FATES OF THE EARLIEST GENERATED CELLS IN THE DEVELOPING MURINE NEOCORTEX

Citation
Dj. Price et al., FATES OF THE EARLIEST GENERATED CELLS IN THE DEVELOPING MURINE NEOCORTEX, Journal of comparative neurology, 377(3), 1997, pp. 414-422
Citations number
18
Categorie Soggetti
Neurosciences
ISSN journal
00219967
Volume
377
Issue
3
Year of publication
1997
Pages
414 - 422
Database
ISI
SICI code
0021-9967(1997)377:3<414:FOTEGC>2.0.ZU;2-T
Abstract
In mammalian species studied to date, the first-born neocortical cells normally form two layers, one above and one below the cortical plate, called the marginal zone (future layer 1) and the subplate. In primat es and carnivores, many of these first-born cells die early in postnat al life. Whether this also occurs in rodents is highly controversial. In this study, we injected pregnant mice with bromodeoxyuridine on emb ryonic days (E) 11-14 to label the earliest generated neocortical cell s, and examined their fates between birth and postnatal day 21. At bir th, most cells born on embryonic day 11 were below the cortical plate, and a smaller proportion were above it. Very few of these cells remai ned by postnatal day 3 and there were none at any depth in the neocort ex at older ages. At birth, the largest proportion of cells born on em bryonic days 12 and 13 were in the subplate and smaller proportions we re in the cortical plate and marginal zone. At older ages, almost all of these cells had disappeared from the marginal zone and from below t he cortical plate, although some were retained in the cortical plate. The density of the remaining E12- and E13-born cells decreased more th an could be explained by neocortical expansion alone. As a control, we studied cells born on embryonic day 14. These cells were restricted t o the cortical plate at birth. By postnatal day 21, their density had decreased by an amount that could be explained by neocortical expansio n alone. We conclude that, as in other species, many of the earliest g enerated cells of the murine neocortex die. J. Comp. Neurol. 377:414-4 22, 1997. (C) 1997 Wiley-Liss, Inc.