Taylor Y C, Zhang X F, Parsian A J, Duncan P G
Cancer Biology Section, Washington University School of Medicine, St. Louis, Missouri 63108.
Exp Cell Res. 1991 Dec;197(2):222-8. doi: 10.1016/0014-4827(91)90426-u.
An image analysis system was used to visualize and measure the changes in nucleoid diameter (nuclear matrix core plus extruded DNA loops) which occur when increasing concentrations of propidium iodide are used to titrate the DNA supercoiling response. Parallel core size measurements allow estimates of the changes in apparent DNA loop size. Unlike sedimentation assays, DNA loop size estimates are not influenced by particle mass, require no prior cell labeling, and can be performed on a per cell basis. This technique was used to examine changes in DNA loop characteristics which may occur when cells are transformed or undergo changes in their proliferative state. SV40-transformation of human diploid fibroblast lines resulted in a significant increase in both the nucleoid core and average DNA loop size. Lymphoblast cell lines also had larger nucleoid dimensions than normal lymphocytes. The response of several established human tumor cell lines indicated slightly increased loop but not core sizes as compared to normal human diploid fibroblasts. Changes in proliferative state also resulted in changes in DNA loop characteristics as measured in this assay. Both quiescent fibroblasts and unstimulated lymphocytes appeared to have smaller or more condensed DNA loop structures than their proliferating counterparts. These results demonstrate the utility of this assay in detecting changes in DNA loop structure which occur in association with changes in the proliferative activity of cells in culture.
使用图像分析系统来可视化并测量当用递增浓度的碘化丙啶滴定DNA超螺旋反应时,核仁直径(核基质核心加上挤出的DNA环)的变化。并行的核心大小测量可以估计表观DNA环大小的变化。与沉降分析不同,DNA环大小的估计不受颗粒质量的影响,无需预先对细胞进行标记,并且可以在单个细胞的基础上进行。该技术用于检查细胞转化或增殖状态发生变化时可能出现的DNA环特征的变化。人二倍体成纤维细胞系的SV40转化导致核仁核心和平均DNA环大小均显著增加。淋巴母细胞系的核仁尺寸也比正常淋巴细胞大。与正常人二倍体成纤维细胞相比,几种已建立的人肿瘤细胞系的反应表明,环大小略有增加,但核心大小没有增加。增殖状态的变化也导致了本试验中所测量的DNA环特征的变化。静止的成纤维细胞和未受刺激的淋巴细胞似乎比其增殖的对应细胞具有更小或更浓缩的DNA环结构。这些结果证明了该试验在检测与培养细胞增殖活性变化相关的DNA环结构变化方面的实用性。