King's College London, Institute of Psychiatry, Old Age Psychiatry and Dementia, London, SE5 8AF, UK.
Mol Neurobiol. 2011 Apr;43(2):139-46. doi: 10.1007/s12035-011-8172-6. Epub 2011 Mar 8.
p73, a transcription factor of the p53 family, plays a key role in many biological processes including neuronal development. Indeed, mice deficient for both TAp73 and ΔNp73 isoforms display neuronal pathologies, including hydrocephalus and hippocampal dysgenesis, with defects in the CA1-CA3 pyramidal cell layers and the dentate gyrus. TAp73 expression increases in parallel with neuronal differentiation and its ectopic expression induces neurite outgrowth and expression of neuronal markers in neuroblastoma cell lines and neural stem cells, suggesting that it has a pro-differentiation role. In contrast, ΔNp73 shows a survival function in mature cortical neurons as selective ΔNp73 null mice have reduced cortical thickness. Recent evidence has also suggested that p73 isoforms are deregulated in neurodegenerative pathologies such as Alzheimer's disease, with abnormal tau phosphorylation. Thus, in addition to its increasingly accepted contribution to tumorigenesis, the p73 subfamily also plays a role in neuronal development and neurodegeneration.
p73 是 p53 家族的转录因子,在许多生物学过程中发挥着关键作用,包括神经元发育。事实上,同时缺乏 TAp73 和 ΔNp73 异构体的小鼠表现出神经元病理学,包括脑积水和海马发育不良,在 CA1-CA3 锥体细胞层和齿状回中存在缺陷。TAp73 的表达随着神经元分化而增加,其异位表达在神经母细胞瘤细胞系和神经干细胞中诱导轴突生长和神经元标记物的表达,表明其具有促进分化的作用。相反,ΔNp73 在成熟皮质神经元中具有生存功能,因为选择性 ΔNp73 缺失小鼠的皮质厚度减少。最近的证据还表明,p73 异构体在神经退行性疾病(如阿尔茨海默病)中失调,出现异常的 tau 磷酸化。因此,除了其在肿瘤发生中的日益被接受的贡献外,p73 亚家族还在神经元发育和神经退行性变中发挥作用。