Golsteyn E J, Po C, Lefebvre Y A
Can J Biochem Cell Biol. 1985 Dec;63(12):1231-40. doi: 10.1139/o85-154.
We have isolated and purified, with good yields, nuclear envelopes from an androgen-responsive and from two androgen-unresponsive cell lines of the Shionogi mouse mammary carcinoma after subjecting purified nuclei to DNase at high pH and characterized them morphologically, chemically, and enzymatically. Phase-contrast microscopy revealed the nuclei to be free of cytoplasmic tags and that the nuclear envelopes were isolated as membrane "ghosts." Electron micrographs clearly showed the double-membrane system with nuclear pore complexes which illustrates that the nuclear envelopes were ultrastructurally intact. The nuclear envelopes contained little DNA, low levels of arylesterase or acid phosphatase activity, and undetectable levels of succinate dehydrogenase and 5'-nucleotidase activity. Coomassie blue staining of the nuclear envelope fractions on sodium dodecyl sulfate-polyacrylamide gels for all three cell lines revealed that most of the polypeptides were similar. However, we have identified androgen-dependent peptides of molecular weights 29 000, 32 000, and 34 000 in nuclear envelopes of the androgen-responsive cell line peptide profiles by comparing the nuclear envelopes prepared from the androgen-responsive cell line grown in intact mice, in castrated mice, and in mice which had been injected with testosterone after castration. Further investigation of the androgen regulation of these nuclear envelope peptides may help us understand the molecular mechanisms involved during morphological changes of the nucleus which occur in response to different hormonal environments.
我们通过在高pH值下用脱氧核糖核酸酶处理纯化的细胞核,从雄性激素反应性和两种雄性激素无反应性的日本住友小鼠乳腺癌细胞系中,以高产量分离并纯化了核膜,并对其进行了形态学、化学和酶学表征。相差显微镜显示细胞核没有细胞质标记,并且核膜以膜“空壳”形式被分离出来。电子显微镜照片清楚地显示了带有核孔复合体的双层膜系统,这表明核膜在超微结构上是完整的。核膜含有少量DNA、低水平的芳基酯酶或酸性磷酸酶活性,以及无法检测到的琥珀酸脱氢酶和5'-核苷酸酶活性。对所有三种细胞系的核膜组分在十二烷基硫酸钠-聚丙烯酰胺凝胶上进行考马斯亮蓝染色,结果显示大多数多肽是相似的。然而,通过比较在完整小鼠、去势小鼠以及去势后注射睾酮的小鼠中生长的雄性激素反应性细胞系制备的核膜,我们在雄性激素反应性细胞系的核膜肽谱中鉴定出了分子量分别为29000、32000和34000的雄激素依赖性肽。对这些核膜肽的雄激素调节进行进一步研究,可能有助于我们了解在不同激素环境下发生的细胞核形态变化过程中所涉及的分子机制。