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.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
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
“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
Cited by
Sorted by citations
Items 501–600 of 1,006
Dual Role of CD38 in Microglial Activation and Activation-Induced Cell Death
Mayo, L., Jacob‐Hirsch, J., Amariglio, N., Rechavi, G., Moutin, M., Lund, F. E., & Stein, R. (2008) · The Journal of Immunology · doi:10.4049/jimmunol.181.1.92 · Cited by 100
Minten, C., Terry, R., Deffrasnes, C., King, N. J. C., & Campbell, I. L. (2012) · PLoS ONE · doi:10.1371/journal.pone.0049851 · Cited by 100
Intrastriatal lipopolysaccharide injection induces parkinsonism in C57/B6 mice
Hunter, R. L., Cheng, B., Choi, D., Liu, M., Liu, S., Cass, W. A., & Bing, G. (2009) · Journal of Neuroscience Research · doi:10.1002/jnr.22012 · Cited by 100
Fibronectin and laminin regulate thein vitro differentiation of microglial cells
Chamak, B., & Mallat, M. (1991) · Neuroscience · doi:10.1016/0306-4522(91)90267-r · Cited by 100
Further Studies on Motor and Sensory Nerve Regeneration in Mice With Delayed Wallerian Degeneration
Brown, M. C., Perry, V. H., Hunt, S. P., & Lapper, S. R. (1994) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1994.tb00285.x · Cited by 100
Self-citationSandvig, I., Augestad, I. L., Håberg, A. K., & Sandvig, A. (2018) · European Journal of Neuroscience · doi:10.1111/ejn.13959 · Cited by 94
Smeets, W. J. A. J., Alonso, J. R., & Gonz�lez, A. (1997) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19970106)377:1 · Cited by 71
Zhou, H.-F., Liu, X., Niu, D.-B., Li, F., He, Q., & Wang, X.-M. (2005) · Neurobiology of Disease · doi:10.1016/j.nbd.2004.12.005 · Cited by 99
Miller, R. L., Sun, G. Y., & Sun, A. Y. (2007) · Brain Research · doi:10.1016/j.brainres.2007.06.046 · Cited by 99
Shaik, S., Combs, C. K., & Ebadi, M. (2006) · Neurochemical Research · doi:10.1007/s11064-005-9233-x · Cited by 104
Circulating interleukin-10 and interleukin-12 in Parkinson’s disease
Rentzos, M., Nikolaou, C., Andreadou, E., Paraskevas, G. P., Rombos, A., Zoga, M., Tsoutsou, A., Boufidou, F., Kapaki, E., & Vassilopoulos, D. (2009) · Acta Neurologica Scandinavica · doi:10.1111/j.1600-0404.2008.01103.x · Cited by 99
Lafrenaye, A. D., Todani, M., Walker, S. A., & Povlishock, J. T. (2015) · Journal of Neuroinflammation · doi:10.1186/s12974-015-0405-6 · Cited by 98
Alzheimer’s Disease and Inflammaging
Kosyreva, A., Sentyabreva, A., Tsvetkov, I., & Makarova, O. (2022) · Brain Sciences · doi:10.3390/brainsci12091237 · Cited by 98
Greig, N. H., Mattson, M. P., Perry, T., Chan, S. L., Giordano, T., Sambamurti, K., Rogers, J. T., Ovadia, H., & Lahiri, D. K. (2004) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1332.018 · Cited by 99
Immunotherapy for Parkinson’s disease
Schwab, A. D., Thurston, M. J., Machhi, J., Olson, K. E., Namminga, K. L., Gendelman, H. E., & Mosley, R. L. (2020) · Neurobiology of Disease · doi:10.1016/j.nbd.2020.104760 · Cited by 101
Kumar, A., Muzik, O., Shandal, V., Chugani, D. C., Chakraborty, P. K., & Chugani, H. T. (2012) · Journal of Neuroinflammation · doi:10.1186/1742-2094-9-232 · Cited by 98
Jinno, S., Fleischer, F., Eckel, S., Schmidt, V., & Kosaka, T. (2007) · Glia · doi:10.1002/glia.20552 · Cited by 98
Gyoneva, S., Shapiro, L. P., Lazo, C. R., Garnier‐Amblard, E. C., Smith, Y., Miller, G. W., & Traynelis, S. F. (2014) · Neurobiology of Disease · doi:10.1016/j.nbd.2014.03.004 · Cited by 102
The immunology of Parkinson’s disease
Zhu, B., Yin, D., Zhao, H., & Zhang, L. (2022) · Seminars in Immunopathology · doi:10.1007/s00281-022-00947-3 · Cited by 108
Roles of microglia in adult hippocampal neurogenesis in depression and their therapeutics
Fang, S., Wu, Z., Guo, Y., Zhu, W., Wan, C., Yuan, N., Chen, J., Hao, W., Mo, X., Guo, X., et al. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1193053 · Cited by 107
From development to dysfunction: Microglia and the complement cascade in CNS homeostasis
Zabel, M. K., & Kirsch, W. M. (2013) · Ageing Research Reviews · doi:10.1016/j.arr.2013.02.001 · Cited by 100
Abel, T. W., Voytko, M. L., & Rance, N. E. (1999) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem.84.6.5689 · Cited by 97
Human-specific features of spatial gene expression and regulation in eight brain regionsPreprint
Xu, C., Li, Q., Efimova, O., He, L., Tatsumoto, S., Stepanova, V. V., Oishi, T., Udono, T., Yamaguchi, K., Shigenobu, S., et al. (2018) · Genome Research · doi:10.1101/gr.231357.117 · Cited by 95
Sheffield, L. G., Marquis, J. G., & Berman, N. E. J. (2000) · Neuroscience Letters · doi:10.1016/s0304-3940(00)01037-5 · Cited by 96
Post-Ischaemic Immunological Response in the Brain: Targeting Microglia in Ischaemic Stroke Therapy
Rawlinson, C., Jenkins, S. I., Thei, L., Dallas, M. L., & Chen, R. (2020) · Brain Sciences · doi:10.3390/brainsci10030159 · Cited by 99
Santos, S. E. D., Medeiros, M., Porfírio, J., Tavares, W. C., Pessôa, L. M., Grinberg, L. T., Leite, R. E. P., Ferretti‐Rebustini, R. E. D. L., Suemoto, C. K., Filho, W. J., et al. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.2339-19.2020 · Cited by 104
miR-155 Is Essential for Inflammation-Induced Hippocampal Neurogenic Dysfunction
Woodbury, M. E., Freilich, R. W., Cheng, C. J., Asai, H., Ikezu, S., Boucher, J. D., Slack, F. J., & Ikezu, T. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.4790-14.2015 · Cited by 96
Diverse activation of microglia by chemokine (C-C motif) ligand 2 overexpression in brain
Selenica, M. B., Alvarez, J. A., Nash, K. R., Lee, D. C., Cao, C., Lin, X., Reid, P., Mouton, P. R., Morgan, D., & Gordon, M. N. (2013) · Journal of Neuroinflammation · doi:10.1186/1742-2094-10-86 · Cited by 99
Maatouk, L., Compagnion, A.-C., Sauvage, M.-A. C.-D., Bemelmans, A.-P., Leclere-Turbant, S., Cirotteau, V., Tohme, M., Beke, A., Trichet, M., Bazin, V., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-04569-y · Cited by 95
Role of pyroptosis in the pathogenesis of various neurological diseases
Oladapo, A., Jackson, T., Menolascino, J., & Periyasamy, P. (2024) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2024.02.001 · Cited by 101
Perry, V. H., Crocker, P. R., & Gordon, S. (1992) · Journal of Cell Science · doi:10.1242/jcs.101.1.201 · Cited by 95
Self-citationRoqué, P. J., Dao, K., & Costa, L. G. (2016) · NeuroToxicology · doi:10.1016/j.neuro.2016.08.006 · Cited by 95
Region-specific vulnerability in neurodegeneration: lessons from normal ageing
Pandya, V. A., & Patani, R. (2021) · Ageing Research Reviews · doi:10.1016/j.arr.2021.101311 · Cited by 98
TRPM7 and TRPM2—Candidate susceptibility genes for Western Pacific ALS and PD?
Hermosura, M. C., & Garruto, R. M. (2007) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2007.02.008 · Cited by 94
Wu, C., Wen, C. Y., Shieh, J., & Ling, E. (1992) · Europe PMC (PubMed Central) · Cited by 94
Cellular therapy to target neuroinflammation in amyotrophic lateral sclerosis
Rizzo, F., Riboldi, G. M., Salani, S., Nizzardo, M., Simone, C., Corti, S. P., & Hedlund, E. (2013) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-013-1480-4 · Cited by 93
Two phenotypically and functionally distinct microglial populations in adult zebrafish
Wu, S., Nguyen, L. T. M., Pan, H., Hassan, S., Dai, Y., Xu, J., & Wen, Z. (2020) · Science Advances · doi:10.1126/sciadv.abd1160 · Cited by 98
Berezovskaya, O. L., Maysinger, D., & FEDOROFF, S. (1995) · International Journal of Developmental Neuroscience · doi:10.1016/0736-5748(95)00013-7 · Cited by 94
Differential distribution and activation of microglia in the brain of male C57BL/6J mice
Yang, T.-T., Lin, C., Hsu, C.-T., Wang, T.-F., Ke, F.-Y., & Kuo, Y.-M. (2013) · Brain Structure and Function · doi:10.1007/s00429-012-0446-x · Cited by 92
Zhou, F., Wang, X., Han, B.-Y., Tang, X., Liu, R., Ji, Q., Zhou, Z., & Zhang, L. (2021) · Molecular Pain · doi:10.1177/1744806921996520 · Cited by 96
The Inflammatory Response in Alzheimer's Disease
Rogers, J. (2008) · Journal of Periodontology · doi:10.1902/jop.2008.080171 · Cited by 92
Microglia energy metabolism in metabolic disorder
Kalsbeek, M. J. T., Mulder, L., & Yi, C. (2016) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2016.09.028 · Cited by 93
FcγRIIB mediates the inhibitory effect of aggregated α-synuclein on microglial phagocytosis
Choi, Y. R., Kang, S., Kim, J.-M., Lee, S., Jou, I., Joe, E.-H., & Park, S. M. (2015) · Neurobiology of Disease · doi:10.1016/j.nbd.2015.08.025 · Cited by 88
Modeling neuroinflammatory pathogenesis of Parkinson’s disease
Barnum, C. J., & Tansey, M. G. (2010) · Progress in brain research · doi:10.1016/s0079-6123(10)84006-3 · Cited by 91
The P2X7 Receptor in Microglial Cells Modulates the Endolysosomal Axis, Autophagy, and Phagocytosis
Campagno, K. E., & Mitchell, C. H. (2021) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2021.645244 · Cited by 94
Microglia Diversity in Healthy and Diseased Brain: Insights from Single-Cell Omics
Ochocka, N., & Kaminska, B. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22063027 · Cited by 97
Epigenetic Regulation of Neuroinflammation in Parkinson’s Disease
Rasheed, M., Liang, J., Wang, C., Deng, Y., & Chen, Z. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22094956 · Cited by 96
Ren, L.-Q., Lubrich, B., Biber, K. P. H., & Gebicke‐Haerter, P. J. (1999) · Molecular Brain Research · doi:10.1016/s0169-328x(99)00016-9 · Cited by 90
Decreased microglial activation in MS patients treated with glatiramer acetate
Ratchford, J. N., Endres, C. J., Hammoud, D. A., Pomper, M. G., Shiee, N., McGready, J., Pham, D. L., & Calabresi, P. A. (2011) · Journal of Neurology · doi:10.1007/s00415-011-6337-x · Cited by 91
Genetic contributions to Parkinson's disease
Huang, Y. M., Cheung, L., Rowe, D. B., & Halliday, G. M. (2004) · Brain Research Reviews · doi:10.1016/j.brainresrev.2004.04.007 · Cited by 91
Matyszak, M. K., Lawson, L. J., Perry, V. H., & Gordon, S. (1992) · Journal of Neuroimmunology · doi:10.1016/0165-5728(92)90131-4 · Cited by 91
Self-citationLiu, W., Brosnan, C. F., Dickson, D. W., & Lee, S. C. (1994) · PubMed Central · Cited by 91
Patir, A., Shih, B., McColl, B. W., & Freeman, T. C. (2019) · Glia · doi:10.1002/glia.23572 · Cited by 90
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
Phosphoinositides Regulate P2X4ATP-Gated Channels through Direct Interactions
Bernier, L., Ase, A. R., Chevallier, S., Blais, D., Zhao, Q., Boué‐Grabot, É., Logothetis, D. E., & Séguéla, P. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.3038-08.2008 · Cited by 92
The emerging tale of microglia in psychiatric disorders
Rahimian, R., Wakid, M., O’Leary, L. A., & Mechawar, N. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2021.09.023 · Cited by 96
Antioxidant treatment protects striatal neurons against excitotoxic insults
Nakao, N., Grasbon-Frodl, E. M., Widner, H., & Brundin, P. (1996) · Neuroscience · doi:10.1016/0306-4522(96)00034-6 · Cited by 90
Lipopolysaccharides Upregulate Hepcidin in Neuron via Microglia and the IL-6/STAT3 Signaling Pathway
Qian, Z.-M., He, X., Liang, T., Wu, K.-C., Yan, Y.-C., Lu, L.-N., Yang, G., Luo, Q. Q., Yung, W.-H., & Ke, Y. (2014) · Molecular Neurobiology · doi:10.1007/s12035-014-8671-3 · Cited by 89
Lu, X., Bing, G., & Hagg, T. (2000) · Neuroscience · doi:10.1016/s0306-4522(00)00033-6 · Cited by 89
Defining the Microglia Response during the Time Course of Chronic Neurodegeneration
Vincenti, J. E., Murphy, L., Grabert, K., McColl, B. W., Cancellotti, E., Freeman, T. C., & Manson, J. C. (2016) · Journal of Virology · doi:10.1128/jvi.02613-15 · Cited by 88
Effects of Microglial Activation and Polarization on Brain Injury After Stroke
Dong, R., Huang, R., Wang, J., Liu, H., & Xu, Z. (2021) · Frontiers in Neurology · doi:10.3389/fneur.2021.620948 · Cited by 87
Dynamic Changes in the Nigrostriatal Pathway in the MPTP Mouse Model of Parkinson’s Disease
Huang, D., Xu, J., Wang, J., Tong, J., Bai, X., Li, H., Wang, Z., Huang, Y., Wu, Y., Yu, M., et al. (2017) · Parkinson s Disease · doi:10.1155/2017/9349487 · Cited by 89
Human retinal microglia: Expression of immune markers and relationship to the Glia limitans
Provis, J. M., Penfold, P. L., Edwards, A. J., & van Driel, D. (1995) · Glia · doi:10.1002/glia.440140402 · Cited by 89
Friend, Foe or Both? Immune Activity in Alzheimer’s Disease
Frost, G. R., Jonas, L. A., & Li, Y. (2019) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2019.00337 · Cited by 88
Behrstock, S. P., Anantharam, V., Thompson, K. W., Schweitzer, E. S., & Tobin, A. J. (2000) · Journal of Neuroscience Research · doi:10.1002/(sici)1097-4547(20000501)60:3 · Cited by 17
Mao, J., Yang, J., Zhang, Y., Li, T., Wang, C., Xu, L., Hu, Q., Wang, X., Jiang, S., Nie, X., et al. (2016) · Toxicology and Applied Pharmacology · doi:10.1016/j.taap.2016.05.003 · Cited by 87
Recent Advances in the Study of Bipolar/Rod-Shaped Microglia and their Roles in Neurodegeneration
Au, N. P. B., & Ma, C. H. E. (2017) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2017.00128 · Cited by 87
Microglia heterogeneity along a spatio–temporal axis: More questions than answers
Silvin, A., & Ginhoux, F. (2018) · Glia · doi:10.1002/glia.23458 · Cited by 90
Diabetes, a Contemporary Risk for Parkinson’s Disease: Epidemiological and Cellular Evidences
Sergi, D., Renaud, J., Simola, N., & Martinoli, M. (2019) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2019.00302 · Cited by 87
Wilms, H., Hartmann, D., & Sievers, J. (1997) · Cell and Tissue Research · doi:10.1007/s004410050769 · Cited by 86
α-Synuclein-carrying extracellular vesicles in Parkinson’s disease: deadly transmitters
Chistiakov, D. A., & Chistiakov, A. A. (2016) · Acta Neurologica Belgica · doi:10.1007/s13760-016-0679-1 · Cited by 87
Exosomes-associated neurodegeneration and progression of Parkinson's disease.
Russo, I., Bubacco, L., & Greggio, E. (2012) · Europe PMC (PubMed Central) · Cited by 85
The Mononuclear Phagocytic System. Generation of Diversity
Gordon, S., & Plüddemann, A. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.01893 · Cited by 89
Self-citationThe old guard: Age-related changes in microglia and their consequences
Costa, J., Martins, S., Ferreira, P. A., Cardoso, A. M., Guedes, J. R., Peça, J., & Cardoso, A. L. (2021) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2021.111512 · Cited by 88
Neurotoxicity by microglia: Mechanisms and potential therapeutic strategy
Takeuchi, H. (2010) · Clinical and Experimental Neuroimmunology · doi:10.1111/j.1759-1961.2009.00001.x · Cited by 88
Stereological estimation of total microglia number in mouse hippocampus
Long, J. M., Kalehua, A. N., Muth, N. J., Hengemihle, J. M., Jucker, M., Calhoun, M. E., Ingram, D. K., & Mouton, P. R. (1998) · Journal of Neuroscience Methods · doi:10.1016/s0165-0270(98)00100-9 · Cited by 87
Effect of Allopurinol Supplementation on Nitric Oxide Levels in Asphyxiated Newborns
Güneş, T., Ozturk, M. A., Köklü, E., Köse, K., & Güneş, I. (2006) · Pediatric Neurology · doi:10.1016/j.pediatrneurol.2006.08.005 · Cited by 85
Åkerblom, M., Sachdeva, R., Quintino, L., Wettergren, E. E., Chapman, K. Z., Manfre, G., Lindvall, O., Lundberg, C., & Jakobsson, J. (2013) · Nature Communications · doi:10.1038/ncomms2801 · Cited by 85
Quantification of the mononuclear phagocyte response to Wallerian degeneration of the optic nerve
Lawson, L. J., Frost, L., Risbridger, J., Fearn, S., & Perry, V. H. (1994) · Journal of Neurocytology · doi:10.1007/bf01268086 · Cited by 86
Self-citationDecoding Mast Cell-Microglia Communication in Neurodegenerative Diseases
Sandhu, J. K., & Kulka, M. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22031093 · Cited by 90
Banati, R. B. (2002) · Journal of Physiology-Paris · doi:10.1016/s0928-4257(02)00018-9 · Cited by 84
Pathological differences between white and grey matter multiple sclerosis lesions
Prins, M., Schul, E., Geurts, J. J. G., van der Valk, P., Drukarch, B., & van Dam, A. (2015) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.12841 · Cited by 89
Role of Microglia in Regulation of Ethanol Neurotoxic Action
Chastain, L. G., & Sarkar, D. K. (2014) · International review of neurobiology · doi:10.1016/b978-0-12-801284-0.00004-x · Cited by 85
Roth, A. B., Schaffner, W., & Hertel, C. (1999) · Journal of Neuroscience Research · doi:10.1002/(sici)1097-4547(19990801)57:3 · Cited by 81
Morrison, H. W., & Filosa, J. A. (2016) · Neuroscience · doi:10.1016/j.neuroscience.2016.09.047 · Cited by 85
Verina, T., Kiihl, S. F., Schneider, J. S., & Guilarte, T. R. (2010) · NeuroToxicology · doi:10.1016/j.neuro.2010.11.003 · Cited by 82
Reshef, R., Kreisel, T., Kay, D. B., & Yirmiya, R. (2014) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2014.04.009 · Cited by 84
Benameur, T., Soleti, R., & Porro, C. (2021) · Nutrients · doi:10.3390/nu13041318 · Cited by 85
The Evolving Biology of Microglia in Alzheimer's Disease
Malm, T. M., Jay, T. R., & Landreth, G. E. (2015) · Neurotherapeutics · doi:10.1007/s13311-014-0316-8 · Cited by 85
Suzuki, M., & Raisman, G. (1992) · Glia · doi:10.1002/glia.440060310 · Cited by 82
De Haas, A. H., Boddeke, H. W. G. M., Brouwer, N., & Biber, K. (2007) · Glia · doi:10.1002/glia.20554 · Cited by 81
Impact of age-related neuroglial cell responses on hippocampal deterioration
Ojo, J. O., Rezaie, P., Gabbott, P. L. A., & Stewart, M. G. (2015) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2015.00057 · Cited by 83
Jurcău, M. C., Jurcău, A., Cristian, A., Hogea, V. O., Diaconu, R. G., & Nunkoo, V. S. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms251910535 · Cited by 100
An optimized protocol for the acute isolation of human microglia from autopsy brain samples
Olah, M., Raj, D. D. A., Brouwer, N., Haas, A. H. D., Eggen, B. J. L., den Dunnen, W. F. A., Biber, K. P. H., & Boddeke, H. W. G. M. (2011) · Glia · doi:10.1002/glia.21251 · Cited by 84
Vizuete, M., Merino, M., Venero, J. L., Santiago, M., Cano, J., & Machado, A. (2000) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2000.0750540.x · Cited by 81
Wang, X., Chen, S., Ma, G., Ye, M., & Lü, G. (2005) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2005.06.012 · Cited by 81
Morphology and distribution of microglial cells in the young and adult mouse cerebellum
Vela, J. M., Dalmau, I., González, B., & Castellano, B. (1995) · The Journal of Comparative Neurology · doi:10.1002/cne.903610405 · Cited by 81
Ismaiel, A. A., Espinosa‐Oliva, A. M., Santiago, M., García-Quintanilla, A., Oliva-Martín, M. J., Herrera, A. J., Venero, J. L., & de Pablos, R. M. (2016) · Toxicology and Applied Pharmacology · doi:10.1016/j.taap.2016.03.004 · Cited by 81
Microglia: origins, homeostasis, and roles in myelin repair
Lloyd, A. F., Davies, C. L., & Miron, V. E. (2017) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2017.10.001 · Cited by 85
Purinoceptors in microglia and neuropathic pain
Trang, T., Beggs, S., & Salter, M. (2006) · Pflügers Archiv · doi:10.1007/s00424-006-0074-5 · Cited by 85
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
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