首页> 美国卫生研究院文献>Journal of Visualized Experiments : JoVE >Assessing Cell Cycle Progression of Neural Stem and Progenitor Cells in the Mouse Developing Brain after Genotoxic Stress
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Assessing Cell Cycle Progression of Neural Stem and Progenitor Cells in the Mouse Developing Brain after Genotoxic Stress

机译:评估遗传毒性应激后发育中的小鼠大脑中神经干细胞和祖细胞的细胞周期进程

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摘要

Neurons of the cerebral cortex are generated during brain development from different types of neural stem and progenitor cells (NSPC), which form a pseudostratified epithelium lining the lateral ventricles of the embryonic brain. Genotoxic stresses, such as ionizing radiation, have highly deleterious effects on the developing brain related to the high sensitivity of NSPC. Elucidation of the cellular and molecular mechanisms involved depends on the characterization of the DNA damage response of these particular types of cells, which requires an accurate method to determine NSPC progression through the cell cycle in the damaged tissue. Here is shown a method based on successive intraperitoneal injections of EdU and BrdU in pregnant mice and further detection of these two thymidine analogues in coronal sections of the embryonic brain. EdU and BrdU are both incorporated in DNA of replicating cells during S phase and are detected by two different techniques (azide or a specific antibody, respectively), which facilitate their simultaneous detection. EdU and BrdU staining are then determined for each NSPC nucleus in function of its distance from the ventricular margin in a standard region of the dorsal telencephalon. Thus this dual labeling technique allows distinguishing cells that progressed through the cell cycle from those that have activated a cell cycle checkpoint leading to cell cycle arrest in response to DNA damage.An example of experiment is presented, in which EdU was injected before irradiation and BrdU immediately after and analyzes performed within the 4 hr following irradiation. This protocol provides an accurate analysis of the acute DNA damage response of NSPC in function of the phase of the cell cycle at which they have been irradiated. This method is easily transposable to many other systems in order to determine the impact of a particular treatment on cell cycle progression in living tissues.
机译:大脑皮层的神经元是在大脑发育过程中由不同类型的神经干细胞和祖细胞(NSPC)生成的,这些细胞形成了伪分层的上皮细胞,位于胚胎脑的侧脑室。遗传毒性应激(例如电离辐射)对发育中的大脑具有高度有害的作用,这与NSPC的高敏感性有关。对涉及的细胞和分子机制的阐明取决于这些特定类型细胞的DNA损伤反应的特征,这需要一种准确的方法来确定NSPC在受损组织中整个细胞周期中的进程。这里显示了一种方法,该方法基于在怀孕小鼠中连续腹膜内注射EdU和BrdU并进一步检测胚胎脑冠状部分中的这两种胸苷类似物。 EdU和BrdU都在S期掺入复制细胞的DNA中,并通过两种不同的技术(分别是叠氮化物或特异性抗体)进行检测,这有助于同时进行检测。然后,根据每个NSPC核距背脑标准区域心室边缘的距离来确定EdU和BrdU染色。因此,这种双重标记技术可以将经历了细胞周期进程的细胞与已经激活了细胞周期检查点的细胞区分开来,从而响应于DNA损伤而导致细胞周期停滞。给出了一个实验示例,其中在辐照之前注射了EdU,BrdU注射了照射后4小时内立即进行分析。该协议提供了对NSPC的急性DNA损伤反应的精确分析,该反应取决于受到照射的细胞周期的阶段。为了确定特定治疗对活组织中细胞周期进程的影响,该方法可轻松转换为许多其他系统。

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