Apical versus basal neurogenesis directs cortical interneuron subclass fate
Open accessAbstract
Fate determination in the mammalian telencephalon, with its diversity of neuronal subtypes and relevance to neuropsychiatric disease, remains a critical area of study in neuroscience. Most studies investigating this topic focus on the diversity of neural progenitors within spatial and temporal domains along the lateral ventricles. Often overlooked is whether the location of neurogenesis within a fate-restricted domain is associated with, or instructive for, distinct neuronal fates. Here, we use in vivo fate mapping and the manipulation of neurogenic location to demonstrate that apical versus basal neurogenesis influences the fate determination of major subgroups of cortical interneurons derived from the subcortical telencephalon. Somatostatin-expressing interneurons arise mainly from apical divisions along the ventricular surface, whereas parvalbumin-expressing interneurons originate predominantly from basal divisions in the subventricular zone. As manipulations that shift neurogenic location alter interneuron subclass fate, these results add an additional dimension to the spatial-temporal determinants of neuronal fate determination.
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Nr2f1 and Nr2f2 influence neuronal specification by regulating cell cycle dynamics, which may explain why cell cycle factors have been implicated in interneuron diversity.
“Nr2f1 and Nr2f2 influence neuronal specification by regulating cell cycle dynamics”
From Development and Functional Diversification of Cortical Interneurons (2018) · cites this paper as Petros et al., 2015
Previous work suggested that SST+ interneurons are preferentially generated from ventricular zone progenitors through direct neurogenesis.
“previous work suggesting that SST+ interneurons are preferentially generated from VZ progenitors through direct neurogenesis”
From Development and Functional Diversification of Cortical Interneurons (2018) · cites this paper as Petros et al., 2015
The mode of progenitor mitosis critically influences MGE-derived interneuron fate determination.
“the mode of progenitor mitosis critically influences MGE-derived interneuron fate determination”
From Hippocampal GABAergic Inhibitory Interneurons (2017) · cites this paper as [904]
BP neurogenesis within the SVZ yields primarily PV interneurons.
“BP neurogenesis within the SVZ yields primarily PV interneurons”
From Hippocampal GABAergic Inhibitory Interneurons (2017) · cites this paper as [904]
ApP neurogenesis within the MGE VZ is strongly biased to produce SST interneurons.
“ApP neurogenesis within the MGE VZ is strongly biased to produce SST interneurons”
From Hippocampal GABAergic Inhibitory Interneurons (2017) · cites this paper as [904]
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Cites
Shrestha, S., & Offer, S. M. (2016) · Medical Epigenetics · doi:10.1159/000444713 · Cited by 8,949 · see citing works
Development and Evolution of the Human Neocortex
Lui, J. H., Hansen, D. V., & Kriegstein, A. R. (2011) · Cell · doi:10.1016/j.cell.2011.06.030 · Cited by 1,342 · see citing works
Interneuron dysfunction in psychiatric disorders
Marín, O. (2012) · Nature Reviews Neuroscience · doi:10.1038/nrn3155 · Cited by 1,190 · see citing works
A developmental and genetic classification for malformations of cortical development: update 2012
Barkovich, A. J., Guerrini, R., Kuzniecky, R., Jackson, G. D., & Dobyns, W. B. (2012) · Brain · doi:10.1093/brain/aws019 · Cited by 1,110 · see citing works
Origins of Cortical Interneuron Subtypes
Xu, Q., Cobos, I., De La Cruz, E., Rubenstein, J. L., & Anderson, S. A. (2004) · The Journal of Neuroscience · doi:10.1523/jneurosci.5667-03.2004 · Cited by 639 · see citing works
Self-citationThe temporal and spatial origins of cortical interneurons predict their physiological subtype
Butt, S. J. B., Fuccillo, M., Nery, S., Noctor, S., Kriegstein, A., Corbin, J. G., & Fishell, G. (2005) · Neuron · doi:10.1016/j.neuron.2005.09.034 · Cited by 587 · see citing works
Self-citationFate mapping Nkx2.1‐lineage cells in the mouse telencephalon
Xu, Q., Tam, M., & Anderson, S. A. (2007) · The Journal of Comparative Neurology · doi:10.1002/cne.21529 · Cited by 560 · see citing works
Self-citationFlames, N., Pla, R., Gelman, D. M., Rubenstein, J. L. R., Puelles, L., & Marín, O. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.2750-07.2007 · Cited by 560 · see citing works
Anderson, S. A., Qiu, M. S., Bulfone, A., Eisenstat, D. D., Meneses, J. J., Pedersen, R. A., & Rubenstein, J. L. R. (1997) · Neuron · doi:10.1016/s0896-6273(00)80345-1 · Cited by 541 · see citing works
Self-citationDifferential Notch signalling distinguishes neural stem cells from intermediate progenitors
Mizutani, K., Yoon, K., Dang, L. T., Tokunaga, A., & Gaiano, N. (2007) · Nature · doi:10.1038/nature06090 · Cited by 521 · see citing works
Xu, X., Roby, K. D., & Callaway, E. M. (2010) · Journal of Comparative Neurology · doi:10.1002/cne.22229 · Cited by 429 · see citing works
Kowalczyk, T., Pontious, A., Englund, C., Daza, R. A. M., Bedogni, F., Hodge, R. D., Attardo, A., Bell, C., Huttner, W. Β., & Hevner, R. F. (2009) · Cerebral Cortex · doi:10.1093/cercor/bhn260 · Cited by 407 · see citing works
Sessa, A., Mao, C., Hadjantonakis, A., Klein, W. H., & Broccoli, V. (2008) · Neuron · doi:10.1016/j.neuron.2008.09.028 · Cited by 372 · see citing works
Growth Suppression of Pre-T Acute Lymphoblastic Leukemia Cells by Inhibition of Notch Signaling
Weng, A. P., Nam, Y., Wolfe, M. S., Pear, W. S., Griffin, J. D., Blacklow, S. C., & Aster, J. C. (2003) · Molecular and Cellular Biology · doi:10.1128/mcb.23.2.655-664.2003 · Cited by 369 · see citing works
Bultje, R. S., Castañeda-Castellanos, D. R., Jan, L. Y., Jan, Y. N., Kriegstein, A. R., & Shi, S. (2009) · Neuron · doi:10.1016/j.neuron.2009.07.004 · Cited by 346 · see citing works
Self-citationGal, J. S., Morozov, Y. M., Ayoub, A. E., Chatterjee, M., RAKIC, P. T., & Haydar, T. F. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.4499-05.2006 · Cited by 343 · see citing works
Fate-Restricted Neural Progenitors in the Mammalian Cerebral Cortex
Franco, S. J., Gil, C., Martínez‐Garay, I., Espinosa, A., Harkins-Perry, S. R., Ramos, C., & Müller, U. (2012) · Science · doi:10.1126/science.1223616 · Cited by 334 · see citing works
Non-epithelial stem cells and cortical interneuron production in the human ganglionic eminences
Hansen, D. V., Lui, J. H., Flandin, P., Yoshikawa, K., Rubenstein, J. L., Alvarez-Buylla, A., & Kriegstein, A. R. (2013) · Nature Neuroscience · doi:10.1038/nn.3541 · Cited by 328 · see citing works
The embryonic preoptic area is a novel source of cortical GABAergic interneurons
Gelman, D. M., Martini, F. J., Nóbrega-Pereira, S., Pierani, A., Kessaris, N., & Marín, O. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.0604-09.2009 · Cited by 280 · see citing works
Xu, Q., Guo, L., Moore, H., Waclaw, R. R., Campbell, K., & Anderson, S. A. (2010) · Neuron · doi:10.1016/j.neuron.2010.01.004 · Cited by 218 · see citing works
Self-citationA spatial bias for the origins of interneuron subgroups within the medial ganglionic eminence
Wonders, C. P., Taylor, L. A., Welagen, J., Mbata, I. C., Xiang, J., & Anderson, S. A. (2007) · Developmental Biology · doi:10.1016/j.ydbio.2007.11.018 · Cited by 215 · see citing works
Self-citationAmplification of progenitors in the mammalian telencephalon includes a new radial glial cell type
Pilz, G.-A., Shitamukai, A., Reillo, I., Pacary, E., Schwausch, J., Stahl, R., Ninkovic, J., Snippert, H. J. G., Clevers, H. C., Godinho, L., et al. (2013) · Nature Communications · doi:10.1038/ncomms3125 · Cited by 212 · see citing works
Yoon, K., Koo, B., Im, S.-K., Jeong, H., Ghim, J., Kwon, M.-C., Moon, J.-S., Miyata, T., & Kong, Y. (2008) · Neuron · doi:10.1016/j.neuron.2008.03.018 · Cited by 198 · see citing works
Stancik, E. K., Navarro-Quiroga, I., Sellke, R., & Haydar, T. F. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.6131-09.2010 · Cited by 186 · see citing works
Genetics and Function of Neocortical GABAergic Interneurons in Neurodevelopmental Disorders
Rossignol, E. (2011) · Neural Plasticity · doi:10.1155/2011/649325 · Cited by 183 · see citing works
Postiglione, M. P., Jüschke, C., Xie, Y., Haas, G. A., Charalambous, C., & Knoblich, J. A. (2011) · Neuron · doi:10.1016/j.neuron.2011.09.022 · Cited by 169 · see citing works
Inan, M., Welagen, J., & Anderson, S. A. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhr148 · Cited by 161 · see citing works
Self-citationClonal production and organization of inhibitory interneurons in the neocortex
Brown, K. N., Chen, S., Han, Z., Lu, C.-H., Tan, X., Zhang, X.-J., Ding, L., Lopez-Cruz, A., Saur, D., Anderson, S. A., et al. (2011) · Science · doi:10.1126/science.1208884 · Cited by 152 · see citing works
Self-citationOrigin and molecular specification of globus pallidus neurons
Nóbrega-Pereira, S., Gelman, D., Bartolini, G., Pla, R., Pierani, A., & Marín, O. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.4023-09.2010 · Cited by 142 · see citing works
Lineage-specific laminar organization of cortical GABAergic interneurons
Ciceri, G., Dehorter, N., Sols, I., Huang, Z. J., Maravall, M., & Marín, O. (2013) · Nature Neuroscience · doi:10.1038/nn.3485 · Cited by 124 · see citing works
Mayer, C., Jaglin, X. H., Cobbs, L. V., Bandler, R. C., Streicher, C., Cepko, C. L., Hippenmeyer, S., & Fishell, G. (2015) · Neuron · doi:10.1016/j.neuron.2015.07.011 · Cited by 113 · see citing works
Self-citationLodato, S., Tomassy, G. S., De Leonibus, E., Uzcategui, Y. G., Andolfi, G., Armentano, M., Touzot, A., Gaztelu, J. M., Arlotta, P., Menendez de la Prida, L., et al. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.6580-10.2011 · Cited by 112 · see citing works
The role of Notch and Rho GTPase signaling in the control of dendritic development
Redmond, L., & Ghosh, A. (2001) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(00)00181-1 · Cited by 111 · see citing works
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 · see citing works
Selective cortical interneuron and GABA deficits in cyclin D2-null mice
Glickstein, S. B., Moore, H., Slowinska, B., Racchumi, J., Suh, M., Chuhma, N., & Ross, M. E. (2007) · Development · doi:10.1242/dev.008524 · Cited by 89 · see citing works
Self-citationDifferences in Cyclin D2 and D1 Protein Expression Distinguish Forebrain Progenitor Subsets
Glickstein, S. B., Alexander, S., & Ross, M. E. (2006) · Cerebral Cortex · doi:10.1093/cercor/bhk008 · Cited by 85 · see citing works
Self-citationSawamoto, K., Yamamoto, A., Kawaguchi, A., Yamaguchi, M., Mori, K., Goldman, S. A., & Okano, H. (2001) · Journal of Neuroscience Research · doi:10.1002/jnr.1145 · Cited by 66 · see citing works
Guirado, S., D�vila, J. C., Real, M. A., & Medina, L. M. (1999) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19990301)405:1 · Cited by 33 · see citing works
Culurgioni, S., & Mapelli, M. (2013) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-013-1319-z · Cited by 17 · see citing works
Sukhov, R. R., Cayouette, M. H., Radeke, M. J., Feinstein, S. C., Blumberg, D., Rosenthal, A., Price, D. L., & Koliatsos, V. E. (1997) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19970630)383:2 · Cited by 11 · see citing works
Flagged first, then by citations
Research works printed but not linked: 2
- Gloster A El-Bizri H Bamji SX Rogers D Miller FD 1999 Early induction of Talpha1 alpha-tubulin transcription in neurons of the developing nervous system J Comp Neurol 405 45 60 10022195
- Sheth AN Bhide P 1997 Concurrent cellular output from two proliferative populations in the early embryonic mouse corpus striatum Journal of Comparative Neurology 383 220 230 9182850
Cited by
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Hippocampal GABAergic Inhibitory Interneurons
Pelkey, K. A., Chittajallu, R., Craig, M. T., Tricoire, L., Wester, J. C., & McBain, C. J. (2017) · Physiological Reviews · doi:10.1152/physrev.00007.2017 · Cited by 889 · see citing works
Development and Functional Diversification of Cortical Interneurons
Lim, L., Mi, D., Llorca, A., & Marín, O. (2018) · Neuron · doi:10.1016/j.neuron.2018.10.009 · Cited by 714 · see citing works
“…is consistent with the observation that intermediate progenitor cells in the MGE and CGE are transcriptionally heterogeneous (Mi et al., 2018; Petryniak et al., 2007), but it contrasts with previous work suggesting that SST+ interneurons are preferentially generated from VZ progenitors…”
Developmental diversification of cortical inhibitory interneurons
Mayer, C., Hafemeister, C., Bandler, R. C., Machold, R., Batista Brito, R., Jaglin, X., Allaway, K., Butler, A., Fishell, G., & Satija, R. (2018) · Nature · doi:10.1038/nature25999 · Cited by 492 · see citing works
Self-citationCortical interneuron development: a tale of time and space
Hu, J. S., Vogt, D., Sandberg, M., & Rubenstein, J. L. (2017) · Development · doi:10.1242/dev.132852 · Cited by 189 · see citing works
Cortical interneuron specification: the juncture of genes, time and geometry
Bandler, R. C., Mayer, C., & Fishell, G. (2017) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2016.10.003 · Cited by 125 · see citing works
Self-citationInterneuron origin and molecular diversity in the human fetal brain
Yu, Y., Zeng, Z., Xie, D., Chen, R., Sha, Y., Huang, S., Cai, W., Chen, W., Li, W., Ke, R., et al. (2021) · Nature Neuroscience · doi:10.1038/s41593-021-00940-3 · Cited by 101 · see citing works
The Ciliary Margin Zone of the Mammalian Retina Generates Retinal Ganglion Cells
Marcucci, F., Murcia‐Belmonte, V., Wang, Q., Coca, Y., Ferreiro‐Galve, S., Kuwajima, T., Khalid, S., Ross, M. E., Mason, C. A., & Herrera, E. (2016) · Cell Reports · doi:10.1016/j.celrep.2016.11.016 · Cited by 95 · see citing works
Self-citationSingle-cell RNA sequencing identifies distinct mouse medial ganglionic eminence cell types
Chen, Y.-J. J., Friedman, B. A., Ha, C., Durinck, S., Liu, J., Rubenstein, J. L. R., Seshagiri, S., & Modrusan, Z. D. (2017) · Scientific Reports · doi:10.1038/srep45656 · Cited by 79 · see citing works
Beyond Axon Guidance: Roles of Slit-Robo Signaling in Neocortical Formation
Gonda, Y., Namba, T., & Hanashima, C. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.607415 · Cited by 75 · see citing works
Local Thyroid Hormone Action in Brain Development
Alcaide, M. A., & Mayerl, S. E. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241512352 · Cited by 70 · see citing works
Coup-TF1 and Coup-TF2 control subtype and laminar identity of MGE-derived neocortical interneurons
Hu, J. S., Vogt, D. L., Lindtner, S., Sandberg, M., Silberberg, S. N., & Rubenstein, J. L. R. (2017) · Development · doi:10.1242/dev.150664 · Cited by 63 · see citing works
Pai, E. L.-L., Vogt, D. L., Clemente-Perez, A., McKinsey, G. L., Cho, F. S., Hu, J. S., Wimer, M., Paul, A., Darbandi, S. F., Pla, R., et al. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.01.031 · Cited by 63 · see citing works
Radial glia in the ventral telencephalon
Turrero García, M., & Harwell, C. C. (2017) · FEBS Letters · doi:10.1002/1873-3468.12829 · Cited by 62 · see citing works
Yu, D., Li, T., Delpech, J.-C., Zhu, B., Kishore, P., Koshi, T., Luo, R., Pratt, K. J. B., Popova, G., Nowakowski, T. J., et al. (2022) · Science Advances · doi:10.1126/sciadv.abm2545 · Cited by 58 · see citing works
Wang, Q., Marcucci, F., Cerullo, I., & Mason, C. A. (2016) · eNeuro · doi:10.1523/eneuro.0169-16.2016 · Cited by 56 · see citing works
Sp9 Regulates Medial Ganglionic Eminence-Derived Cortical Interneuron Development
Liu, Z., Zhang, Z., Lindtner, S., Li, Z., Xu, Z., Wei, S., Liang, Q., Wen, Y. F., Tao, G., You, Y., et al. (2018) · Cerebral Cortex · doi:10.1093/cercor/bhy133 · Cited by 53 · see citing works
Close, J., Yao, Z., Levi, B. P., Miller, J. A., Bakken, T. E., Menon, V., Ting, J. T., Wall, A., Krostag, A.-R., Thomsen, E. R., et al. (2017) · Neuron · doi:10.1016/j.neuron.2017.02.014 · Cited by 51 · see citing works
Generation of diverse cortical inhibitory interneurons
Sultan, K. T., & Shi, S. (2017) · Wiley Interdisciplinary Reviews Developmental Biology · doi:10.1002/wdev.306 · Cited by 48 · see citing works
From Progenitors to Progeny: Shaping Striatal Circuit Development and Function
Knowles, R., Dehorter, N., & Ellender, T. J. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.0620-21.2021 · Cited by 45 · see citing works
Temporal Dynamics and Neuronal Specificity of Grin3a Expression in the Mouse Forebrain
Murillo, A., Navarro, A. I., Puelles, E., Zhang, Y., Petros, T. J., & Pérez‐Otaño, I. (2020) · Cerebral Cortex · doi:10.1093/cercor/bhaa330 · Cited by 46 · see citing works
Self-citationPensold, D., Symmank, J., Hahn, A., Lingner, T., Salinas, G., Downie, B., Ludewig, F., Rotzsch, A., Haag, N., Andreas, N., et al. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhw341 · Cited by 43 · see citing works
Transcriptional regulation of intermediate progenitor cell generation during hippocampal development
Harris, L., Zalucki, O. H., Gobius, I., McDonald, H., Osinki, J., Harvey, T. J., Essebier, A., Vidovic, D., Gladwyn-Ng, I. E., Burne, T. H. J., et al. (2016) · Development · doi:10.1242/dev.140681 · Cited by 42 · see citing works
McKenzie, M. G., Cobbs, L., Dummer, P. D., Petros, T. J., Halford, M. M., Stacker, S. A., Zou, Y., Fishell, G., & Au, E. (2019) · Neuron · doi:10.1016/j.neuron.2019.06.003 · Cited by 40 · see citing works
Self-citationPai, E. L.-L., Chen, J., Darbandi, S. F., Cho, F. S., Chen, J., Lindtner, S., Chu, J. S. F., Paz, J. T., Vogt, D. L., Paredes, M. F., et al. (2020) · eLife · doi:10.7554/elife.54903 · Cited by 43 · see citing works
Falk, S., Bugeon, S., Ninkovic, J., Pilz, G.-A., Postiglione, M. P., Cremer, H., Knoblich, J. A., & Götz, M. (2017) · Neuron · doi:10.1016/j.neuron.2017.02.009 · Cited by 39 · see citing works
Origin, Development, and Synaptogenesis of Cortical Interneurons
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Lee, D. R., Rhodes, C. T., Mitra, A., Zhang, Y., Maric, D., Dale, R. K., & Petros, T. J. (2022) · eLife · doi:10.7554/elife.71864 · Cited by 39 · see citing works
Self-citationAn epigenome atlas of neural progenitors within the embryonic mouse forebrain
Rhodes, C. T., Thompson, J. J., Mitra, A., Asokumar, D., Lee, D. R., Lee, D. J., Zhang, Y., Jason, E., Dale, R., Rocha, P. P., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-31793-4 · Cited by 33 · see citing works
Self-citationTranscriptional profiling of sequentially generated septal neuron fates
García, M. T., Stegmann, S. K., Lacey, T. E., Reid, C. M., Hrvatin, S., Weinreb, C., Adam, M. A., Nagy, M. A., & Harwell, C. C. (2021) · eLife · doi:10.7554/elife.71545 · Cited by 29 · see citing works
Magno, L., Asgarian, Z., Pendolino, V., Velona, T., Mackintosh, A. I., Lee, F., Stryjewska, A., Zimmer, C., Guillemot, F., Farrant, M., et al. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.109249 · Cited by 28 · see citing works
Heterotopic Transplantations Reveal Environmental Influences on Interneuron Diversity and Maturation
Quattrocolo, G., Fishell, G., & Petros, T. J. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.09.075 · Cited by 28 · see citing works
Self-citationElucidating the developmental trajectories of GABAergic cortical interneuron subtypes
Miyoshi, G. (2018) · Neuroscience Research · doi:10.1016/j.neures.2018.09.012 · Cited by 28 · see citing works
Development, Diversity, and Death of MGE-Derived Cortical Interneurons
Williams, R. H., & Riedemann, T. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22179297 · Cited by 24 · see citing works
Angara, K., Pai, E. L.-L., Bilinovich, S. M., Stafford, A. M., Nguyen, J. T., Li, K. X., Paul, A., Rubenstein, J. L. R., & Vogt, D. L. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1915458117 · Cited by 24 · see citing works
Slavi, N., Balasubramanian, R., Lee, M. A., Liapin, M., Oaks-Leaf, R., Peregrin, J., Potenski, A. M., Troy, C. M., Ross, M. E., Herrera, E., et al. (2022) · Neuron · doi:10.1016/j.neuron.2022.10.025 · Cited by 23 · see citing works
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Generation of cerebral cortical GABAergic interneurons from pluripotent stem cells
Fitzgerald, M., Sotuyo, N. P., Tischfield, D. J., & Anderson, S. A. (2020) · Stem Cells · doi:10.1002/stem.3252 · Cited by 20 · see citing works
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Chohan, M. O., & Moore, H. M. (2016) · Frontiers in Neural Circuits · doi:10.3389/fncir.2016.00064 · Cited by 22 · see citing works
Ansen-Wilson, L. J., & Lipinski, R. J. (2016) · NeuroToxicology · doi:10.1016/j.neuro.2016.12.002 · Cited by 22 · see citing works
O’Shaughnessy, K. L., McMichael, B. D., Sasser, A. L., Bell, K. S., Riutta, C., Ford, J., Stoker, T. E., Grindstaff, R. D., Pandiri, A. R., & Gilbert, M. E. (2023) · Frontiers in Endocrinology · doi:10.3389/fendo.2023.1090081 · Cited by 18 · see citing works
Sultan, K. T., Liu, W. A., Li, Z.-L., Shen, Z., Li, Z., Zhang, X., Dean, O. R., Ma, J., & Shi, S. (2018) · Nature Communications · doi:10.1038/s41467-018-07055-7 · Cited by 18 · see citing works
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Sheehan, C. J., McMahon, J. J., Serdar, L. D., & Silver, D. L. (2019) · Development · doi:10.1242/dev.182295 · Cited by 16 · see citing works
Ramos, S. I., Makeyev, E. V., Salierno, M. J., Kodama, T., Kawakami, Y., & Sahara, S. (2020) · Developmental Cell · doi:10.1016/j.devcel.2020.01.036 · Cited by 15 · see citing works
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Self-citationFate determination of cerebral cortical GABAergic interneurons and their derivation from stem cells
DeBoer, E., & Anderson, S. A. (2015) · Brain Research · doi:10.1016/j.brainres.2015.12.031 · Cited by 13 · see citing works
Self-citationDistinct hyperactive RAS/MAPK alleles converge on common GABAergic interneuron core programs
Knowles, S. J., Stafford, A. M., Zaman, T., Angara, K., Williams, M. R., Newbern, J. M., & Vogt, D. L. (2023) · Development · doi:10.1242/dev.201371 · Cited by 13 · see citing works
Mason, C. A., & Guillery, R. W. (2019) · European Journal of Neuroscience · doi:10.1111/ejn.14396 · Cited by 12 · see citing works
Fin, N. A. S. H., Yip, A., Scott, J. T., Teo, L., Homman‐Ludiye, J., & Bourne, J. A. (2025) · Development · doi:10.1242/dev.204254 · Cited by 13 · see citing works
Temporal control of progenitor competence shapes maturation in GABAergic neuron development in mice
Bright, A. R., Kotlyarenko, Y., Neuhaus, F., Rodrigues, D., Feng, C., Peters, C., Vitali, I., Dönmez, E., Myoga, M. H., Dvoretskova, E., et al. (2025) · Nature Neuroscience · doi:10.1038/s41593-025-01999-y · Cited by 11 · see citing works
Garcίa, M. T., Baizabal, J., Tran, D. N., Peixoto, R. T., Wang, W., Xie, Y., Adam, M. A., English, L. A., Reid, C. M., Brito, S. I., et al. (2020) · Development · doi:10.1242/dev.187526 · Cited by 11 · see citing works
Kelly, S. M., Raudales, R., Moissidis, M., & Huang, Z. J. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/735019 · Cited by 9 · see citing works
Loss of the centrosomal protein Cenpj leads to dysfunction of the hypothalamus and obesity in mice
Ding, W., Zhang, C., Wang, B., Zhou, X., Sun, L., Zhong, S., Liu, J., Zhang, J., Wang, X., & Wu, Q. (2020) · Science China Life Sciences · doi:10.1007/s11427-020-1767-5 · Cited by 12 · see citing works
DOT1L deletion impairs the development of cortical parvalbumin-expressing interneurons
Cheffer, A., Garcia‐Miralles, M., Maier, E., Akol, I., Franz, H., Srinivasan, V. S. V., & Vogel, T. (2023) · Cerebral Cortex · doi:10.1093/cercor/bhad281 · Cited by 7 · see citing works
Tischfield, D. J., Kim, J., & Anderson, S. A. (2017) · Stem Cell Reports · doi:10.1016/j.stemcr.2017.03.015 · Cited by 7 · see citing works
Self-citationGrowth/differentiation factor 15 controls ependymal and stem cell number in the V-SVZ
Baur, K., García, C. C., Şan, Ş., von Hahn, M., Strelau, J., Hölzl‐Wenig, G., Mandl, C., & Ciccolini, F. (2024) · Stem Cell Reports · doi:10.1016/j.stemcr.2024.01.008 · Cited by 6 · see citing works
Kaushik, K., Chapman, G., Prakasam, R., Batool, F., Saleh, M., Determan, J. J., Huettner, J. E., & Kroll, K. L. (2025) · Cell Reports · doi:10.1016/j.celrep.2025.115597 · Cited by 6 · see citing works
Transcriptional Regulation of Cortical Interneuron Development
Pai, E. L.-L., Vogt, D. L., Hu, J. S., & Rubenstein, J. L. R. (2024) · Oxford University Press eBooks · doi:10.1093/med/9780197549469.003.0047 · Cited by 5 · see citing works
Developmental emergence of cortical neurogliaform cell diversity
Gomez, L., Cadilhac, C., Prados, J., Mule, N., Jabaudon, D., & Dayer, A. G. (2023) · Development · doi:10.1242/dev.201830 · Cited by 4 · see citing works
Subventricular zone radial glial cells maintain inhibitory neuron production in the human brain
Jia, L., Li, X., Yan, Y., Xu, L., Guo, J., Wang, W., Zhang, W., Li, L., Shang, B., Zhang, Y., et al. (2026) · Science · doi:10.1126/science.adw1803 · Cited by 4 · see citing works
Rhodes, C. T., Asokumar, D., Sohn, M., Naskar, S., Elisha, L., Stevenson, P. K., Lee, D. R., Zhang, Y., Rocha, P. P., Dale, R., et al. (2024) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2024.1334244 · Cited by 4 · see citing works
Self-citationBechelli, L., Tomasella, E., Cardoso, S. L., Belmonte, M., & Gelman, D. M. (2023) · Scientific Reports · doi:10.1038/s41598-023-46954-8 · Cited by 3 · see citing works
Fin, N. A. S. H., Yip, A., Teo, L., Homman‐Ludiye, J., & Bourne, J. A. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.07.10.602904 · Cited by 3 · see citing works
Esumi, S., Nasu, M., Kawauchi, T., Miike, K., Morooka, K., Yanagawa, Y., Seki, T., Sakimura, K., Fukuda, T., & Tamamaki, N. (2021) · Frontiers in Neuroscience · doi:10.3389/fnins.2021.607908 · Cited by 2 · see citing works
Knowles, S. J., Holter, M. C., Li, G., Bjorklund, G. R., Rees, K. P., Martinez-Fuentes, J. S., Nishimura, K. J., Afshari, A. E., Fry, N., Stafford, A. M., et al. (2023) · doi:10.7554/elife.88313.1 · Cited by 2 · see citing works
Lu, I.-L., Song, M., Rangel-Sandoval, C., Palacios, J. M., Kim, J., Huang, E. J., Álvarez-Buylla, A., Kriegstein, A. R., Paredes, M. F., & Rowitch, D. H. (2026) · Developmental Cell · doi:10.1016/j.devcel.2026.01.007 · Cited by 1 · see citing works
A Butterfly Effect on Neural Stem Cells
Vanderhaeghen, P. (2017) · Neuron · doi:10.1016/j.neuron.2017.02.015 · Cited by 1 · see citing works
Differentiation of Mouse Embryonic Stem Cells into Cortical Interneuron Precursors
Tischfield, D. J., & Anderson, S. A. (2017) · Journal of Visualized Experiments · doi:10.3791/56358 · Cited by 1 · see citing works
Self-citationHomochronic Transplantation of Interneuron Precursors into Early Postnatal Mouse Brains
Quattrocolo, G., Isaac, M., Zhang, Y., & Petros, T. J. (2018) · Journal of Visualized Experiments · doi:10.3791/57723 · Cited by 1 · see citing works
Self-citationSpecific Functions of ERK/MAPK Signaling in Brain Development and Neurocognition
Holter, M. C. (2019) · Cited by 1 · see citing works
Petros, T. J. (2018) · Journal of Experimental Neuroscience · doi:10.1177/1179069518758656 · Cited by 1 · see citing works
Self-citationKnowles, S. J., Holter, M. C., Li, G., Bjorklund, G. R., Rees, K. P., Martinez-Fuentes, J. S., Nishimura, K. J., Afshari, A. E., Fry, N., Stafford, A. M., et al. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.08.02.502073 · Cited by 1 · see citing works
Baur, K., Carrillo-García, C., Şan, Ş., von Hahn, M., Strelau, J., Hölzl-Wenig, G., Mandl, C., & Ciccolini, F. (2023) · bioRxiv · doi:10.1101/2022.12.02.518869 · Cited by 1 · see citing works
Knowles, S. J., Holter, M. C., Li, G., Bjorklund, G. R., Rees, K. P., Martinez-Fuentes, J. S., Nishimura, K. J., Afshari, A. E., Fry, N., Stafford, A. M., et al. (2023) · doi:10.7554/elife.88313 · Cited by 1 · see citing works
Marshall, A. H., Boyle, D. J., Hanson, M. A., Nagarajan, D., Bibi, N., Safa, A., Johantges, A. C., & Wester, J. C. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.06.07.597984 · Cited by 1 · see citing works
McKenzie, M. G., Cobbs, L., Petros, T. J., Halford, M. M., Stacker, S. A., Zou, Y., Fishell, G., & Au, E. (2018) · SSRN Electronic Journal · doi:10.2139/ssrn.3155597
Self-citationTranscription factor ZBTB20: What expression is telling us of its cellular function?
Stoyanov, D. S., & Tonchev, A. B. (2020) · Biomedical Reviews · doi:10.14748/bmr.v31.7700
The construction of 3D cognitive networks from iPSCs through precise spatiotemporal specification
Miu, K.-K., Cao, D., Wang, Z., Hao, S., & Chan, W. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-823809-7.00012-8
Noguchi, H., Li, G., & Pleasure, S. J. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-814407-7.00017-1
Genesis and Migration of Cerebral Cortical Inhibitory Interneurons: An Overview
Cook, K., & Anderson, S. A. (2022) · Springer eBooks · doi:10.1007/978-1-4614-6434-1_186-1
Self-citationHomochronic Transplantation of Interneuron Precursors into Early Postnatal Mouse Brains
Quattrocolo, G., Isaac, M., Zhang, Y., & Petros, T. J. (2018) · Journal of Visualized Experiments · doi:10.3791/57723-v
Self-citationGenesis and Migration of Cerebral Cortical Inhibitory Interneurons: An Overview
Cook, K., & Anderson, S. A. (2022) · Springer eBooks · doi:10.1007/978-3-030-88832-9_186
Self-citationCortical Neuron Migration in Health and Disease
Javier‐Torrent, M., & Nguyen, L. (2023) · Wiley eBooks · doi:10.1002/9781119860914.ch17
Knowles, S. J., Holter, M. C., Li, G., et al. (2023) · doi:10.7554/elife.88313.1.sa0
NFIB influences progenitor competence in maturation of GABAergic neurons in micePreprint
Bright, A. R., Kotlyarenko, Y., Neuhaus, F., Rodrigues, D., Feng, C., Peters, C., Vitali, I., Dönmez, E., Myoga, M. H., Dvoretskova, E., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.03.18.585524
Garg, V., Beyene, S., Tanzillo, A. F., Tucker, A., Johantges, A. C., Abebe, D. T., Zhang, Y., & Petros, T. J. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.07.28.667082 · Cited by 1 · see citing works
Self-citationSelective Lis1 inactivation disrupts migration and positioning of cortical somatostatin interneurons
Pombero, A., García-López, R., Geijo‐Barrientos, E., & Martı́nez, S. (2026) · Scientific Reports · doi:10.1038/s41598-026-38316-x
Rapid and reproducible in vitro generation of human parvalbumin-expressing cortical interneuronsPreprint
Azzouni, K., D’Andrea, D., Ghazwani, A., Wilson, S., Pocklington, A. J., & Shin, E. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.03.09.710579
Etude du rôle de la kinésine KIF21B au cours du développement cortical
Asselin, L. (2019) · theses.fr (ABES) · doi:10.70675/bd543948zdb0fz4298zae3fzf4fc50923d78
- Authors
- Petros, T. J., Bultje, R. S., Ross, M. E., Fishell, G., & Anderson, S. A.
- Affiliations
- Weill Cornell Medicine (US)
- New York University (US)
- Children's Hospital of Philadelphia (US)
- Corresponding author
- Anderson, Stewart A.
- Venue
- Cell Reports
- Publisher
- Elsevier BV
- Published
- 2015-11
- Volume
- 13
- Issue
- 6
- Pages
- 1090-1095
- ISSN
- 2211-1247 (ISSN-L)
- PMC
- PMC4704102
- OpenAlex
- W1924943590
- Cited by
- 91
- References
- 40
- Citations by year
- 2026: 4 · 2025: 4 · 2024: 6 · 2023: 11 · 2022: 9 · 2021: 7 · 2020: 10 · 2019: 7 · 2018: 11 · 2017: 13 · 2016: 8 · 2015: 1
- FWCI
- 4.42
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Cell Reports (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion)
- Funders
- National Institutes of Health
- National Institute of Mental Health (K02MH070031, R01MH066912, K99MH104595, R01MH070031)
- National Institute of Neurological Disorders and Stroke (P01NS074972, F32NS074742, P01NS048120, R01NS081297)
- 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 › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Congenital heart defects research
- Keywords
- cortical interneurons, neuronal fate determination, somatostatin interneurons, parvalbumin interneurons, subventricular zone, ventricular zone
- MeSH terms
- Animals, Cerebral Cortex, Interneurons, Mice, Inbred C57BL, Parvalbumins, Somatostatin, Telencephalon, Cell Lineage, Mice, Neurogenesis
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