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Exploiting the dynamics of S-phase tracers in developing brain: interkinetic nuclear migration for cells entering versus leaving the S-phase.利用发育中大脑S期示踪剂的动态变化:进入与离开S期的细胞的核内有丝分裂运动
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The role of cell death in regulating the size and shape of the mammalian forebrain.细胞死亡在调节哺乳动物前脑大小和形状中的作用。
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Changes in cell-cycle kinetics during the development and evolution of primate neocortex.灵长类动物新皮层发育和进化过程中细胞周期动力学的变化。
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Radiation-induced, lamina-specific deletion of neurons in the primate visual cortex.辐射诱导的灵长类动物视觉皮层中特定板层神经元的缺失。
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原始细胞缺陷和神经元发生延迟在16三体小鼠小头畸形中的作用。

Role of founder cell deficit and delayed neuronogenesis in microencephaly of the trisomy 16 mouse.

作者信息

Haydar T F, Nowakowski R S, Yarowsky P J, Krueger B K

机构信息

Department of Physiology, University of Maryland School of Medicine, Baltimore, Maryland 21201, USA.

出版信息

J Neurosci. 2000 Jun 1;20(11):4156-64. doi: 10.1523/JNEUROSCI.20-11-04156.2000.

DOI:10.1523/JNEUROSCI.20-11-04156.2000
PMID:10818151
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6772637/
Abstract

Development of the neocortex of the trisomy 16 (Ts16) mouse, an animal model of Down syndrome (DS), is characterized by a transient delay in the radial expansion of the cortical wall and a persistent reduction in cortical volume. Here we show that at each cell cycle during neuronogenesis, a smaller proportion of Ts16 progenitors exit the cell cycle than do control, euploid progenitors. In addition, the cell cycle duration was found to be longer in Ts16 than in euploid progenitors, the Ts16 growth fraction was reduced, and an increase in apoptosis was observed in both proliferative and postmitotic zones of the developing Ts16 neocortical wall. Incorporation of these changes into a model of neuronogenesis indicates that they are sufficient to account for the observed delay in radial expansion. In addition, the number of neocortical founder cells, i.e., precursors present just before neuronogenesis begins, is reduced by 26% in Ts16 mice, leading to a reduction in overall cortical size at the end of Ts16 neuronogenesis. Thus, altered proliferative characteristics during Ts16 neuronogenesis result in a delay in the generation of neocortical neurons, whereas the founder cell deficit leads to a proportional reduction in the overall number of neurons. Such prenatal perturbations in either the timing of neuron generation or the final number of neurons produced may lead to significant neocortical abnormalities such as those found in DS.

摘要

唐氏综合征(DS)动物模型——16三体(Ts16)小鼠新皮质的发育特点是皮质壁径向扩展出现短暂延迟以及皮质体积持续减小。我们在此表明,在神经元发生过程的每个细胞周期中,与对照的整倍体祖细胞相比,Ts16祖细胞退出细胞周期的比例更小。此外,发现Ts16祖细胞的细胞周期持续时间比整倍体祖细胞更长,Ts16生长分数降低,并且在发育中的Ts16新皮质壁的增殖区和有丝分裂后区均观察到细胞凋亡增加。将这些变化纳入神经元发生模型表明,它们足以解释所观察到的径向扩展延迟。此外,Ts16小鼠新皮质奠基细胞(即就在神经元发生开始前存在的前体细胞)的数量减少了26%,导致Ts16神经元发生结束时整体皮质大小减小。因此,Ts16神经元发生过程中增殖特征的改变导致新皮质神经元生成延迟,而奠基细胞数量不足导致神经元总数成比例减少。在神经元生成时间或所产生的神经元最终数量方面的这种产前扰动可能会导致显著的新皮质异常,如在唐氏综合征中发现的那些异常。