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...
Saved in:
Published in | Cerebral cortex (New York, N.Y. 1991) Vol. 13; no. 2; pp. 115 - 122 |
---|---|
Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Oxford University Press
01.02.2003
Oxford Publishing Limited (England) |
Subjects | |
Online Access | Get full text |
Cover
Loading…
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. istex:AFFC7CA860ACB728524595030D8D3591833B64AA local:0130115 ark:/67375/HXZ-30L0T380-Q ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 ObjectType-Article-1 ObjectType-Feature-2 |
ISSN: | 1047-3211 1460-2199 1460-2199 |
DOI: | 10.1093/cercor/13.2.115 |