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小鼠新皮质增殖上皮中G1期持续时间的梯度变化。

A gradient in the duration of the G1 phase in the murine neocortical proliferative epithelium.

作者信息

Miyama S, Takahashi T, Nowakowski R S, Caviness V S

机构信息

Department of Neurology, Massachusetts General Hospital, Harvard Medical School, Boston 02114, USA.

出版信息

Cereb Cortex. 1997 Oct-Nov;7(7):678-89. doi: 10.1093/cercor/7.7.678.

Abstract

Neuronogenesis in the neocortical pseudostratified ventricular epithelium (PVE) is initiated rostrolaterally and progresses caudo-medially as development progresses. Here we have measured the cytokinetic parameters and the fractional neuronal output parameter, Q, 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 the PVE. Laterally, as medially, the duration of the neuronogenetic interval is 6 days and comprises 11 integer cell cycles. Also, in both lateral and medial areas the length of G1 phase (TG1) increases nearly 4-fold and is the only cell cycle parameter to change. Q 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 TG1. The gradient is due both to the lateral to medial graded stage of neuronogenesis and to the stepwise increase in TG1 with each integer cycle during the neuronogenetic interval. To our knowledge this gradient in TG1 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 TG1 is the cellular mechanism for positionally encoding a protomap of the neocortex within the PVE.

摘要

新皮质假复层室管膜上皮(PVE)中的神经发生从 rostrolaterally 开始,并随着发育的进行向 caudo - 内侧推进。在这里,我们测量了小鼠新皮质神经发生主要胚胎期(E12 - E15)期间位于外侧的早熟区域的细胞动力学参数和分数神经元输出参数 Q。这些测量结果与之前对 PVE 内侧晚熟部分所做的测量结果进行了比较。在外侧,与内侧一样,神经发生间隔的持续时间为 6 天,包括 11 个整数细胞周期。此外,在外侧和内侧区域,G1 期(TG1)的长度增加了近 4 倍,并且是唯一发生变化的细胞周期参数。就整数细胞周期的连续而言,Q 在外侧和内侧的进展基本相同。最重要的是,从 E12 到 E13,TG1 存在从外侧到内侧急剧下降的梯度。这种梯度既归因于神经发生从外侧到内侧的分级阶段,也归因于在神经发生间隔期间每个整数周期 TG1 的逐步增加。据我们所知,大脑 PVE 中 TG1 的这种梯度是在如此广泛的增殖上皮片中通过实验证明的第一个细胞生物学梯度。我们认为,TG1 中的这种梯度是在 PVE 内对新皮质原地图进行位置编码的细胞机制。

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