GRADIENT IN THE DURATION OF THE G1 PHASE IN THE MURINE NEOCORTICAL PROLIFERATIVE EPITHELIUM

Citation
S. Miyama et al., GRADIENT IN THE DURATION OF THE G1 PHASE IN THE MURINE NEOCORTICAL PROLIFERATIVE EPITHELIUM, Cerebral cortex, 7(7), 1997, pp. 678-689
Citations number
63
Categorie Soggetti
Neurosciences
Journal title
ISSN journal
10473211
Volume
7
Issue
7
Year of publication
1997
Pages
678 - 689
Database
ISI
SICI code
1047-3211(1997)7:7<678:GITDOT>2.0.ZU;2-L
Abstract
Neuronogenesis in the neocortical pseudostratified ventricular epithel ium (PVE) is initiated rostrolaterally acid progresses caudo-medially as development progresses. Here we have measured the cytokinetic param eters and the fractional neuronal output parameter, a, of laterally lo cated early-maturing regions over the principal embryonic days (E12-E1 5) of neocortical neuronogenesis in the mouse. These measures are comp ared with ones previously made of a medial, late-maturing portion of f ire PVE. Laterally, as medially, the duration of the neuronogenetic in terval is 6 days and comprises 11 integer cell cycles. Also, in both l ateral acid medial areas the length of G1 phase (T-G1) increases nearl y 4-fold and is the only cell cycle parameter to change, a progresses essentially identically laterally and medially with respect to the suc cession of integer cell cycles. Most importantly, from E12 to E13 ther e is a steeply declining lateral to medial gradient in T-G1. The gradi ent is due both to the lateral to medial graded stage of neuronogenesi s and to the stepwise increase in T-G1 with each integer cycle during the neuronogenetic interval. To our knowledge this gradient in T-G1 of the cerebral PVE is the first cell biological gradient to be demonstr ated experimentally in such an extensive proliferative epithelial shee t. We suggest that this gradient in T-G1 is the cellular mechanism for positionally encoding a protomap of the neocortex within the PVE.