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The Glial Nature of Embryonic and Adult Neural Stem Cells
Open accessAbstract
Glial cells were long considered end products of neural differentiation, specialized supportive cells with an origin very different from that of neurons. New studies have shown that some glial cells—radial glia (RG) in development and specific subpopulations of astrocytes in adult mammals—function as primary progenitors or neural stem cells (NSCs). This is a fundamental departure from classical views separating neuronal and glial lineages early in development. Direct visualization of the behavior of NSCs and lineage-tracing studies reveal how neuronal lineages emerge. In development and in the adult brain, many neurons and glial cells are not the direct progeny of NSCs, but instead originate from transit amplifying, or intermediate, progenitor cells (IPCs). Within NSCs and IPCs, genetic programs unfold for generating the extraordinary diversity of cell types in the central nervous system. The timing in development and location of NSCs, a property tightly linked to their neuroepithelial origin, appear to be the key determinants of the types of neurons generated. Identification of NSCs and IPCs is critical to understand brain development and adult neurogenesis and to develop new strategies for brain repair.
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“GFAP is also expressed by progenitor cells15 and its expression depends on developmental stages16,17.”
From Reactive astrocyte nomenclature, definitions, and future directions (2021) · cites this paper as [15]
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In the citing paper
“In particular, and by taking advantage of Btg2 and Tubb3 expression, our group has generated a combinatorial, double-reporter mouse line in which RFP and or GFP expression allowed the isolation specifically of PP, DP and N based on their endogenous fluorescence (RFP-, RFP+ and GFP+, respectively) (31).”
From MicroRNA profiling of mouse cortical progenitors and neurons reveals miR-486-5p as a regulator of neurogenesis (2020) · cites this paper as [31]
Experimental — accuracy not yet measuredThe check wasn’t confident either way, so it gives no verdict — never disputed.
In the citing paper
“Unsurprisingly, when analyzing the expression pattern of the host genes of switch miRNAs (data retrieved from ( 31)), we found a high degree of overlap in their differential expression within different cell populations (Figure 3).”
From MicroRNA profiling of mouse cortical progenitors and neurons reveals miR-486-5p as a regulator of neurogenesis (2020) · cites this paper as [31]
Experimental — accuracy not yet measuredIn the citing paper
“There is evidence of neurogenesis from adult neural stem cells deriving from the subventricular zone (SVZ) and the subgranular zone (SGZ) of the hippocampal dentate gyrus, that can give rise to neurons, oligodendrocytes and astrocytes [107,108].”
From Ageing, Cellular Senescence and Neurodegenerative Disease (2018) · cites this paper as [108]
In the citing paper
“The predicted progenitors expressed proliferation (Mki67) and known markers (Pax6, Rspo2/3, Wnt5a/3a/1, Fabp7, clusters 7 and 8 in Figure 2A,B S2B; STAR Methods), previously reported for precursors of ependymal cells and cortical neurons (Kriegstein and Alvarez-Buylla, 2009), with Wnt1 having the most specific expression (Figure S2G).”
From A cellular and spatial map of the choroid plexus across brain ventricles and ages (2021) · cites this paper as Kriegstein and Alvarez-Buylla, 2009
In the citing paper
“In embryos, subsets of glial cells expressed markers of neural progenitor/stem-like cells (e.g. Pax6, Nes, Sox2, Rspo2/3) or of oligodendrocyte precursor cells (OPCs, e.g. Olig1, Olig2) (Kriegstein and Alvarez-Buylla, 2009) (Figure 2A, S2A,B).”
From A cellular and spatial map of the choroid plexus across brain ventricles and ages (2021) · cites this paper as Kriegstein and Alvarez-Buylla, 2009
In the citing paper
“Validation and use of this mouse line revealed to be very powerful in the identification of several new genes and biological processes regulating cortical development (31).”
From MicroRNA profiling of mouse cortical progenitors and neurons reveals miR-486-5p as a regulator of neurogenesis (2020) · cites this paper as [31]
In the citing paper
“our group previously concluded that a transient up-or down-regulation specifically in DP compared to both their PP progenitors and N progeny (on-and off-switch transcripts, respectively) represented a hallmark of functional commitment to the neurogenic lineage (31,36).”
From MicroRNA profiling of mouse cortical progenitors and neurons reveals miR-486-5p as a regulator of neurogenesis (2020) · cites this paper as [31]
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Citations
Cites
Neurogenesis in the adult human hippocampus
Eriksson, P. S., Perfilieva, E., Björk-Eriksson, T., Alborn, A.-M., Nordborg, C., Peterson, D. A., & Gage, F. H. (1998) · Nature Medicine · doi:10.1038/3305 · Cited by 6,369
Gage, F. H. (2000) · Science · doi:10.1126/science.287.5457.1433 · Cited by 4,786
Requirement of hippocampal neurogenesis for the behavioral effects of antidepressants
Santarelli, L., Saxe, M., Gross, C., Surget, A., Battaglia, F., Dulawa, S., Weisstaub, N., Lee, J., Duman, R., Arancio, O., et al. (2003) · Science · doi:10.1126/science.1083328 · Cited by 4,321
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
Autoradiographic and histological evidence of postnatal hippocampal neurogenesis in rats
Altman, J., & Das, G. D. (1965) · Journal of Comparative Neurology · doi:10.1002/cne.901240303 · Cited by 3,592
More hippocampal neurons in adult mice living in an enriched environment
Kempermann, G., Kuhn, H. G., & Gage, F. H. (1997) · Nature · doi:10.1038/386493a0 · Cited by 3,586
Specification of Cerebral Cortical Areas
Rakic, P. (1988) · Science · doi:10.1126/science.3291116 · Cited by 3,127 · cited 1×
“Astrocytes may retain fundamental properties and positional information linked to the original array of RG in the developing brain (Rakic 1988).”
BackgroundMechanisms and Functional Implications of Adult Neurogenesis
Zhao, C., Deng, W., & Gage, F. H. (2008) · Cell · doi:10.1016/j.cell.2008.01.033 · Cited by 3,007
Running enhances neurogenesis, learning, and long-term potentiation in mice
van Praag, H., Christie, B. R., Sejnowski, T. J., & Gage, F. H. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.23.13427 · Cited by 2,904
Inflammatory Blockade Restores Adult Hippocampal Neurogenesis
Monje, M. L., Toda, H., & Palmer, T. D. (2003) · Science · doi:10.1126/science.1088417 · Cited by 2,426
Research works printed but not linked: 7
- 10.1016/S0092-8674(00)80783-7 · DOI · Paper page
- Hajós F, 1981, Acta Morphol. Acad. Sci. Hung., 29, 361
- Magini J, 1888, Arch. Ital. Biol., 10, 384
- Miyata T, 2008, Dev. Growth Differ., 50, S105
- Retzius G, 1894, Biol. Unters., 6, 1
- Smart IH, 1973, J. Anat., 116, 67
- 10.1523/JNEUROSCI.18-20-08331.1998 · DOI
Cited by
Sorted by citations
Items 401–500 of 1,011
Radial Glia: Progenitor, Pathway, and Partner
Sild, M., & Ruthazer, E. S. (2011) · The Neuroscientist · doi:10.1177/1073858410385870 · Cited by 83
D-cysteine is an endogenous regulator of neural progenitor cell dynamics in the mammalian brain
Semenza, E. R., Harraz, M. M., Abramson, E., Malla, A. P., Vasavda, C., Gadalla, M. M., Kornberg, M. D., Snyder, S. H., & Roychaudhuri, R. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2110610118 · Cited by 80
Kim, H. J., & Chuang, D. (2014) · Europe PMC (PubMed Central) · Cited by 79
Transcriptional control of vertebrate neurogenesis by the proneural factor Ascl1
Vasconcelos, F. F., & Castro, D. S. (2014) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2014.00412 · Cited by 81
Endesfelder, S., Makki, H., von Haefen, C., Spies, C., Bührer, C., & Sifringer, M. (2017) · PLoS ONE · doi:10.1371/journal.pone.0171498 · Cited by 79
FOXP1 Promotes Embryonic Neural Stem Cell Differentiation by Repressing Jagged1 Expression
Braccioli, L., Vervoort, S. J., Adolfs, Y., Heijnen, C. J., Başak, O., Pasterkamp, R. J., Nijboer, C. H. A., & Coffer, P. J. (2017) · Stem Cell Reports · doi:10.1016/j.stemcr.2017.10.012 · Cited by 79
Cellular and Molecular Mechanisms Linking Human Cortical Development and Evolution
Libé-Philippot, B., & Vanderhaeghen, P. (2021) · Annual Review of Genetics · doi:10.1146/annurev-genet-071719-020705 · Cited by 78
MicroRNA Function in the Nervous System
Fiore, R., Khudayberdiev, S., Saba, R., & Schratt, G. M. (2011) · Progress in molecular biology and translational science · doi:10.1016/b978-0-12-415795-8.00004-0 · Cited by 80
Mechanisms that regulate the number of neurons during mouse neocortical development
Miyata, T., Kawaguchi, D., Kawaguchi, A., & Gotoh, Y. (2010) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2010.01.001 · Cited by 78
Isolation and differentiation properties of neural crest stem cells
Dupin, É., & Coelho‐Aguiar, J. M. (2012) · Cytometry Part A · doi:10.1002/cyto.a.22098 · Cited by 81
Selvaraj, V., Plane, J. M., Williams, A. J., & Deng, W. (2010) · Trends in biotechnology · doi:10.1016/j.tibtech.2010.01.002 · Cited by 83
New neurons in adult brain: distribution, molecular mechanisms and therapies
Pino, A., Fumagalli, G. F., Bifari, F., & Decimo, I. (2017) · Biochemical Pharmacology · doi:10.1016/j.bcp.2017.07.003 · Cited by 83
Pellegrino, G., Trubert, C., Terrien, J., Pifferi, F., Leroy, D., Loyens, A., Migaud, M., Baroncini, M., Maurage, C., Fontaine, C., et al. (2017) · The Journal of Comparative Neurology · doi:10.1002/cne.24376 · Cited by 78
Astrocytes: Heterogeneous and Dynamic Phenotypes in Neurodegeneration and Innate Immunity
Cunningham, C. M., Dunne, A., & López-Rodríguez, A. B. (2018) · The Neuroscientist · doi:10.1177/1073858418809941 · Cited by 80
Cohen, E., Allen, S. R., Sawyer, J. K., & Fox, D. T. (2018) · eLife · doi:10.7554/elife.38327 · Cited by 77
Developmental and evolutionary dynamics of cis-regulatory elements in mouse cerebellar cells
Sarropoulos, I., Sepp, M., Frömel, R., Leiss, K., Trost, N., Leushkin, E. V., Okonechnikov, K., Joshi, P. K., Giere, P., Kutscher, L. M., et al. (2021) · Science · doi:10.1126/science.abg4696 · Cited by 79
van Bruggen, D., Pohl, F. B., Langseth, C. M., Kukanja, P., Lee, H., Albiach, A. M., Kabbe, M., Meijer, M., Linnarsson, S., Hilscher, M. M., et al. (2022) · Developmental Cell · doi:10.1016/j.devcel.2022.04.016 · Cited by 87
The impact of neuroinflammation on neuronal integrity
Tastan, B., & Heneka, M. T. (2024) · Immunological Reviews · doi:10.1111/imr.13419 · Cited by 81
Avet‐Rochex, A., Kaul, A. K., Gatt, A. P., McNeill, H., & Bateman, J. E. (2012) · Development · doi:10.1242/dev.074179 · Cited by 77
Characterization of the ventricular-subventricular stem cell niche during human brain development
Coletti, A., Singh, D., Kumar, S., Shafin, T. N., Briody, P. J., Babbitt, B. F., Pan, D., Norton, E. S., Brown, E. C., Kahle, K. T., et al. (2018) · Development · doi:10.1242/dev.170100 · Cited by 76
Astrocytes in Multiple Sclerosis—Essential Constituents with Diverse Multifaceted Functions
Aharoni, R., Eilam, R., & Arnon, R. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22115904 · Cited by 81
Mechanisms for complexity in the brain: generating the insect central complex
Boyan, G., & Reichert, H. (2011) · Trends in Neurosciences · doi:10.1016/j.tins.2011.02.002 · Cited by 76
Dillen, Y., Kemps, H., Gervois, P., Wolfs, E., & Bronckaers, A. (2019) · Translational Stroke Research · doi:10.1007/s12975-019-00717-8 · Cited by 79
Lv, X., Ren, S., Zhang, X., Shen, Z., Ghosh, T., Xianyu, A., Gao, P., Li, Z., Lin, S., Yu, Y., et al. (2019) · Nature Communications · doi:10.1038/s41467-019-11854-x · Cited by 79
Function-related structural plasticity of the GnRH system
Prévot, V., Hanchate, N. K., Bellefontaine, N., Sharif, A., Parkash, J., Estrella, C., Allet, C., Seranno, S. D., Campagne, C., de Tassigny, X. D., et al. (2010) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2010.05.003 · Cited by 82
Qin, S., & Zhang, C. (2012) · Molecular and Cellular Biology · doi:10.1128/mcb.00838-12 · Cited by 78
Samuels, T. J., Järvelin, A. I., Ish‐Horowicz, D., & Davis, I. (2020) · eLife · doi:10.7554/elife.51529 · Cited by 75
Convergent microRNA actions coordinate neocortical development
Barca‐Mayo, O., & Tonelli, D. D. P. (2014) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-014-1576-5 · Cited by 79
The regulation of cortical neurogenesis
Villalba, A., Götz, M., & Borrell, V. (2020) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/bs.ctdb.2020.10.003 · Cited by 80
Expression of the Norrie disease gene (Ndp) in developing and adult mouse eye, ear, and brain
Ye, X., Smallwood, P. M., & Nathans, J. (2010) · Gene Expression Patterns · doi:10.1016/j.gep.2010.10.007 · Cited by 76
Cancer Stem Cells in Glioblastoma Multiforme
Bradshaw, A., Wickremesekera, A., Brasch, H. D., Chibnall, A. M., Davis, P. F., Tan, S. T., & Itinteang, T. (2016) · Frontiers in Surgery · doi:10.3389/fsurg.2016.00048 · Cited by 81
Imp and Syp RNA-binding proteins govern decommissioning of Drosophila neural stem cells
Yang, C.-P., Samuels, T. J., Huang, Y., Yang, L., Ish‐Horowicz, D., Davis, I., & Lee, T. (2017) · Development · doi:10.1242/dev.149500 · Cited by 74
Santana, J., & Marzolo, M. (2017) · Biochemical Journal · doi:10.1042/bcj20160628 · Cited by 76
Shin, J. E., Jung, K., Kim, M., Hwang, K., Lee, H.-J., Kim, I., Lee, B. H., Lee, I.-S., & Park, K. I. (2018) · Experimental & Molecular Medicine · doi:10.1038/s12276-018-0054-9 · Cited by 73
Notter, T. (2021) · Brain and Neuroscience Advances · doi:10.1177/23982128211009148 · Cited by 75
Developmental Origins of Human Cortical Oligodendrocytes and Astrocytes
Yang, L., Li, Z., Liu, G., Li, X., & Yang, Z. (2021) · Neuroscience Bulletin · doi:10.1007/s12264-021-00759-9 · Cited by 75
Astrocyte development in the cerebral cortex: Complexity of their origin, genesis, and maturation
Clavreul, S., Dumas, L., & Loulier, K. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2022.916055 · Cited by 80
Neocortical neurogenesis and neuronal migration
Tan, X., & Shi, S. (2012) · Wiley Interdisciplinary Reviews Developmental Biology · doi:10.1002/wdev.88 · Cited by 85
Astrocytes in neurodegenerative diseases (I): function and molecular description
Guillamón-Vivancos, T., Gómez‐Pinedo, U., & Matías‐Guiu, J. (2015) · Neurología (English Edition) · doi:10.1016/j.nrleng.2014.12.005 · Cited by 75
Herzog, D., Lötscher, P., van Hengel, J., Knüsel, S., Brakebusch, C., Taylor, V., Suter, U., & Relvas, J. B. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.4807-10.2011 · Cited by 75
DeBoer, E. M., Azevedo, R., Vega, T. A., Brodkin, J., Akamatsu, W., Okano, H., Wagner, G. C., & Rasin, M.-R. (2014) · The Journal of Neuroscience · doi:10.1523/jneurosci.3703-13.2014 · Cited by 72
Hedgehog trafficking, cilia and brain functions
Ruat, M., Roudaut, H., Ferent, J., & Traiffort, É. (2011) · Differentiation · doi:10.1016/j.diff.2011.11.011 · Cited by 81
Genetic Architectures and Cell-of-Origin in Glioblastoma
Kim, H. J., Park, J. W., & Lee, J. H. (2021) · Frontiers in Oncology · doi:10.3389/fonc.2020.615400 · Cited by 69
Xie, Y., Jüschke, C., Esk, C., Hirotsune, S., & Knoblich, J. A. (2013) · Neuron · doi:10.1016/j.neuron.2013.05.027 · Cited by 75
Doobin, D. J., Kemal, S., Dantas, T. J., & Vallee, R. B. (2016) · Nature Communications · doi:10.1038/ncomms12551 · Cited by 73
The Role of Lipid Metabolism for Neural Stem Cell Regulation
Knobloch, M. (2017) · Brain Plasticity · doi:10.3233/bpl-160035 · Cited by 78
Ex vivo gene therapy for the treatment of neurological disorders
Gowing, G., Svendsen, S. P., & Svendsen, C. N. (2017) · Progress in brain research · doi:10.1016/bs.pbr.2016.11.003 · Cited by 74
Melrose, J. (2018) · Journal of Neurochemistry · doi:10.1111/jnc.14652 · Cited by 72
Blood Vessels as Regulators of Neural Stem Cell Properties
Karakatsani, A., Shah, B., & de Almodóvar, C. R. (2019) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2019.00085 · Cited by 77
Prospective isolation of adult neural stem cells from the mouse subependymal zone
Fischer, J., Beckervordersandforth, R., Tripathi, P., Steiner-Mezzadri, A., Ninkovic, J., & Götz, M. (2011) · Nature Protocols · doi:10.1038/nprot.2011.412 · Cited by 71
Neuroinflammation and Glial Phenotypic Changes in Alpha-Synucleinopathies
Refolo, V., & Stefanova, N. (2019) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2019.00263 · Cited by 72
Multiplexed spatial mapping of chromatin features, transcriptome and proteins in tissues
Guo, P., Mao, L., Chen, Y., Lee, C. N., Cardilla, A., Li, M., Bartošovič, M., & Deng, Y. (2025) · Nature Methods · doi:10.1038/s41592-024-02576-0 · Cited by 71
klumpfuss distinguishes stem cells from progenitor cells during asymmetric neuroblast division
Qi, X., Komori, H., & Lee, C. (2012) · Development · doi:10.1242/dev.081687 · Cited by 71
Distinct and separable roles for EZH2 in neurogenic astroglia
Hwang, W. W., Salinas, R. D., Siu, J. J., Kelley, K. W., Delgado, R. N., Paredes, M. F., Álvarez-Buylla, A., Oldham, M. C., & Lim, D. A. (2014) · eLife · doi:10.7554/elife.02439 · Cited by 76
Large-scale live imaging of adult neural stem cells in their endogenous niche
Dray, N., Bedu, S., Vuillemin, N., Alunni, A., Coolen, M., Krecsmarik, M., Supatto, W., Beaurepaire, E., & Bally‐Cuif, L. (2015) · Development · doi:10.1242/dev.123018 · Cited by 71
Optimizing neuronal differentiation from induced pluripotent stem cells to model ASD
Kim, D.-S., Ross, P. J., Zaslavsky, K., & Ellis, J. (2014) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2014.00109 · Cited by 70
Li, W., Chen, G., Liu, M., Zheng, J., Xu, Y., & He, Q. (2019) · Neural Regeneration Research · doi:10.4103/1673-5374.265185 · Cited by 72
Dong, X., Zhang, Q., Yu, X., Wang, D., Ma, J., Ma, J., & Shi, S. (2022) · Nature Neuroscience · doi:10.1038/s41593-022-01093-7 · Cited by 70
Distinctive effects of arachidonic acid and docosahexaenoic acid on neural stem /progenitor cells
Sakayori, N., Maekawa, M., Numayama‐Tsuruta, K., Katura, T., Moriya, T., & Osumi, N. (2011) · Genes to Cells · doi:10.1111/j.1365-2443.2011.01527.x · Cited by 70
MicroRNA Regulation of Embryonic Stem Cell Self-Renewal and Differentiation
Melton, C. A., & Blelloch, R. H. (2010) · Advances in experimental medicine and biology · doi:10.1007/978-1-4419-7037-4_8 · Cited by 72
Garcίa, M. T., Chang, Y., Arai, Y., & Huttner, W. Β. (2015) · The Journal of Comparative Neurology · doi:10.1002/cne.23801 · Cited by 77
Visualization and genetic manipulation of adult neurogenesis using transgenic mice
Dhaliwal, J., & Lagace, D. C. (2011) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2011.07600.x · Cited by 74
Llorens, F., Gil, V., & del Río, J. A. (2010) · The FASEB Journal · doi:10.1096/fj.10-162792 · Cited by 72
P2X7 receptors at adult neural progenitor cells of the mouse subventricular zone
Messemer, N., Kunert, C., Grohmann, M., Sobottka, H., Nieber, K., Zimmermann, H., Franke, H., Nörenberg, W., Straub, I., Schaefer, M., et al. (2013) · Neuropharmacology · doi:10.1016/j.neuropharm.2013.05.017 · Cited by 70
Genetic Methods to Identify and Manipulate Newly Born Neurons in the Adult Brain
Imayoshi, I., Sakamoto, M., & Kageyama, R. (2011) · Frontiers in Neuroscience · doi:10.3389/fnins.2011.00064 · Cited by 73
RNA on the brain: emerging layers of post‐transcriptional regulation in cerebral cortex development
Lennox, A. L., Mao, H., & Silver, D. L. (2017) · Wiley Interdisciplinary Reviews Developmental Biology · doi:10.1002/wdev.290 · Cited by 73
Neural responses to electrical stimulation in 2D and 3D in vitro environments
Bertucci, C., Koppes, R. A., Dumont, C. M., & Koppes, A. N. (2019) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2019.07.016 · Cited by 71
Radial glia and radial glia-like cells: Their role in neurogenesis and regeneration
Miranda-Negrón, Y., & García‐Arrarás, J. E. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2022.1006037 · Cited by 74
Inside-Out Radial Migration Facilitates Lineage-Dependent Neocortical Microcircuit Assembly
He, S., Li, Z., Ge, S., Yu, Y., & Shi, S. (2015) · Neuron · doi:10.1016/j.neuron.2015.05.002 · Cited by 74
The roles and regulation of Polycomb complexes in neural development
Corley, M., & Kroll, K. L. (2014) · Cell and Tissue Research · doi:10.1007/s00441-014-2011-9 · Cited by 76
Robo1 Modulates Proliferation and Neurogenesis in the Developing Neocortex
Yeh, M. L., Gonda, Y., Mommersteeg, M. T. M., Barber, M., Ypsilanti, A. R., Hanashima, C., Parnavelas, J. G., & Andrews, W. D. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.4256-13.2014 · Cited by 76
Adherens Junctions: Guardians of Cortical Development
Veeraval, L., O’Leary, C. J., & Cooper, H. M. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.00006 · Cited by 74
Liu, W. A., Chen, S., Li, Z., Lee, C. H., Mirzaa, G., Dobyns, W. B., Ross, M. E., Zhang, J., & Shi, S. (2018) · Genes & Development · doi:10.1101/gad.313171.118 · Cited by 77
Long-term culture of astrocytes attenuates the readily releasable pool of synaptic vesicles
Kawano, H., Katsurabayashi, S., Kakazu, Y., Yamashita, Y., Kubo, N., Kubo, M., Okuda, H., Takasaki, K., Kubota, K., Mishima, K., et al. (2012) · PLoS ONE · doi:10.1371/journal.pone.0048034 · Cited by 68
More Than Mortar: Glia as Architects of Nervous System Development and Disease
Lago‐Baldaia, I., Fernandes, V. M., & Ackerman, S. D. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.611269 · Cited by 74
Distinct progenitor behavior underlying neocortical gliogenesis related to tumorigenesis
Shen, Z., Lin, Y., Yang, J., Jörg, D. J., Peng, Y., Zhang, X., Xu, Y., Hernandez, L., Ma, J., Simons, B. D., et al. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.108853 · Cited by 70
SREBPs: SREBP function in glia–neuron interactions
Camargo, N., Smit, A. B., & Verheijen, M. H. G. (2008) · FEBS Journal · doi:10.1111/j.1742-4658.2008.06808.x · Cited by 76
Leone, D. P., Srinivasan, K., Brakebusch, C., & McConnell, S. K. (2010) · Developmental Neurobiology · doi:10.1002/dneu.20804 · Cited by 70
Huang, Z., Sun, D., Hu, J., Tang, F., Lee, D., Wang, Y., Hu, G., Zhu, X., Zhou, J., Mei, L., et al. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.4487-15.2016 · Cited by 68
Andreu, Z., Khan, M. A., González‐Gómez, P., Negueruela, S., Hortigüela, R., Emeterio, J. S., Ferrón, S. R., Martínez, G., Vidal, A., Fariñas, I., et al. (2014) · Stem Cells · doi:10.1002/stem.1832 · Cited by 67
Spinal cord tumours: advances in genetics and their implications for treatment
Zadnik, P. L., Gokaslan, Z. L., Burger, P. C., & Bettegowda, C. (2013) · Nature Reviews Neurology · doi:10.1038/nrneurol.2013.48 · Cited by 67
Ma, S., Kwon, H. J., & Huang, Z. (2012) · PLoS ONE · doi:10.1371/journal.pone.0048001 · Cited by 67
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Hu, X.-L., Chen, G., Zhang, S., Zheng, J., Wu, J., Bai, Q., Wang, Y., Li, J., Wang, H., Han, F., et al. (2017) · Neuron · doi:10.1016/j.neuron.2017.06.047 · Cited by 70
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Mora‐Bermúdez, F., Matsuzaki, F., & Huttner, W. Β. (2014) · eLife · doi:10.7554/elife.02875 · Cited by 73
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Gorris, R., Fischer, J., Erwes, K. L., Kesavan, J., Peterson, D. A., Alexander, M., Nöthen, M. M., Peitz, M., Quandel, T., Karus, M., et al. (2015) · Glia · doi:10.1002/glia.22882 · Cited by 66
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Metadata
- Authors
- Kriegstein, A., & Alvarez-Buylla, A.
- Affiliations
- University of California, San Francisco (US)
- The Eli and Edythe Broad Center of Regeneration Medicine and Stem Cell Research, Departments of Neurology, Neurological Surgery, and School of Medicine, University of California, San Francisco, California 94143-0525;,
- ORCID
- Kriegstein, Arnold
- Venue
- Annual Review of Neuroscience
- Publisher
- Annual Reviews
- Published
- 2009-06-01
- Volume
- 32
- Issue
- 1
- Pages
- 149-184
- ISSN
- 0147-006X (ISSN-L)
- 1545-4126
- PMC
- PMC3086722
- OpenAlex
- W2172266256
- Cited by
- 2,475
- References
- 263
- Citations by year
- 2026: 87 · 2025: 141 · 2024: 138 · 2023: 131 · 2022: 133 · 2021: 168 · 2020: 162 · 2019: 147 · 2018: 166 · 2017: 155 · 2016: 162 · 2015: 129 · 2014: 167 · 2013: 172 · 2012: 155
- FWCI
- 12.34
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Annual Review of Neuroscience (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institute of Neurological Disorders and Stroke (R01NS035710, R01NS028478, R01NS021223)
- Topics
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Keywords
- neural stem cells, radial glia, astrocytes, intermediate progenitor cells, transit amplifying cells, neuronal lineage, neuroepithelium, adult neurogenesis, brain development, lineage tracing, brain repair
- MeSH terms
- Animals, Cell Differentiation, Central Nervous System, Humans, Neuroglia, Neurons, Stem Cells, Gene Expression Regulation, Developmental, Cell Lineage, Adult Stem Cells, Neurogenesis
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