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The caudal ganglionic eminence is a source of distinct cortical and subcortical cell populations
Abstract
During development, the mammalian ventral telencephalon is comprised of three major proliferative zones: the medial (MGE), lateral (LGE) and caudal (CGE) ganglionic eminences. Through gene expression studies, in vitro migration assays, genetic mutant analysis and in vivo fate mapping in mice, we found that the CGE is a progenitor region that is distinct from both the MGE and LGE. Notably, CGE cells showed a unique in vivo pattern of migration, and the CGE contributed cells to nuclei distinct from those populated by the MGE and LGE. Moreover, we report that the migratory fate of cells from the CGE is intrinsically determined by embryonic day 13.5 (E13.5). Together, these results provide the first insights into the development and fate of the CGE.
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“the CGE produces all VIP+ and CCK+ cortical interneurons along with several other less abundant types of interneurons such as single bouquet cells”
From Development and Functional Diversification of Cortical Interneurons (2018) · cites this paper as Nery et al., 2002
In the citing paper
“in vitro culture and in vivo transplant studies implicated the CGE as a source of cortical interneurons that assumed mature fates distinct from MGE-derived interneurons”
From Hippocampal GABAergic Inhibitory Interneurons (2017) · cites this paper as [829]
In the citing paper
“MGE- and CGE-derived interneurons reach the dorsal telencephalon via separate pathways: those from the MGE travel via dorsolateral routes while those from the CGE follow three distinct routes laterally, medially, and caudally.”
From Hippocampal GABAergic Inhibitory Interneurons (2017) · cites this paper as [829]
In the citing paper
“interneurons from both GEs converge and then disperse widely via two streams running in parallel, separated by the cortical plate (CPl) or hippocampal primordium: a deep stream in the intermediate/subventricular zones (IZ/SVZ) and a superficial one in the marginal zone (MZ)”
From Hippocampal GABAergic Inhibitory Interneurons (2017) · cites this paper as [829]
In the citing paper
“MGE progenitors preferentially express the transcription factor Nkx2.1 (147, 148, 829, 1233), which must be downregulated in migrating postmitotic cells in order for them to avoid the striatum and reach the cortex”
From Hippocampal GABAergic Inhibitory Interneurons (2017) · cites this paper as [829]
In the citing paper
“The choice of migratory path appears to be an intrinsic property of cells dependent on their region of origin and ultimate destination, and governed by different transcription factors”
From Hippocampal GABAergic Inhibitory Interneurons (2017) · cites this paper as [829]
In the citing paper
“The MGE and CGE generate different groups of cortical interneurons (17–19).”
From Early emergence of cortical interneuron diversity in the mouse embryo (2018) · cites this paper as [18]
In the citing paper
“Part of the BNST has embryonic origins in the CGE (Nery et al., 2002), suggesting that this structure may harbor such cell types.”
From Single-Cell Multi-omic Integration Compares and Contrasts Features of Brain Cell Identity (2019) · cites this paper as Nery et al., 2002
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Self-citation
Metadata
- Authors
- Nery, S., Fishell, G., & Corbin, J. G.
- Affiliations
- NYU Langone Health (US)
- Venue
- Nature Neuroscience
- Published
- 2002-11-04
- Volume
- 5
- Issue
- 12
- Pages
- 1279-1287
- ISSN
- 1097-6256 (ISSN-L)
- 1546-1726
- OpenAlex
- W2084114120
- Cited by
- 558
- References
- 48
- Citations by year
- 2026: 9 · 2025: 14 · 2024: 15 · 2023: 23 · 2022: 16 · 2021: 18 · 2020: 26 · 2019: 19 · 2018: 16 · 2017: 23 · 2016: 20 · 2015: 19 · 2014: 23 · 2013: 39 · 2012: 29
- FWCI
- 5.33
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature Neuroscience (publishedVersion)
- PubMed (publishedVersion)
- ANU Open Research (Australian National University) (submittedVersion)
- Funders
- National Institutes of Health (5f32ns010962-02)
- National Institute of Neurological Disorders and Stroke (R01 NS39007-03, R01NS039007, NS10962-03)
- 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
- caudal ganglionic eminence, ganglionic eminence, ventral telencephalon, cortical development, neuronal migration, progenitor cells, medial ganglionic eminence, lateral ganglionic eminence, cell fate determination, fate mapping, mouse embryo
- MeSH terms
- Animals, Cell Differentiation, Cell Movement, Cerebral Cortex, Corpus Striatum, Genetic Markers, Immunohistochemistry, Interneurons, Limbic System, Mice, Transgenic, Mutation, Neurons, Stem Cells, Telencephalon, Transcription Factors, Homeodomain Proteins, Gene Expression Regulation, Developmental, Cell Lineage, Stem Cell Transplantation, Mice
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