Tennessee State University, Nashville, TN 37209, USA.
Cell Tissue Res. 2011 Oct;346(1):43-51. doi: 10.1007/s00441-011-1247-x. Epub 2011 Oct 11.
Pluripotent mouse embryonal carcinoma (mEC) and mouse embryonic stem (mES) cells differentiate into several cell lineages upon retinoic acid (RA) addition. Differentiation is facilitated, in part, by RA activation of nuclear RA receptors (RARs) that bind to DNA response elements located in the promoters of target genes. The purpose of the studies reported here was to immunolocalize RARα and RARγ protein in mEC and mES cells and in their RA-induced differentiated progeny. Fixed cells were reacted with three different RARα antibodies and one RARγ antibody. Pluripotent and differentiated mEC and mES cells showed positive nuclear immunoreactivity with all antibodies tested. Two RARα antibodies also showed positive reactivity in the cytoplasm. Surprisingly, our results revealed variability in immunofluorescence intensity and in RARα and RARγ distribution from one cell to the other, suggesting that RARα and RARγ protein levels were not synchronous throughout the cell population. The results indicate that RARα and RARγ are present in pluripotent and differentiating mEC and mES cells and suggest that the expression of these proteins is dynamic.
多能性小鼠胚胎癌细胞 (mEC) 和小鼠胚胎干细胞 (mES) 在添加视黄酸 (RA) 后会分化为几种细胞谱系。RA 激活核 RA 受体 (RARs),与靶基因启动子中位于 DNA 反应元件的结合,在一定程度上促进了分化。本研究的目的是在 mEC 和 mES 细胞及其 RA 诱导的分化后代中免疫定位 RARα 和 RARγ 蛋白。固定细胞用三种不同的 RARα 抗体和一种 RARγ 抗体进行反应。多能性和分化的 mEC 和 mES 细胞用所有测试的抗体均显示出阳性核免疫反应性。两种 RARα 抗体在细胞质中也显示出阳性反应性。令人惊讶的是,我们的结果显示,从一个细胞到另一个细胞,免疫荧光强度和 RARα 和 RARγ 分布存在可变性,这表明 RARα 和 RARγ 蛋白水平在整个细胞群体中并非同步。结果表明,RARα 和 RARγ 存在于多能性和分化的 mEC 和 mES 细胞中,并表明这些蛋白的表达是动态的。