji, K., Eu, M. Y., Kang, S., Gwag, B. J., Jou, I., & Joe, E.-H. (2008) · Glia · doi:10.1002/glia.20677 · Cited by 69
SPARC Regulates Microgliosis and Functional Recovery following Cortical Ischemia
Lloyd-Burton, S. M., York, E. M., Anwar, M. A., Vincent, A. J., & Roskams, A. J. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.3585-12.2013 · Cited by 67
Matyszak, M. K., & Perry, V. H. (1996) · Journal of Neuroimmunology · doi:10.1016/0165-5728(96)00082-3 · Cited by 69
Self-citationCzapski, G. A., Gajkowska, B., & Strosznajder, J. B. (2010) · Brain Research · doi:10.1016/j.brainres.2010.07.096 · Cited by 68
Zhang, P., Wong, T. A., Lokuta, K. M., Turner, D. E., Vujisic, K., & Liu, B. (2009) · Experimental Neurology · doi:10.1016/j.expneurol.2009.02.013 · Cited by 68
Nau, R., Ribes, S., Djukic, M., & Eiffert, H. (2014) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2014.00138 · Cited by 73
A Robust Image Registration Interface for Large Volume Brain Atlas
Ni, H., Tan, C., Feng, Z., Chen, S., Zhang, Z., Li, W., Guan, Y., Gong, H., Luo, Q., & Li, A. (2020) · Scientific Reports · doi:10.1038/s41598-020-59042-y · Cited by 71
microRNAs Orchestrate Pathophysiology of Breast Cancer Brain Metastasis: Advances in Therapy
Kanchan, R. K., Siddiqui, J. A., Mahapatra, S., Batra, S. K., & Nasser, M. W. (2020) · Molecular Cancer · doi:10.1186/s12943-020-1140-x · Cited by 70
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Anfinogenova, Y., Quinn, M. T., Schepetkin, I. A., & Atochin, D. N. (2020) · Cells · doi:10.3390/cells9112350 · Cited by 68
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Metadata
- Authors
- Lawson, L. J., Perry, V. H., Dri, P., & Gordon, S.
- Affiliations
- University of Oxford (GB)
- Corresponding author
- Lawson, L.J.
- Venue
- Neuroscience
- Publisher
- Elsevier BV
- Published
- 1990-01
- Volume
- 39
- Issue
- 1
- Pages
- 151-170
- ISSN
- 0306-4522 (ISSN-L)
- OpenAlex
- W1991805788
- Cited by
- 2,045
- References
- 55
- Citations by year
- 2026: 61 · 2025: 77 · 2024: 92 · 2023: 107 · 2022: 115 · 2021: 166 · 2020: 120 · 2019: 110 · 2018: 85 · 2017: 88 · 2016: 76 · 2015: 80 · 2014: 91 · 2013: 79 · 2012: 71
- FWCI
- 10.58
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Neuroscience (publishedVersion)
- PubMed (publishedVersion)
- ePrints Soton (University of Southampton) (submittedVersion)
- Funders
- Wellcome Trust
- Topics
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Keywords
- microglia, microglial morphology, F4/80, mouse brain, regional variation, gray matter, white matter, developmental cell death, monocyte recruitment, microenvironment, Kupffer cells, brain macrophages, substantia nigra, hippocampus, basal ganglia
- MeSH terms
- Animals, Brain, Female, Immunoenzyme Techniques, Immunohistochemistry, Macrophages, Membrane Glycoproteins, Mesoderm, Mice, Inbred BALB C, Neuroglia, Organ Specificity, Reference Values, Mice
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