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p53调节神经前体细胞的自我更新和分化。

p53 regulates the self-renewal and differentiation of neural precursors.

作者信息

Armesilla-Diaz A, Bragado P, Del Valle I, Cuevas E, Lazaro I, Martin C, Cigudosa J C, Silva A

机构信息

Department of Cellular and Molecular Physiopathology, Consejo Superior de Investigaciones Científicas, Ramiro de Maeztu, 9, 28040 Madrid, Spain.

出版信息

Neuroscience. 2009 Feb 18;158(4):1378-89. doi: 10.1016/j.neuroscience.2008.10.052. Epub 2008 Nov 7.

Abstract

During embryo neurogenesis, neurons that originate from stem cells located in the forebrain subventricular zone (SVZ) continuously migrate to the olfactory bulb (OB). However, other authors describe the occurrence of resident stem cells in the OB. In the present work we report that the absence of tumor suppressor protein p53 increases the number of neurosphere-forming cells and the proliferation of stem cells derived from 13.5-day embryo OB. Interestingly, differentiation of p53 knockout-derived neurospheres was biased toward neuronal precursors, suggesting a role for p53 in the differentiation process. Moreover, we demonstrate the relevance of p53 in maintaining chromosomal stability in response to genotoxic insult. Finally, our data show that neurosphere stem cells are highly resistant to long-term epidermal growth factor (EGF) and basic fibroblast growth factor (bFGF) deprivation in a p53-independent fashion, and they preserve their differentiation potential. Thus, these data demonstrate that p53 controls the proliferation, chromosomal stability and differentiation pattern of embryonic mouse olfactory bulb stem cells.

摘要

在胚胎神经发生过程中,起源于前脑脑室下区(SVZ)干细胞的神经元持续迁移至嗅球(OB)。然而,其他作者描述了嗅球中存在常驻干细胞。在本研究中,我们报告称肿瘤抑制蛋白p53的缺失增加了神经球形成细胞的数量以及源自13.5天胚胎嗅球的干细胞的增殖。有趣的是,p53基因敲除衍生的神经球的分化偏向于神经元前体,表明p53在分化过程中发挥作用。此外,我们证明了p53在响应基因毒性损伤时维持染色体稳定性的相关性。最后,我们的数据表明,神经球干细胞以不依赖p53的方式对长期表皮生长因子(EGF)和碱性成纤维细胞生长因子(bFGF)剥夺具有高度抗性,并且它们保留了分化潜能。因此,这些数据表明p53控制着胚胎小鼠嗅球干细胞的增殖、染色体稳定性和分化模式。

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