Moutsatsos I K, Wade M, Schindler M, Wang J L
Proc Natl Acad Sci U S A. 1987 Sep;84(18):6452-6. doi: 10.1073/pnas.84.18.6452.
Proliferating 3T3 mouse fibroblasts contain higher levels of the lectin carbohydrate-binding protein 35 (CBP35) than do quiescent cultures of the same cells. An immunofluorescence study was carried out with a rabbit antiserum directed against CBP35 to map the cellular fluorescence distribution in a large population of cells under different growth conditions. This cytometric analysis showed that the lectin is predominantly localized in the nucleus of the proliferating cells. In quiescent 3T3 cultures, the majority of the cells lost their nuclear staining and underwent a general decrease in the overall fluorescence intensity. Stimulation of serum-starved quiescent 3T3 cells by the addition of serum resulted in an increase in the level of CBP35. The percentage of cells showing distinct punctate intranuclear staining reached a maximum at about the same time as the onset of the first S-phase of the cell cycle. All of these results suggest that CBP35 may be a protein whose presence in the nucleus, in discrete punctate distribution, is coordinated with the proliferation state of the cell.
与相同细胞的静止培养物相比,增殖的3T3小鼠成纤维细胞中凝集素碳水化合物结合蛋白35(CBP35)的水平更高。用针对CBP35的兔抗血清进行了免疫荧光研究,以绘制不同生长条件下大量细胞中的细胞荧光分布。这种细胞计数分析表明,凝集素主要定位于增殖细胞的细胞核中。在静止的3T3培养物中,大多数细胞失去了核染色,并且总体荧光强度普遍下降。通过添加血清刺激血清饥饿的静止3T3细胞会导致CBP35水平升高。显示明显点状核内染色的细胞百分比在细胞周期第一个S期开始时达到最大值。所有这些结果表明,CBP35可能是一种蛋白质,其在细胞核中的存在以离散的点状分布与细胞的增殖状态相协调。