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A Specialized Vascular Niche for Adult Neural Stem Cells
Open accessAbstract
Stem cells reside in specialized niches that regulate their self-renewal and differentiation. The vasculature is emerging as an important component of stem cell niches. Here, we show that the adult subventricular zone (SVZ) neural stem cell niche contains an extensive planar vascular plexus that has specialized properties. Dividing stem cells and their transit-amplifying progeny are tightly apposed to SVZ blood vessels both during homeostasis and regeneration. They frequently contact the vasculature at sites that lack astrocyte endfeet and pericyte coverage, a modification of the blood-brain barrier unique to the SVZ. Moreover, regeneration often occurs at these sites. Finally, we find that circulating small molecules in the blood enter the SVZ. Thus, the vasculature is a key component of the adult SVZ neural stem cell niche, with SVZ stem cells and transit-amplifying cells uniquely poised to receive spatial cues and regulatory signals from diverse elements of the vascular system.
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“They contact the cerebrospinal fluid in the ventricles at the center of pinwheels formed by ependymal cells and extend a long process to the vasculature (Mirzadeh et al., 2008; Shen et al., 2008; Tavazoie et al., 2008).”
From Single-Cell Analysis of Regional Differences in Adult V-SVZ Neural Stem Cell Lineages (2019) · cites this paper as Tavazoie et al., 2008
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Cites
Astrocyte-endothelial interactions at the blood-brain barrier
Abbott, N. J., Rönnbäck, L., & Hansson, E. (2006) · Nature Reviews Neuroscience · doi:10.1038/nrn1824 · Cited by 5,595
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 Blood-Brain Barrier in Health and Chronic Neurodegenerative Disorders
Zlokovic, B. V. (2008) · Neuron · doi:10.1016/j.neuron.2008.01.003 · Cited by 3,280
Kiel, M. J., Yilmaz, Ö. H., Iwashita, T., Yilmaz, O. H., Terhorst, C., & Morrison, S. J. (2005) · Cell · doi:10.1016/j.cell.2005.05.026 · Cited by 3,168
Purification and Characterization of Mouse Hematopoietic Stem Cells
Spangrude, G. J., Heimfeld, S., & Weissman, I. L. (1988) · Science · doi:10.1126/science.2898810 · Cited by 2,908
A Perivascular Niche for Brain Tumor Stem Cells
Calabrese, C. R., Poppleton, H., Koçak, M., Hogg, T. L., Fuller, C. E., Hamner, J. B., Oh, E. Y., Gaber, M. W., Finklestein, D., Allen, M., et al. (2007) · Cancer Cell · doi:10.1016/j.ccr.2006.11.020 · Cited by 2,253
Doetsch, F. K., García‐Verdugo, J. M., & Álvarez-Buylla, A. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-13-05046.1997 · Cited by 1,909
Hellström, M., Kalén, M., Lindahl, P., Abramsson, A., & Betsholtz, C. (1999) · Development · doi:10.1242/dev.126.14.3047 · Cited by 1,734
Endothelial Cells Stimulate Self-Renewal and Expand Neurogenesis of Neural Stem Cells
Shen, Q., Goderie, S. K., Jin, L., Karanth, N., Sun, Y., Abramova, N. E., Vincent, P. A., Pumiglia, K. M., & Temple, S. (2004) · Science · doi:10.1126/science.1095505 · Cited by 1,574
Vascular endothelial growth factor (VEGF) stimulates neurogenesis in vitro and in vivo
Jin, K., Zhu, Y., Sun, Y., Mao, X. O., Xie, L., & Greenberg, D. A. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.182296499 · Cited by 1,507
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Ryu, B., Sekine, H., Homma, J., Kobayashi, T., Kobayashi, E., Kawamata, T., & Shimizu, T. (2019) · Journal of neurosurgery · doi:10.3171/2018.11.jns182331 · Cited by 68
Caspase-1 Inhibition Attenuates Hyperoxia-induced Lung and Brain Injury in Neonatal Mice
Dapaah-Siakwan, F. M., Zambrano, R. A. P., Luo, S., Duncan, M. R., Kerr, N. A., Donda, K., Vaccari, J. P. D. R., Keane, R. W., Dietrich, W. D., Benny, M., et al. (2019) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.2018-0192oc · Cited by 71
CRISPR–Cas9 screens reveal regulators of ageing in neural stem cells
Ruetz, T. J., Pogson, A. N., Kashiwagi, C. M., Gagnon, S. D., Morton, B., Sun, E., Na, J., Yeo, R. W., Leeman, D. S., Morgens, D. W., et al. (2024) · Nature · doi:10.1038/s41586-024-07972-2 · Cited by 75
The balance of Id3 and E47 determines neural stem/precursor cell differentiation into astrocytes
Bohrer, C., Pfurr, S., Mammadzada, K., Schildge, S., Plappert, L., Hils, M., Pous, L., Rauch, K. S., Dumit, V. I., Pfeifer, D., et al. (2015) · The EMBO Journal · doi:10.15252/embj.201591118 · Cited by 70
CXCR4/CXCR7 Molecular Involvement in Neuronal and Neural Progenitor Migration: Focus in CNS Repair
Merino, J. J., Bellver‐Landete, V., Oset‐Gasque, M. J., & Cubelos, B. (2014) · Journal of Cellular Physiology · doi:10.1002/jcp.24695 · Cited by 65
Angiocrine endothelium: from physiology to cancer
Pasquier, J., Ghiabi, P., Chouchane, L., Razzouk, K., Rafii, S., & Rafii, A. (2020) · Journal of Translational Medicine · doi:10.1186/s12967-020-02244-9 · Cited by 68
Neurogenesis From Embryo to Adult – Lessons From Flies and Mice
Mira, H., & Morante, J. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.00533 · Cited by 71
Function of neural stem cells in ischemic brain repair processes
Zhang, R., Zhang, Z., & Chopp, M. (2016) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1177/0271678x16674487 · Cited by 68
Bioprinting Cell- and Spheroid-Laden Protein-Engineered Hydrogels as Tissue-on-Chip Platforms
Campos, D. F. D., Lindsay, C. D., Roth, J. G., LeSavage, B. L., Seymour, A. J., Krajina, B. A., Ribeiro, R. D. C., Costa, P. F., Blaeser, A., & Heilshorn, S. C. (2020) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2020.00374 · Cited by 68
Magueresse, C. L., Alfonso, J., Bark, C., Eliava, M., Khrulev, S., & Monyer, H. (2011) · Cerebral Cortex · doi:10.1093/cercor/bhr302 · Cited by 66
Shin, Y., Yang, K., Han, S., Park, H., Heo, Y. S., Cho, S., & Chung, S. H. (2014) · Advanced Healthcare Materials · doi:10.1002/adhm.201300569 · Cited by 65
Sirko, S., Neitz, A., Mittmann, T., Horvat-Broecker, A., von Holst, A., Eysel, U. T., & Faissner, A. (2009) · Brain · doi:10.1093/brain/awp043 · Cited by 66
Cellular Kinetics of Perivascular MSC Precursors
Chen, W. C. W., Park, T. S., Murray, I. R., Zimmerlin, L., Lazzari, L., Huard, J., & Péault, B. (2013) · Stem Cells International · doi:10.1155/2013/983059 · Cited by 68
Home sweet home: the neural stem cell niche throughout development and after injury
Ruddy, R. M., & Morshead, C. M. (2017) · Cell and Tissue Research · doi:10.1007/s00441-017-2658-0 · Cited by 72
Blood-brain barrier-supported neurogenesis in healthy and diseased brain
Пожиленкова, Е. А., Lopatina, O. L., Komleva, Y. K., Salmin, V. V., & Salmina, A. B. (2017) · Reviews in the Neurosciences · doi:10.1515/revneuro-2016-0071 · Cited by 66
Snijders, G. J. L., Sneeboer, M. A. M., Fernández-Andreu, A., Udine, E., (NBB-Psy), P. D. P. O. T. N. B. B., Boks, M. P., Ormel, P. R., van Berlekom, A. B., van Mierlo, H. C., Böttcher, C., et al. (2020) · Molecular Psychiatry · doi:10.1038/s41380-020-00896-z · Cited by 66
Roles for HIF-1α in neural stem cell function and the regenerative response to stroke
Cunningham, L. A., Candelario, K. M., & Li, L. (2011) · Behavioural Brain Research · doi:10.1016/j.bbr.2011.08.002 · Cited by 66
Blood vessels as a scaffold for neuronal migration
Fujioka, T., Kaneko, N., & Sawamoto, K. (2019) · Neurochemistry International · doi:10.1016/j.neuint.2019.03.001 · Cited by 67
Migaud, M., Butrille, L., & Batailler, M. (2014) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2014.11.004 · Cited by 65
Developmental regulation of barrier‐ and non‐barrier blood vessels in the CNS
Ben‐Zvi, A., & Liebner, S. (2021) · Journal of Internal Medicine · doi:10.1111/joim.13263 · Cited by 67
The Incredible Elastic Brain: How Neural Stem Cells Expand Our Minds
Kokovay, E., Shen, Q., & Temple, S. (2008) · Neuron · doi:10.1016/j.neuron.2008.10.025 · Cited by 64
Brain homeostasis: VEGF receptor 1 and 2—two unequal brothers in mind
Wittko-Schneider, I. M., Schneider, F. T., & Plate, K. H. (2013) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-013-1279-3 · Cited by 62
Epigenetic regulation of adult neural stem cells: implications for Alzheimer’s disease
Fitzsimons, C. P., van Bodegraven, E. J., Schouten, M., Lardenoije, R., Kompotis, K., Kenis, G., van den Hurk, M., Boks, M. P., Biojone, C., Joca, S. R. L., et al. (2014) · Molecular Neurodegeneration · doi:10.1186/1750-1326-9-25 · Cited by 67
Inhibition of EGFR Induces a c-MET-Driven Stem Cell Population in Glioblastoma
Jun, H. J., Bronson, R. T., & Charest, A. (2013) · Stem Cells · doi:10.1002/stem.1554 · Cited by 64
The Molecular Profiles of Neural Stem Cell Niche in the Adult Subventricular Zone
Lee, C., Hu, J., Ralls, S., Kitamura, T., Loh, Y. P., Yang, Y., Mukouyama, Y., & Ahn, S. (2012) · PLoS ONE · doi:10.1371/journal.pone.0050501 · Cited by 63
Aging and neurogenesis in the adult forebrain: what we have learned and where we should go from here
Hamilton, L. K., Joppé, S. E., Cochard, L. M., & Fernandes, K. J. L. (2013) · European Journal of Neuroscience · doi:10.1111/ejn.12207 · Cited by 74
Cell adhesion and signaling networks in brain neurovascular units
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The Stem Cell Niche Should be a Key Issue for Cell Therapy in Regenerative Medicine
Becerra, J., Santos‐Ruiz, L., Andrades, J. A., & Marí‐Beffa, M. (2010) · Stem Cell Reviews and Reports · doi:10.1007/s12015-010-9195-5 · Cited by 64
Impaired Hippocampal Neurogenesis and Vascular Formation in Ephrin-A5 -Deficient Mice
Hara, Y., Nomura, T., Yoshizaki, K., Frisén, J., & Osumi, N. (2010) · Stem Cells · doi:10.1002/stem.427 · Cited by 63
Bain, J., Moore, L., Ren, Z., Simonishvili, S., & Levison, S. W. (2012) · Translational Stroke Research · doi:10.1007/s12975-012-0213-6 · Cited by 61
Glioblastoma stem cells: Molecular characteristics and therapeutic implications
Bayin, N. S. (2014) · World Journal of Stem Cells · doi:10.4252/wjsc.v6.i2.230 · Cited by 66
Nascimento, M. A., Sorokin, L. M., & Coelho‐Sampaio, T. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.3064-17.2018 · Cited by 64
Lindsey, B. W., Hall, Z. J., Heuzé, A., Joly, J., Tropepe, V., & Kaslin, J. (2018) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2018.06.004 · Cited by 62
Jacquet, B. V., Muthusamy, N., Sommerville, L. J., Xiao, G., Liang, H., Zhang, Y., Holtzman, M. J., & Ghashghaei, H. T. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.0171-11.2011 · Cited by 58
A Chimeric Egfr Protein Reporter Mouse Reveals Egfr Localization and Trafficking In Vivo
Yang, Y.-P., Ma, H., Starchenko, A., Huh, W. J., Li, W., Hickman, F. E., Zhang, Q., Franklin, J. L., Mortlock, D. P., Fuhrmann, S., et al. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.04.048 · Cited by 57
Characteristics of glioma stem cells
Sampetrean, O., & Saya, H. (2013) · Brain Tumor Pathology · doi:10.1007/s10014-013-0141-5 · Cited by 59
Zujovic, V., Thibaud, J., Bachelin, C., Vidal, M., Deboux, C., Coulpier, F., Stadler, N., Charnay, P., Topilko, P., & Evercooren, A. B. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1018687108 · Cited by 62
Komabayashi‐Suzuki, M., Yamanishi, E., Watanabe, C., Okamura, M., Tabata, H., Iwai, R., Ajioka, I., Matsushita, J., Kidoya, H., Takakura, N., et al. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.09.048 · Cited by 61
Generation of Cortical Brain Organoid with Vascularization by Assembling with Vascular Spheroid
Kook, M. G., Lee, S., Shin, N., Kong, D., Kim, D., Kim, M., Kang, H. K., Choi, S. W., & Kang, K. (2022) · International Journal of Stem Cells · doi:10.15283/ijsc21157 · Cited by 59
Neurogenic and non-neurogenic functions of endogenous neural stem cells
Butti, E., Cusimano, M., Bacigaluppi, M., & Martino, G. (2014) · Frontiers in Neuroscience · doi:10.3389/fnins.2014.00092 · Cited by 58
Concurrent Vasculogenesis and Neurogenesis From Adult Neural Stem Cells
Ii, M., Nishimura, H., Sekiguchi, H., Kamei, N., Yokoyama, A., Horii, M., & Asahara, T. (2009) · Circulation Research · doi:10.1161/circresaha.109.199299 · Cited by 58
Sintoni, S., Benton, J. L., Beltz, B. S., Hansson, B. S., & Harzsch, S. (2012) · Neural Development · doi:10.1186/1749-8104-7-1 · Cited by 58
Lauvrud, A. T., Kelk, P., Wiberg, M., & Kingham, P. J. (2016) · Journal of Tissue Engineering and Regenerative Medicine · doi:10.1002/term.2147 · Cited by 57
Post-stroke Neurogenesis: Friend or Foe?
Cuartero, M. I., García‐Culebras, A., Torres‐López, C., Medina, V., Fraga, E., Vázquez‐Reyes, S., Jareño-Flores, T., García-Segura, J. M., Lizasoaín, I., & Moro, M. Á. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.657846 · Cited by 64
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Xiao, Y., Woo, W., Nagao, K., Li, W., Terunuma, A., Mukouyama, Y., Oro, A. E., Vogel, J. C., & Brownell, I. (2013) · Journal of Investigative Dermatology · doi:10.1038/jid.2013.167 · Cited by 56
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Villeda, S., & Wyss‐Coray, T. (2012) · Autoimmunity Reviews · doi:10.1016/j.autrev.2012.10.014 · Cited by 57
Bone marrow-derived mesenchymal stem cells enhance angiogenesis via their α6β1 integrin receptor
Carrion, B., Kong, Y. P., Kaigler, D., & Putnam, A. J. (2013) · Experimental Cell Research · doi:10.1016/j.yexcr.2013.09.007 · Cited by 56
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Kim, D., Rhee, I., & Paik, J. (2014) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-014-1686-0 · Cited by 59
Valdovinos-Flores, C., & Gonsebatt, M. E. (2012) · Neurochemistry International · doi:10.1016/j.neuint.2012.05.019 · Cited by 55
Mas, A., Stone, L., O'Connor, P. M., Yang, Q., Kleven, D. T., Simón, C., Walker, C. L., & Al-Hendy, A. A. (2016) · Stem Cells · doi:10.1002/stem.2519 · Cited by 55
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Adult neurogenesis and its role in brain injury and psychiatric diseases
Hayashi, Y., Jinnou, H., Sawamoto, K., & Hitoshi, S. (2018) · Journal of Neurochemistry · doi:10.1111/jnc.14557 · Cited by 56
DeCarolis, N. A., Kirby, E. D., Wyss‐Coray, T., & Palmer, T. D. (2015) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a025874 · Cited by 55
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Six3 is required for ependymal cell maturation
Lavado, A., & Oliver, G. C. (2011) · Development · doi:10.1242/dev.067470 · Cited by 54
Gilley, J. A., Yang, C., & Kernie, S. G. (2009) · Hippocampus · doi:10.1002/hipo.20719 · Cited by 54
Addington, C. P., Dharmawaj, S., Heffernan, J. M., Sirianni, R. W., & Stabenfeldt, S. E. (2016) · Matrix Biology · doi:10.1016/j.matbio.2016.09.007 · Cited by 54
Calorie restriction protects neural stem cells from age-related deficits in the subventricular zone
Apple, D. M., Mahesula, S., Fonseca, R. S., Zhu, C., & Kokovay, E. (2019) · Aging · doi:10.18632/aging.101731 · Cited by 56
Ah-Pine, F., Khettab, M., Bedoui, Y., Slama, Y., Daniel, M., Doray, B., & Gasque, P. (2023) · Acta Neuropathologica Communications · doi:10.1186/s40478-023-01605-x · Cited by 66
Grimm, I., Ullsperger, S. N., & Zimmermann, H. (2010) · Acta Physiologica · doi:10.1111/j.1748-1716.2010.02092.x · Cited by 53
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Stolp, H. B., & Molnár, Z. (2015) · Frontiers in Neuroscience · doi:10.3389/fnins.2015.00020 · Cited by 56
Jiang, Y., Berry, D. C., Jo, A.-Y., Tang, W., Arpke, R. W., Kyba, M., & Graff, J. M. (2017) · Nature Communications · doi:10.1038/ncomms15926 · Cited by 55
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Solozobova, V., Wyvekens, N., & Pruszak, J. (2012) · Stem Cell Reviews and Reports · doi:10.1007/s12015-012-9381-8 · Cited by 54
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Conover, J. C., & Todd, K. L. (2016) · Experimental Gerontology · doi:10.1016/j.exger.2016.11.007 · Cited by 53
Hauser, K. F., & Knapp, P. E. (2018) · Frontiers in Pediatrics · doi:10.3389/fped.2017.00294 · Cited by 57
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Azari, H., & Reynolds, B. A. (2015) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a021279 · Cited by 54
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Differences Between Niche Cells and Limbal Stromal Cells in Maintenance of Corneal Limbal Stem Cells
Li, Y., Inoue, T., Takamatsu, F., Kobayashi, T., Shiraishi, A., Maeda, N., Ohashi, Y., & Nishida, K. (2014) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.13-13698 · Cited by 51
Young, C. C., van der Harg, J. M., Lewis, N. J., Brooks, K. J., Buchan, A. M., & Szele, F. G. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhs049 · Cited by 53
CD133+ niches and single cells in glioblastoma have different phenotypes
Christensen, K. G., Schrøder, H. D., & Kristensen, B. W. (2010) · Journal of Neuro-Oncology · doi:10.1007/s11060-010-0488-y · Cited by 54
Exercise protects against methamphetamine-induced aberrant neurogenesis
Park, M., LEVINE, H. D., & Toborek, M. J. (2016) · Scientific Reports · doi:10.1038/srep34111 · Cited by 49
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Sultan, K. T., & Shi, S. (2017) · Wiley Interdisciplinary Reviews Developmental Biology · doi:10.1002/wdev.306 · Cited by 57
Diversity of Neural Precursors in the Adult Mammalian BrainPreprint
Bonaguidi, M. A., Stadel, R. P., Berg, D. A., Sun, J., Ming, G., & Song, H. (2016) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a018838 · Cited by 51
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Neurogenesis in the circumventricular organs of adult mouse brains
Hourai, A., & Miyata, S. (2013) · Journal of Neuroscience Research · doi:10.1002/jnr.23206 · Cited by 52
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Tata, M., Wall, I. B., Joyce, A., Vieira, J. M., Kessaris, N., & Ruhrberg, C. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1613113113 · Cited by 49
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Pasqualini, C., Kozaki, T., Bruschi, M., Nguyen, T. H. H., Minard‐Colin, V., Castel, D., Grill, J., & Ginhoux, F. (2020) · Neuron · doi:10.1016/j.neuron.2020.09.018 · Cited by 55
Developmental dysregulation of adult neurogenesis
Kuhn, H. G., & Blomgren, K. (2011) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2011.07610.x · Cited by 50
Angiogenesis Potential of Human Limbal Stromal Niche Cells
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Sattiraju, A., Sai, K. K. S., & Mintz, A. (2017) · Advances in experimental medicine and biology · doi:10.1007/978-3-319-69194-7_7 · Cited by 51
Zhou, S.-T., Gao, B., Sun, C., Bai, Y., Cheng, D., Zhang, Y., Li, X., Zhao, J., & Xu, D. (2020) · Neuroscience · doi:10.1016/j.neuroscience.2020.05.046 · Cited by 50
Ontogeny of adult neural stem cells in the mammalian brain
Bond, A. M., Ming, G., & Song, H. (2020) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/bs.ctdb.2020.11.002 · Cited by 51
Stem cells niches during development — lessons from the cerebral cortex
Johansson, P. A., Cappello, S., & Götz, M. (2010) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2010.04.003 · Cited by 49
Ephrin-A1-Mediated Dopaminergic Neurogenesis and Angiogenesis in a Rat Model of Parkinson's Disease
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Metadata
- Authors
- Tavazoie, M., Van der Veken, L., Silva-Vargas, V., Louissaint, M., Colonna, L., Zaidi, B., Garcia-Verdugo, J. M., & Doetsch, F.
- Affiliations
- Columbia University (US)
- Corresponding author
- Doetsch, Fiona
- Venue
- Cell stem cell
- Publisher
- Elsevier BV
- Published
- 2008-09
- Volume
- 3
- Issue
- 3
- Pages
- 279-288
- ISSN
- 1875-9777 (ISSN-L)
- 1934-5909
- PMC
- PMC6864413
- OpenAlex
- W2108340830
- Cited by
- 1,033
- References
- 55
- Citations by year
- 2026: 13 · 2025: 21 · 2024: 31 · 2023: 22 · 2022: 35 · 2021: 48 · 2020: 59 · 2019: 61 · 2018: 49 · 2017: 60 · 2016: 59 · 2015: 71 · 2014: 88 · 2013: 79 · 2012: 95
- FWCI
- 24.41
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- www.elsevier.com/tdm/userlicense/1.0/ (tdm)
- www.elsevier.com/legal/tdmrep-license (tdm)
- www.elsevier.com/open-access/userlicense/1.0/ (vor, 1816 d)
- doi.org/10.15223/policy-017 (stm-asf)
- doi.org/10.15223/policy-037 (stm-asf)
- doi.org/10.15223/policy-012 (stm-asf)
- doi.org/10.15223/policy-029 (stm-asf)
- doi.org/10.15223/policy-004 (stm-asf)
- Locations
- Cell stem cell (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institute of General Medical Sciences (T32GM008224, T32GM007367)
- National Institute of Neurological Disorders and Stroke (R01NS053884)
- Topics
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Life Sciences › Neuroscience › Neurology › Barrier Structure and Function Studies
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Angiogenesis and VEGF in Cancer
- Keywords
- neural stem cells, stem cell niche, subventricular zone, vascular system, blood-brain barrier, pericytes, astrocyte endfeet, transit amplifying cells, self-renewal, tissue regeneration
- MeSH terms
- Animals, Blood Vessels, Brain, Cell Differentiation, Cell Division, Humans, Mice, Inbred Strains, Lateral Ventricles, Mice, Adult Stem Cells
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