Contributions of cortical subventricular zone to the development of the human cerebral cortex
Open accessAbstract
The cortical subventricular zone (SVZ), a proliferative compartment in the forebrain, has a uniquely important role during the second half of intrauterine development in human. This is best observed in numerous neonatal pathologies that result from prenatal SVZ damage. These conditions highlight a need to better understand the contribution of the SVZ to the development of the human cerebral cortex. With this goal in mind, we analyzed histological organization, cell proliferation, and molecular diversity in the human fetal SVZ from 7-27 gestational weeks (gw) using light and electron microscopy, immunohistochemistry, and in vitro methods. Complex histological organization distinguishes human cortical SVZ from that of other mammals. In vitro quantification showed that approximately 50% of cells in the VZ/SVZ region are neurons, 30% are astroglia, 15% are nestin+ cells, with other cell types representing smaller fractions. Immunolabeling with BrdU showed that a considerable number of cells ( approximately 10%) are generated in the human cortical SVZ during midgestation (18-24 gw) under in vitro conditions. Immunofluorescence with cell type-specific markers and BrdU revealed that all major cell types, neural precursors (nestin+), astroglia including radial glia (GFAP+, vimentin+), and oligodendrocyte progenitors (PDGFR-alpha+) were proliferating. An increase in the ratio of the size of the SVZ to VZ, protracted period of cell proliferation, as well as cellular and histological complexity of the human fetal SVZ are directly related to the evolutionary expansion of the human cerebral cortex.
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oRGs are present in large numbers in gyrencephalic primates and are considered pivotal to the evolutionary increase in human cortex size and complexity.
“oRGs are present in large numbers in gyrencephalic primates22,23,40–44 and are considered pivotal to the evolutionary increase in human cortex size and complexity45,46.”
From The use of brain organoids to investigate neural development and disease (2017) · cites this paper as [42]
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References 85 · Cited by 269
- Authors
- Zecevic, N., Chen, Y., & Filipovic, R.
- Affiliations
- UConn Health (US)
- Venue
- The Journal of Comparative Neurology
- Publisher
- Wiley
- Published
- 2005
- Volume
- 491
- Issue
- 2
- Pages
- 109-122
- ISSN
- 0021-9967 (ISSN-L)
- 1096-9861
- PMC
- PMC2628573
- OpenAlex
- W2021399360
- Cited by
- 269
- References
- 85
- Citations by year
- 2026: 2 · 2025: 2 · 2024: 6 · 2023: 11 · 2022: 14 · 2021: 14 · 2020: 20 · 2019: 16 · 2018: 10 · 2017: 16 · 2016: 15 · 2015: 16 · 2014: 24 · 2013: 24 · 2012: 14
- FWCI
- 2.38
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- The Journal of Comparative Neurology (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institute of Neurological Disorders and Stroke (R01NS041489, R01NS41489-03)
- Topics
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Health Sciences › Medicine › Pediatrics, Perinatology and Child Health › Fetal and Pediatric Neurological Disorders
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
- Keywords
- human fetal brain development, cerebral cortex evolution, cell proliferation, neuronal precursors, nestin, radial glia, oligodendrocyte progenitors, astroglia, ventricular zone, gestational age
- MeSH terms
- Cerebral Cortex, Humans, Nerve Tissue Proteins, Neurons, Organ Culture Techniques, Prosencephalon, Microglia, Lateral Ventricles, Cell Proliferation
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