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The P2Y12 receptor regulates microglial activation by extracellular nucleotides
Abstract
Microglia are primary immune sentinels of the CNS. Following injury, these cells migrate or extend processes toward sites of tissue damage. CNS injury is accompanied by release of nucleotides, serving as signals for microglial activation or chemotaxis. Microglia express several purinoceptors, including a G(i)-coupled subtype that has been implicated in ATP- and ADP-mediated migration in vitro. Here we show that microglia from mice lacking G(i)-coupled P2Y(12) receptors exhibit normal baseline motility but are unable to polarize, migrate or extend processes toward nucleotides in vitro or in vivo. Microglia in P2ry(12)(-/-) mice show significantly diminished directional branch extension toward sites of cortical damage in the living mouse. Moreover, P2Y(12) expression is robust in the 'resting' state, but dramatically reduced after microglial activation. These results imply that P2Y(12) is a primary site at which nucleotides act to induce microglial chemotaxis at early stages of the response to local CNS injury.
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“Thus, preservation of the CNS environment can delay loss of microglial signature gene expression ex vivo although microglial identity does eventually decay in cultured brain slices (Haynes et al., 2006).”
From Diverse Requirements for Microglial Survival, Specification, and Function Revealed by Defined-Medium Cultures (2017) · cites this paper as Haynes et al., 2006
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“Moreover, P2RY12 expression is decreased and lost in macrophages that exhibit an inflammatory phenotype [19, 31].”
From Loss of homeostatic microglial phenotype in CSF1R-related Leukoencephalopathy (2020) · cites this paper as [19]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Microglia express a broad spectrum of neurotransmitter receptors and ion channels that critically regulate microglial functions such as surveillance (Madry et al., 2018), cytokine release (Nguyen et al., 2017), chemotaxis, and phagocytosis (Haynes et al., 2006; Koizumi et al., 2007; Ohsawa et al., 2007).”
From Overexpressing low‐density lipoprotein receptor reduces tau‐associated neurodegeneration in relation to apoE‐linked mechanisms (2021) · cites this paper as Haynes et al., 2006
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“Mature pMGLs stained positive for markers of murine and human microglia 10,11,29,30, with both TMEM119 and P2RY12 displaying a broad membrane and punctate vesicular expression pattern”
From Efficient derivation of microglia-like cells from human pluripotent stem cells (2016) · cites this paper as [30]
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“P2Y12 is highly sensitive to adenosine diphosphate, abundantly and selectively expressed in homeostatic microglia, rapidly downregulated following the initiation of inflammation and elicits rapid and pronounced chemotactic responses of microglial processes2122.”
From Microglial P2Y12 is necessary for synaptic plasticity in mouse visual cortex (2016) · cites this paper as [21]
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“P2RY12 expression is lost upon microglia activation74, culture34”
From Genetic analysis of the human microglial transcriptome across brain regions, aging and disease pathologies (2022) · cites this paper as [74]
In the citing paper
“They use the products of nearly 100 genes to sense changes in their microenvironment (their sensome) including P2yr12, AXL, and MER4,7,19”
From Microglia in neurodegeneration (2018) · cites this paper as [4]
In the citing paper
“we focused on the P2Y12 purinergic receptor, which is selectively expressed in non-activated microglia and mediates process motility during early injury responses.”
From Microglial P2Y12 is necessary for synaptic plasticity in mouse visual cortex (2016) · cites this paper as [21]
In the citing paper
“we focused on the P2Y12 purinergic receptor, which is selectively expressed in non-activated microglia and mediates process motility during early injury responses.”
From Microglial P2Y12 is necessary for synaptic plasticity in mouse visual cortex (2016) · cites this paper as [21]
In the citing paper
“In addition, its expression correlates strongly with a ramified microglial morphology characteristic of healthy neurophysiology, indicating that it primarily functions during rapid responses to perturbations of brain homeostasis2123.”
From Microglial P2Y12 is necessary for synaptic plasticity in mouse visual cortex (2016) · cites this paper as [21]
In the citing paper
“P2Y12 is highly sensitive to adenosine diphosphate, abundantly and selectively expressed in homeostatic microglia, rapidly downregulated following the initiation of inflammation and elicits rapid and pronounced chemotactic responses of microglial processes2122.”
From Microglial P2Y12 is necessary for synaptic plasticity in mouse visual cortex (2016) · cites this paper as [21]
In the citing paper
“The microglial expression of most of these receptors has been demonstrated in vitro, but activation of the Gi/o-coupled purinergic receptor, P2Y12, has been shown to powerfully alter microglial dynamics in vivo21.”
From Microglial P2Y12 is necessary for synaptic plasticity in mouse visual cortex (2016) · cites this paper as [21]
In the citing paper
“P2Y12 is highly sensitive to adenosine diphosphate, abundantly and selectively expressed in homeostatic microglia, rapidly downregulated following the initiation of inflammation and elicits rapid and pronounced chemotactic responses of microglial processes2122.”
From Microglial P2Y12 is necessary for synaptic plasticity in mouse visual cortex (2016) · cites this paper as [21]
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Citations
Cites
The capsaicin receptor: a heat-activated ion channel in the pain pathway
Caterina, M. J., Schumacher, M. A., Tominaga, M., Rosen, T. A., Levine, J. D., & Julius, D. J. (1997) · Nature · doi:10.1038/39807 · Cited by 9,132
Self-citationResting 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
Microglia: a sensor for pathological events in the CNS
Kreutzberg, G. W. (1996) · Trends in Neurosciences · doi:10.1016/0166-2236(96)10049-7 · Cited by 4,396
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
Self-citationJung, 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
BDNF from microglia causes the shift in neuronal anion gradient underlying neuropathic pain
Coull, J. A. M., Beggs, S., Boudreau, D., Boivin, D., Tsuda, M., Inoue, K., Gravel, C., Salter, M. W., & De Koninck, Y. (2005) · Nature · doi:10.1038/nature04223 · Cited by 1,965
P2X4 receptors induced in spinal microglia gate tactile allodynia after nerve injury
Tsuda, M., Shigemoto‐Mogami, Y., Koizumi, S., Mizokoshi, A., Kohsaka, S., Salter, M. W., & Inoue, K. (2003) · Nature · doi:10.1038/nature01786 · Cited by 1,567
Identification of the platelet ADP receptor targeted by antithrombotic drugs
Hollopeter, G., Jantzen, H., Vincent, D., Li, G., England, L. J., Ramakrishnan, V., Yang, R., Nurden, P., Nurden, A. T., Julius, D. J., et al. (2001) · Nature · doi:10.1038/35051599 · Cited by 1,421
Self-citationCharacterization of ameboid microglia isolated from developing mammalian brain
Giulian, D., & Baker, T. J. (1986) · Journal of Neuroscience · doi:10.1523/jneurosci.06-08-02163.1986 · Cited by 1,300
Activated microglia mediate neuronal cell injury via a nitric oxide mechanism
Chao, C. C., Hu, S., Molitor, T. W., Shaskan, E. G., & Peterson, P. K. (1992) · The Journal of Immunology · doi:10.4049/jimmunol.149.8.2736 · Cited by 1,138
Research works printed but not linked: 1
- Burnstock, G. in P2 Purinoceptors: Localization, Funciton, and Transduction Mechanisms (eds. Chadwick, D. & Goode, J.) 1–34 (Wiley, New York, 1996).
Cited by
Sorted by citations
Items 501–600 of 1,005
Hattori, Y., Kato, D., Murayama, F., Koike, S., Asai, H., Yamasaki, A., Naito, Y., Kawaguchi, A., Konishi, H., Prinz, M., et al. (2022) · Cell Reports · doi:10.1016/j.celrep.2023.112092 · Cited by 66
Role of glia and extracellular matrix in controlling neuroplasticity in the central nervous system
Dzyubenko, E., & Hermann, D. M. (2023) · Seminars in Immunopathology · doi:10.1007/s00281-023-00989-1 · Cited by 73
P2X4 purinoceptor signaling in chronic pain
Trang, T., & Salter, M. W. (2012) · Purinergic Signalling · doi:10.1007/s11302-012-9306-7 · Cited by 66
Clearance by Microglia Depends on Packaging of Phagosomes into a Unique Cellular Compartment
Villani, A., Benjaminsen, J., Moritz, C., Henke, K., Hartmann, J., Norlin, N., Richter, K., Schieber, N. L., Franke, T., Schwab, Y., et al. (2019) · Developmental Cell · doi:10.1016/j.devcel.2019.02.014 · Cited by 60
Single Cell RNA-Seq Analysis Reveals Compartment-Specific Heterogeneity and Plasticity of Microglia
Zheng, J., Ru, W., Adolacion, J. R. T., Spurgat, M. S., Liu, X., Yuan, S., Liang, R. X., Dong, J., Potter, A. S., Potter, S. S., et al. (2020) · iScience · doi:10.1016/j.isci.2021.102186 · Cited by 64
Bi, Q., Wang, C., Cheng, G., Chen, N., Wei, B., Liu, X., Li, L., Lu, C. C., He, J., Weng, Y., et al. (2022) · Immunity · doi:10.1016/j.immuni.2022.06.018 · Cited by 66
The role of the immunoproteasome in interferon-γ-mediated microglial activation
Moritz, K. E., McCormack, N. M., Abera, M. B., Viollet, C., Yauger, Y. J., Sukumar, G., Dalgard, C. L., & Burnett, B. G. (2017) · Scientific Reports · doi:10.1038/s41598-017-09715-y · Cited by 68
Microglia gone awry: linking immunometabolism to neurodegeneration
Afridi, R., Lee, W.-H., & Suk, K. (2020) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2020.00246 · Cited by 64
How microglia contribute to the induction and maintenance of neuropathic pain
Malcangio, M., & Sideris-Lampretsas, G. (2025) · Nature reviews. Neuroscience · doi:10.1038/s41583-025-00914-5 · Cited by 69
Dibaj, P., Steffens, H., Zschüntzsch, J., Nadrigny, F., Schomburg, E. D., Kirchhoff, F., & Neusch, C. (2011) · PLoS ONE · doi:10.1371/journal.pone.0017910 · Cited by 67
Proteomic profiling of epileptogenesis in a rat model: Focus on inflammation
Walker, A., Russmann, V., Deeg, C. A., von Toerne, C., Kleinwort, K. J. H., Szober, C. M., Rettenbeck, M. L., von Rüden, E., Goc, J., Ongerth, T., et al. (2015) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2015.12.007 · Cited by 66
TMEM16F Regulates Spinal Microglial Function in Neuropathic Pain States
Batti, L., Sundukova, M., Murana, E., Pimpinella, S., Reis, F. D. C., Pagani, F., Wang, H., Pellegrino, E., Perlas, E., Angelantonio, S. D., et al. (2016) · Cell Reports · doi:10.1016/j.celrep.2016.05.039 · Cited by 67
Microglial motility in Alzheimer’s disease and after Aβ42 immunotherapy: a human post-mortem study
Franco-Bocanegra, D. K., George, B., Lau, L. C., Holmes, C., Nicoll, J. A. R., & Boche, D. (2019) · Acta Neuropathologica Communications · doi:10.1186/s40478-019-0828-x · Cited by 64
Jairaman, A., McQuade, A., Granzotto, A., Kang, Y. J., Chadarevian, J. P., Gandhi, S., Parker, I., Smith, I., Cho, H., Sensi, S. L., et al. (2022) · eLife · doi:10.7554/elife.73021 · Cited by 62
Tay, T. L., Carrier, M., & Tremblay, M. (2019) · Advances in experimental medicine and biology · doi:10.1007/978-981-13-9913-8_6 · Cited by 61
Role of ATP in Extracellular Vesicle Biogenesis and Dynamics
Lombardi, M., Gabrielli, M., Adinolfi, E., & Verderio, C. (2021) · Frontiers in Pharmacology · doi:10.3389/fphar.2021.654023 · Cited by 63
Microglial Function and Regulation during Development, Homeostasis and Alzheimer’s Disease
Casali, B. T., & Reed-Geaghan, E. G. (2021) · Cells · doi:10.3390/cells10040957 · Cited by 70
Ferreira, R., & Schlichter, L. C. (2013) · PLoS ONE · doi:10.1371/journal.pone.0062345 · Cited by 66
Miller, A. M., & Stella, N. (2008) · Glia · doi:10.1002/glia.20813 · Cited by 62
Wilkaniec, A., Gąssowska, M., Czapski, G. A., Cieślik, M., Sulkowski, G., & Adamczyk, A. (2017) · Purinergic Signalling · doi:10.1007/s11302-017-9567-2 · Cited by 61
Fernández‐Albarral, J. A., Salazar, J. J., de Hoz, R., Marco, E. M., Martín‐Sánchez, B., Flores-Salguero, E., Salobrar‐García, E., López‐Cuenca, I., Barrios, V., Avilés‐Trigueros, M., et al. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22042066 · Cited by 61
Single-Cell RNA-Sequencing: Astrocyte and Microglial Heterogeneity in Health and Disease
Spurgat, M. S., & Tang, S. (2022) · Cells · doi:10.3390/cells11132021 · Cited by 67
Mechanisms of microglia-mediated synapse turnover and synaptogenesis
Ball, J. B., Green‐Fulgham, S. M., & Watkins, L. R. (2022) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2022.102336 · Cited by 64
Tadmouri, A., Champagnat, J., & Morin-Surun, M. P. (2014) · Journal of Neuroscience Research · doi:10.1002/jnr.23336 · Cited by 60
Animal models for studying microglia: The first, the popular, and the new
Sieger, D., & Peri, F. (2012) · Glia · doi:10.1002/glia.22385 · Cited by 60
Rayah, A., Kanellopoulos, J., & Virgilio, F. D. (2012) · Microbes and Infection · doi:10.1016/j.micinf.2012.07.006 · Cited by 63
Hamilton, L., Astell, K. R., Velikova, G., & Sieger, D. (2016) · Zebrafish · doi:10.1089/zeb.2016.1339 · Cited by 60
P2Y12 Receptors in Tumorigenesis and Metastasis
Ballerini, P., Dovizio, M., Bruno, A., Tacconelli, S., & Patrignani, P. (2018) · Frontiers in Pharmacology · doi:10.3389/fphar.2018.00066 · Cited by 61
Healthy Brain Aging Modifies Microglial Calcium Signaling In Vivo
Olmedillas, M., Asavapanumas, N., Uzcategui, N. L., & Garaschuk, O. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20030589 · Cited by 60
Sabogal-Guáqueta, A. M., Marmolejo-Garza, A., de Pádua, V. P., Eggen, B. J. L., Boddeke, E., & Dolga, A. M. (2020) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2020.101805 · Cited by 65
Shukla, A., McIntyre, L. L., Marsh, S. E., Schneider, C. A., Hoover, E. M., Walsh, C. M., Lodoen, M. B., Blurton-Jones, M. M., & Inlay, M. A. (2018) · Glia · doi:10.1002/glia.23575 · Cited by 59
Gut-innervating TRPV1+ Neurons Drive Chronic Visceral Pain via Microglial P2Y12 Receptor
Defaye, M., Abdullah, N. S., Iftinca, M., Hassan, A., Agosti, F., Zhang, Z., Cuménal, M., Zamponi, G. W., & Altier, C. (2021) · Cellular and Molecular Gastroenterology and Hepatology · doi:10.1016/j.jcmgh.2021.12.012 · Cited by 60
Differential regulation of microglial motility by ATP/ADP and adenosine
Gyoneva, S., Orr, A. G., & Traynelis, S. F. (2009) · Parkinsonism & Related Disorders · doi:10.1016/s1353-8020(09)70813-2 · Cited by 64
The neuroendocrine control of the innate immune system in health and brain diseases
Bellavance, M., & Rivest, S. (2012) · Immunological Reviews · doi:10.1111/j.1600-065x.2012.01129.x · Cited by 61
Madry, C., Arancibia‐Cárcamo, I. L., Kyrargyri, V., Chan, V. T. T., Hamilton, N. B., & Attwell, D. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1715354115 · Cited by 63
The Role of Glial Cells in Synaptic Dysfunction: Insights into Alzheimer's Disease Mechanisms
Yu, Y., Chen, R., Mao, K., Deng, M., & Li, Z. (2023) · Aging and Disease · doi:10.14336/ad.2023.0718 · Cited by 62
Hu, Y., & Tao, W. (2024) · Journal of Advanced Research · doi:10.1016/j.jare.2024.01.006 · Cited by 64
Braganhol, E., Kukulski, F., Lévesque, S. A., Fausther, M., Lavoie, É. G., Zanotto‐Filho, A., Bergamin, L. S., Pelletier, J., Bahrami, F., Yebdri, F. B., et al. (2014) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2014.10.014 · Cited by 59
Fang, K., Yang, C., Sun, S. H., & Tzeng, S. (2009) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2009.06409.x · Cited by 59
Environmental stimuli shape microglial plasticity in glioma
Garofalo, S., Porzia, A., Mainiero, F., Di Angelantonio, S., Cortese, B., Basilico, B., Pagani, F., Cignitti, G., Chece, G., Maggio, R., et al. (2017) · eLife · doi:10.7554/elife.33415 · Cited by 58
Harnessing Microglia and Macrophages for the Treatment of Glioblastoma
Prionisti, I., Bühler, L. H., Walker, P. R., & Jolivet, R. (2019) · Frontiers in Pharmacology · doi:10.3389/fphar.2019.00506 · Cited by 63
Exploring the Role of Apigenin in Neuroinflammation: Insights and Implications
Charrière, K., Schneider, V., Perrignon-Sommet, M., Lizard, G., Bénani, A., Jacquin, A., & Véjux, A. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25095041 · Cited by 65
Apolipoprotein E isoform‐dependent microglia migration
Cudaback, E., Li, X., Montine, K. S., Montine, T. J., & Keene, C. D. (2011) · The FASEB Journal · doi:10.1096/fj.10-176891 · Cited by 58
The GluN2A Subunit Regulates Neuronal NMDA receptor-Induced Microglia-Neuron Physical Interactions
Eyo, U. B., Bispo, A., Liu, J., Sabu, S., Wu, R., DiBona, V. L., Zheng, J., Murugan, M., Zhang, H., Tang, Y., et al. (2018) · Scientific Reports · doi:10.1038/s41598-018-19205-4 · Cited by 57
Role of Chondroitin Sulfation Following Spinal Cord Injury
Hussein, R. K., Mencio, C. P., Katagiri, Y., Brake, A., & Geller, H. M. (2020) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2020.00208 · Cited by 60
P2 receptor-mediated modulation of neurotransmitter release—an update
Sperlágh, B., Heinrich, A., & Csölle, C. (2007) · Purinergic Signalling · doi:10.1007/s11302-007-9080-0 · Cited by 56
Jeong, H.-J., Na, Y.-J., Lee, K., Kim, Y. H., Lee, Y., Kang, M., Jiang, B., Yeom, Y. I., Wu, L., Gao, Y., et al. (2016) · Pain · doi:10.1097/j.pain.0000000000000470 · Cited by 55
A story of birth and death: Insights into the formation and dynamics of the microglial population
Askew, K. E., & Gómez‐Nicola, D. (2017) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2017.03.009 · Cited by 59
Role of Glia in the Regulation of Sleep in Health and Disease
Garofalo, S., Picard, K., Limatola, C., Nadjar, A., Pascual, O., & Tremblay, M. (2020) · Comprehensive physiology · doi:10.1002/cphy.c190022 · Cited by 64
The G protein-coupled receptor GPR34 – The past 20 years of a grownup
Schöneberg, T., Meister, J., Knierim, A. B., & Schulz, A. (2018) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2018.04.008 · Cited by 54
How Stress Shapes Neuroimmune Function: Implications for the Neurobiology of Psychiatric Disorders
Koo, J. W., & Wohleb, E. S. (2020) · Biological Psychiatry · doi:10.1016/j.biopsych.2020.11.007 · Cited by 60
Reich, M., Paris, I., Ebeling, M., Dahm, N., Schweitzer, C., Reinhardt, D., Schmucki, R., Prasad, M., Köchl, F., Leist, M., et al. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2020.617860 · Cited by 49
Purinergic signaling in epilepsy
Rassendren, F., & Audinat, É. (2016) · Journal of Neuroscience Research · doi:10.1002/jnr.23770 · Cited by 54
Toll-Like Receptor 4 Is a Regulator of Monocyte and Electroencephalographic Responses to Sleep Loss
Wisor, J. P., Clegern, W. C., & Schmidt, M. A. (2011) · Sleep · doi:10.5665/sleep.1274 · Cited by 54
In Vivo Targeting of the Neurovascular Unit: Challenges and Advancements
Naranjo, O., Osborne, O., Torices, S., & Toborek, M. J. (2021) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-021-01113-3 · Cited by 57
Martins, T. A., Kaymak, D., Tatari, N., Gerster, F., Hogan, S., Ritz, M.-F., Sabatino, V., Wieboldt, R., Bartoszek, E. M., McDaid, M., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-54129-w · Cited by 54
Impaired microglia process dynamics post‐stroke are specific to sites of secondary neurodegeneration
Kluge, M. G., Kracht, L., Abdolhoseini, M., Ong, L. K., Johnson, S. J., Nilsson, M., & Walker, F. R. (2017) · Glia · doi:10.1002/glia.23201 · Cited by 52
Bedolla, A. M., McKinsey, G. L., Ware, K., Santander, N., Arnold, T. D., & Luo, Y. (2024) · Cell Reports · doi:10.1016/j.celrep.2023.113660 · Cited by 53
“P2RY12 signaling is responsible for inflammation-induced microglia process extension 36 and microglia containment of leakage following cerebrovascular injury.”
Bollinger, J. L., Dadosky, D. T., Flurer, J. K., Rainer, I. L., Woodburn, S. C., & Wohleb, E. S. (2022) · Neuropsychopharmacology · doi:10.1038/s41386-022-01519-7 · Cited by 55
Importance of GPCR-Mediated Microglial Activation in Alzheimer’s Disease
Haque, M. E., Kim, I., Jakaria, M., Akther, M., & Choi, D. (2018) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2018.00258 · Cited by 55
Tozaki‐Saitoh, H., Masuda, J., Kawada, R., Kojima, C., Yoneda, S., Masuda, T., Inoue, K., & Tsuda, M. (2019) · Glia · doi:10.1002/glia.23570 · Cited by 52
Khan, K. M., Rosa, G. B.-D. L., Biggerstaff, N., Selvakumar, G. P., Wang, R., Mason, S., Dailey, M. E., & Marcinkiewcz, C. A. (2022) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2022.07.160 · Cited by 54
Self-citationAltered motility of plaque-associated microglia in a model of Alzheimer’s disease
Gyoneva, S., Swanger, S. A., Zhang, J., Weinshenker, D., & Traynelis, S. F. (2016) · Neuroscience · doi:10.1016/j.neuroscience.2016.05.061 · Cited by 51
Microglia: Lifelong modulator of neural circuits
Ikegami, A., Haruwaka, K., & Wake, H. (2019) · Neuropathology · doi:10.1111/neup.12560 · Cited by 49
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Parusel, S., Yi, M., Hunt, C., & Wu, L. (2022) · Neuroscience Bulletin · doi:10.1007/s12264-022-00937-3 · Cited by 53
Brain region- and sex-specific transcriptional profiles of microglia
Barko, K., Shelton, M. A., Xue, X., Afriyie-Agyemang, Y., Puig, S., Freyberg, Z., Tseng, G. C., Logan, R. W., & Seney, M. L. (2022) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2022.945548 · Cited by 56
Purinergic system, microglia and neuropathic pain
Tsuda, M., Tozaki‐Saitoh, H., & Inoue, K. (2011) · Current Opinion in Pharmacology · doi:10.1016/j.coph.2011.10.014 · Cited by 51
Ueno, M., & Yamashita, T. (2014) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2014.02.004 · Cited by 56
Isfort, K., Ebert, F., Bornhorst, J., Sargin, S., Kardakaris, R., Pasparakis, M., Bähler, M., Schwerdtle, T., Schwab, A., & Hanley, P. J. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.289793 · Cited by 51
Overview of pleiotropic effects of platelet P2Y12 receptor inhibitors
Koziński, M., Ostrowska, M., Fabiszak, T., Navarese, E. P., Paciorek, P., Grześk, G., Kubica, J., & Adamski, P. (2014) · Thrombosis and Haemostasis · doi:10.1160/th13-11-0915 · Cited by 51
Hayashi, Y. (2013) · Journal of Neurological Disorders · doi:10.4172/2329-6895.1000120 · Cited by 49
Blume, Z. I., Lambert, J. M., Lovel, A. G., & Mitchell, D. M. (2020) · Developmental Dynamics · doi:10.1002/dvdy.163 · Cited by 52
Purinergic Receptors in Neurological Diseases With Motor Symptoms: Targets for Therapy
Oliveira-Giacomelli, Á., Naaldijk, Y., Sardá-Arroyo, L., Gonçalves, M. C. B., Corrêa-Velloso, J., Pillat, M. M., de Souza, H. D. N., & Ulrich, H. (2018) · Frontiers in Pharmacology · doi:10.3389/fphar.2018.00325 · Cited by 50
Berdowski, W. M., van der Linde, H. C., Breur, M., Oosterhof, N., Beerepoot, S., Sanderson, L. E., Wijnands, L. I., de Jong, P., Tsai-Meu-Chong, E., de Valk, W. G., et al. (2022) · Acta Neuropathologica · doi:10.1007/s00401-022-02440-5 · Cited by 52
MicroRNAs in platelet biogenesis and function
Dangwal, S., & Thum, T. (2012) · Thrombosis and Haemostasis · doi:10.1160/th12-03-0211 · Cited by 51
Neuroprotective roles of the P2Y2 receptor
Weisman, G. A., Ajit, D., Garrad, R. C., Peterson, T. S., Woods, L. T., Thebeau, C. N., Camden, J. M., & Erb, L. (2012) · Purinergic Signalling · doi:10.1007/s11302-012-9307-6 · Cited by 55
P2Y Receptors in Immune Response and Inflammation
Duc, D. L., Schulz, A., Lede, V., Schulze, A., Thor, D., Brüser, A., & Schöneberg, T. (2017) · Advances in immunology · doi:10.1016/bs.ai.2017.05.006 · Cited by 51
Neuroimmune interaction in seizures and epilepsy: focusing on monocyte infiltration
Bosco, D. B., Tian, D., & Wu, L. (2020) · FEBS Journal · doi:10.1111/febs.15428 · Cited by 49
Sleep decreases neuronal activity control of microglial dynamics in mice
Hristovska, I., Robert, M., Combet, K., Honnorat, J., Comte, J.-C., & Pascual, O. (2022) · Nature Communications · doi:10.1038/s41467-022-34035-9 · Cited by 52
Extracellular ATP/adenosine dynamics in the brain and its role in health and disease
Shigetomi, E., Sakai, K., & Koizumi, S. (2024) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2023.1343653 · Cited by 57
Levard, D., Seillier, C., Bellemain-Sagnard, M., Fournier, A. P., Lemarchand, E., Dembech, C., Riou, G., McDade, K., Smith, C., McQuaid, C., et al. (2024) · Nature Neuroscience · doi:10.1038/s41593-024-01695-3 · Cited by 57
Blossom, V., Ullal, S. D., D’Souza, M. M., Ranade, A. V., Kumar, N. A., & Rai, R. (2025) · 3 Biotech · doi:10.1007/s13205-025-04468-2 · Cited by 57
Disease-associated microglia in neurodegenerative diseases: Friend or foe?
Cheng, Y.-H., & Ho, M. S.-C. (2025) · PLoS Biology · doi:10.1371/journal.pbio.3003426 · Cited by 57
IRF8 is a transcriptional determinant for microglial motility
Masuda, T., Nishimoto, N., Tomiyama, D., Matsuda, T., Tozaki‐Saitoh, H., Tamura, T., Kohsaka, S., Tsuda, M., & Inoue, K. (2014) · Purinergic Signalling · doi:10.1007/s11302-014-9413-8 · Cited by 51
Bollinger, J. L., & Wohleb, E. S. (2019) · Neuroscience Letters · doi:10.1016/j.neulet.2019.134369 · Cited by 51
P2Y Receptors in the Mammalian Nervous System: Pharmacology, Ligands and Therapeutic Potential
Weisman, G. A., Woods, L. T., Erb, L., & Seye, C. I. (2012) · CNS & Neurological Disorders - Drug Targets · doi:10.2174/187152712803581047 · Cited by 52
Penney, J., Ralvenius, W. T., Loon, A., Cerit, O., Dileep, V., Milo, B., Pao, P., Woolf, H., & Tsai, L. (2024) · Glia · doi:10.1002/glia.24485 · Cited by 52
The aging mouse CNS is protected by an autophagy-dependent microglia population promoted by IL-34
Berglund, R., Cheng, Y., Piket, E., Adzemovic, M. Z., Zeitelhofer, M., Olsson, T. P., Guerreiro‐Cacais, A. O., & Jagodic, M. (2024) · Nature Communications · doi:10.1038/s41467-023-44556-6 · Cited by 49
Central Nervous System Macrophages in Health and Disease
Hove, H. V., Feo, D. D., Greter, M., & Becher, B. (2025) · Annual Review of Immunology · doi:10.1146/annurev-immunol-082423-041334 · Cited by 53
Fekete, R., Simats, A., Bíró, E., Pósfai, B., Cserép, C., Schwarcz, A. D., Szabadits, E., Környei, Z., Tóth, K., Fichó, E., et al. (2025) · Nature Neuroscience · doi:10.1038/s41593-025-01871-z · Cited by 59
Fang, K., Wang, Y., Huang, M., Sun, S. H., Cheng, H., & Tzeng, S. (2010) · Journal of Neuroscience Research · doi:10.1002/jnr.22538 · Cited by 48
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Stefani, J., Tschesnokowa, O., Parrilla, M., Robaye, B., Boeynaems, J. M., Acker‐Palmer, A., Zimmermann, H., & Gampe, K. (2018) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2018.00134 · Cited by 50
Chaves-Filho, A. J. M., Macêdo, D. S., de Lucena, D. F., & Maes, M. H. J. (2019) · Behavioural Brain Research · doi:10.1016/j.bbr.2019.111975 · Cited by 47
Fujita, Y., Nakanishi, T., Ueno, M., Itohara, S., & Yamashita, T. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.107580 · Cited by 48
The Safeguarding Microglia: Central Role for P2Y12 Receptors
Lin, S.-S., Tang, Y., Illés, P., & Verkhratsky, A. (2021) · Frontiers in Pharmacology · doi:10.3389/fphar.2020.627760 · Cited by 51
Glial Purinergic Signaling in Neurodegeneration
Pietrowski, M. J., Gabr, A. A., Kozlov, S. O., Blum, D. L., Halle, A., & Carvalho, K. (2021) · Frontiers in Neurology · doi:10.3389/fneur.2021.654850 · Cited by 49
Involvement of P2X and P2Y receptors in microglial activation in vivo
Franke, H., Schepper, C., Illés, P., & Krügel, U. (2007) · Purinergic Signalling · doi:10.1007/s11302-007-9082-y · Cited by 49
George, J., Gonçalves, F. Q., Cristóvão, G., Rodrigues, L., Meyer‐Fernandes, J. R., Gonçalves, T., Cunha, R. A., & Gomes, C. A. (2015) · Glia · doi:10.1002/glia.22833 · Cited by 47
Sweepers in the CNS: Microglial Migration and Phagocytosis in the Alzheimer Disease Pathogenesis
Noda, M., & Suzumura, A. (2012) · International Journal of Alzheimer s Disease · doi:10.1155/2012/891087 · Cited by 52
Tian, L., Hui, C. W., Bisht, K., Tan, Y., Sharma, K. P., Chen, S., Zhang, X., & Tremblay, M. (2017) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2017.01.007 · Cited by 52
Metadata
- Authors
- Haynes, S. E., Hollopeter, G., Yang, G., Kurpius, D., Dailey, M. E., Gan, W.-B., & Julius, D.
- Affiliations
- University of California, San Francisco (US)
- New York University (US)
- University of Iowa (US)
- Corresponding author
- Julius, David
- Venue
- Nature Neuroscience
- Published
- 2006-11-19
- Volume
- 9
- Issue
- 12
- Pages
- 1512-1519
- ISSN
- 1097-6256 (ISSN-L)
- 1546-1726
- OpenAlex
- W2131686384
- Cited by
- 1,542
- References
- 34
- Citations by year
- 2026: 91 · 2025: 80 · 2024: 126 · 2023: 94 · 2022: 122 · 2021: 138 · 2020: 104 · 2019: 93 · 2018: 80 · 2017: 71 · 2016: 63 · 2015: 68 · 2014: 64 · 2013: 67 · 2012: 69
- FWCI
- 19.53
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature Neuroscience (publishedVersion)
- PubMed (publishedVersion)
- eScholarship (California Digital Library) (submittedVersion)
- Funders
- University of California, San Francisco
- National Institute of Neurological Disorders and Stroke (R01NS043468, NS434468)
- National Center for Research Resources (S10RR017941)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Physiology › Adenosine and Purinergic Signaling
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Health Sciences › Medicine › Clinical Neurology › Traumatic Brain Injury and Neurovascular Disturbances
- Keywords
- P2Y12 receptor, microglial activation, extracellular nucleotides, microglial chemotaxis, microglial polarization, microglial motility, purinergic signaling, G protein-coupled receptors, central nervous system injury, cortical injury
- MeSH terms
- Adenosine Diphosphate, Adenosine Triphosphate, Animals, Brain Injuries, Central Nervous System, Chemotaxis, Membrane Proteins, Microglia, Receptors, Purinergic P2, Mice, Knockout, Mice, Receptors, Purinergic P2Y12
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