The DOI matches its Crossref record; 142 of the 142 references it cites were found in a registry or an index.
The origin and specification of cortical interneurons
Abstract
GABA-containing interneurons are crucial to both the development and function of the cerebral cortex. Unlike cortical projection neurons, which have a relatively conserved set of characteristics, interneurons include multiple phenotypes that vary on morphological, physiological and neurochemical axes. This diversity, and the relatively late, context-dependent maturation of defining features, has challenged efforts to uncover the transcriptional control of cortical interneuron development. Here, we discuss recent data that are beginning to illuminate the origins and specification of distinct subgroups of cortical interneurons.
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“Their 'parvalbumin' fate seems to be established at their origin, as the progenitors leave the cell cycle [127, 128].”
From Parvalbumin interneuron vulnerability and brain disorders (2021) · cites this paper as [127]
In the citing paper
“In contrast, Martinotti cells and 5-HT3AR-lacking O-LM cells arise from MGE progenitors with specification driven by the homeodomain transcription factor Nkx2.1 (10% of MGE-derived hippocampal interneurons based on assumptions outlined above combined with the fact that O-LMs represent 40% of SST interneurons) (102, 203, 651, 794, 1042, 1134, 1138, 1213).”
From Hippocampal GABAergic Inhibitory Interneurons (2017) · cites this paper as [1213]
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“We also observed that over-expression of Maf at the peak of PV neurogenesis (E14.5) (23) repress PV+ interneuron fates (fig. S24, D and E).”
From Early emergence of cortical interneuron diversity in the mouse embryo (2018) · cites this paper as [23]
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Neuronal subtype specification in the cerebral cortex
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“Multiple lines of evidence suggest that cortical interneuron diversity arises during development through the interaction of specific genetic and environmental factor”
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“…rodents and primates, the projection neurons, which utilize the excitatory neurotransmitter glutamate, and the local circuit neurons, many of which use the inhibitory neurotransmitter gamma-amino butyric acid (GABA), arise in part from different regions of the forebrain (Wonders & Anderson, 2007).”
Hippocampal GABAergic Inhibitory Interneurons
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“…interneurons, which account for about 20% of all cortical neurons, are GABAergic and also typically express distinct neuropeptides that help define subclasses (Cherubini and Conti, 2001; Krimer and Goldman-Rakic, 2001; Kawaguchi and Kondo, 2002; Butt et al., 2005; Wonders and Anderson, 2006).”
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“…studies, to give rise to the globus pallidus (Pakzaban et al., 1993), subclasses of interneurons of the striatum and cortex (Metin et al., 2006; Wonders and Anderson, 2006), and cholinergic projection neurons of the nucleus basalis (Fragkouli et al., 2005; Sussel et al., 1999; Zhao et al.,…”
BackgroundSelf-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
“In addition, analysis of interneuron populations derived from the MGE and CGE suggests that these two regions may contain different progenitor pools (Xu et al., 2004; Butt et al., 2005; Wonders and Anderson, 2006).”
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“…to lie in the growing body of evidence suggesting that the subtype identity of a given interneuron can be predicted by its place and time of origin (Xu et al., 2004; Butt et al., 2005; Wonders and Anderson, 2006; Flames et al., 2007; Fogarty et al., 2007; Ghanem et al., 2007; Miyoshi et al., 2007).”
BackgroundHardwiring the Brain: Endocannabinoids Shape Neuronal Connectivity
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“One mechanism for generating neuronal diversity that is employed during CNS development is the specification of a particular type of neuron in one region, followed by their subsequent migration away from this region to occupy appropriate functional position”
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“Cortical interneurons originate within the subcortical telencephalon (for PV-cells the medial ganglionic eminence) and then migrate tangentially into the overlying cortex but never express Otx2 (Butt et al., 2007; Wonders and Anderson, 2006).”
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Control of cortical GABA circuitry development by Nrg1 and ErbB4 signalling
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“generation of regular- and burst-spiking interneurons [29], we”
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“, place and timing of neuron birth, transcription factors regulating cell fate, etc; see (Wonders and Anderson, 2006) for review] might also contribute to cell type-specific vulnerability.”
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“In addition, both time of birth (30) and transcription factors that regulate early differentiation (31) differ across these subpopulations of GABA neurons.”
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“However, the bulk of data support a major subpallial origin for cortical interneurons in rodents (for review, see Wonders and Anderson, 2006).”
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“…neuronal cultures highly enriched for these neurons by taking advantage of the fact that, early in their development, inhibitory neurons are localized to specialized regions of the embryonic brain, the ganglionic eminences, that are devoid of excitatory neurons (Wonders and Anderson, 2006).”
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New insights into the development of the human cerebral cortex
Molnár, Z., Clowry, G. J., Šestan, N., Alzu’bi, A., Bakken, T. E., Hevner, R. F., Hüppi, P. S., Kostović, I., RAKIC, P. T., Anton, E. S., et al. (2019) · Journal of Anatomy · doi:10.1111/joa.13055 · Cited by 426
“The neuronal progenitor marker GSX2, proposed to specify CalR+ interneurons generation in the CGE, has been found to be expressed in proliferating cells in the VZ/SVZ of the human fetal cortex (Radonji c et al. 2014).”
BackgroundInfluentialGeneral Cortical and Special Prefrontal Connections: Principles from Structure to Function
Barbas, H. (2015) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-071714-033936 · Cited by 408
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“Fate-mapping studies of the ventral telencephalon have revealed that the medial (MGE) and caudal (CGE) ganglionic eminences produce most of these GABAergic cortical interneurons (Wichterle et al., 2001; Nery et al., 2002; Xu et al., 2004; Butt et al., 2005; Wonders and Anderson, 2006).”
BackgroundTranscriptional co-regulation of neuronal migration and laminar identity in the neocortex
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“The molecular mechanisms that regulate these developmental processes are being unraveled and remain a highly active area of research (Marín and Rubenstein, 2003; Rash and Grove, 2006; Wonders and Anderson, 2006; Molyneaux et al., 2007; Leone et al., 2008; Batista-Brito and Fishell, 2009).”
BackgroundCell Densities in the Mouse Brain: A Systematic Review
Keller, D., Erö, C., & Markram, H. (2018) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2018.00083 · Cited by 380
Characterizing transcriptional heterogeneity through pathway and gene set overdispersion analysis
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“During development CR, NPY and VIP neurons originate in the CGE (Flames and Marín, 2005; but, see Anderson et al., 2001; Wonders and Anderson, 2006), whereas SOM progenitors are born in the MGE (Butt et al., 2005; Miyoshi et al., 2007; Xu et al., 2004).”
BackgroundInfluentialThe determination of projection neuron identity in the developing cerebral cortex
Leone, D. P., Srinivasan, K., Chen, B., Alcamo, E., & McConnell, S. K. (2008) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2008.05.006 · Cited by 382
“The regulation of interneuron fates has been reviewed recently and will not be discussed here [1,2].”
BackgroundThe genetics of early telencephalon patterning: some assembly required
Hébert, J. M., & Fishell, G. (2008) · Nature reviews. Neuroscience · doi:10.1038/nrn2463 · Cited by 377
“By contrast, the LGE produces a substantial population of olfactory bulb interneurons, as well as inhibitory projection neurons that populate several ventral regions including the striatum and limbic area”
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“1 and Gsh2, as well the signaling molecules Sonic hedgehog (Shh) and fibroblast growth factors (FGFs), establish the regional identity of the ganglionic eminences and AEP (Wonders and Anderson, 2006).”
InfluentialAdult generation of glutamatergic olfactory bulb interneurons
Brill, M. S., Ninkovic, J., Winpenny, E. M., Hodge, R. D., Ozen, I., Yang, R., Lepier, A., Gascón, S., Erdélyi, F., Szabó, G., et al. (2009) · Nature Neuroscience · doi:10.1038/nn.2416 · Cited by 364
“A large part of these interneurons arise from the lateral SEZ, which derives from the ventral telencephalon, producing mostly telencephalic GABAergic neurons during developmen”
BackgroundIntrinsically determined cell death of developing cortical interneurons
Southwell, D. G., Paredes, M. F., Galvao, R. P., Jones, D. L., Froemke, R. C., Sebe, J. Y., Alfaro-Cervello, C., Tang, Y., Garcia-Verdugo, J. M., Rubenstein, J. L., et al. (2012) · Nature · doi:10.1038/nature11523 · Cited by 365
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“To target gene expression in GABAergic neurons selectively, we have taken advantage of the Dlx gene family, which encodes homeobox transcription factors that are required for specification, maturation, and survival of forebrain GABAergic neurons (20, 21).”
BackgroundNon-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
“In the LGE OSVZ, only ~25% of cells expressed COUP-TFII, almost none of which were proliferating.”
BackgroundInfluentialSubcortical origins of human and monkey neocortical interneurons
Ma, T., Wang, C., Wang, L., Zhou, X., Tian, M., Zhang, Q., Zhang, Y., Li, J., Liu, Z., Cai, Y., et al. (2013) · Nature Neuroscience · doi:10.1038/nn.3536 · Cited by 322
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“6I), besides suggesting deficient or altered neuronal subtype specification, could also reflect an increased entry into the cortex of interneurons that were generated in germinal zones not affected by Dicer ablation (i.e. outside of the Emx1 domain) (Wonders and Anderson, 2006).”
Single-cell analysis of long non-coding RNAs in the developing human neocortex
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“With these methods, we identified the cell clusters to be endothelial cells (FLT1), radial glia (VIM, GFAP), dividing radial glia (MKI67, TOP2A), intermediate progenitors (EOMES), newborn neurons (SEMA3C, DCC), maturing excitatory neurons (SATB2, ADCY1), and inhibitory interneurons (DLX2, GAD1) [28, 34–36].”
MethodAstrocyte Development and HeterogeneityPreprint
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“…of the striatum and olfactory bulb (OB) interneurons, whereas MGE progenitors give rise to the interneurons that populate the different regions of the telencephalon, as well as projection neurons of the pallidum and basal forebrain (Campbell 2003; Wonders and Anderson 2006; Flames et al. 2007).”
BackgroundOkaty, B. W., Miller, M. N., Sugino, K., Hempel, C. M., & Nelson, S. B. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.0105-09.2009 · Cited by 309
“…evidence suggests that the location and time of birth of prospective interneurons dictates their mature phenotype in part by initiating divergent transcriptional cascades in the embryo (Xu et al., 2004; Butt et al., 2005, 2007; Cobos et al., 2006; Wonders and Anderson, 2006; Flames et al., 2007).”
BackgroundResultNeuronal activity is required for the development of specific cortical interneuron subtypes
De Marco García, N. V., Karayannis, T., & Fishell, G. (2011) · Nature · doi:10.1038/nature09865 · Cited by 294
Autism: A “Critical Period” Disorder?
LeBlanc, J. J., & Fagiolini, M. (2011) · Neural Plasticity · doi:10.1155/2011/921680 · Cited by 301
“In particular, progenitors of PV-cells derive from the medial ganglionic eminence with a relatively late birth date, and their differentiation and migration into specific cortical layers can be regulated by homeoproteins like Lhx6 [88, 89], or excitatory projection neurons [90].”
Dishing out mini-brains: Current progress and future prospects in brain organoid research
Kelava, I., & Lancaster, M. A. (2016) · Developmental Biology · doi:10.1016/j.ydbio.2016.06.037 · Cited by 323
“Additionally, organoids exhibit some of the features of regional connections, with interneurons, which in vivo are partly produced in the ventral forebrain and migrate to the dorsal cortex (Nakajima, 2012; Wonders and Anderson, 2006), showing a similar pattern of migration in the organoids.”
BackgroundEvaluating cell reprogramming, differentiation and conversion technologies in neuroscience
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CXCR4 and CXCR7 Have Distinct Functions in Regulating Interneuron Migration
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“Therefore, DLX2 + /Lhx6- GFP + cells (yellow) represented MGE-derived interneurons, whereas DLX2 + /Lhx6-GFP À cells (red) represented dCGEderived interneurons (Figure 2U).”
InfluentialSchulz, D. J., Goaillard, J.-M., & Marder, E. E. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0705827104 · Cited by 288
A Blueprint for the Spatiotemporal Origins of Mouse Hippocampal Interneuron Diversity
Tricoire, L., Pelkey, K. A., Erkkila, B. E., Jeffries, B. W., Yuan, X., & McBain, C. J. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.0323-11.2011 · Cited by 292
“Although distinct interneurons require weeks of postnatal maturation to fully attain their subtype-defining characteristics, genetic restriction of neuronal potential at the progenitor stage is a major determinant of interneuron diversity (Wonders and Anderson, 2006; Batista-Brito and Fishell, 2009).”
BackgroundInfluentialCxcr7 controls neuronal migration by regulating chemokine responsiveness
Sánchez-Alcañiz, J. A., Haege, S., Mueller, W., Pla, R., Mackay, F., Schulz, S., López-Bendito, G., Stumm, R., & Marín, O. (2011) · Neuron · doi:10.1016/j.neuron.2010.12.006 · Cited by 290
“Most cortical interneurons derive from the medial ganglionic eminence (MGE, Batista-Brito and Fishell, 2009; Wonders and Anderson, 2006), a transient structure in the developing basal telencephalon, and migrate toward the cortex in response to a combination of chemoattractive and chemorepulsive cues (Marı́n et al.”
BackgroundThe 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
“…to cells that migrate to the cortex Despite the substantial number of studies analyzing the derivatives of the ganglionic eminences (Corbin et al., 2001; Marín and Rubenstein, 2001; Wonders and Anderson, 2006), virtually nothing is known about the destiny of neurons generated in the embryonic POA.”
BackgroundInfluentialDevelopment of GABA innervation in the cerebral and cerebellar cortices
Huang, Z. J., Cristo, G. D., & Ango, F. (2007) · Nature reviews. Neuroscience · doi:10.1038/nrn2188 · Cited by 294
Cortical Plasticity Induced by Inhibitory Neuron Transplantation
Southwell, D. G., Froemke, R. C., Alvarez-Buylla, A., Stryker, M. P., & Gandhi, S. P. (2010) · Science · doi:10.1126/science.1183962 · Cited by 271
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“Lhx6 and Lhx7 are essential regulators of the fate of several types of GABAergic and cholinergic neurons derived from Nkx2-1-expressing progenitors (Fragkouli et al., 2005; Mori et al., 2004; Wonders and Anderson, 2006; Zhao et al., 1999), reinforcing the idea that Nkx2-1 expression prior to cell cycle exit influences…”
BackgroundSelf-citationInta, D., Alfonso, J., von Engelhardt, J., Kreuzberg, M. M., Meyer, A. H., van Hooft, J. A., & Monyer, H. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0807059105 · Cited by 267
“In agreement with other studies (14), a large fraction of cortical EGFP-positive interneurons were born during embryogenesis in the GE (Table 1 and Fig.”
BackgroundThinning of sensorimotor cortices in children with Tourette syndrome
Sowell, E. R., Kan, E., Yoshii, J., Thompson, P. M., Bansal, R., Xu, D., Toga, A. W., & Peterson, B. S. (2008) · Nature Neuroscience · doi:10.1038/nn.2121 · Cited by 254
Early emergence of cortical interneuron diversity in the mouse embryo
Mi, D., Li, Z., Lim, L., Li, M., Moissidis, M., Yang, Y., Gao, T., Hu, T. X., Pratt, T., Price, D. J., et al. (2018) · Science · doi:10.1126/science.aar6821 · Cited by 259
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Lodato, S., Rouaux, C., Quast, K. B., Jantrachotechatchawan, C., Studer, M., Hensch, T. K., & Arlotta, P. (2011) · Neuron · doi:10.1016/j.neuron.2011.01.015 · Cited by 244
Dlx transcription factors promote migration through repression of axon and dendrite growth
Cobos, I., Borello, U., & Rubenstein, J. L. R. (2007) · Neuron · doi:10.1016/j.neuron.2007.05.024 · Cited by 246
“Their differentiation program involves the outgrowth of neurites and tangential migration (yellow arrow) toward the cortical plate (Marin and Rubenstein, 2003; Metin et al., 2006; Wonders and Anderson, 2006).”
Chromatin accessibility dynamics in a model of human forebrain development
Trevino, A. E., Sinnott-Armstrong, N., Andersen, J., Yoon, S.-J., Huber, N., Pritchard, J. K., Chang, H. Y., Greenleaf, W. J., & Pașca, S. P. (2020) · Science · doi:10.1126/science.aay1645 · Cited by 251
“g-aminobutyric acid (GABA)– ergic interneurons, born in the subpallium, migrate into the cerebral cortex, where they integrate to form circuits (2, 3).”
BackgroundEarly somatostatin interneuron connectivity mediates the maturation of deep layer cortical circuits
Tuncdemir, S. N., Wamsley, B., Stam, F. J., Osakada, F., Goulding, M., Callaway, E. M., Rudy, B., & Fishell, G. (2016) · Neuron · doi:10.1016/j.neuron.2015.11.020 · Cited by 224
Direct lineage conversions: unnatural but useful?
Vierbuchen, T., & Wernig, M. (2011) · Nature Biotechnology · doi:10.1038/nbt.1946 · Cited by 259
Microglial Dynamics During Human Brain Development
Menassa, D. A., & Gómez‐Nicola, D. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.01014 · Cited by 259
Neurodevelopment, GABA System Dysfunction, and Schizophrenia
Schmidt, M. J., & Mirnics, K. (2014) · Neuropsychopharmacology · doi:10.1038/npp.2014.95 · Cited by 243
“Similarly, GABAergic interneuron types are predetermined based on unique transcription factor combinations in different progenitor types in the subpallial ganglionic eminences (Flames et al, 2007; Wonders and Anderson, 2006).”
BackgroundWirth, E. K., Conrad, M., Winterer, J., Wozny, C., Carlson, B. A., Roth, S., Schmitz, D., Bornkamm, G. W., Coppola, V., Tessarollo, L., et al. (2010) · The FASEB Journal · doi:10.1096/fj.09-143974 · Cited by 237
“origin with NPY and SOM interneurons (34), whose”
BackgroundKawase‐Koga, Y., Otaegi, G., & Sun, T. (2009) · Developmental Dynamics · doi:10.1002/dvdy.22109 · Cited by 241
Mechanisms of Inhibition within the Telencephalon: “Where the Wild Things Are”
Fishell, G., & Rudy, B. (2011) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-061010-113717 · Cited by 233
“In total, the two most numerous populations of interneurons are the PV-expressing FS cells and the Martinotti cells, both of which originate embryonically within the medial ganglionic eminence (MGE) (Butt et al. 2005; Fishell 2007; Xu et al. 2004, 2008).”
Chapter 3 The Developmental Integration of Cortical Interneurons into a Functional Network
Batista‐Brito, R., & Fishell, G. (2009) · Current Topics in Developmental Biology · doi:10.1016/s0070-2153(09)01203-4 · Cited by 223
“Notably, this is the precise developmental stage during which cortical interneuron diversity is being established (Butt et al., 2005; Wonders and Anderson, 2006).”
NKX2.1 specifies cortical interneuron fate by activatingLhx6
Du, T., Xu, Q., Ocbina, P. J. R., & Anderson, S. A. (2008) · Development · doi:10.1242/dev.015123 · Cited by 220
“, 2004), distinct subgroups that are known to originate primarily from the MGE (Wonders and Anderson, 2006).”
BackgroundSelf-citationLeveling Waddington: the emergence of direct programming and the loss of cell fate hierarchies
Ladewig, J., Koch, P., & Brüstle, O. (2013) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3543 · Cited by 236
Developmental origins of brain disorders: roles for dopamine
Money, K. M., & Stanwood, G. D. (2013) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2013.00260 · Cited by 221
“…forebrain in the medial and Frontiers in Cellular Neuroscience www.frontiersin.org December 2013 | Volume 7 | Article 260 | 4 “fncel-07-00260” — 2013/12/17 — 17:09 — page 5 — #5 caudal ganglionic eminences migrate tangentially to the cortex (de Carlos et al., 1996; Wonders and Anderson, 2006).”
BackgroundA 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 224
“1 for their specification (for review see Wonders and Anderson, 2006).”
BackgroundSelf-citationParvalbumin interneuron vulnerability and brain disorders
Ruden, J. B., Dugan, L. L., & Konradi, C. (2021) · Neuropsychopharmacology · doi:10.1038/s41386-020-0778-9 · Cited by 194
Zhao, Y., Flandin, P., Long, J. E., Cuesta, M. D., Westphal, H., & Rubenstein, J. L. R. (2008) · Journal of Comparative Neurology · doi:10.1002/cne.21772 · Cited by 207
“Molecular regulation of interneuron specification, differentiation, and migration has begun to be elucidated (reviewed in Marin and Rubenstein, 2003; Flames and Marin, 2005; Wonders and Anderson, 2006).”
BackgroundInfluentialCanetta, S., Bolkan, S., Padilla-Coreano, N., Song, L. J., Sahn, R., Harrison, N. L., Gordon, J. A., Brown, A., & Kellendonk, C. (2016) · Molecular Psychiatry · doi:10.1038/mp.2015.222 · Cited by 201
Morris, H. M., Hashimoto, T., & Lewis, D. A. (2008) · Cerebral Cortex · doi:10.1093/cercor/bhm186 · Cited by 216
“Thus, factors shared by SST and PV neurons that differ from CR neurons (e.g., place and timing of neuron birth, transcription factors regulating cell fate, etc.; see Wonders and Anderson 2006, for review) might also contribute to cell typespecific vulnerability.”
BackgroundCortical 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
“Our recent study showed that conditional deletion ofCoupTF2 in theMGE and POA, via Nkx2-1–Cre, reduces SST+ CIN numbers and increases PV+ CIN numbers (Hu et al., 2017), revealing a role for this TF in controlling the SST+/PV+ ratio.”
BackgroundInfluentialOlig1 and Olig2 triplication causes developmental brain defects in down syndrome.
Chakrabarti, L., Best, T. K., Cramer, N. P., Carney, R. S. E., Isaac, J. T. R., Galdzicki, Z., & Haydar, T. F. (2010) · Nature Neuroscience · doi:10.1038/nn.2600 · Cited by 258
SOX6 controls dorsal progenitor identity and interneuron diversity during neocortical development
Azim, E., Jabaudon, D., Fame, R. M., & Macklis, J. D. (2009) · Nature Neuroscience · doi:10.1038/nn.2387 · Cited by 209
“This strongly suggests that there are at least two pathways that restrict Mash1 expression to the subpallium: (1) a classic Pax6→ Ngn2 pathway, and (2) a cooperative pathway in which SOX6 is expressed independently of Pax6 and Ngn2.”
InfluentialWu, H., Luo, J., Yu, H. M., Rattner, A., Mo, A., Wang, Y., Smallwood, P. M., Avigdor, B. E., Wheelan, S. J., & Nathans, J. (2014) · Neuron · doi:10.1016/j.neuron.2013.10.051 · Cited by 211
GABAergic Inhibitory Interneuron Deficits in Alzheimer’s Disease: Implications for Treatment
Xu, Y., Zhao, M., Han, Y., & Zhang, H. (2020) · Frontiers in Neuroscience · doi:10.3389/fnins.2020.00660 · Cited by 203
“TARGETING INCREASED NUMBERS OF GABA INHIBITORY INTERNEURONS Previous studies have shown that neuronal loss is common in AD (Wright et al., 2013; Figures 1, 2 and Tables 1, 2).”
MethodInterneuron Types as Attractors and Controllers
Fishell, G., & Kepecs, Á. (2019) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-070918-050421 · Cited by 212
“…subtypes (reviewed in Fishell & Rudy 2011), the developmental and molecular cascades that generate them (Bandler et al. 2017, Batista-Brito & Fishell 2009, Wonders & Anderson 2006), and the circuit motifs to which they contribute (Hangya et al. 2014, Moore et al. 2010, Turkheimer et al. 2015).”
BackgroundHedgehog signaling is involved in development of the neocortex
Komada, M., Saitsu, H., Kinboshi, M., Miura, T., Shiota, K., & Ishibashi, M. (2008) · Development · doi:10.1242/dev.015891 · Cited by 195
Somatostatinergic systems in brain: Networks and functions
Viollet, C., Lepousez, G., Loudes, C., Videau, C., Simon, A., & Epelbaum, J. (2007) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2007.09.007 · Cited by 195
“Somatostatinergic interneurons, detected at early stages of ontogenesis in both hippocampus and neocortex (Shiosaka, 1992), mainly derive from a common proliferative zone, the medial ganglionic eminence (reviewed by Wonders and Anderson, 2006).”
BackgroundXu, R., Brawner, A. T., Li, S., Liu, J.-J., Kim, H., Xue, H., Pang, Z. P., Kim, W.-Y., Hart, R. P., Liu, Y., et al. (2019) · Cell Stem Cell · doi:10.1016/j.stem.2019.04.014 · Cited by 193
Integration of GABAergic interneurons into cortical cell assemblies: lessons from embryos and adults
Bartolini, G., Ciceri, G., & Marín, O. (2013) · Neuron · doi:10.1016/j.neuron.2013.08.014 · Cited by 185
Metadata
- Authors
- Wonders, C. P., & Anderson, S. A.
- Affiliations
- Cornell University (US)
- Corresponding author
- Anderson, Stewart A.
- ORCID
- Anderson, Stewart A.
- Venue
- Nature Reviews Neuroscience
- Published
- 2006-08-02
- Volume
- 7
- Issue
- 9
- Pages
- 687-696
- ISSN
- 1471-003X (ISSN-L)
- 1471-0048
- OpenAlex
- W2007034511
- Cited by
- 980
- References
- 142
- Citations by year
- 2026: 32 · 2025: 49 · 2024: 39 · 2023: 47 · 2022: 32 · 2021: 42 · 2020: 66 · 2019: 53 · 2018: 43 · 2017: 52 · 2016: 49 · 2015: 49 · 2014: 53 · 2013: 54 · 2012: 50
- FWCI
- 3.02
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature reviews. Neuroscience (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health
- National Institute of Mental Health
- National Institute of Neurological Disorders and Stroke
- 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 › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Keywords
- cortical interneurons, interneuron specification, GABAergic neurons, cortical development, transcriptional regulation, interneuron subtypes, neuronal maturation
- MeSH terms
- Animals, Cell Differentiation, Cell Movement, Cerebral Cortex, Humans, Interneurons, Nerve Tissue Proteins, Stem Cells, Telencephalon, Biomarkers, Gene Expression Regulation, Developmental, Cell Lineage
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