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Local generation of glia is a major astrocyte source in postnatal cortex
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Glial cells constitute nearly 50% of the cells in the human brain. Astrocytes, which make up the largest glial population, are crucial to the regulation of synaptic connectivity during postnatal development. Because defects in astrocyte generation are associated with severe neurological disorders such as brain tumours, it is important to understand how astrocytes are produced. Astrocytes reportedly arise from two sources: radial glia in the ventricular zone and progenitors in the subventricular zone, with the contribution from each region shifting with time. During the first three weeks of postnatal development, the glial cell population, which contains predominantly astrocytes, expands 6-8-fold in the rodent brain. Little is known about the mechanisms underlying this expansion. Here we show that a major source of glia in the postnatal cortex in mice is the local proliferation of differentiated astrocytes. Unlike glial progenitors in the subventricular zone, differentiated astrocytes undergo symmetric division, and their progeny integrate functionally into the existing glial network as mature astrocytes that form endfeet with blood vessels, couple electrically to neighbouring astrocytes, and take up glutamate after neuronal activity.
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“Astrocytes being the most abundant type of glial cells within cortical areas, are generated from the radial glial cells in the VZ and from the intermediate progenitors in the SVZ after the peak of neurogenesis [53].”
From Development of prefrontal cortex (2022) · cites this paper as [53]
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Cites
A robust and high-throughput Cre reporting and characterization system for the whole mouse brain
Madisen, L., Zwingman, T. A., Sunkin, S. M., Oh, S. W., Zariwala, H. A., Gu, H., Ng, L. L., Palmiter, R. D., Hawrylycz, M. J., Jones, A. R., et al. (2010) · Nature Neuroscience · doi:10.1038/nn.2467 · Cited by 6,907
Subventricular zone astrocytes are neural stem cells in the adult mammalian brain
Doetsch, F., Caillé, I., Lim, D. A., García-Verdugo, J. M., & Alvarez-Buylla, A. (1999) · Cell · doi:10.1016/s0092-8674(00)80783-7 · Cited by 3,898
The Glial Nature of Embryonic and Adult Neural Stem Cells
Kriegstein, A., & Alvarez-Buylla, A. (2009) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.051508.135600 · Cited by 2,475
Azevedo, F. A. C., Carvalho, L. R. B., Grinberg, L. T., Farfel, J. M., Ferretti, R. E. L., Leite, R. E. P., Filho, W. J., Lent, R., & Herculano‐Houzel, S. (2009) · Journal of Comparative Neurology · doi:10.1002/cne.21974 · Cited by 2,337
Visualizing Spatiotemporal Dynamics of Multicellular Cell-Cycle Progression
Sakaue-Sawano, A., Kurokawa, H., Morimura, T., Hanyu, A., Hama, H., Osawa, H., Kashiwagi, S., Fukami, K., Miyata, T., Miyoshi, H., et al. (2008) · Cell · doi:10.1016/j.cell.2007.12.033 · Cited by 2,194
Self-citationCell death and control of cell survival in the oligodendrocyte lineage
Barres, B. A., Hart, I. K., Coles, H. S. R., Burne, J. F., Voyvodic, J. T., Richardson, W. D., & Raff, M. C. (1992) · Cell · doi:10.1016/0092-8674(92)90531-g · Cited by 1,345
Astrocyte-mediated control of cerebral blood flow
Takano, T., Tian, G.-F., Peng, W., Lou, N., Libionka, W., Han, X., & Nedergaard, M. (2005) · Nature Neuroscience · doi:10.1038/nn1623 · Cited by 1,137
Epidemiology and molecular pathology of glioma
Schwartzbaum, J., Fisher, J. L., Aldape, K., & Wrensch, M. (2006) · Nature Clinical Practice Neurology · doi:10.1038/ncpneuro0289 · Cited by 951
Astroglial Metabolic Networks Sustain Hippocampal Synaptic Transmission
Rouach, N., Koulakoff, A., Abudara, V., Willecke, K., & Giaume, C. (2008) · Science · doi:10.1126/science.1164022 · Cited by 912
Suh, H., Consiglio, A., Ray, J., Sawai, T., D’Amour, K. A., & Gage, F. H. (2007) · Cell stem cell · doi:10.1016/j.stem.2007.09.002 · Cited by 851
Self-citation
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Sorted by citations
Zhang, Y., Sloan, S. A., Clarke, L. E., Caneda, C., Plaza, C. A., Blumenthal, P. D., Vogel, H., Steinberg, G. K., Edwards, M. S. B., Li, G., et al. (2016) · Neuron · doi:10.1016/j.neuron.2015.11.013 · Cited by 2,295
Verkhratsky, A., & Nedergaard, M. (2018) · Physiological Reviews · doi:10.1152/physrev.00042.2016 · Cited by 1,678
Astrocyte Crosstalk in CNS Inflammation
Linnerbauer, M., Wheeler, M. A., & Quintana, F. J. (2020) · Neuron · doi:10.1016/j.neuron.2020.08.012 · Cited by 989
Astrocyte reactivity and reactive astrogliosis: costs and benefits
Pekny, M., & Pekna, M. (2014) · Physiological Reviews · doi:10.1152/physrev.00041.2013 · Cited by 934
Guo, Z., Zhang, L., Wu, Z., Chen, Y., Wang, F., & Chen, G. (2013) · Cell stem cell · doi:10.1016/j.stem.2013.12.001 · Cited by 849
Identification of region-specific astrocyte subtypes at single cell resolution
Batiuk, M. Y., Martirosyan, A., Wahis, J., de Vin, F., Marneffe, C., Kusserow, C., Koeppen, J., Viana, J. F., Oliveira, J. F., Voet, T., et al. (2020) · Nature Communications · doi:10.1038/s41467-019-14198-8 · Cited by 805
Astrocytes and disease: a neurodevelopmental perspective
Molofsky, A. V., Krenick, R., Ullian, E., Tsai, H.-H., Deneen, B., Richardson, W. D., Barres, B. A., & Rowitch, D. H. (2012) · Genes & Development · doi:10.1101/gad.188326.112 · Cited by 682
Function and therapeutic value of astrocytes in neurological diseases
Lee, H.-G., Wheeler, M. A., & Quintana, F. J. (2022) · Nature Reviews Drug Discovery · doi:10.1038/s41573-022-00390-x · Cited by 662
Molecular basis of astrocyte diversity and morphology across the CNS in health and disease
Endo, F., Kasai, A., Soto, J. S., Yu, X., Qu, Z., Hashimoto, H., Gradinaru, V., Kawaguchi, R., & Khakh, B. S. (2022) · Science · doi:10.1126/science.adc9020 · Cited by 560
Chinta, S. J., Woods, G., Demaria, M., Rane, A., Zou, Y., McQuade, A., Rajagopalan, S., Limbad, C., Madden, D. T., Campisi, J., et al. (2018) · Cell Reports · doi:10.1016/j.celrep.2017.12.092 · Cited by 530
Regional Astrocyte Allocation Regulates CNS Synaptogenesis and Repair
Tsai, H., Li, H., Fuentealba, L. C., Molofsky, A. V., Taveira‐Marques, R., Zhuang, H., Tenney, A., Murnen, A. T., Fancy, S. P. J., Merkle, F. T., et al. (2012) · Science · doi:10.1126/science.1222381 · Cited by 555
Identification of diverse astrocyte populations and their malignant analogs
John Lin, C.-C., Yu, K., Hatcher, A., Huang, T.-W., Lee, H. K., Carlson, J., Weston, M. C., Chen, F., Zhang, Y., Zhu, W., et al. (2017) · Nature Neuroscience · doi:10.1038/nn.4493 · Cited by 525
The Indispensable Roles of Microglia and Astrocytes during Brain Development
Reemst, K., Noctor, S. C., Lucassen, P. J., & Hol, E. M. (2016) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2016.00566 · Cited by 516
Bayraktar, O. A., Bartels, T., Holmqvist, S., Kleshchevnikov, V., Martirosyan, A., Polioudakis, D., Ben Haim, L., Young, A. M. H., Batiuk, M. Y., Prakash, K., et al. (2020) · Nature Neuroscience · doi:10.1038/s41593-020-0602-1 · Cited by 489
In vivo reprogramming of astrocytes to neuroblasts in the adult brain
Niu, W., Zang, T., Zou, Y., Fang, S., Smith, D. K., Bachoo, R. M., & Zhang, C. (2013) · Nature Cell Biology · doi:10.1038/ncb2843 · Cited by 501
The Emerging Nature of Astrocyte Diversity
Khakh, B. S., & Deneen, B. (2019) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-070918-050443 · Cited by 512
Live imaging of astrocyte responses to acute injury reveals selective juxtavascular proliferation
Bardehle, S., Krüger, M., Buggenthin, F., Schwausch, J., Ninkovic, J., Clevers, H. C., Snippert, H. J. G., Theis, F. J., Meyer‐Luehmann, M., Bechmann, I., et al. (2013) · Nature Neuroscience · doi:10.1038/nn.3371 · Cited by 448
Astrocytes, neurons, synapses: a tripartite view on cortical circuit development
Farhy-Tselnicker, I., & Allen, N. J. (2018) · Neural Development · doi:10.1186/s13064-018-0104-y · Cited by 417
Development of prefrontal cortex
Kolk, S. M., & Rakic, P. (2022) · Neuropsychopharmacology · doi:10.1038/s41386-021-01137-9 · Cited by 378
“Astrocytes being the most abundant type of glial cells within cortical areas, are generated from the radial glial cells in the VZ and from the intermediate progenitors in the SVZ after the peak of neurogenesis [53].”
BackgroundAstrocyte regulation of synaptic behavior
Allen, N. J. (2014) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev-cellbio-100913-013053 · Cited by 343
Astrocyte Development and HeterogeneityPreprint
Bayraktar, O. A., Fuentealba, L. C., Álvarez-Buylla, A., & Rowitch, D. H. (2014) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a020362 · Cited by 365
Astrocyte-encoded positional cues maintain sensorimotor circuit integrity
Molofsky, A. V., Kelley, K. W., Tsai, H., Redmond, S., Chang, S., Madireddy, L., Chan, J. R., Baranzini, S. E., Ullian, E. M., & Rowitch, D. H. (2014) · Nature · doi:10.1038/nature13161 · Cited by 322
Astrocyte development: A Guide for the Perplexed
Molofsky, A. V., & Deneen, B. (2015) · Glia · doi:10.1002/glia.22836 · Cited by 323
Synaptic Integration of Adult-Born Hippocampal Neurons Is Locally Controlled by Astrocytes
Sultan, S., Li, L., Moss, J., Petrelli, F., Cassé, F., Gebara, E., Lopatar, J., Pfrieger, F. W., Bezzi, P., Bischofberger, J., et al. (2015) · Neuron · doi:10.1016/j.neuron.2015.10.037 · Cited by 284
Reactive gliosis in the pathogenesis of CNS diseases
Pekny, M., & Pekna, M. (2015) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2015.11.014 · Cited by 289
Cell of Origin for Malignant Gliomas and Its Implication in Therapeutic DevelopmentPreprint
Zong, H., Parada, L. F., & Baker, S. J. (2015) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a020610 · Cited by 281
Glial Cells as Progenitors and Stem Cells: New Roles in the Healthy and Diseased Brain
Dimou, L., & Götz, M. (2014) · Physiological Reviews · doi:10.1152/physrev.00036.2013 · Cited by 285
Mechanisms of astrocyte development and their contributions to neurodevelopmental disorders
Sloan, S. A., & Barres, B. A. (2014) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2014.03.005 · Cited by 260
Astrocyte Endfeet in Brain Function and Pathology: Open Questions
Díaz-Castro, B., Robel, S., & Mishra, A. (2023) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-091922-031205 · Cited by 238
Hertz, L. (2013) · Frontiers in Endocrinology · doi:10.3389/fendo.2013.00059 · Cited by 250
Baldwin, K. T., Murai, K. K., & Khakh, B. S. (2023) · Trends in Cell Biology · doi:10.1016/j.tcb.2023.09.006 · Cited by 237
Maintaining genome stability in the nervous system
McKinnon, P. J. (2013) · Nature Neuroscience · doi:10.1038/nn.3537 · Cited by 229
Schiweck, J., Eickholt, B. J., & Murk, K. (2018) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2018.00261 · Cited by 223
Protective Functions of Reactive Astrocytes Following Central Nervous System Insult
Linnerbauer, M., & Rothhammer, V. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.573256 · Cited by 235
Götz, M., Sirko, S., Beckers, J., & Irmler, M. (2015) · Glia · doi:10.1002/glia.22850 · Cited by 237
Glial Development: The Crossroads of Regeneration and Repair in the CNS
Gallo, V., & Deneen, B. (2014) · Neuron · doi:10.1016/j.neuron.2014.06.010 · Cited by 232
Vascularization and Engraftment of Transplanted Human Cerebral Organoids in Mouse Cortex
Daviaud, N., Friedel, R. H., & Zou, H. (2018) · eNeuro · doi:10.1523/eneuro.0219-18.2018 · Cited by 219
Nishiyama, J., Mikuni, T., & Yasuda, R. (2017) · Neuron · doi:10.1016/j.neuron.2017.10.004 · Cited by 215
Role of EGFR in the Nervous System
Romanò, R., & Bucci, C. (2020) · Cells · doi:10.3390/cells9081887 · Cited by 214
Weng, Q., Wang, J., Wang, J., He, D., Cheng, Z., Zhang, F., Verma, R., Xu, L., Dong, X., Liao, Y., et al. (2019) · Cell stem cell · doi:10.1016/j.stem.2019.03.006 · Cited by 206
Birey, F., Kloc, M. L., Chavali, M., Hussein, I., Wilson, M., Christoffel, D. J., Chen, T., Frohman, M. A., Robinson, J. K., Russo, S. J., et al. (2015) · Neuron · doi:10.1016/j.neuron.2015.10.046 · Cited by 214
Capsid Serotype and Timing of Injection Determines AAV Transduction in the Neonatal Mice Brain
Chakrabarty, P., Rosario, A. M., Cruz, P. E., Siemienski, Z. B., Ceballos‐Diaz, C., Crosby, K. W., Jansen, K. R., Borchelt, D., Kim, J., Jankowsky, J. L., et al. (2013) · PLoS ONE · doi:10.1371/journal.pone.0067680 · Cited by 212
Cellular and molecular introduction to brain development
Jiang, X., & Nardelli, J. (2015) · Neurobiology of Disease · doi:10.1016/j.nbd.2015.07.007 · Cited by 222
Single-cell delineation of lineage and genetic identity in the mouse brain
Bandler, R. C., Vitali, I., Delgado, R. N., Ho, M. C., Dvoretskova, E., Molinas, J. S. I., Frazel, P. W., Mohammadkhani, M., Machold, R. P., Mädler, S. C., et al. (2021) · Nature · doi:10.1038/s41586-021-04237-0 · Cited by 206
Masserdotti, G., Gillotin, S., Sutor, B., Drechsel, D., Irmler, M., Jørgensen, H. F., Sass, S., Theis, F. J., Beckers, J., Berninger, B., et al. (2015) · Cell stem cell · doi:10.1016/j.stem.2015.05.014 · Cited by 194
Evolving Concepts of Gliogenesis: A Look Way Back and Ahead to the Next 25 Years
Freeman, M. R., & Rowitch, D. H. (2013) · Neuron · doi:10.1016/j.neuron.2013.10.034 · Cited by 202
Diverse subtypes of astrocytes and their development during corticogenesis
Tabata, H. (2015) · Frontiers in Neuroscience · doi:10.3389/fnins.2015.00114 · Cited by 213
Multiplex Cell and Lineage Tracking with Combinatorial Labels
Loulier, K., Barry‐Martinet, R., Mahou, P., Franc, Y. L., Supatto, W., Matho, K. S., Ieng, S.-H., Fouquet, S., Dupin, É., Benosman, R. B., et al. (2014) · Neuron · doi:10.1016/j.neuron.2013.12.016 · Cited by 205
Astrocytes in Alzheimer's disease: pathological significance and molecular pathways
Preman, P., Alfonso-Triguero, M., Alberdi, E., Verkhratsky, A., & Arranz, A. M. (2021) · Cells · doi:10.3390/cells10030540 · Cited by 176
MEK Is a Key Regulator of Gliogenesis in the Developing Brain
Li, X., Newbern, J. M., Wu, Y., Morgan-Smith, M., Zhong, J., Charron, J., & Snider, W. D. (2012) · Neuron · doi:10.1016/j.neuron.2012.08.031 · Cited by 174
Cortical astrocytes develop in a plastic manner at both clonal and cellular levels
Clavreul, S., Abdeladim, L., Hernández-Garzón, E., Niculescu, D., Durand, J., Ieng, S.-H., Barry‐Martinet, R., Bonvento, G., Beaurepaire, E., Livet, J., et al. (2019) · Nature Communications · doi:10.1038/s41467-019-12791-5 · Cited by 181
An improved monomeric infrared fluorescent protein for neuronal and tumour brain imaging
Yu, D., Gustafson, W. C., Han, C., Lafaye, C., Noirclerc‐Savoye, M., Ge, W., Thayer, D. A., Huang, H., Kornberg, T. B., Royant, A., et al. (2014) · Nature Communications · doi:10.1038/ncomms4626 · Cited by 162
Self-citationRegion-Specific Transcriptional Control of Astrocyte Function Oversees Local Circuit Activities
Huang, A. Y.-S., Woo, J., Sardar, D., Lozzi, B., Huerta, N. A. B., Lin, C.-C. J., Felice, D., Jain, A., Paulucci-Holthauzen, A. A., & Deneen, B. (2020) · Neuron · doi:10.1016/j.neuron.2020.03.025 · Cited by 162
Chandrasekaran, A., Avci, H. X., Leist, M., Kobolák, J., & Dinnyés, A. (2016) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2016.00215 · Cited by 159
Asymmetric cell division of stem and progenitor cells during homeostasis and cancer
Gómez‐López, S., Lerner, R. G., & Petritsch, C. K. (2013) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-013-1386-1 · Cited by 159
Morphological plasticity of astroglia: Understanding synaptic microenvironment
Heller, J. P., & Rusakov, D. A. (2015) · Glia · doi:10.1002/glia.22821 · Cited by 160
FUCCI sensors: powerful new tools for analysis of cell proliferation
Zielke, N., & Edgar, B. A. (2015) · Wiley Interdisciplinary Reviews Developmental Biology · doi:10.1002/wdev.189 · Cited by 145
PDGF-B Is Required for Development of the Glymphatic System
Munk, A. S. F., Wang, W., Bèchet, N. B., Eltanahy, A. M., Cheng, A. X., Sigurðsson, B., Benraiss, A., Mäe, M. A., Kress, B. T., Kelley, D. H., et al. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.02.050 · Cited by 147
Postnatal development of cerebrovascular structure and the neurogliovascular unit
Coelho‐Santos, V., & Shih, A. Y. (2019) · Wiley Interdisciplinary Reviews Developmental Biology · doi:10.1002/wdev.363 · Cited by 151
A glial blueprint for gliomagenesis
Laug, D., Glasgow, S. M., & Deneen, B. (2018) · Nature reviews. Neuroscience · doi:10.1038/s41583-018-0014-3 · Cited by 143
Windrem, M. S., Schanz, S. J., Morrow, C., Munir, J., Chandler-Militello, D., Wang, S., & Goldman, S. A. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.1510-14.2014 · Cited by 141
Heterogeneity of Astrocytes: From Development to Injury – Single Cell Gene Expression
Rusnakova, V., Honsa, P., Džamba, D., Ståhlberg, A., Kubista, M., & Anděrová, M. (2013) · PLoS ONE · doi:10.1371/journal.pone.0069734 · Cited by 132
Developmental Cell Death in the Cerebral Cortex
Wong, F. K., & Marín, Ó. (2019) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev-cellbio-100818-125204 · Cited by 139
Mechanisms of radial glia progenitor cell lineage progression
Beattie, R., & Hippenmeyer, S. (2017) · FEBS Letters · doi:10.1002/1873-3468.12906 · Cited by 136
Neurovascular Coupling in Development and Disease: Focus on Astrocytes
Stackhouse, T. L., & Mishra, A. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.702832 · Cited by 132
Astrocyte heterogeneity in the brain: from development to disease
Schitine, C., Nogaroli, L., Costa, M. R., & Hedin‐Pereira, C. (2015) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2015.00076 · Cited by 131
Herrero-Navarro, Á., Puche-Aroca, L., Moreno-Juan, V., Sempere-Ferràndez, A., Espinosa, A., Susín, R., Torres-Masjoan, L., Leyva-Díaz, E., Karow, M., Figueres-Oñate, M., et al. (2021) · Science Advances · doi:10.1126/sciadv.abe8978 · Cited by 117
“At this developmental stage, retroviruses only transduce proliferative glia (17).”
BackgroundZbtb20 promotes astrocytogenesis during neocortical development
Nagao, M., Ogata, T., Sawada, Y., & Gotoh, Y. (2016) · Nature Communications · doi:10.1038/ncomms11102 · Cited by 121
YAP stabilizes SMAD1 and promotes BMP2-induced neocortical astrocytic differentiation
Huang, Z., Hu, J., Pan, J., Wang, Y., Hu, G., Zhou, J., Mei, L., & Xiong, W. (2016) · Development · doi:10.1242/dev.130658 · Cited by 116
Astrocytogenesis: where, when, and how
Akdemir, E. S., Huang, A. Y.-S., & Deneen, B. (2020) · F1000Research · doi:10.12688/f1000research.22405.1 · Cited by 119
Decoding Cortical Glial Cell Development
Li, X., Liu, G., Yang, L., Li, Z., Zhang, Z., Xu, Z., Cai, Y., Du, H., Su, Z., Wang, Z., et al. (2021) · Neuroscience Bulletin · doi:10.1007/s12264-021-00640-9 · Cited by 124
Mossink, B., Negwer, M., Schubert, D., & Nadif Kasri, N. (2021) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-020-03714-5 · Cited by 114
Developmental Origins of Astrocyte Heterogeneity: The final frontier of CNS development
Chaboub, L. S., & Deneen, B. (2012) · Developmental Neuroscience · doi:10.1159/000343723 · Cited by 103
Zehnder, T., Petrelli, F., Romanos, J., Figueiredo, E. C. D. O., Lewis, T. L., Déglon, N., Polleux, F., Santello, M., & Bezzi, P. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.108952 · Cited by 112
Verkhratsky, A., Augusto‐Oliveira, M., Pivoriūnas, A., Popov, A., Brazhe, A., & Semyanov, A. V. (2020) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-020-02465-3 · Cited by 110
Cell-type specific mechanisms of D-serine uptake and release in the brain
Martineau, M., Parpura, V., & Mothet, J. (2014) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2014.00012 · Cited by 116
A star is born: new insights into the mechanism of astrogenesis
Kanski, R., van Strien, M. E., van Tijn, P., & Hol, E. M. (2013) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-013-1435-9 · Cited by 119
YAP Is a Critical Inducer of SOCS3, Preventing Reactive Astrogliosis
Huang, Z., Wang, Y., Hu, G., Zhou, J., Mei, L., & Xiong, W. (2015) · Cerebral Cortex · doi:10.1093/cercor/bhv292 · Cited by 110
Wide dispersion and diversity of clonally related inhibitory interneurons
Harwell, C. C., Fuentealba, L. C., Gonzalez-Cerrillo, A., Parker, P. R. L., Gertz, C. C., Mazzola, E., Garcia, M. T., Alvarez-Buylla, A., Cepko, C. L., & Kriegstein, A. R. (2015) · Neuron · doi:10.1016/j.neuron.2015.07.030 · Cited by 106
Activity-dependent modulation of synapse-regulating genes in astrocytes
Farhy-Tselnicker, I., Boisvert, M., Liu, H., Dowling, C. C., Erikson, G. A., Blanco‐Suárez, E., Farhy, C., Shokhirev, M. N., Ecker, J. R., & Allen, N. J. (2021) · eLife · doi:10.7554/elife.70514 · Cited by 108
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Yu, G., Zhang, Y., & Ning, B. (2021) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2021.792764 · Cited by 107
Higashimori, H., Schin, C. S., Chiang, M. S. R., Morel, L., Shoneye, T. A., Nelson, D. L., & Yang, Y. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.1069-16.2016 · Cited by 105
Neuronal and tumourigenic boundaries of glioblastoma plasticity
Silva, M. I. D., Stringer, B. W., & Bardy, C. (2022) · Trends in cancer · doi:10.1016/j.trecan.2022.10.010 · Cited by 110
Lrp4 in astrocytes modulates glutamatergic transmission
Sun, X.-D., Li, L., Liu, F., Huang, Z.-H., Bean, J. C., Jiao, H.-F., Barik, A., Kim, S.-M., Wu, H., Shen, C., et al. (2016) · Nature Neuroscience · doi:10.1038/nn.4326 · Cited by 102
“(c,d) Quantitative analysis of sEPSC frequency (c) and amplitude (d) (3 coculture experiments were performed; n = 11 control neurons co-cultured with control astrocytes; n = 9 control neurons co-cultured with mutant astrocytes; n = 8 mutant neurons co-cultured with control astrocytes; n = 8 mutant neurons co-cultured…”
MethodPuñal, V. M., Paisley, C. E., Brecha, F. S., Lee, M. A., Perelli, R. M., Wang, J., O’Koren, E. G., Ackley, C. R., Saban, D. R., Reese, B. E., et al. (2019) · PLoS Biology · doi:10.1371/journal.pbio.3000492 · Cited by 107
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Sohn, J., Orosco, L. A., Guo, F., Chung, S., Bannerman, P. G. C., Ko, E. M., Zarbalis, K., Deng, W., & Pleasure, D. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.3454-14.2015 · Cited by 98
Beattie, R., Postiglione, M. P., Burnett, L. E., Laukoter, S., Streicher, C., Pauler, F. M., Xiao, G., Klezovitch, O., Vasioukhin, V. I., Ghashghaei, T., et al. (2017) · Neuron · doi:10.1016/j.neuron.2017.04.012 · Cited by 100
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Abdeladim, L., Matho, K. S., Clavreul, S., Mahou, P., Sintès, J.-M., Solinas, X., Arganda‐Carreras, I., Turney, S. G., Lichtman, J. W., Chessel, A., et al. (2019) · Nature Communications · doi:10.1038/s41467-019-09552-9 · Cited by 103
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Cohen‐Salmon, M., Slaoui, L., Mazaré, N., Gilbert, A., Oudart, M., Alvear‐Perez, R., Elorza‐Vidal, X., Chever, O., & Boulay, A. (2021) · Glia · doi:10.1002/glia.23924 · Cited by 93
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Namihira, M., & Nakashima, K. (2013) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2013.06.002 · Cited by 93
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Yang, Y., Higashimori, H., & Morel, L. (2013) · Journal of Neurodevelopmental Disorders · doi:10.1186/1866-1955-5-22 · Cited by 99
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Abbink, M. R., van Deijk, A. F., Heine, V. M., Verheijen, M. H. G., & Kőrösi, A. (2019) · Glia · doi:10.1002/glia.23625 · Cited by 95
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Gao, X., Zhang, Z., Mashimo, T., Shen, B., Nyagilo, J. O., Wang, H., Wang, Y., Liu, Z., Mulgaonkar, A., Hu, X.-L., et al. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.01.089 · Cited by 90
Self-citationSex differences in developmental patterns of neocortical astroglia: A mouse translatome database
Rurak, G. M., Simard, S., Andrade, M. F., Lacoste, B., Charih, F., Geel, A. V., Stead, J. D. H., Woodside, B. C., Green, J. R., Coppola, G., et al. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.110310 · Cited by 91
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Gil, C., Espinosa, A., Fregoso, S. P., Bluske, K. K., Cunningham, C. L., Martínez‐Garay, I., Zeng, H., Franco, S. J., & Müller, U. (2015) · Neuron · doi:10.1016/j.neuron.2015.04.019 · Cited by 95
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Figueiredo, E. C. D. O., Calì, C., Petrelli, F., & Bezzi, P. (2022) · Glia · doi:10.1002/glia.24221 · Cited by 87
Metadata
- Authors
- Ge, W.-P., Miyawaki, A., Gage, F. H., Jan, Y. N., & Jan, L. Y.
- Affiliations
- Howard Hughes Medical Institute (US)
- Japan Science and Technology Agency (JP)
- Salk Institute for Biological Studies (US)
- Corresponding author
- Jan, Lily Yeh
- Venue
- Nature
- Published
- 2012-03-28
- Volume
- 484
- Issue
- 7394
- Pages
- 376-380
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- PMC
- PMC3777276
- OpenAlex
- W2163958669
- Cited by
- 507
- References
- 36
- Citations by year
- 2026: 20 · 2025: 30 · 2024: 44 · 2023: 47 · 2022: 44 · 2021: 40 · 2020: 40 · 2019: 37 · 2018: 30 · 2017: 21 · 2016: 32 · 2015: 42 · 2014: 29 · 2013: 36 · 2012: 14
- FWCI
- 13.02
- Type
- journal article
- Language
- en
- Open access
- green
- europepmc.org
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- Funders
- Howard Hughes Medical Institute
- National Institute on Aging (P01AG010435)
- National Institute of Mental Health (R01MH090258, R01MH084234, R37MH065334, MH090258)
- National Institute of Neurological Disorders and Stroke (R00NS073735, K99NS073735)
- Topics
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Keywords
- astrocyte proliferation, astrocyte endfeet, glutamate uptake, radial glia, symmetric cell division, astrocyte development, mouse brain
- MeSH terms
- Animals, Animals, Newborn, Astrocytes, Cell Differentiation, Cell Division, Cerebral Cortex, Mice, Transgenic, Neuroglia, Glutamic Acid, Cell Lineage, Cell Proliferation, Mice, Time-Lapse Imaging
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