The Changing Number of Cells in the Human Fetal Forebrain and its Subdivisions: A Stereological Analysis

The total number of cells – including both neurons and glial cells – was estimated in the neocortical part of the human fetal telencephalon in 22 normal brains within four major developmental zones: the cortical plate/marginal zone, the subplate, the intermediate zone and the ventricular/subventricu...

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Published inCerebral cortex (New York, N.Y. 1991) Vol. 13; no. 2; pp. 115 - 122
Main Authors Samuelsen, Grethe Badsberg, Larsen, Karen Bonde, Bogdanovic, Nenad, Laursen, Henning, Græm, Niels, Larsen, Jørgen Falck, Pakkenberg, Bente
Format Journal Article
LanguageEnglish
Published United States Oxford University Press 01.02.2003
Oxford Publishing Limited (England)
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Summary:The total number of cells – including both neurons and glial cells – was estimated in the neocortical part of the human fetal telencephalon in 22 normal brains within four major developmental zones: the cortical plate/marginal zone, the subplate, the intermediate zone and the ventricular/subventricular zone. The fetal ages ranged from 13 to 41 weeks of gestation. The cellular growth in the human fetal forebrain appears to be two-phased: one rapid, exponential phase from 13 to 20 weeks of gestation and a second and slower phase, which increases linearly, from approximately 22 weeks of gestation to term. From 13 to 20 weeks of gestation the total number of cells increases by a factor of 4.3 from 3 × 109 cells to 13 × 109 cells at 20 weeks of gestation. From mid-gestation to term, the total cell number increases by a factor of 2.9 to 38 × 109 cells in the newborn infant. Studying cellular growth in the normal human fetal brain is important since it may serve as a useful parameter for the assessment of cortical growth in non-invasive and histological studies, and thus improve the analysis of fetal brain disturbances.
Bibliography:PII:1460-2199
Address correspondence to Bente Pakkenberg, Research Laboratory for Stereology and Neuroscience, Bispebjerg University Hospital, Bispebjerg Bakke 23, DK-2400 Copenhagen NV, Denmark. Email: forsklab@bbh.hosp.dk.
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ISSN:1047-3211
1460-2199
1460-2199
DOI:10.1093/cercor/13.2.115