Chen Shanyi, Fariss Robert N, Kutty R Krishnan, Nelson Ralph, Wiggert Barbara
Biochemistry Section, Laboratory of Retinal Cell and Molecular Biology, National Eye Institute, National Institutes of Health, Bethesda, Maryland 20892-0706, USA.
Mol Vis. 2006 Nov 1;12:1355-63.
We reported earlier that fenretinide can induce neuronal differentiation of ARPE-19 human retinal pigment epithelial cells in culture. The purpose of this study was to investigate the potential involvement of key proteins involved in gene transcription, signal transduction, cell cycle check point, differentiation, neuronal cell survival, and stress response in the neuronal differentiation of ARPE-19 cells by fenretinide.
Cells in culture were treated with 1.0 microM fenretinide. Cells were analyzed using antibodies against pax-6, neuronal specific enolase (NSE), tubulin beta-III, 14-3-3, bag-1, and Hsp-70 proteins using immunocytochemistry, western blot and ELISA methodologies.
We found that pax-6 and NSE were both expressed in the control ARPE-19 cells. Fenretinide induced neuronal differentiation of ARPE-19 cells led to a decrease in pax-6 protein and an increase in tubulin beta-III protein expression after 5 days fenretinide treatment. There was a translocation of 14-3-3 from the cytoplasm to the nucleus, and an increase in nuclear expression of bag-1 after treatment. We also found a time-dependent increase in Hsp70 protein expression in ARPE-19 cells treated with fenretinide. D-407, another human retinal pigment epithelial cell line, but not either Y-79 or PC-12 cells, was also able to be induced into neuronal morphologies by fenretinide.
The fenretinide-induced neuronal differentiation of ARPE-19 cells is associated with an increase in expression of the neuronal specific protein tubulin beta-III, and a decrease in expression of the progenitor cell marker pax-6. Neuronal differentiation of ARPE-19 cells is also associated with nuclear translocation of 14-3-3, a protein involved in signal transduction, cell cycle check point and cell growth, and an increase in expression of bag-1, a protein involved in neuronal cell survival and axon elongation. These results suggest that ARPE-19 cells could be a progenitor cell line that can be differentiated into neuronal cells when treated with factors such as fenretinide.
我们之前报道过,维甲酸能在培养中诱导ARPE - 19人视网膜色素上皮细胞发生神经元分化。本研究的目的是调查参与基因转录、信号转导、细胞周期检查点、分化、神经元细胞存活和应激反应的关键蛋白在维甲酸诱导ARPE - 19细胞神经元分化过程中的潜在作用。
用1.0微摩尔/升的维甲酸处理培养中的细胞。使用免疫细胞化学、蛋白质印迹法和酶联免疫吸附测定法,用针对pax - 6、神经元特异性烯醇化酶(NSE)、微管蛋白β - III、14 - 3 - 3、bag - 1和热休克蛋白70(Hsp - 70)蛋白的抗体对细胞进行分析。
我们发现pax - 6和NSE在对照ARPE - 19细胞中均有表达。维甲酸诱导ARPE - 19细胞发生神经元分化,在维甲酸处理5天后导致pax - 6蛋白减少,微管蛋白β - III蛋白表达增加。处理后14 - 3 - 3从细胞质转位至细胞核,且bag - 1的核表达增加。我们还发现,用维甲酸处理的ARPE - 19细胞中Hsp70蛋白表达呈时间依赖性增加。另一种人视网膜色素上皮细胞系D - 407,但不是Y - 79或PC - 12细胞,也能被维甲酸诱导形成神经元形态。
维甲酸诱导的ARPE - 19细胞神经元分化与神经元特异性蛋白微管蛋白β - III表达增加以及祖细胞标志物pax - 6表达减少有关。ARPE - 19细胞的神经元分化还与14 - 3 - 3的核转位有关,14 - 3 - 3是一种参与信号转导、细胞周期检查点和细胞生长的蛋白,并且与bag - 1表达增加有关,bag - 1是一种参与神经元细胞存活和轴突伸长的蛋白。这些结果表明,ARPE - 19细胞可能是一种祖细胞系,在用维甲酸等因子处理时可分化为神经元细胞。