Grzanka Alina, Grzanka Dariusz
Department of Clinical Pathomorphology, L. Rydygier Medical University, Bydgoszcz, Poland.
Med Sci Monit. 2003 Jan;9(1):BR66-9.
In the last decade there has been increasing interest in cytoskeletal research in relation to important process of cell biology. However, after decades of debate many issues remain unsettled. The aim of our study was to estimate the distribution of tubulin in etoposide-induced HL-60 cells and address the question of whether the reorganization of tubulin may be involved in apoptosis.
MATERIAL/METHODS: HL-60 cells were incubated with etoposide (0.02-200 mM/L) for 72 hours. Tubulin was estimated by the indirect immunofluorescence method. TRITC-labeled goat anti rabbit IgG was used to label tubulin.
Significant changes occurred in cell morphology of and tubulin organization at 200 mM/L etoposide: large cells, brightly labeled for tubulin, in cytoplasm. At 200 uM/L etoposide, we also observed an increase in apoptotic cells with bright staining for tubulin at the site of apoptotic body formations. Cells with features of apoptosis were frequently seen also at 20 mM/L etoposide. The exposure of cells to 0.02, 0.2, or 2 mM/L etoposide did not result in any visible changes in morphology or tubulin organization. Cell size, the number of viable cells, and the percentage of apoptotic cells correlated significantly with the dose of etoposide (p<0.001).
These results indicate that etoposide promotes changes in the distribution of tubulin in HL-60 cells, depending on the dose, and that the reorganization of tubulin seems to be involved in apoptosis
在过去十年中,细胞骨架研究与细胞生物学的重要过程相关,受到越来越多的关注。然而,经过数十年的争论,许多问题仍未解决。我们研究的目的是估计微管蛋白在依托泊苷诱导的HL-60细胞中的分布,并探讨微管蛋白的重组是否可能参与细胞凋亡。
材料/方法:HL-60细胞与依托泊苷(0.02 - 200 mM/L)孵育72小时。通过间接免疫荧光法估计微管蛋白。用TRITC标记的山羊抗兔IgG标记微管蛋白。
在200 mM/L依托泊苷处理下,细胞形态和微管蛋白组织发生了显著变化:细胞变大,细胞质中的微管蛋白标记明亮。在200 μM/L依托泊苷处理下,我们还观察到凋亡细胞增加,凋亡小体形成部位的微管蛋白染色明亮。在20 mM/L依托泊苷处理下也经常可见具有凋亡特征的细胞。细胞暴露于0.02、0.2或2 mM/L依托泊苷未导致形态或微管蛋白组织出现任何可见变化。细胞大小、活细胞数量和凋亡细胞百分比与依托泊苷剂量显著相关(p<0.001)。
这些结果表明,依托泊苷可促进HL-60细胞中微管蛋白分布的变化,这取决于剂量,并且微管蛋白的重组似乎参与了细胞凋亡。