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p53抑制诱导的神经元加速分化。

Accelerated neuronal differentiation induced by p53 suppression.

作者信息

Ferreira A, Kosik K S

机构信息

Department of Medicine (Division Neurology) Brigham and Women's Hospital, Boston MA 02115, USA.

出版信息

J Cell Sci. 1996 Jun;109 ( Pt 6):1509-16. doi: 10.1242/jcs.109.6.1509.

Abstract

p53, a tumor suppressor gene product, has been implicated in the control of cell growth and malignant transformation in different cell types. Here we studied the role of p53 in normal central nervous system development. We show that p53 is expressed in neuroblasts and is down regulated when migrating neurons reach their destination. The suppression of p53 either by the addition of antisense oligonucleotides to culture medium or by the culture of neurons from p53-/- mice accelerated their differentiation. This effect is accompanied by an early induction of MAP1b and a premature dephosphorylation of tau. p53 suppression also reduced levels of p21. Taken collectively these results suggest that the expression of p53 in neuroblasts might prevent neuronal terminal differentiation.

摘要

p53是一种肿瘤抑制基因产物,已被证明参与调控不同细胞类型中的细胞生长和恶性转化。在此,我们研究了p53在正常中枢神经系统发育中的作用。我们发现p53在神经母细胞中表达,当迁移的神经元到达目的地时其表达下调。通过向培养基中添加反义寡核苷酸或培养来自p53基因敲除小鼠的神经元来抑制p53,可加速其分化。这种效应伴随着MAP1b的早期诱导和tau蛋白的过早去磷酸化。p53的抑制还降低了p21的水平。综合这些结果表明,神经母细胞中p53的表达可能会阻止神经元的终末分化。

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