Microglia, seen from the CX3CR1 angle

Resting microglial cells are highly dynamic surveillants of brain parenchyma in vivo

Nimmerjahn, A., Kirchhoff, F., & Helmchen, F. (2005) · Science · doi:10.1126/science.1110647 · Cited by 5,827

Fate 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

Synaptic Pruning by Microglia Is Necessary for Normal Brain Development

Paolicelli, R. C., Bolasco, G., Pagani, F., Maggi, L., Scianni, M., Panzanelli, P., Giustetto, M., Ferreira, T. A., Guiducci, E., Dumas, L., et al. (2011) · Science · doi:10.1126/science.1202529 · Cited by 4,244

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

ATP mediates rapid microglial response to local brain injury in vivo

Davalos, D., Grutzendler, J., Yang, G., Kim, J. V., Zuo, Y., Jung, S., Littman, D. R., Dustin, M. L., & Gan, W.-B. (2005) · Nature Neuroscience · doi:10.1038/nn1472 · Cited by 3,913

Microglia: Active sensor and versatile effector cells in the normal and pathologic brain

Hanisch, U.-K., & Kettenmann, H. (2007) · Nature Neuroscience · doi:10.1038/nn1997 · Cited by 3,676

Fate Mapping Reveals Origins and Dynamics of Monocytes and Tissue Macrophages under Homeostasis

Yona, S., Kim, K.-W., Wolf, Y., Mildner, A., Varol, D., Breker, M., Strauss-Ayali, D., Viukov, S., Guilliams, M., Misharin, A., et al. (2013) · Immunity · doi:10.1016/j.immuni.2012.12.001 · Cited by 3,245

Cre reporter strains produced by targeted insertion of EYFP and ECFP into the ROSA26 locus

Srinivas, S., Watanabe, T., Lin, C.-S., William, C. M., Tanabe, Y., Jessell, T. M., & Costantini, F. (2001) · BMC Developmental Biology · doi:10.1186/1471-213x-1-4 · Cited by 3,121

Development of Monocytes, Macrophages, and Dendritic Cells

Geissmann, F., Manz, M. G., Jung, S., Sieweke, M. H., Merad, M., & Ley, K. (2010) · Science · doi:10.1126/science.1178331 · Cited by 3,049

Analysis of Fractalkine Receptor CX3CR1 Function by Targeted Deletion and Green Fluorescent Protein Reporter Gene Insertion

Jung, S., Aliberti, J., Graemmel, P., Sunshine, M. J., Kreutzberg, G. W., Sher, A., & Littman, D. R. (2000) · Molecular and Cellular Biology · doi:10.1128/mcb.20.11.4106-4114.2000 · Cited by 2,632

Fractalkine (CX3CL1) enhances hippocampal N-methyl-d-aspartate receptor (NMDAR) function via d-serine and adenosine receptor type A2 (A2AR) activity

Scianni, M., Antonilli, L., Chece, G., Cristalli, G., Castro, M. A. D., Limatola, C., & Maggi, L. (2013) · Journal of Neuroinflammation · doi:10.1186/1742-2094-10-108 · Cited by 70

New Insights Into Tissue Macrophages: From Their Origin to the Development of Memory

Italiani, P., & Boraschi, D. (2015) · Immune Network · doi:10.4110/in.2015.15.4.167 · Cited by 68

Mu opioid receptor in microglia contributes to morphine analgesic tolerance, hyperalgesia, and withdrawal in mice

Reiss, D. J., Maduna, T., Maurin, H., Audouard, E., & Gavériaux‐Ruff, C. (2020) · Journal of Neuroscience Research · doi:10.1002/jnr.24626 · Cited by 62

FACS analysis of neuronal–glial interactions in the nucleus accumbens following morphine administration

Schwarz, J. M., Smith, S. H., & Bilbo, S. D. (2013) · Psychopharmacology · doi:10.1007/s00213-013-3180-z · Cited by 61

Neuroinflammation in retinitis pigmentosa: Therapies targeting the innate immune system

Zhao, L., Hou, C., & Yan, N. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.1059947 · Cited by 65

The impact of neuroimmune changes on development of amyloid pathology; relevance to A lzheimer's disease

Lynch, M. A. (2013) · Immunology · doi:10.1111/imm.12156 · Cited by 64

ETV3 and ETV6 enable monocyte differentiation into dendritic cells by repressing macrophage fate commitment

Villar, J., Cros, A., de Juan, A., Alaoui, L., Bonté, P., Lau, C. M., Tiniakou, I., Reizis, B., & Segura, É. (2022) · Nature Immunology · doi:10.1038/s41590-022-01374-0 · Cited by 63

Leucine-Rich Repeat Kinase 2 Modulates Neuroinflammation and Neurotoxicity in Models of Human Immunodeficiency Virus 1-Associated Neurocognitive Disorders

Puccini, J. M., Marker, D. F., Fitzgerald, T., Barbieri, J., Kim, C. S., Miller‐Rhodes, P., Lu, S., Dewhurst, S., & Gelbard, H. A. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.0650-14.2015 · Cited by 59

Genetic manipulation of microglia during brain development and disease

Wieghofer, P., & Prinz, M. (2015) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2015.09.019 · Cited by 60

Neuronal apoptosis drives remodeling states of microglia and shifts in survival pathway dependence

Anderson, S. R., Roberts, J. M., Ghena, N., Irvin, E., Schwakopf, J., Cooperstein, I. B., Bosco, A., & Vetter, M. L. (2022) · eLife · doi:10.7554/elife.76564 · Cited by 57

Role of glia in optic nerve

Yazdankhah, M., Shang, P., Ghosh, S., Hose, S., Liu, H., Weiss, J., Fitting, C. S., Bhutto, I. A., Zigler, J. S., Qian, J. X., et al. (2020) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2020.100886 · Cited by 57

Activation of the human chemokine receptor CX3CR1 regulated by cholesterol

Lu, M., Zhao, W., Han, S., Lin, X., Xu, T., Tan, Q., Wang, M., Yi, C., Chu, X., Yang, W., et al. (2022) · Science Advances · doi:10.1126/sciadv.abn8048 · Cited by 56

Redefining our vision: an updated guide to the ocular immune system

Wu, M., Fletcher, E. L., Chinnery, H. R., Downie, L. E., & Mueller, S. N. (2024) · Nature reviews. Immunology · doi:10.1038/s41577-024-01064-y · Cited by 60

Antibiotic-induced gut dysbiosis leads to activation of microglia and impairment of cholinergic gamma oscillations in the hippocampus

Çalışkan, G., French, T., Lacalle, S. E., del Ángel, M., Steffen, J., Heimesaat, M. M., Dunay, I. R., & Stork, O. (2021) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2021.10.007 · Cited by 58

Glucocorticoids as Regulators of Macrophage-Mediated Tissue Homeostasis

Díaz-Jiménez, D., Kolb, J. P., & Cidlowski, J. A. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.669891 · Cited by 60

Chronic antidepressant treatments resulted in altered expression of genes involved in inflammation in the rat hypothalamus

Alboni, S., Benatti, C., Montanari, C., Tascedda, F., & Brunello, N. (2013) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2013.08.046 · Cited by 54

CX3CR1 deficiency accelerates the development of retinopathy in a rodent model of type 1 diabetes

Beli, E., Dominguez, J. M., Hu, P., Thinschmidt, J. S., Caballero, S., Calzi, S. L., Luo, D., Shanmugam, S., Salazar, T. E., Duan, Y., et al. (2016) · Journal of Molecular Medicine · doi:10.1007/s00109-016-1433-0 · Cited by 52

Bidirectional tuning of microglia in the developing brain: from neurogenesis to neural circuit formation

Ueno, M., & Yamashita, T. (2014) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2014.02.004 · Cited by 56

Inhibition of the Activation and Recruitment of Microglia-Like Cells Protects Against Neomycin-Induced Ototoxicity

Sun, S., Yu, H., Yu, H., Mei, H., Ni, W., Zhang, Y., Guo, L., He, Y., Xue, Z., Ni, Y., et al. (2014) · Molecular Neurobiology · doi:10.1007/s12035-014-8712-y · Cited by 53

Spinal microglial activation in a murine surgical model of knee osteoarthritis

Tran, P. B., Miller, R. E., Ishihara, S., Miller, R. E., & Malfait, A. (2016) · Osteoarthritis and Cartilage · doi:10.1016/j.joca.2016.09.007 · Cited by 50

Evidence for a Gender-Specific Protective Role of Innate Immune Receptors in a Model of Perinatal Brain Injury

Pimentel‐Coelho, P. M., Michaud, J.-P., & Rivest, S. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.0535-13.2013 · Cited by 51

CCL17 exerts a neuroimmune modulatory function and is expressed in hippocampal neurons

Fülle, L., Offermann, N., Hansen, J. N., Breithausen, B., Erazo, A. B., Schanz, O., Radau, L., Gondorf, F., Knöpper, K., Alferink, J., et al. (2018) · Glia · doi:10.1002/glia.23507 · Cited by 52

Early Sex Differences in the Immune-Inflammatory Responses to Neonatal Ischemic Stroke

Villapol, S., Faivre, V., Joshi, P., Moretti, R., Besson, V. C., & Charriaut‐Marlangue, C. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20153809 · Cited by 50

Microglia Signatures: A Cause or Consequence of Microglia-Related Brain Disorders?

Mirarchi, A., Albi, E., & Arcuri, C. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms252010951 · Cited by 52

Microglial activation during epileptogenesis in a mouse model of tuberous sclerosis complex

Zhang, B., Zou, J., Han, L., Rensing, N. R., & Wong, M. (2016) · Epilepsia · doi:10.1111/epi.13429 · Cited by 50

The specificity and role of microglia in epileptogenesis in mouse models of tuberous sclerosis complex

Zhang, B., Zou, J., Han, L., Beeler, B., Friedman, J. L., Griffin, E., Piao, Y., Rensing, N. R., & Wong, M. (2018) · Epilepsia · doi:10.1111/epi.14526 · Cited by 50

CX3CL1 (Fractalkine) Protein Expression in Normal and Degenerating Mouse Retina: In Vivo Studies

Zieger, M. V., Ahnelt, P. K., & Uhrín, P. (2014) · PLoS ONE · doi:10.1371/journal.pone.0106562 · Cited by 46

Cysteine cathepsins as therapeutic targets in inflammatory diseases

Vizovišek, M., Vidak, E., Javoršek, U., Mikhaylov, G., Bratovš, A., & Turk, B. (2020) · Expert opinion on therapeutic targets · doi:10.1080/14728222.2020.1746765 · Cited by 39

Microglial-specific depletion of TAK1 is neuroprotective in the acute phase after ischemic stroke

Zeyen, T., Noristani, R., Habib, S., Heinisch, O., Slowik, A., Huber, M., Schulz, J., Reich, A., & Habib, P. (2020) · Journal of molecular medicine · doi:10.1007/s00109-020-01916-9 · Cited by 41

Brain region-specific microglial and astrocytic activation in response to systemic lipopolysaccharides exposure

Brandi, E., Torres-Garcia, L., Svanbergsson, A., Haikal, C., Liu, D., Li, W., & Li, J. (2022) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2022.910988 · Cited by 48

Microglial cGAS–STING signaling underlies glaucoma pathogenesis

Liu, Y., Wang, A., Chen, C., Zhang, Q., Shen, Q., Zhang, D., Xiao, X., Chen, S., Lian, L., Le, Z., et al. (2024) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2409493121 · Cited by 47

The impact of chronic blackberry intake on the neuroinflammatory status of rats fed a standard or high-fat diet

Meireles, M., Marques, C., Norberto, S., Fernandes, I., Mateus, N. F. D. C. B., Rendeiro, C., Spencer, J. P. E., Faria, A., & Calhau, C. (2015) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2015.05.008 · Cited by 45

Lipopolysaccharide-induced maternal immune activation modulates microglial CX3CR1 protein expression and morphological phenotype in the hippocampus and dentate gyrus, resulting in cognitive inflexibility during late adolescence

de Cossío, L. F., Lacabanne, C., Bordeleau, M., Castino, G., Kyriakakis, P., & Tremblay, M. (2021) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2021.07.025 · Cited by 43

Endocannabinoids regulate the activity of astrocytic hemichannels and the microglial response against an injury: In vivo studies

Vázquez, C., Tolón, R. M., Pazos, M. R., Moreno, M., Koester, E. C., Cravatt, B. F., Hillard, C. J., & Romero, J. (2015) · Neurobiology of Disease · doi:10.1016/j.nbd.2015.04.005 · Cited by 42

ADAM17-deficiency on microglia but not on macrophages promotes phagocytosis and functional recovery after spinal cord injury

Sommer, D., Corstjens, I., Sanchez, S., Dooley, D., Lemmens, S., Broeckhoven, J. V., Bogie, J. F. J., Vanmierlo, T., Vidal, P. M., Rose‐John, S., et al. (2019) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2019.02.032 · Cited by 42

Stem cells in neuroinjury and neurodegenerative disorders: challenges and future neurotherapeutic prospects

Mouhieddine, T. H., Wang, K., Kobeissy, F. H., Itani, M. M., & Nokkari, A. (2014) · Neural Regeneration Research · doi:10.4103/1673-5374.133129 · Cited by 42

Microglial contribution to the pathology of neurodevelopmental disorders in humans

Matulevičiūtė, R., Akinluyi, E. T., Muntslag, T. A. O., Dewing, J. M., Long, K. R., Vernon, A. C., Tremblay, M., & Menassa, D. A. (2023) · Acta Neuropathologica · doi:10.1007/s00401-023-02629-2 · Cited by 41

Human amnion epithelial cells rescue cell death via immunomodulation of microglia in a mouse model of perinatal brain injury

Leaw, B., Zhu, D., Tan, J. L., Muljadi, R. C. M., Saad, M. I., Mockler, J. C., Wallace, E. M., Lim, R., & Tolcos, M. (2017) · Stem Cell Research & Therapy · doi:10.1186/s13287-017-0496-3 · Cited by 40

Beneficial impact of intracerebroventricular fractalkine administration on behavioral and biochemical changes induced by prenatal stress in adult rats: Possible role of NLRP3 inflammasome pathway

Ślusarczyk, J., Trojan, E., Wydra, K., Głombik, K., Chamera, K., Kucharczyk, M. W., Budziszewska, B., Kubera, M., Lasoń, W., Filip, M., et al. (2016) · Biochemical Pharmacology · doi:10.1016/j.bcp.2016.05.008 · Cited by 41

Microglial diversity along the hippocampal longitudinal axis impacts synaptic plasticity in adult male mice under homeostatic conditions

De Felice, E., Gonçalves de Andrade, E., Golia, M. T., González Ibáñez, F., Khakpour, M., Di Castro, M. A., Garofalo, S., Di Pietro, E., Benatti, C., Brunello, N., et al. (2022) · Journal of Neuroinflammation · doi:10.1186/s12974-022-02655-z · Cited by 39

Microglia and Brain Disorders: The Role of Vitamin D and Its Receptor

Mirarchi, A., Albi, E., Beccari, T., & Arcuri, C. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241511892 · Cited by 47

Resident immune responses to spinal cord injury: role of astrocytes and microglia

Brockie, S. T., Zhou, C., & Fehlings, M. G. (2023) · Neural Regeneration Research · doi:10.4103/1673-5374.389630 · Cited by 41

Injury Leads to the Appearance of Cells with Characteristics of Both Microglia and Astrocytes in Mouse and Human Brain

Wilhelmsson, U., Andersson, D., de Pablo, Y., Pekny, R., Ståhlberg, A., Mulder, J., Mitsios, N., Hortobágyi, T., Pekny, M., & Pekna, M. (2017) · Cerebral Cortex · doi:10.1093/cercor/bhx069 · Cited by 38

Differential Neuroinflammatory Response in Male and Female Mice: A Role for BDNF

Rossetti, A. C., Paladini, M. S., Trepci, A., Mallien, A. S., Riva, M. A., Gass, P., & Molteni, R. (2019) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2019.00166 · Cited by 41

Ischemic preconditioning induces cortical microglial proliferation and a transcriptomic program of robust cell cycle activation

McDonough, A., Noor, S., Lee, R. V., Dodge, R. E., Strosnider, J. S., Shen, J., Davidson, S., Möller, T., Garden, G. A., & Weinstein, J. R. (2019) · Glia · doi:10.1002/glia.23701 · Cited by 40

Fractalkine Induces Hepcidin Expression of BV-2 Microglia and Causes Iron Accumulation in SH-SY5Y Cells

Pandur, E., Tamási, K., Pap, R., Varga, E., Miseta, A., & Sipos, K. (2019) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-019-00694-4 · Cited by 37

Androgens show sex-dependent differences in myelination in immune and non-immune murine models of CNS demyelination

Zahaf, A., Kassoussi, A., Hutteau-Hamel, T., Mellouk, A., Marie, C., Zoupi, L., Tsouki, F., Mattern, C., Bobé, P., Schumacher, M., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-36846-w · Cited by 37

Sanguisorba officinalis L. derived from herbal medicine prevents intestinal inflammation by inducing autophagy in macrophages

Yasueda, A., Kayama, H., Murohashi, M., Nishimura, J., Wakame, K., Komatsu, K., Ogino, T., Miyoshi, N., Takahashi, H., Uemura, M., et al. (2020) · Scientific Reports · doi:10.1038/s41598-020-65306-4 · Cited by 37

Association of the CX3CR1-V249I Variant with Neurofibrillary Pathology Progression in Late-Onset Alzheimer’s Disease

López-López, A., Gelpí, E., Lopategui, D. M., & Vidal-Taboada, J. M. (2017) · Molecular Neurobiology · doi:10.1007/s12035-017-0489-3 · Cited by 35

Kososan, a Kampo medicine, prevents a social avoidance behavior and attenuates neuroinflammation in socially defeated mice

Ito, N., Hirose, E., Ishida, T., Hori, A., Nagai, T., Kobayashi, Y., Kiyohara, H., Oikawa, T., Hanawa, T., & Odaguchi, H. (2017) · Journal of Neuroinflammation · doi:10.1186/s12974-017-0876-8 · Cited by 36

Regulation of microglia phagocytosis and potential involvement of exercise

Li, C., Wang, Y., Xing, Y., Han, J., Zhang, Y., Zhang, A., Hu, J., Hua, Y., & Bai, Y. (2022) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2022.953534 · Cited by 37

The serotonin 2B receptor is required in neonatal microglia to limit neuroinflammation and sickness behavior in adulthood

Béchade, C., D’Andrea, I., Etienne, F., Verdonk, F., Moutkine, I., Banas, S. M., Kolodziejczak, M., Diaz, S. L., Parkhurst, C. N., Gan, W., et al. (2020) · Glia · doi:10.1002/glia.23918 · Cited by 37

Delivery Platforms for CRISPR/Cas9 Genome Editing of Glial Cells in the Central Nervous System

Meneghini, V., Peviani, M., Luciani, M., Zambonini, G., & Gritti, A. (2021) · Frontiers in Genome Editing · doi:10.3389/fgeed.2021.644319 · Cited by 36

Proneurogenic and neuroprotective effect of a multi strain probiotic mixture in a mouse model of acute inflammation: Involvement of the gut-brain axis

Petrella, C., Strimpakos, G., Torcinaro, A., Middei, S., Ricci, V., Gargari, G., Mora, D., Santa, F. D., & Vecchioli, S. F. (2021) · Pharmacological Research · doi:10.1016/j.phrs.2021.105795 · Cited by 39

Loss of Fractalkine Signaling Exacerbates Axon Transport Dysfunction in a Chronic Model of Glaucoma

Breen, K., Anderson, S., Steele, M. R., Calkins, D. J., Bosco, A., & Vetter, M. L. (2016) · Frontiers in Neuroscience · doi:10.3389/fnins.2016.00526 · Cited by 35

Monitoring in vivo function of cortical microglia

Brawek, B., & Garaschuk, O. (2017) · Cell Calcium · doi:10.1016/j.ceca.2017.02.011 · Cited by 35

Ifit2 deficiency restricts microglial activation and leukocyte migration following murine coronavirus (m-CoV) CNS infection

Sarma, J. D., Burrows, A. C., Rayman, P. A., Hwang, M., Kundu, S., Sharma, N., Bergmann, C. C., & Sen, G. C. (2020) · PLoS Pathogens · doi:10.1371/journal.ppat.1009034 · Cited by 34

Defining Microglial States and Nomenclature: A Roadmap to 2030Preprint

Paolicelli, R. C., Sierra, A., Stevens, B., Tremblay, M., Aguzzi, A., Ajami, B., Amit, I., Audinat, É., Bechmann, I., Bennett, M. L., et al. (2022) · SSRN Electronic Journal · doi:10.2139/ssrn.4065080 · Cited by 33

Deplete and repeat: microglial CSF1R inhibition and traumatic brain injury

Boland, R., & Kokiko‐Cochran, O. N. (2024) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2024.1352790 · Cited by 32

Functional cooperation of the hedgehog and androgen signaling pathways during developmental and repairing myelination

Laouarem, Y., Kassoussi, A., Zahaf, A., Hutteau-Hamel, T., Mellouk, A., Bobé, P., Mattern, C., Schumacher, M., & Traiffort, É. (2021) · Glia · doi:10.1002/glia.23967 · Cited by 31

Serotonin sensing by microglia conditions the proper development of neuronal circuits and of social and adaptive skills

Albertini, G., D’Andrea, I., Druart, M., Béchade, C., Nieves-Rivera, N., Etienne, F., Magueresse, C. L., Rebsam, A., Heck, N., Maroteaux, L., et al. (2023) · Molecular Psychiatry · doi:10.1038/s41380-023-02048-5 · Cited by 37

A novel molecular class that recruits HDAC/MECP2 complexes to PU.1 motifs reduces neuroinflammation

Ralvenius, W. T., Mungenast, A. E., Woolf, H., Huston, M. M., Gillingham, T. Z., Godin, S. K., Penney, J., Cam, H. P., Gao, F., Fernandez, C. G., et al. (2023) · Journal of Experimental Medicine · doi:10.1084/jem.20222105 · Cited by 29

Distinct spatial distribution of microglia and macrophages following mesenchymal stem cell implantation in mouse brain

Blon, D. L., Hoornaert, C., Daans, J., Santermans, E., Hens, N., Goossens, H., Berneman, Z. N., & Ponsaerts, P. (2014) · Immunology and Cell Biology · doi:10.1038/icb.2014.49 · Cited by 31

Voluntary exercise ameliorates synaptic pruning deficits in sleep-deprived adolescent mice

Tuan, L., Tsao, C.-Y., Lee, L. J., & Lee, L.-J. (2020) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2020.12.017 · Cited by 34

Microglia lacking a peroxisomal β-oxidation enzyme chronically alter their inflammatory profile without evoking neuronal and behavioral deficits

Beckers, L., Geric, I., Stroobants, S., Beel, S., Van Damme, P., D’Hooge, R., & Baes, M. (2019) · Journal of Neuroinflammation · doi:10.1186/s12974-019-1442-3 · Cited by 30

Interferon-gamma ameliorates experimental autoimmune encephalomyelitis by inducing homeostatic adaptation of microglia

Tichauer, J. E., Arellano, G., Acuña, E., González, L. F., Kannaiyan, N. R., Murgas, P., Panadero-Medianero, C., Ibañez-Vega, J., Burgos, P. I., Loda, E., et al. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1191838 · Cited by 33

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

Microglial Cx3cr1knockout reduces prion disease incubation time in mice

Grizenkova, J., Akhtar, S., Brandner, S., Collinge, J., & Lloyd, S. E. (2014) · BMC Neuroscience · doi:10.1186/1471-2202-15-44 · Cited by 29

Microglial cells: Sensors for neuronal activity and microbiota-derived molecules

D’Alessandro, G., Marrocco, F., & Limatola, C. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.1011129 · Cited by 31

A Distinct Microglial Cell Population Expressing Both CD86 and CD206 Constitutes a Dominant Type and Executes Phagocytosis in Two Mouse Models of Retinal Degeneration

Zhang, Y., Park, Y. S., & Kim, I. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241814236 · Cited by 31

Interaction of microglia with the microenvironment in spinal cord injury

Timofeeva, A. V., Akhmetzyanova, E. R., Rizvanov, A. A., & Mukhamedshina, Y. O. (2024) · Neuroscience · doi:10.1016/j.neuroscience.2024.11.074 · Cited by 29

The Neuro-Immune-Regulators (NIREGs) Promote Tissue Resilience; a Vital Component of the Host’s Defense Strategy against Neuroinflammation

Bedoui, Y., Neal, J. W., & Gasque, P. (2018) · Journal of Neuroimmune Pharmacology · doi:10.1007/s11481-018-9793-6 · Cited by 28

Modulators of microglia: a patent review

Papa, S., Caron, I., Rossi, F., & Veglianese, P. (2016) · Expert Opinion on Therapeutic Patents · doi:10.1517/13543776.2016.1135901 · Cited by 26

The Shh receptor Boc is important for myelin formation and repair

Zakaria, M., Ferent, J., Hristovska, I., Laouarem, Y., Zahaf, A., Kassoussi, A., Mayeur, M.-E., Pascual, O., Charron, F., & Traiffort, É. (2019) · Development · doi:10.1242/dev.172502 · Cited by 28

Social defeat-induced increase in the conditioned rewarding effects of cocaine: Role of CX3CL1

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Reviewed by:

Wolf, Y., Yona, S., Kim, K.-W., Jung, S., Legendre, P., Pierre, U., Université, M.-E. T., Department Of, Kim, K.-W., & Department Of (2013)

Role of CX3CL1 in Synaptic Activity and Neuroprotection

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Chemokine CX3C motif receptor 1 ( CX3CR1 ) promoter–dependent gene expression in microglia

(2013) · Science-Business eXchange · doi:10.1038/scibx.2013.1170

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Role for Neuronally Derived Fractalkine in Mediating Interactions between Neurons and CX3CR1-Expressing Microglia

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