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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]
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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 901–1,000 of 1,011
Calvo‐Ochoa, E., Byrd-Jacobs, C. A., & Fuss, S. H. (2020) · Cell and Tissue Research · doi:10.1007/s00441-020-03334-2 · Cited by 35
Cell Polarity and Neurogenesis in Embryonic Stem Cell-Derived Neural Rosettes
Banda, E. C., McKinsey, A. G., Germain, N. D., Carter, J., Anderson, N. C., & Grabel, L. B. (2014) · Stem Cells and Development · doi:10.1089/scd.2014.0415 · Cited by 35
Viktorin, G., Riebli, N., & Reichert, H. (2013) · Developmental Biology · doi:10.1016/j.ydbio.2013.04.020 · Cited by 33
A new approach to manipulate the fate of single neural stem cells in tissue
Taverna, E., Haffner, C., Pepperkok, R., & Huttner, W. Β. (2011) · Nature Neuroscience · doi:10.1038/nn.3008 · Cited by 33
Transcriptional Regulation of Olfactory Bulb Neurogenesis
Díaz‐Guerra, E., Pignatelli, J., Nieto‐Estévez, V., & Vicario‐Abejón, C. (2013) · The Anatomical Record · doi:10.1002/ar.22733 · Cited by 33
Wu, Z., Li, D., Huang, Y., Chen, X., Huang, W., Liu, C., Zhao, H., Xu, R., Cheng, M., Schachner, M., et al. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhv318 · Cited by 34
Sá, J. V., Kleiderman, S., Brito, C., Sonnewald, U., Leist, M., Teixeira, A. P., & Alves, P. M. (2016) · Neurochemical Research · doi:10.1007/s11064-016-1907-z · Cited by 33
Xu, Z. C., Wang, W., Ren, Y., Zhang, W., Fang, P., Huang, L., Wang, X., & Shi, P. (2017) · Biomaterials · doi:10.1016/j.biomaterials.2017.12.010 · Cited by 33
Involvement of Wnt7a in the role of M2c microglia in neural stem cell oligodendrogenesis
Mecha, M., Yanguas‐Casás, N., Feliú, A., Mestre, L., Carrillo-Salinas, F. J., Riecken, K., Gómez‐Nicola, D., & Guaza, C. (2020) · Journal of Neuroinflammation · doi:10.1186/s12974-020-01734-3 · Cited by 33
Brains in metamorphosis: reprogramming cell identity within the central nervous system
Arlotta, P., & Berninger, B. (2014) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2014.04.007 · Cited by 32
Radial Glia, the Keystone of the Development of the Hippocampal Dentate Gyrus
Xu, L., Tang, X., Wang, Y., Xu, H., & Fan, X. (2014) · Molecular Neurobiology · doi:10.1007/s12035-014-8692-y · Cited by 36
Wu, S., Esumi, S., Watanabe, K., Chen, J., Nakamura, K., Nakamura, K., Kometani, K., Minato, N., Yanagawa, Y., Akashi, K., et al. (2011) · Development · doi:10.1242/dev.063032 · Cited by 35
Welker, A. M., Jaros, B. D., An, M. J., & Beattie, C. E. (2017) · Neuroscience · doi:10.1016/j.neuroscience.2017.05.010 · Cited by 35
Wang, Y., Guo, Y., Tang, C., Han, X. W., Xu, M., Sun, J., Zhao, Y., Zhang, Y., Wang, M., Cao, X., et al. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.10.127 · Cited by 33
Perinatal Opioid Exposure Primes the Peripheral Immune System Toward Hyperreactivity
Newville, J., Maxwell, J. R., Kitase, Y., Robinson, S., & Jantzie, L. L. (2020) · Frontiers in Pediatrics · doi:10.3389/fped.2020.00272 · Cited by 32
The Effects of YAP and Its Related Mechanisms in Central Nervous System Diseases
Jin, J., Zhao, X., Fu, H., & Gao, Y. (2020) · Frontiers in Neuroscience · doi:10.3389/fnins.2020.00595 · Cited by 36
Seki, T. (2020) · Frontiers in Neuroscience · doi:10.3389/fnins.2020.00839 · Cited by 32
Stem cells for the treatment of glioblastoma: a 20-year perspective
Calinescu, A., Kauss, M. C., Sultan, Z., Al‐Holou, W. N., & O’Shea, S. (2021) · CNS Oncology · doi:10.2217/cns-2020-0026 · Cited by 33
Gillotin, S., Sahni, V., Lepko, T., Hanspal, M. A., Swartz, J., Alexopoulou, Z., & Marshall, F. H. (2021) · Ageing Research Reviews · doi:10.1016/j.arr.2021.101447 · Cited by 34
Sonic hedgehog as a chemoattractant for adult NPCs
Hor, C. H. H., & Tang, B. L. (2010) · Cell Adhesion & Migration · doi:10.4161/cam.4.1.9914 · Cited by 32
Deregulated proliferation and differentiation in brain tumors
Swartling, F. J., Čančer, M., Frantz, A., Weishaupt, H., & Persson, A. I. (2014) · Cell and Tissue Research · doi:10.1007/s00441-014-2046-y · Cited by 32
Yu, D., Dong, Z., Gustafson, W. C., Ruiz‐González, R., Signor, L., Marzocca, F., Borel, F., Klassen, M. P., Makhijani, K., Royant, A., et al. (2015) · Protein Science · doi:10.1002/pro.2843 · Cited by 32
Cabras, S., Saba, F., Reali, C., Scorciapino, L., Sirigu, A., Talani, G., Biggio, G., & Sogos, V. (2010) · The International Journal of Neuropsychopharmacology · doi:10.1017/s1461145710000210 · Cited by 33
Usp9x-deficiency disrupts the morphological development of the postnatal hippocampal dentate gyrus
Oishi, S., Premarathne, S., Harvey, T. J., Iyer, S. P., Dixon, C. M., Alexander, S., Burne, T. H. J., Wood, S. A., & Piper, M. (2016) · Scientific Reports · doi:10.1038/srep25783 · Cited by 32
Endogenous neurogenesis in adult mammals after spinal cord injury
Duan, H., Song, W., Zhao, W., Gao, Y., Yang, Z., & Li, X. (2016) · Science China Life Sciences · doi:10.1007/s11427-016-0205-2 · Cited by 32
The clock is ticking. Ageing of the circadian system: From physiology to cell cycle
Terzibasi-Tozzini, E., Martínez-Nicolás, A., & Lucas-Sánchez, A. (2017) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2017.06.011 · Cited by 33
Alonso, M. I., Lamus, F., Carnicero, E., Moro, J. A., la Mano, A. D., Fernández, J. M. F., Desmond, M. E., & Gato, A. (2017) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2017.00124 · Cited by 32
Essential Role of PDZ-RGS3 in the Maintenance of Neural Progenitor Cells
Qiu, R., Wang, J., Tsark, W. M. K., & Lü, Q. (2010) · Stem Cells · doi:10.1002/stem.478 · Cited by 33
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Yang, L., Liu, S., Liu, Y., Zhu, F.-Q., Xiong, M.-J., Hu, D.-X., & Zhang, W.-J. (2024) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2024.1329712 · Cited by 32
Kamath, A. P., Nayak, P. G., John, J., Mutalik, S., Balaraman, A. K., & Nandakumar, K. (2024) · Neuropharmacology · doi:10.1016/j.neuropharm.2024.110096 · Cited by 32
Dual lineage origins contribute to neocortical astrocyte diversity
Zhou, J., Vitali, I., Roig‐Puiggros, S., Javed, A., Cantando, I., Puglisi, M., Bezzi, P., Jabaudon, D., Mayer, C., & Bocchi, R. (2025) · Nature Communications · doi:10.1038/s41467-025-61829-4 · Cited by 31
Small-molecule blocks malignant astrocyte proliferation and induces neuronal gene expression
Zhang, L., Peng, L., Hsu, T., Aguilar, H. R., Frantz, D. E., Schneider, J. W., Bachoo, R. M., & Hsieh, J. (2011) · Differentiation · doi:10.1016/j.diff.2011.02.005 · Cited by 31
Gli3 Repressor Controls Cell Fates and Cell Adhesion for Proper Establishment of Neurogenic Niche
Wang, H., Kane, A. W., Lee, C., & Ahn, S. (2014) · Cell Reports · doi:10.1016/j.celrep.2014.07.006 · Cited by 31
Adult neural stem cells: plastic or restricted neuronal fates?
Sequerra, E. B., Costa, M. R., Menezes, J. R. L., & Hedin‐Pereira, C. (2013) · Development · doi:10.1242/dev.093096 · Cited by 31
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Weng, M., & Lee, C. (2010) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2010.09.005 · Cited by 31
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Bonfanti, L. (2016) · Frontiers in Neuroscience · doi:10.3389/fnins.2016.00044 · Cited by 32
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Guichet, P., Guelfi, S., Ripoll, C., Teigell, M., Sabourin, J.-C., Bauchet, L., Rigau, V., Rothhut, B., & Hugnot, J. (2016) · PLoS ONE · doi:10.1371/journal.pone.0151274 · Cited by 31
Pathobiology of Neurodegeneration: The Role for Astroglia
Verkhratsky, A., Zorec, R., Rodriguez, J. J., & Parpura, V. (2016) · PubMed · doi:10.20388/omp2016.001.0019 · Cited by 31
The PROK2/PROKR2 signaling pathway is required for the migration of most olfactory bulb interneurons
Wen, Y. F., Zhang, Z., Li, Z., Liu, G., Tao, G., Song, X., Xu, Z., Shang, Z., Guo, T., Su, Z., et al. (2019) · The Journal of Comparative Neurology · doi:10.1002/cne.24719 · Cited by 32
Li, L., Ruan, X., Wen, C., Chen, P., Liu, W., Zhu, L., Xiang, P., Zhang, X., Wei, Q., Hou, L., et al. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.06.055 · Cited by 32
Tissue mechanical properties modulate cell extrusion in the Drosophila abdominal epidermis
Michel, M., & Dahmann, C. (2020) · Development · doi:10.1242/dev.179606 · Cited by 31
Maternal cariprazine exposure inhibits embryonic and postnatal brain cholesterol biosynthesis
Genaro‐Mattos, T. C., Anderson, A. C., Allen, L. B., Tallman, K. A., Porter, N. A., Korade, Ž., & Mirnics, K. (2020) · Molecular Psychiatry · doi:10.1038/s41380-020-0801-x · Cited by 31
Impacts of bisphenol A analogues on zebrafish post‐embryonic brain
Coumailleau, P., Trempont, S., Pellegrini, E., & Charlier, T. D. (2020) · Journal of Neuroendocrinology · doi:10.1111/jne.12879 · Cited by 31
Notch1 and Notch2 collaboratively maintain radial glial cells in mouse neurogenesis
Mase, S., Shitamukai, A., Wu, Q., Morimoto, M., Gridley, T., & Matsuzaki, F. (2020) · Neuroscience Research · doi:10.1016/j.neures.2020.11.007 · Cited by 31
The promise of the TGF-β superfamily as a therapeutic target for Parkinson's disease
Karampetsou, M., Vekrellis, K., & Melachroinou, K. (2022) · Neurobiology of Disease · doi:10.1016/j.nbd.2022.105805 · Cited by 31
Li, Z., Liu, G., Yang, L., Sun, M., Zhang, Z., Xu, Z., Gao, Y., Jiang, X., Su, Z., Li, X., et al. (2023) · Protein & Cell · doi:10.1093/procel/pwad036 · Cited by 32
SVCT2 vitamin C transporter expression in progenitor cells of the postnatal neurogenic niche
Pastor, P., Cisternas, P., Salazar, K., Silva-Álvarez, C., Oyarce, K., Jara, N., Espinoza, F., Martı́nez, A. D., & Nualart, F. (2013) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2013.00119 · Cited by 31
Neural and Oligodendrocyte Progenitor Cells: Transferrin Effects on Cell Proliferation
Silvestroff, L., Franco, P. G., & Pasquini, J. M. (2013) · ASN NEURO · doi:10.1042/an20120075 · Cited by 31
Yang, N., Dong, Z., & Guo, S. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.2216-12.2012 · Cited by 31
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Ulrich, H., do Nascimento, I. C., Bocsi, J., & Tárnok, A. (2014) · Stem Cell Reviews and Reports · doi:10.1007/s12015-014-9556-6 · Cited by 31
Adult neurogenesis: Examples from the decapod crustaceans and comparisons with mammals
Sandeman, D. C., Bazin, F., & Beltz, B. S. (2011) · Arthropod Structure & Development · doi:10.1016/j.asd.2011.03.001 · Cited by 32
Endocytic receptor-mediated control of morphogen signaling
Willnow, T. E., Christ, A., & Hammes, A. (2012) · Development · doi:10.1242/dev.084467 · Cited by 35
Spinal Cord Stem Cells In Their Microenvironment: The Ependyma as a Stem Cell Niche
Marichal, N., Reali, C., Trujillo-Cenóz, O., & Russo, R. E. (2017) · Advances in experimental medicine and biology · doi:10.1007/978-3-319-69194-7_5 · Cited by 32
Fast neurogenesis from carotid body quiescent neuroblasts accelerates adaptation to hypoxia
Sobrino, V., González‐Rodríguez, P., Annese, V., López‐Barneo, J., & Pardal, R. (2018) · EMBO Reports · doi:10.15252/embr.201744598 · Cited by 31
EZH2-Mediated H3K27me3 Targets Transcriptional Circuits of Neuronal Differentiation
Buontempo, S., Laise, P., Hughes, J. M., Trattaro, S., Das, V., Rencurel, C., & Testa, G. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2022.814144 · Cited by 33
Neuroglia in cognitive reserve
Verkhratsky, A., & Zorec, R. (2024) · Molecular Psychiatry · doi:10.1038/s41380-024-02644-z · Cited by 34
Huttner, H. B., Corbeil, D., Thirmeyer, C., Coras, R., Köhrmann, M., Mauer, C., Kuramatsu, J. B., Kloska, S. P., Doerfler, A., Weigel, D., et al. (2011) · Epilepsy Research · doi:10.1016/j.eplepsyres.2011.10.029 · Cited by 30
Orphan nuclear receptor TLX regulates astrogenesis by modulating BMP signaling
Qin, S., Niu, W., Iqbal, N. S., Smith, D. K., & Zhang, C. (2014) · Frontiers in Neuroscience · doi:10.3389/fnins.2014.00074 · Cited by 30
Çelikkaya, H., Coşacak, M. İ., Papadimitriou, C., Popova, S. D., Bhattarai, P., Biswas, S. N., Siddiqui, T., Wistorf, S., Nevado-Alcalde, I., Naumann, L., et al. (2019) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2019.00023 · Cited by 31
Demirci, Y., Cucun, G., Poyraz, Y. K., Mohammed, S., Heger, G., Papatheodorou, I., & Özhan, G. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.584604 · Cited by 33
Edwards‐Faret, G., González‐Pinto, K., Cebrián‐Silla, A., Peñailillo, J., García‐Verdugo, J. M., & Larraı́n, J. (2021) · Neural Development · doi:10.1186/s13064-021-00152-2 · Cited by 30
Microstructural Periventricular White Matter Injury in Post-hemorrhagic Ventricular Dilatation
Isaacs, A. M., Neil, J. J., McAllister, J. P., Dahiya, S., Castañeyra-Ruiz, L., Merisaari, H., Botteron, H. E., Alexopoulos, D., George, A., Sun, P., et al. (2021) · Neurology · doi:10.1212/wnl.0000000000013080 · Cited by 30
Emergence of a geometric pattern of cell fates from tissue-scale mechanics in the Drosophila eye
Gallagher, K. D., Mani, M., & Carthew, R. W. (2022) · eLife · doi:10.7554/elife.72806 · Cited by 30
Schaberg, E., Götz, M., & Faissner, A. (2022) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-022-04259-5 · Cited by 32
Verkhratsky, A., & Butt, A. M. (2023) · Elsevier eBooks · doi:10.1016/b978-0-12-821565-4.00008-0 · Cited by 31
Cesetti, T., Fila, T., Obernier, K., Bengtson, C. P., Li, Y., Mandl, C., Hölzl‐Wenig, G., & Ciccolini, F. (2010) · Stem Cells · doi:10.1002/stem.573 · Cited by 30
Suetterlin, P., Williams, E. J., Chambers, D. J., Saraf, K. A., von Schack, D., Reisenberg, M., Doherty, P., & Williams, G. H. (2012) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2012.10.006 · Cited by 30
Neonatal Subventricular Zone Electroporation
Feliciano, D. M., Lafourcade, C., & Bordey, A. (2013) · Journal of Visualized Experiments · doi:10.3791/50197 · Cited by 30
Adult neurogenesis without germinal layers: the "atypical" cerebellum of rabbits.
Ponti, G., Crociara, P., Armentano, M., & Bonfanti, L. (2010) · PubMed · Cited by 30
High-throughput clonal analysis of neural stem cells in microarrayed artificial niches
Roccio, M., Gobaa, S., & Lütolf, M. P. (2012) · Integrative Biology · doi:10.1039/c2ib00070a · Cited by 30
Bioelectric State and Cell Cycle Control of Mammalian Neural Stem Cells
Aprea, J., & Calegari, F. (2012) · Stem Cells International · doi:10.1155/2012/816049 · Cited by 30
Cell migration in the developing rodent olfactory system
Huilgol, D., & Tole, S. (2016) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-016-2172-7 · Cited by 34
Oligodendrogenesis after traumatic brain injury
Takase, H., Washida, K., Hayakawa, K., Arai, K., Wang, X., Lo, E. H., & Lok, J. M. (2016) · Behavioural Brain Research · doi:10.1016/j.bbr.2016.10.042 · Cited by 30
Mechanisms of Cortical Differentiation
Adnani, L., Han, S., Li, S., Mattar, P. A., & Schuurmans, C. (2017) · International review of cytology · doi:10.1016/bs.ircmb.2017.07.005 · Cited by 33
OTX1 regulates cell cycle progression of neural progenitors in the developing cerebral cortex
Huang, B., Li, X., Tu, X., Zhao, W., Zhu, D., Feng, Y., Si, X., & Chen, J.-G. (2017) · Journal of Biological Chemistry · doi:10.1074/jbc.ra117.001249 · Cited by 30
Maeda, Y. K., Nakagomi, N., Nakano‐Doi, A., Ishikawa, H., Tatsumi, Y., Bandô, Y., Yoshikawa, H., Matsuyama, T., Gomi, F., & Nakagomi, T. (2019) · Cells · doi:10.3390/cells8091025 · Cited by 30
Zrf1 is required to establish and maintain neural progenitor identityPreprint
Aloia, L., Stefano, B. D., Sessa, A., Morey, L., Santanach, A., Gutiérrez, A., Cozzuto, L., Benitah, S. A., Graf, T., Broccoli, V., et al. (2014) · Genes & Development · doi:10.1101/gad.228510.113 · Cited by 30
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Coller, H. A. (2019) · Comprehensive physiology · doi:10.1002/cphy.c190014 · Cited by 33
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Salazar, K., Jara, N., Ramírez, E., de Lima, I., Smith-Ghigliotto, J., Muñoz, V., Ferrada, L., & Nualart, F. (2023) · Frontiers in Neuroscience · doi:10.3389/fnins.2023.1155758 · Cited by 29
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Kunoh, S., Nakashima, H., & Nakashima, K. (2024) · Epigenomes · doi:10.3390/epigenomes8020022 · Cited by 33
Madsen, S., Delgado, A. C., Cadilhac, C., Maillard, V., Battiston, F., Igelbüscher, C. M., Neck, S. D., Magrinelli, E., Jabaudon, D., Telley, L., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-49449-w · Cited by 29
North, H. A., Clifford, M. A., & Donoghue, M. J. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhs183 · Cited by 29
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Encinas, J. M., & Fitzsimons, C. P. (2017) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2017.07.016 · Cited by 32
Herculano‐Houzel, S., & Santos, S. D. (2018) · Neuroglia · doi:10.3390/neuroglia1010014 · Cited by 30
Robotic platform for microinjection into single cells in brain tissue
Shull, G. M., Haffner, C., Huttner, W. Β., Taverna, E., & Kodandaramaiah, S. B. (2019) · EMBO Reports · doi:10.15252/embr.201947880 · Cited by 30
Masood, M. I., Schäfer, K. H., Naseem, M., Weyland, M., & Meiser, P. (2020) · PLoS ONE · doi:10.1371/journal.pone.0237025 · Cited by 29
Smith, M. J., Paton, M. C. B., Fahey, M. C., Jenkin, G., Miller, S., Finch‐Edmondson, M., & McDonald, C. (2021) · Stem Cells Translational Medicine · doi:10.1002/sctm.21-0243 · Cited by 29
Recent advances in tissue stem cells
Fu, X., He, Q., Tao, Y., Wang, M., Wang, W., Wang, Y., Yu, Q. C., Zhang, F., Zhang, X., Chen, Y., et al. (2021) · Science China Life Sciences · doi:10.1007/s11427-021-2007-8 · Cited by 30
Schweingruber, C., & Hedlund, E. (2022) · Biology · doi:10.3390/biology11081191 · Cited by 29
Jaylet, T., Quintens, R., Benotmane, M. A., Luukkonen, J., Tanaka, I. B., Ibanez, C., Durand, C., Sachana, M., Azimzadeh, O., Adam‐Guillermin, C., et al. (2022) · International Journal of Radiation Biology · doi:10.1080/09553002.2022.2110312 · Cited by 29
Ye, D., Walsh, J. T., Junker, I. P., & Ding, Y. (2024) · Current Biology · doi:10.1016/j.cub.2024.04.020 · Cited by 30
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Sakaguchi, M., Imaizumi, Y., Shingo, T., Tada, H., Hayama, K., Yamada, O., Morishita, T., Kadoya, T., Uchiyama, N., Shimazaki, T., et al. (2010) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2010.06712.x · Cited by 29
Reprogramming of Postnatal Astroglia of the Mouse Neocortex into Functional, Synapse-Forming Neurons
Heinrich, C., Götz, M., & Berninger, B. (2011) · Methods in molecular biology · doi:10.1007/978-1-61779-452-0_32 · Cited by 29
Weng, M., Haenfler, J. M., & Lee, C. (2011) · Developmental Neurobiology · doi:10.1002/dneu.20995 · Cited by 29
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Koutmani, Y., & Karalis, K. P. (2015) · Frontiers in Physiology · doi:10.3389/fphys.2015.00077 · Cited by 31
Xie, Y., Li, X., Zhang, X., Mei, S., Li, H., Urso, A., & Zhu, S. (2014) · eLife · doi:10.7554/elife.03596 · Cited by 29
Self‐induced accumulation of glutamate in striatal astrocytes and basal ganglia excitotoxicity
Moráles, I., & Rodríguez, M. (2012) · Glia · doi:10.1002/glia.22368 · Cited by 31
Zhu, X., Li, B., Ai, Z., Xiang, Z., Zhang, K., Qiu, X., Chen, Y., Li, Y., Rizak, J. D., Niu, Y., et al. (2015) · Stem Cell Reports · doi:10.1016/j.stemcr.2015.10.007 · Cited by 29
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Ribeiro, D. E., Glaser, T., Oliveira‐Giacomelli, Á., & Ulrich, H. (2018) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2018.12.013 · Cited by 29
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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