Cited by 402Neurogenesis and neuroplasticity mechanismsDevelopmental Biology and Gene RegulationCongenital heart defects research

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Retinoic acid from the meninges regulates cortical neuron generation.

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Siegenthaler, Julie A., Ashique, Amir M., Zarbalis, Konstantinos, Patterson, Katelin P., Hecht, Jonathan H., Kane, Maureen A., Folias, Alexandra E., Choe, Youngshik, May, Scott R., Kume, Tsutomu, Napoli, Joseph L., Peterson, Andrew S., Pleasure, Samuel J.·2009·Cell

DOI 10.1016/j.cell.2009.10.004PMC PMC2772834

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Abstract

Extrinsic signals controlling generation of neocortical neurons during embryonic life have been difficult to identify. In this study we demonstrate that the dorsal forebrain meninges communicate with the adjacent radial glial endfeet and influence cortical development. We took advantage of Foxc1 mutant mice with defects in forebrain meningeal formation. Foxc1 dosage and loss of meninges correlated with a dramatic reduction in both neuron and intermediate progenitor production and elongation of the neuroepithelium. Several types of experiments demonstrate that retinoic acid (RA) is the key component of this secreted activity. In addition, Rdh10- and Raldh2-expressing cells in the dorsal meninges were either reduced or absent in the Foxc1 mutants, and Rdh10 mutants had a cortical phenotype similar to the Foxc1 null mutants. Lastly, in utero RA treatment rescued the cortical phenotype in Foxc1 mutants. These results establish RA as a potent, meningeal-derived cue required for successful corticogenesis.

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A decade of molecular biology of retinoic acid receptors
Chambon, P. (1996) · The FASEB Journal · doi:10.1096/fasebj.10.9.8801176 · Cited by 2,889 · cited 6×
“…is a hormone derived from vitamin A (retinol) that signals via binding to its nuclear retinoic acid receptors (RAR) and retinoid X receptors (RXR) (Chambon, 1996). atRA synthesis is a two-step process that requires retinol dehydrogenases (Rdh) and retinaldehyde dehydrogenases (Raldh1, 2, and 3)…”
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Cortical neurons arise in symmetric and asymmetric division zones and migrate through specific phases
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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
Regulation of Cerebral Cortical Size by Control of Cell Cycle Exit in Neural Precursors
Chenn, A., & Walsh, C. A. (2002) · Science · doi:10.1126/science.1074192 · Cited by 1,431
Lack of Pericytes Leads to Endothelial Hyperplasia and Abnormal Vascular Morphogenesis
Hellström, M., Gerhardt, H., Kalén, M., Li, X., Eriksson, U., Wolburg, H., & Betsholtz, C. (2001) · The Journal of Cell Biology · doi:10.1083/jcb.153.3.543 · Cited by 1,132
Embryonic retinoic acid synthesis is essential for early mouse post-implantation development
Niederreither, K., Subbarayan, V., Dollé, P., & Chambon, P. (1999) · Nature Genetics · doi:10.1038/7788 · Cited by 1,111
Retinoids in Embryonal Development
Ross, S. A., McCaffery, P. J. A., Dräger, U. C., & Luca, L. M. D. (2000) · Physiological Reviews · doi:10.1152/physrev.2000.80.3.1021 · Cited by 866
Asymmetric production of surface-dividing and non-surface-dividing cortical progenitor cells
Miyata, T., Kawaguchi, A., Saito, K., Kawano, M., Muto, T., & Ogawa, M. (2004) · Development · doi:10.1242/dev.01173 · Cited by 791
Cleavage orientation and the asymmetric inheritance of notchl immunoreactivity in mammalian neurogenesis
Chenn, A., & McConnell, S. K. (1995) · Cell · doi:10.1016/0092-8674(95)90035-7 · Cited by 766
Function of the retinoic acid receptors (RARs) during development: (I) Craniofacial and skeletal abnormalities in RAR double mutants
Lohnes, D., Mark, M. P., Mendelsohn, C. L., Dollé, P., Dierich, A., Gorry, P., Gansmüller, A., & Chambon, P. (1994) · Development · doi:10.1242/dev.120.10.2723 · Cited by 764

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Bernal, J. (2024) · BENTHAM SCIENCE PUBLISHERS eBooks · doi:10.2174/9789815274226124010016
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Wang, C. (2010) · eScholarship (California Digital Library)
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Zieger, E. (2016) · theses.fr (ABES) · doi:10.70675/afdccbe5z278dz4cf0zabccze0a8df30916f
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Gaborieau, É. (2017) · doi:10.70675/d2746ce9ze26fz44b2zb53dz961b2ce68cdd
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Shabani, K. (2021) · theses.fr (ABES) · doi:10.70675/2deeb337z2d8ez4a8dzaf55z268de3428ac9

Authors: Siegenthaler, J. A., Ashique, A. M., Zarbalis, K., Patterson, K. P., Hecht, J. H., Kane, M. A., Folias, A. E., Choe, Y., May, S. R., Kume, T., Napoli, J. L., Peterson, A. S., & Pleasure, S. J.
Affiliations: University of California, San Francisco (US)
Genentech (US)
University of California, Berkeley (US)
Salk Institute for Biological Studies (US)
Vanderbilt University Medical Center (US)
Corresponding author: Pleasure, Samuel J.
ORCID: Siegenthaler, Julie A.
Ashique, Amir M.
Zarbalis, Konstantinos
Kane, Maureen A.
Choe, Youngshik
Kume, Tsutomu
Napoli, Joseph L.
Peterson, Andrew S.
Pleasure, Samuel J.
Venue: Cell
Publisher: Elsevier BV
Published: 2009-10
Volume: 139
Issue: 3
Pages: 597-609
ISSN: 0092-8674 (ISSN-L)
DOI: 10.1016/j.cell.2009.10.004
PMC: PMC2772834
OpenAlex: W2083131697
Cited by: 402
References: 51
Citations by year: 2026: 7 · 2025: 10 · 2024: 17 · 2023: 21 · 2022: 28 · 2021: 17 · 2020: 26 · 2019: 27 · 2018: 20 · 2017: 33 · 2016: 25 · 2015: 24 · 2014: 29 · 2013: 37 · 2012: 34
FWCI: 8.47
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, 1385 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 (publishedVersion)
PubMed (publishedVersion)
PubMed Central (acceptedVersion)
Funders: Autism Speaks (AS1625)
National Institute of Mental Health (K02MH074958)
National Institute on Drug Abuse (R56DA017627, R01DA017627)
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: retinoic acid, meninges, cortical development, FOXC1, intermediate progenitor cells, RDH10, Raldh2, dorsal forebrain
MeSH terms: Animals, Meninges, Neurons, Tretinoin, Prosencephalon, Mice, Forkhead Transcription Factors, Neurogenesis, In Vitro Techniques

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Retinoic acid from the meninges regulates cortical neuron generation.

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