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小鼠胚胎癌细胞分化过程中β-淀粉样蛋白前体和微管相关蛋白tau的表达增加。

Increased expression of beta-amyloid protein precursor and microtubule-associated protein tau during the differentiation of murine embryonal carcinoma cells.

作者信息

Fukuchi K, Deeb S S, Kamino K, Ogburn C E, Snow A D, Sekiguchi R T, Wight T N, Piussan H, Martin G M

机构信息

Department of Pathology, University of Washington, Seattle 98195.

出版信息

J Neurochem. 1992 May;58(5):1863-73. doi: 10.1111/j.1471-4159.1992.tb10063.x.

DOI:10.1111/j.1471-4159.1992.tb10063.x
PMID:1560239
Abstract

Expression of the genes encoding the beta/A4 amyloid protein precursor (APP) and microtubule-associated protein tau was studied in an embryonal carcinoma cell line (P19) that differentiates in vitro into cholinergic neurons after treatment with retinoic acid. Expression of APP increased 34- (mRNA) and 50-fold (protein) during neuronal differentiation; APP-695 accounted for most of this increase. These remarkable increases in APP expression coincided with a proliferation of neuronal processes and with an increase in content of tau mRNA. Moreover, subsequent decreases in the levels of APP and tau mRNA coincided with the onset of the degeneration of the neuronal processes. Immunocytochemical staining suggested that greater than 85% of the P19-derived neurons are cholinergic and that APP is present in the neuronal processes and cell bodies. These results suggest that APP may play an important role in construction of neuronal networks and neuronal differentiation and also indicate that this embryonal carcinoma cell line provides an ideal model system to investigate biological functions of APP and the roles of APP and tau protein in development of Alzheimer's disease in cholinergic neurons.

摘要

在一种胚胎癌细胞系(P19)中研究了编码β/A4淀粉样蛋白前体(APP)和微管相关蛋白tau的基因表达,该细胞系在用视黄酸处理后可在体外分化为胆碱能神经元。在神经元分化过程中,APP的表达在mRNA水平增加了34倍,在蛋白质水平增加了50倍;APP-695的增加占了大部分。APP表达的显著增加与神经元突起的增殖以及tau mRNA含量的增加同时出现。此外,随后APP和tau mRNA水平的下降与神经元突起退化的开始同时发生。免疫细胞化学染色表明,超过85%的源自P19的神经元是胆碱能的,并且APP存在于神经元突起和细胞体中。这些结果表明APP可能在神经网络的构建和神经元分化中起重要作用,并且还表明这种胚胎癌细胞系为研究APP的生物学功能以及APP和tau蛋白在胆碱能神经元中阿尔茨海默病发展中的作用提供了理想的模型系统。

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