首页> 美国卫生研究院文献>The Journal of Neuroscience >Sequence of Neuron Origin and Neocortical Laminar Fate: Relation to Cell Cycle of Origin in the Developing Murine Cerebral Wall
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Sequence of Neuron Origin and Neocortical Laminar Fate: Relation to Cell Cycle of Origin in the Developing Murine Cerebral Wall

机译:神经元起源和新皮质层状命运的序列:与发展中的小鼠脑壁起源细胞周期的关系。

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摘要

Neurons destined for each region of the neocortex are known to arise approximately in an “inside-to-outside” sequence from a pseudostratified ventricular epithelium (PVE). This sequence is initiated rostrolaterally and propagates caudomedially. Moreover, independently of location in the PVE, the neuronogenetic sequence in mouse is divisible into 11 cell cycles that occur over a 6 d period. Here we use a novel “birth hour” method that identifies small cohorts of neurons born during a single 2 hr period, i.e., 10–20% of a single cell cycle, which corresponds to ∼1.5% of the 6 d neuronogenetic period. This method shows that neurons arising with the same cycle of the 11 cycle sequence in mouse have common laminar fates even if they arise from widely separated positions on the PVE (neurons of fields 1 and 40) and therefore arise at different embryonic times. Even at this high level of temporal resolution, simultaneously arising cells occupy more than one cortical layer, and there is substantial overlap in the distributions of cells arising with successive cycles. We demonstrate additionally that the laminar representation of cells arising with a given cycle is little if at all modified over the early postnatal interval of histogenetic cell death. We infer from these findings that cell cycle is a neuronogenetic counting mechanism and that this counting mechanism is integral to subsequent processes that determine cortical laminar fate.
机译:已知目的地为新皮质的每个区域的神经元大约从假复层心室上皮(PVE)以“从内到外”的顺序出现。该序列在rosrolateral启动,并在中间传播。此外,与PVE中的位置无关,小鼠中的神经遗传序列可分为6个d周期内发生的11个细胞周期。在这里,我们使用一种新颖的“出生小时”方法,该方法可以识别在单个2小时周期内(即单个细胞周期的10%至20%)出生的神经元的小群,这相当于6 d神经生成周期的约1.5%。此方法显示,在小鼠中以11个循环序列的相同循环产生的神经元具有共同的层状命运,即使它们来自PVE上相距很远的位置(场1和40的神经元),因此也出现在不同的胚胎时期。即使在这种高水平的时间分辨率下,同时出现的细胞也占据了一层以上的皮质层,并且随着连续的循环而出现的细胞分布也存在很大的重叠。我们还证明了,如果在出生后的组织遗传学细胞死亡的早期间隔中进行了修饰,则在给定周期内产生的细胞的层状表示很少。我们从这些发现中推断,细胞周期是一种神经遗传学计数机制,并且该计数机制是确定皮层层命运的后续过程所不可或缺的。

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