Cited by 184Neurogenesis and neuroplasticity mechanismsFetal and Pediatric Neurological DisordersGenetics and Neurodevelopmental Disorders

Human Cortex Development: Estimates of Neuronal Numbers Indicate Major Loss Late During Gestation

Rabinowicz, Theodore, de Courten-Myers, Gabrielle M., Petetot, Jean McDonald-Comber, XI, Guohua, de los Reyes, Emily·1996·Journal of Neuropathology and Experimental Neurology

Abstract

This morphometric study explores temporal and topographic changes in the estimated neuronal number in human neocortex during the latter half of gestation and early infancy. Neuronal estimates are calculated from standardized measurements of cortical layer thickness and neuronal density in 6 neocortical regions in 9 human brains ranging from 17 weeks of gestation to 13 weeks postnatally. Layer thickness increases linearly with age while the average neuronal density first increases, then reaches a maximum at 20 weeks of gestation, and progressively declines. The sum of layer thickness times layer density estimates the number of neurons in a cortical column with a fixed surface area and a length that is equal to the cortical thickness. To derive an estimate of potentially overproduced neurons, the number of neurons in each cortical column was corrected for surface growth and for cortex gyration. These data show that a large percent of cortical neurons present at 20 weeks of gestation are used to populate the expanding cortex. Nevertheless, the growth-corrected data suggest that a substantial overproduction and secondary reduction of cortical neurons takes place mainly during the last quarter of gestation. The corrected mean number of neurons reaches a maximum at 28 weeks of gestation and then declines by approximately 70% to achieve a stable number of neurons around birth. This estimated number of neurons is significantly higher at 28 to 32 weeks of gestation than at 17 to 20 gestational weeks and at 0 to 13 postnatal weeks. These data imply that physiologic neuronal death (apoptosis) may play a major role in early human cortex development.

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Crossref · 10.1097/00005072-199603000-00007

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  • Because proliferation of cortical neurons is exponential between 10 and 20 weeks of gestation and does not occur postnatally, pathological neuron excess cannot be caused by post-natal events and instead indicates neural disorder in ASD has a prenatal origin, likely by the first and/or second trimester.

    “Because proliferation of cortical neurons is exponential between 10 and 20 weeks of gestation [43, 44] and does not occur postnatally, pathological neuron excess cannot be caused by post-natal events and instead indicates neural disorder in ASD has a prenatal origin, likely by the first and/or second trimester.”

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Authors
Rabinowicz, T., de Courten-Myers, G. M., Petetot, J. M.-C., XI, G., & de los Reyes, E.
Venue
Journal of Neuropathology and Experimental Neurology
Published
1996-03
Volume
55
Issue
3
Pages
320-328
ISSN
0022-3069 (ISSN-L)
OpenAlex
W4300577516
Cited by
184
References
0
Citations by year
2026: 2 · 2025: 4 · 2024: 5 · 2023: 4 · 2022: 6 · 2021: 8 · 2020: 3 · 2019: 9 · 2018: 6 · 2017: 10 · 2016: 7 · 2015: 6 · 2014: 6 · 2013: 5 · 2012: 14
FWCI
1.21
Type
journal article
Language
en
Open access
closed
Locations
  • Journal of Neuropathology & Experimental Neurology (publishedVersion)
  • PubMed (publishedVersion)
  • PubMed
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 › Genetics › Genetics and Neurodevelopmental Disorders
Keywords
human cortex, cortical development, neurogenesis, neuronal migration, brain development
MeSH terms
Age Factors, Cell Count, Cerebral Cortex, Embryonic and Fetal Development, Humans, Infant, Infant, Newborn, Neuronal Plasticity, Neurons, Linear Models, Apoptosis

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