The DOI matches its Crossref record; 80 of the 82 references it cites were found in a registry or an index.
Microglia Promote the Death of Developing Purkinje Cells
Open accessAbstract
The loss of neuronal cells, a prominent event in the development of the nervous system, involves regulated triggering of programmed cell death, followed by efficient removal of cell corpses. Professional phagocytes, such as microglia, contribute to the elimination of dead cells. Here we provide evidence that, in addition to their phagocytic activity, microglia promote the death of developing neurons engaged in synaptogenesis. In the developing mouse cerebellum, Purkinje cells die, and 60% of these neurons that already expressed activated caspase-3 were engulfed or contacted by spreading processes emitted by microglial cells. Apoptosis of Purkinje cells in cerebellar slices was strongly reduced by selective elimination of microglia. Superoxide ions produced by microglial respiratory bursts played a major role in this Purkinje cell death. Our study illustrates a mammalian form of engulfment-promoted cell death that links the execution of neuron death to the scavenging of dead cells.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
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?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“In the AD and PD brain, both astrocytes and microglia acquire reactive, inflammatory phenotypes and can effectively phagocytose aggregated proteins and cell debris, as well as secrete various cytokines and inflammatory mediators [8–13].”
From Crosstalk between astrocytes and microglia results in increased degradation of α-synuclein and amyloid-β aggregates (2021) · cites this paper as [13]
Experimental — accuracy not yet measuredThe cited source says what the claim attributes to it.
In the citing paper
“Microglia also contribute to the maintenance of brain homeostasis by clearing apoptotic cells in the brain via efferocytosis (27–29).”
From Reducing microglial lipid load enhances β amyloid phagocytosis in an Alzheimer’s disease mouse model (2025) · cites this paper as [27]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Emerging roles of caspase-3 in apoptosis
Porter, A. G., & Jänicke, R. U. (1999) · Cell Death and Differentiation · doi:10.1038/sj.cdd.4400476 · Cited by 3,921
Bonfoco, E., Krainc, D., Ankarcrona, M., Nicotera, P., & Lipton, S. A. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.16.7162 · Cited by 1,958
Apoptosis in the nervous system
Yuan, J., & Yankner, B. A. (2000) · Nature · doi:10.1038/35037739 · Cited by 1,882
van Rooijen, N., & Sanders, A. (1994) · Journal of Immunological Methods · doi:10.1016/0022-1759(94)90012-4 · Cited by 1,763
A blast from the past: clearance of apoptotic cells regulates immune responses
Savill, J., Dransfield, I., Gregory, C. D., & Haslett, C. (2002) · Nature reviews. Immunology · doi:10.1038/nri957 · Cited by 1,574
Caspase structure, proteolytic substrates, and function during apoptotic cell death
Nicholson, D. (1999) · Cell Death and Differentiation · doi:10.1038/sj.cdd.4400598 · Cited by 1,562
Rothe, J., Lesslauer, W., Loetscher, H., Lang, Y., Koebel, P., Köntgen, F., Althage, A., Zinkernagel, R. M., Steinmetz, M., & Bluethmann, H. (1993) · Nature · doi:10.1038/364798a0 · Cited by 1,246
Killing activity of neutrophils is mediated through activation of proteases by K+ flux
Reeves, E. P., Lu, H., Jacobs, H. L., Messina, C. G. M., Bolsover, S., Gabella, G., Potma, E. O., Warley, A., Roes, J., & Segal, A. W. (2002) · Nature · doi:10.1038/416291a · Cited by 1,153
Cytokines and acute neurodegeneration
Allan, S. M., & Rothwell, N. J. (2001) · Nature reviews. Neuroscience · doi:10.1038/35094583 · Cited by 1,145
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: 2
- Baptista, 1994, Cell-cell interactions influence differentiation of purified Purkinje cells in vitro, Neuron, 2, 243
- Fadok, 2001, Phagocyte receptors for apoptotic cells, J. Clin. Invest., 108, 957, 10.1172/JCI200114122 · DOI
Cited by
Sorted by citations
Items 501–600 of 757
Adequate Time Window and Environmental Factors Supporting Retinal Graft Cell Survival in rd Mice
Mandai, M., Homma, K., Okamoto, S., Yamada, C., Nomori, A., & Takahashi, M. (2012) · Cell Medicine · doi:10.3727/215517912x639315 · Cited by 15
Phagocytic microglia in development: Are they what they eat?
VanRyzin, J. W. (2021) · Brain Behavior & Immunity - Health · doi:10.1016/j.bbih.2021.100373 · Cited by 15
Zanjani, H., Lohof, A. M., McFarland, R. J., Vogel, M. W., & Mariani, J. (2012) · The Cerebellum · doi:10.1007/s12311-012-0427-x · Cited by 14
Cealie, M. Y., Douglas, J. C., Le, L., VonKaenel, E. D., McCall, M. N., Drew, P. D., & Majewska, A. K. (2023) · Frontiers in Neuroscience · doi:10.3389/fnins.2023.1176581 · Cited by 11
Lao, Y., Li, Z., Bai, Y., Li, W., Wang, J., Wang, Y., Li, Q., & Dong, Z. (2023) · Pain Research and Management · doi:10.1155/2023/2061632 · Cited by 13
Yates, R. L., Pansieri, J., Li, Q., Bell, J. S., Yee, S. A., Palace, J. A., Esiri, M. M., & DeLuca, G. C. (2021) · Brain Pathology · doi:10.1111/bpa.13041 · Cited by 14
Domínguez, M. M., González, B., & Zimmer, J. (2009) · Experimental Neurology · doi:10.1016/j.expneurol.2009.03.023 · Cited by 13
Angelim, M. K. S. C., Maia, L. M. S. D. S., Mouffle, C., Ginhoux, F., Low, D., dos Santos, Â. A., Makhoul, J., Corronc, H. L., Mangin, J., & Legendre, P. (2018) · Glia · doi:10.1002/glia.23499 · Cited by 15
The autistic brain in the context of normal neurodevelopment
Ziats, M. N., Edmonson, C. A., & Rennert, O. M. (2015) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2015.00115 · Cited by 15
Cell Death as a Regulator of Cerebellar Histogenesis and Compartmentation
Jankowski, J., Miething, A., Schilling, K., Oberdick, J., & Baader, S. L. (2010) · The Cerebellum · doi:10.1007/s12311-010-0222-5 · Cited by 14
Li, X., Hanson, C. A., Cmarik, J. L., & Ruscetti, S. K. (2009) · Journal of Virology · doi:10.1128/jvi.02343-08 · Cited by 13
Death of injured neurons caused by the precursor of nerve growth factor
Barde, Y. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0401374101 · Cited by 13
Cerebellar microglia: On the edge between neuroinflammation and neuroregulation
Dukhinova, M., Guo, J., Shen, E.-W., Liu, W., Huang, W., Shen, Y., & Wang, L. (2024) · Neural Regeneration Research · doi:10.4103/nrr.nrr-d-24-00550 · Cited by 15
Shi, S., Sun, Y., Zan, G., & Zhao, M. (2025) · Journal of Neuroinflammation · doi:10.1186/s12974-025-03372-z · Cited by 19
Microgliosis: a double‐edged sword in the control of food intake
Salvi, J., Andreoletti, P., Audinat, É., Balland, É., Fradj, S. B., Cherkaoui‐Malki, M., Heurtaux, T., Liénard, F., Nédélec, E., Rovère, C., et al. (2022) · FEBS Journal · doi:10.1111/febs.16583 · Cited by 16
Migration and ramification of microglia in quail embryo retina organotypic cultures
Carrasco, M., Navascués, J., Cuadros, M. Á., Calvente, R., Martín‐Oliva, D., Santos, A. M., Sierra, A., Ferrer‐Martín, R. M., & Marín‐Teva, J. L. (2010) · Developmental Neurobiology · doi:10.1002/dneu.20860 · Cited by 12
Self-citationNaturally-occurring neuron death
Sanes, D. H., Reh, T. A., & Harris, W. A. (2012) · Elsevier eBooks · doi:10.1016/b978-0-12-374539-2.00011-2 · Cited by 12
A new technique for real-time analysis of caspase-3 dependent neuronal cell death
Golbs, A., Heck, N., & Luhmann, H. J. (2007) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2006.11.011 · Cited by 12
A decade of diverse microglial-neuronal physical interactions in the brain (2008–2018)
Uweru, J. O., & Eyo, U. B. (2019) · Neuroscience Letters · doi:10.1016/j.neulet.2019.01.001 · Cited by 13
Kang, Y., Jefferson, A., Sheehan, A. E., Torre, R. D. L., Jay, T. R., Chiao, L. J., Hulegaard, A. L., Corty, M. M., Baconguis, I., Zhou, Z., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.11.06.565932 · Cited by 10
Microglial regulation of cholinergic differentiation in the basal forebrain
Jonakait, G. M., Pratt, L., Acevedo, G., & Ni, L. (2011) · Developmental Neurobiology · doi:10.1002/dneu.20969 · Cited by 11
Cealie, M. Y., Douglas, J. C., Swan, H. K., VonKaenel, E. D., McCall, M. N., Drew, P. D., & Majewska, A. K. (2024) · Cells · doi:10.3390/cells13050386 · Cited by 12
Jacobs, A. J., Castillo‐Ruiz, A., Cisternas, C. D., & Forger, N. G. (2019) · Developmental Neurobiology · doi:10.1002/dneu.22706 · Cited by 11
Delahaye‐Duriez, A., Dufour, A., Bokobza, C., Gressèns, P., & Steenwinckel, J. V. (2021) · Journal of Neuropathology & Experimental Neurology · doi:10.1093/jnen/nlab049 · Cited by 13
Song, G., Liang, H., Song, H., Ding, X., Wang, D., Zhang, X., & Sun, T. (2022) · Journal of Immunology Research · doi:10.1155/2022/3218452 · Cited by 13
Hikosaka, M., Parvez, M. S. A., Yamawaki, Y., Oe, S., Yuan, L., Wada, Y., Hirahara, Y., Koike, T., Imai, H., Oishi, N., et al. (2025) · Communications Biology · doi:10.1038/s42003-025-07566-2 · Cited by 13
Microglia in early brain development: A window of opportunity
Catale, C., & Garel, S. (2025) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2025.103062 · Cited by 13
Kaniuk, J. K., Kumar, D., Mazurek, C. Y., Khavari, S., Sollenberger, C. H., Ahuja, A., Mossner, J. M., & Ahuja, C. S. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26157191 · Cited by 11
Glial Cells and Aging: From the CNS to the Cerebellum
Sala, G. L., & Farini, D. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26157553 · Cited by 12
Clearing Your Mind: Mechanisms of Debris Clearance After Cell Death During Neural Development
Liu, K. E., Raymond, M. H., Ravichandran, K. S., & Kucenas, S. (2022) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-110920-022431 · Cited by 10
Live-cell imaging: new avenues to investigate retinal regeneration
Hyde, D. R., & Lahne, M. (2017) · Neural Regeneration Research · doi:10.4103/1673-5374.213533 · Cited by 10
Headmasters: Microglial regulation of learning and memory in health and disease
Weinhard, L., d’Errico, P., & Tay, T. L. (2018) · AIMS molecular science · doi:10.3934/molsci.2018.1.63 · Cited by 11
A Microglial Function for the Nerve Growth Factor: Predictions of the Unpredictable
Tiberi, A., Capsoni, S., & Cattaneo, A. (2022) · Cells · doi:10.3390/cells11111835 · Cited by 13
Balancing Microglial Density and Activation in Central Nervous System Development and Disease
Wang, S., Pan, L., Sun, C., Ma, C., & Pan, H. (2025) · Current Issues in Molecular Biology · doi:10.3390/cimb47050344 · Cited by 11
The Implication of Glial Metabotropic Glutamate Receptors in Alzheimer’s Disease
de Lima, I. B. Q., & Ribeiro, F. M. (2021) · Current Neuropharmacology · doi:10.2174/1570159x20666211223140303 · Cited by 9
Cell death in development, maintenance, and diseases of the nervous system
Mercau, M. E., Patwa, S., Bhat, K., Ghosh, S., & Rothlin, C. V. (2022) · Seminars in Immunopathology · doi:10.1007/s00281-022-00938-4 · Cited by 9
Microglia Maintain Homeostatic Conditions in the Developing Rostral Migratory Stream
Meller, S. J., Hernandez, L., Martín-López, E., Kloos, Z. A., Liberia, T., & Greer, C. A. (2023) · eNeuro · doi:10.1523/eneuro.0197-22.2023 · Cited by 9
Depletion of Microglia from Primary Cellular Cultures
Pont‐Lezica, L., Colasse, S., & Bessis, A. (2013) · Methods in molecular biology · doi:10.1007/978-1-62703-520-0_7 · Cited by 9
Specific JNK Inhibition by D-JNKI1 Protects Purkinje Cells from Cell Death in Lurcher Mutant Mouse
Repici, M., Zanjani, H., Gautheron, V., Borsello, T., Dusart, I., & Mariani, J. (2008) · The Cerebellum · doi:10.1007/s12311-008-0070-8 · Cited by 9
Self-citationMicroglia perform local protein synthesis at perisynaptic and phagocytic structuresPreprint
Vasek, M. J., Deajon-Jackson, J. D., Liu, Y., Crosby, H. W., Yi, J., & Dougherty, J. D. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.01.13.426577 · Cited by 9
Emerging non-proinflammatory roles of microglia in healthy and diseased brains
Sun, Y., Che, J., & Zhang, J. (2023) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2023.110664 · Cited by 10
Duan, Z., Zheng, L.-Y., Jia, Q., Chen, H., Xu, D., Yang, Y., Qi, Z., Yang, L., & Wu, C. (2024) · Scientific Reports · doi:10.1038/s41598-024-64226-x · Cited by 8
A review of the Bovis Calculus’s intervention mechanism and clinical application in ischemic stroke
Xu, K., Deng, B., Jia, T., Ren, M., Chen, H., Zhang, J., Guo, J., Li, Y., & Wang, J. (2025) · Frontiers in Pharmacology · doi:10.3389/fphar.2024.1510779 · Cited by 8
epDevAtlas: mapping GABAergic cells and microglia in the early postnatal mouse brain
Liwang, J. K., Kronman, F. N., Pi, H.-J., Wu, Y.-T., Vanselow, D. J., Manjila, S. B., Parmaksiz, D., Shin, D., Ben‐Simon, Y., Taormina, M. J., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-64549-x · Cited by 16
Natoli, R., Mason, E. A., Jiao, H., Chuah, A., Patel, H. R., Fernando, N., Valter, K., Wells, C. A., Provis, J. M., & Rutar, M. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.01666 · Cited by 8
RetractedRepici, M., Wehrlé, R., Antoniou, X., Borsello, T., & Dusart, I. (2010) · The Cerebellum · doi:10.1007/s12311-010-0244-z · Cited by 8
Self-citationMicroglial phospholipase D4 deficiency influences myelination during brain development
Chiba, T., Otani, Y., Yamaguchi, Y., Ishibashi, T., Hayashi, A., Tanaka, K. F., Yamazaki, M., Sakimura, K., & Baba, H. (2016) · Proceedings of the Japan Academy Series B · doi:10.2183/pjab.92.237 · Cited by 8
Dulka, K., Nacsa, K., Lajkó, N., & Gulya, K. (2021) · IBRO Neuroscience Reports · doi:10.1016/j.ibneur.2021.01.007 · Cited by 8
Liu, Y., Li, H., Hu, J., Wu, Z., Meng, J., Hayashi, Y., Nakanishi, H., Qing, H., & Ni, J. (2021) · Molecular Neurobiology · doi:10.1007/s12035-021-02594-5 · Cited by 8
Roles of Ca2+ activity in injury-induced migration of microglia in zebrafish in vivo
Du, T., Zhou, X., Zhang, R. D. Y., & Du, X.-F. (2022) · Biochemistry and Biophysics Reports · doi:10.1016/j.bbrep.2022.101340 · Cited by 9
Correlation Analysis between External Factors and Students’ Physics Learning Achievement
Karyadi, K., Sinon, I. L. S., Yusuf, I., & Widyaningsih, S. W. (2018) · Scientiae Educatia · doi:10.24235/sc.educatia.v7i1.2415 · Cited by 9
epDevAtlas: Mapping GABAergic cells and microglia in postnatal mouse brainsPreprint
Liwang, J. K., Kronman, F. N., Minteer, J. A., Wu, Y.-T., Vanselow, D. J., Ben‐Simon, Y., Taormina, M. J., Parmaksiz, D., Way, S. W., Zeng, H., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.11.24.568585 · Cited by 8
Liu, L., Xiao, F., Yang, J., Yao, H.-Q., & Hua, K. Q. (2025) · Cytokine · doi:10.1016/j.cyto.2025.156893 · Cited by 7
Cerebellar pathology contributes to neurodevelopmental deficits in spinal muscular atrophy
Gerstner, F., Wittig, S., Menedo, C., Ruwald, S., Carlini, M. J., Vankova, A., Sowoidnich, L., Martín-López, G., Dreilich, V., Alonso-Collado, A., et al. (2025) · Brain · doi:10.1093/brain/awaf336 · Cited by 10
Attack of the Clones: Microglia in Health and Disease
Manjally, A. V., & Tay, T. L. (2022) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2022.831747 · Cited by 7
Microenvironment and the progress of immunotherapy in clinical practice of NSCLC brain metastasis
Xie, M., & Su, C. (2023) · Frontiers in Oncology · doi:10.3389/fonc.2022.1006284 · Cited by 7
Rethinking Pediatric Gliomas as Developmental Brain Abnormalities
Crouse, N. R., Dahiya, S. M., & Gutmann, D. H. (2011) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/b978-0-12-380916-2.00009-7 · Cited by 7
Bäurle, J., Kučera, J., Frischmuth, S., Lambertz, M., & Kranda, K. (2008) · Brain Pathology · doi:10.1111/j.1750-3639.2008.00200.x · Cited by 7
Zhou, L., Araki, A., Nakano, A., Sezer, C., & Harada, T. (2006) · Pathology International · doi:10.1111/j.1440-1827.2006.01943.x · Cited by 7
Ferreira, P. A., Lebre, C., Costa, J., Amaral, F., Ferreira, R., Martinho, F., Paiva, V. H., Cardoso, A. L., Peça, J., & Guedes, J. R. (2024) · Journal of Neurochemistry · doi:10.1111/jnc.16266 · Cited by 6
Doolittle, T., & Duque‐Wilckens, N. (2025) · Advances in experimental medicine and biology · doi:10.1007/978-3-031-89525-8_11 · Cited by 6
Nguyen, L. T. M., Hassan, S., Pan, H., Wu, S., & Wen, Z. (2024) · Development · doi:10.1242/dev.201829 · Cited by 6
Early postnatal development of rat brain is accompanied by generation of lipofuscin-like pigments
Wilhelm, J., Ivica, J., Kagan, D., & Svoboda, P. (2010) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-010-0623-2 · Cited by 6
Zebrin II Is Ectopically Expressed in Microglia in the Cerebellum of Neurogenin 2 Null Mice
Rahimi-Balaei, M., Jiao, X., Shabanipour, S., Dixit, R., Schuurmans, C. J., & Marzban, H. (2018) · The Cerebellum · doi:10.1007/s12311-018-0944-3 · Cited by 6
Immunometabolic phenotype of BV-2 microglia cells upon murine cytomegalovirus infection
Kučić, N., Rački, V., Jurdana, K., Marcelić, M., & Grabušić, K. (2019) · Journal of NeuroVirology · doi:10.1007/s13365-019-00750-1 · Cited by 6
Brain Cancer-Activated Microglia: A Potential Role for Sphingolipids
Bottai, D., Adami, R., Paroni, R. C., & Ghidoni, R. (2019) · Current Medicinal Chemistry · doi:10.2174/0929867326666190506120213 · Cited by 6
Rahimi-Balaei, M., Jiao, X., Dalvand, A., Shabanipour, S., Chung, S., Amiri, S., Kong, J., & Marzban, H. (2020) · Molecular Biology Reports · doi:10.1007/s11033-020-05614-0 · Cited by 6
Targeting Astrocytomas and Invading Immune Cells with Cannabinoids: A Promising Therapeutic Avenue
Cudaback, E., & Stella, N. (2007) · Molecular Neurobiology · doi:10.1007/s12035-007-0016-z · Cited by 6
Ulrich, H. (2010) · Springer eBooks · doi:10.1007/978-90-481-3375-8 · Cited by 6
Barbierato, M. (2012) · Padua Research Archive (University of Padova) · Cited by 6
Peripheral macrophages in the development and progression of structural cerebrovascular pathologies
Lauzier, D. C., Srienc, A. I., Vellimana, A. K., Dacey, R. G., & Zipfel, G. J. (2023) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1177/0271678x231217001 · Cited by 5
Wu, D., Du, J., Zhao, T., Li, N., Qiao, X., Peng, F., Wang, D., Shi, J., Zhang, S., Diao, C., et al. (2025) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.70347 · Cited by 5
Microgliopathy as a primary mediator of neuronal death in models of Friedreich’s Ataxia
Pernaci, C., Johnson, A., Gillette, S., Warden, A. S., McCormick, C., Novak, S. W., Ramírez, G., Broersma, E. H., Mishra, P., Sivakumar, A., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-66710-y · Cited by 9
p27kip1 Modulates the Morphology and Phagocytic Activity of Microglia
Beeken, J., Kessels, S., Rigo, J., Alpizar, Y. A., Nguyen, L., & Brône, B. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms231810432 · Cited by 5
Microglial inflammation in genome instability: A neurodegenerative perspective
Maliar, N. L., Talbot, E., Edwards, A. R., & Khoronenkova, S. V. (2024) · DNA repair · doi:10.1016/j.dnarep.2024.103634 · Cited by 6
Ulfig, N., Steinbrecher, A., Stoltenburg, G., & Rezaie, P. (2007) · Neuropathology · doi:10.1111/j.1440-1789.2007.00856.x · Cited by 5
Eissa, N., Kermarrec, L., & Ghia, J. (2017) · Contemporary clinical neuroscience · doi:10.1007/978-3-319-59749-2_13 · Cited by 5
Kawai, T., Takao, K., Akter, S., Abe, M., Sakimura, K., Miyakawa, T., & Okamura, Y. (2021) · Journal of Neurochemistry · doi:10.1111/jnc.15292 · Cited by 5
Ghoumari, A. M., Wehrlé, R., Sotelo, C., & Dusart, I. (2005) · Progress in brain research · doi:10.1016/s0079-6123(04)48004-2 · Cited by 5
Self-citationKorhonen, L., Hansson, I., Maugras, C., Wehrlé, R., Kairisalo, M., Borgkvist, A., Jokitalo, E., Sotelo, C., Fisone, G., Dusart, I., et al. (2008) · Neuroscience · doi:10.1016/j.neuroscience.2008.08.005 · Cited by 5
Self-citationCorraliza-Gómez, M., Guilarte, B. B., Sandonís-Camarero, D., Mondejar-Duran, J., Villa, M., Poncela, M., Valero, J., Sánchez, D., & Ganfornina, M. D. (2023) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2023.1112930 · Cited by 4
Sierra, A., Navascués, J., Neubrand, V. E., Sepúlveda, M. R., Martín‐Oliva, D., Cuadros, M. Á., & Marín‐Teva, J. L. (2023) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2023.1120400 · Cited by 4
Self-citationThe role of glial cells in amyotrophic lateral sclerosis
Pandya, V. A., & Patani, R. (2024) · International review of neurobiology · doi:10.1016/bs.irn.2024.04.005 · Cited by 5
Pharmaceutical-mediated neuroimmune modulation in psychiatric/psychological adverse events
Marques, S. I., Sá, S. I., Carmo, H., Carvalho, F. D., & Silva, J. P. (2024) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2024.111114 · Cited by 5
Aging Microglia and Their Impact in the Nervous System
Rommy von Bernhardi, M., & Eugenín, J. L. (2024) · Advances in neurobiology · doi:10.1007/978-3-031-55529-9_21 · Cited by 4
Prasad, J. D., Steenwinckel, J. V., Gunn, A. J., Bennet, L., Korzeniewski, S. J., Gressèns, P., & Dean, J. M. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms252312999 · Cited by 5
Cytotoxicity of Amyloid β1–42 Fibrils to Brain Immune Cells
Matveyenka, M., Шолух, М. В., & Kurouski, D. (2025) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.4c00835 · Cited by 4
Hernández-García, D., García, C., Hernández-Martínez, R., Collazo-Navarrete, O., & Covarrubias, L. (2024) · Biology Open · doi:10.1242/bio.060492 · Cited by 6
Takeuchi, H. (2013) · Advances in Neuroimmune Biology · doi:10.3233/nib-130057 · Cited by 3
Ackman, J. B., & LoTurco, J. J. (2006) · Experimental Neurology · doi:10.1016/j.expneurol.2006.03.007 · Cited by 4
Neurodevelopmental and Neuropsychiatric Disorders
Monji, A., Maezawa, I., Mizoguchi, Y., Kato, T. A., & Jin, L. (2014) · Springer eBooks · doi:10.1007/978-1-4939-1429-6_14 · Cited by 4
The link between early-life adversity and later alcohol use disorder: A role for microglia?
Lichtenstein, H. D., Sequeira, M. K., & Bolton, J. L. (2025) · Neurobiology of Stress · doi:10.1016/j.ynstr.2025.100714 · Cited by 3
Microglial Phagocytosis During Embryonic and Postnatal Development
Marín‐Teva, J. L., Sepúlveda, M. R., Neubrand, V. E., & Cuadros, M. Á. (2024) · Advances in neurobiology · doi:10.1007/978-3-031-55529-9_9 · Cited by 4
Self-citationHomeostatic Functions of Tissue-Resident Macrophages and Their Role in Tissue Maintenance
Crisóstomo, L., Mäkinen, A., Hyseni, B., Bergman, H. ‐., & Mildner, A. (2024) · Results and problems in cell differentiation · doi:10.1007/978-3-031-65944-7_1 · Cited by 3
Plunk, E. C., Navnith, N., Swan, H., Le, L., McCall, M. N., Sobolewski, M., & Majewska, A. K. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26168008 · Cited by 3
Alekseeva, O. S., Gilerovich, E. G., Kirik, O. V., & Korzhevsky, D. E. (2017) · Neuroscience and Behavioral Physiology · doi:10.1007/s11055-017-0447-6 · Cited by 3
Origin and Development of Microglia
Patro, N., & Patro, I. K. (2022) · Springer eBooks · doi:10.1007/978-981-16-8313-8_7 · Cited by 3
Astrocyte-dependent local neurite pruning in Beat-Va neurons
Lehmann, K. S., Hupp, M. T., Abalde-Atristain, L., Jefferson, A., Cheng, Y.-C., Sheehan, A. E., Kang, Y., & Freeman, M. R. (2024) · The Journal of Cell Biology · doi:10.1083/jcb.202312043 · Cited by 3
Elucidation of cytotoxicity of α-Synuclein fibrils on immune cells
Matveyenka, M., Ali, A., Mitchell, C. L., Шолух, М. В., & Kurouski, D. (2024) · Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics · doi:10.1016/j.bbapap.2024.141061 · Cited by 3
A mouse model of microglia-specific ablation in the embryonic central nervous system
Li, C., Konishi, H., Nishiwaki, K., Sato, K., Miyata, T., & Kiyama, H. (2021) · Neuroscience Research · doi:10.1016/j.neures.2021.06.002 · Cited by 3
Metadata
- Authors
- Marı́n-Teva, J. L., Dusart, I., Colin, C., Gervais, A., van Rooijen, N., & Mallat, M.
- Affiliations
- Inserm (FR)
- Vrije Universiteit Amsterdam (NL)
- Corresponding author
- Mallat, Michel
- Venue
- Neuron
- Publisher
- Elsevier BV
- Published
- 2004-02
- Volume
- 41
- Issue
- 4
- Pages
- 535-547
- ISSN
- 0896-6273 (ISSN-L)
- OpenAlex
- W2103711259
- Cited by
- 757
- References
- 82
- Citations by year
- 2026: 13 · 2025: 38 · 2024: 35 · 2023: 45 · 2022: 45 · 2021: 50 · 2020: 30 · 2019: 47 · 2018: 39 · 2017: 29 · 2016: 42 · 2015: 38 · 2014: 42 · 2013: 40 · 2012: 40
- FWCI
- 17.29
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Neuron (publishedVersion)
- PubMed (publishedVersion)
- Pure Amsterdam UMC (publishedVersion)
- Amsterdam UMC (VU Amsterdam) - Institutional Repository (publishedVersion, other-oa)
- HAL (submittedVersion)
- Digital Academic REpository of VU University Amsterdam (Vrije Universiteit Amsterdam) (submittedVersion)
- Data Archiving and Networked Services (DANS) (submittedVersion)
- Data Archiving and Networked Services (DANS) (submittedVersion, other-oa)
- Topics
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Life Sciences › Immunology and Microbiology › Immunology › Phagocytosis and Immune Regulation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Cell death mechanisms and regulation
- Keywords
- microglia, Purkinje cells, neuronal apoptosis, cerebellar development, phagocytosis, caspase-3, superoxide, synaptogenesis, neuronal cell death
- MeSH terms
- Animals, Antibodies, Cell Communication, Cell Differentiation, Cell Survival, Cerebellar Cortex, Enzyme Inhibitors, Mice, Inbred C57BL, Purkinje Cells, Signal Transduction, Free Radical Scavengers, Apoptosis, Microglia, Presynaptic Terminals, Receptors, Tumor Necrosis Factor, Mice, Knockout, Cell Respiration, Caspases, Mice, Caspase 3, In Vitro Techniques
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