Permissive corridor and diffusible gradients direct medial ganglionic eminence cell migration to the neocortex
Open accessAbstract
Young neurons born in the medial ganglionic eminence (MGE) migrate a long distance dorsally, giving rise to several types of interneurons in neocortex. The mechanisms that facilitate selective dorsal dispersion of MGE cells while restricting their movement ventrally into neighboring regions are not known. Using microtransplantation into fetal brain slices and onto dissociated substrate cells on floating filters (spot assay), we demonstrate that ventral forebrain regions neighboring the MGE are nonpermissive for MGE cell migration, whereas the dorsal regions leading to the neocortex are increasingly permissive. Spot assay experiments using filters with different pore sizes indicate that the permissive factors are not diffusible. We also show that MGE cells respond to chemoattractive and inhibitory factors diffusing from the neocortex and ventromedial forebrain, respectively. We propose that the final extent and regional specificity of MGE cell dispersion is largely dictated by contact guidance through a selectively permissive environment, flanked by nonpermissive tissues. In addition, we propose that chemotactic guidance cues superimposed over the permissive corridor facilitate efficient dorsal migration of MGE cells.
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Interneurons move toward the cortex along a gradient of increasing permissivity produced by chemoattractive cues in the developing LGE and pallium.
“Interneurons migrate toward the cortex following a gradient of increasing permissivity generated by chemoattractive cues produced in the developing LGE and pallium (Marín et al., 2003; Wichterle et al., 2003).”
From Development and Functional Diversification of Cortical Interneurons (2018) · cites this paper as Wichterle et al., 2003
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Additional file 4 of Prenatal alcohol exposure is a leading cause of interneuronopathy in humans
Marguet, F., Friocourt, G., Brosolo, M., Sauvestre, F., Marcorelles, P., Lesueur, C., Marret, S., Gonzalez, B. J., & Laquerrière, A. (2020) · Figshare · doi:10.6084/m9.figshare.13310404
Additional file 2 of Prenatal alcohol exposure is a leading cause of interneuronopathy in humans
Marguet, F., Friocourt, G., Brosolo, M., Sauvestre, F., Marcorelles, P., Lesueur, C., Marret, S., Gonzalez, B. J., & Laquerrière, A. (2020) · Figshare · doi:10.6084/m9.figshare.13310392
Additional file 3 of Prenatal alcohol exposure is a leading cause of interneuronopathy in humans
Marguet, F., Friocourt, G., Brosolo, M., Sauvestre, F., Marcorelles, P., Lesueur, C., Marret, S., Gonzalez, B. J., & Laquerrière, A. (2020) · Figshare · doi:10.6084/m9.figshare.13310398
Additional file 1 of Prenatal alcohol exposure is a leading cause of interneuronopathy in humans
Marguet, F., Friocourt, G., Brosolo, M., Sauvestre, F., Marcorelles, P., Lesueur, C., Marret, S., Gonzalez, B. J., & Laquerrière, A. (2020) · Figshare · doi:10.6084/m9.figshare.13310389
Laboratory Models for Central Nervous System Tumor Stem Cell Research
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- Authors
- Wichterle, H., Alvarez-Dolado, M., Erskine, L., & Alvarez-Buylla, A.
- Affiliations
- University of California, San Francisco (US)
- The Rockefeller University, New York, NY 10021; Brain Tumor Research Center, University of California, San Francisco, CA 94143-0520; and Department of Pathology, Columbia University, New York, NY 10032
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 2003-01-06
- Volume
- 100
- Issue
- 2
- Pages
- 727-732
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- PMC
- PMC141064
- OpenAlex
- W2046826788
- Cited by
- 92
- References
- 42
- Citations by year
- 2025: 1 · 2022: 1 · 2021: 4 · 2020: 9 · 2019: 3 · 2018: 6 · 2017: 1 · 2016: 1 · 2015: 3 · 2014: 4 · 2013: 6 · 2012: 3
- FWCI
- 1.95
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Proceedings of the National Academy of Sciences (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- DIGITAL.CSIC (Spanish National Research Council (CSIC)) (submittedVersion)
- UCL Discovery (University College London) (submittedVersion)
- Funders
- National Institute of Child Health and Human Development
- Eunice Kennedy Shriver National Institute of Child Health and Human Development (HD32116, R37HD032116, R01HD032116)
- Topics
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Axon Guidance and Neuronal Signaling
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
- Keywords
- medial ganglionic eminence, neuronal migration, neocortex, contact guidance, chemotaxis, interneurons, ventral forebrain, microtransplantation, chemoattractants, inhibiting factors
- MeSH terms
- Slit Homolog 2 Protein, Animals, Cell Movement, Chemotaxis, Diffusion, Median Eminence, Nerve Tissue Proteins, Neocortex, Intercellular Signaling Peptides and Proteins, Mice
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