Gradient in the duration of the G1 phase in the murine neocortical proliferative epithelium

被引:94
作者
Miyama, S
Takahashi, T
Nowakowski, RS
Caviness, VS
机构
[1] HARVARD UNIV,MASSACHUSETTS GEN HOSP,SCH MED,DEPT NEUROL,BOSTON,MA 02114
[2] KEIO UNIV,SCH MED,DEPT PEDIAT,TOKYO 160,JAPAN
[3] UNIV MED & DENT NEW JERSEY,ROBERT WOOD JOHNSON MED SCH,DEPT NEUROSCI & CELL BIOL,PISCATAWAY,NJ 08854
关键词
D O I
10.1093/cercor/7.7.678
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Neuronogenesis in the neocortical pseudostratified ventricular epithelium (PVE) is initiated rostrolaterally acid progresses caudo-medially as development progresses. Here we have measured the cytokinetic parameters and the fractional neuronal output parameter, a, of laterally located early-maturing regions over the principal embryonic days (E12-E15) of neocortical neuronogenesis in the mouse. These measures are compared with ones previously made of a medial, late-maturing portion of fire PVE. Laterally, as medially, the duration of the neuronogenetic interval is 6 days and comprises 11 integer cell cycles. Also, in both lateral acid medial areas the length of G1 phase (T-G1) increases nearly 4-fold and is the only cell cycle parameter to change, a progresses essentially identically laterally and medially with respect to the succession of integer cell cycles. Most importantly, from E12 to E13 there is a steeply declining lateral to medial gradient in T-G1. The gradient is due both to the lateral to medial graded stage of neuronogenesis 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 demonstrated experimentally in such an extensive proliferative epithelial sheet. We suggest that this gradient in T-G1 is the cellular mechanism for positionally encoding a protomap of the neocortex within the PVE.
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页码:678 / 689
页数:12
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