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HL-60白血病细胞凋亡过程中微管重组的免疫细胞化学研究

Immunocytochemical study on microtubule reorganization in HL-60 leukemia cells undergoing apoptosis.

作者信息

Ahmadian Shahin, Pazhang Yaghub, Shariftabrizi Ahmad

机构信息

Department of Biochemistry, Institute of Biochemistry and Biophysics, University of Tehran, Tehran, Iran.

出版信息

Iran Biomed J. 2007 Oct;11(4):209-14.

Abstract

BACKGROUND

Microtubules (MT) are important components of cell cytoskeleton and play key roles in cell motility mitosis and meiosis. They are also the targets of several anticancer agents which indicating their importance in maintaining cell viability. Microtubular reorganization contributing to apoptotic morphology occurs in normal and neoplastic cells undergoing apoptosis induced by cytotoxic drugs. The aim of this study was to correlate the changes in the MT with behavior of the gamma-tubulin in apoptotic cell, and to see if apoptitic MT showed biochemical characteristics of stable MT.

METHODS

Apoptosis was induced in the human leukemia cells (HL-60) by treatment with 1 microM of all-trans retinoic acid over a 5-day period. The time course of changes was assessed using flow cytometry, DNA fragmentation and immunocytochemistry in cells labeled for alpha-tubulins, acetylated alpha-tubulin and gamma-tubulin.

RESULTS

The results indicated that gamma-tubulin content is increased after cells have gone through the apoptosis with a diffuse cytoplasmic pattern. Alpha-tubulin did not reveal any specific pattern of polymerization in apoptotic cells and acetylated alpha-tubulin content was also decreased in comparison with non-apoptotic cells.

CONCLUSION

Our results support the idea that microtubule reorganization is an important factor of the mammalian cells response to apoptosis, and the altered properties of the MT did not reflect changes in function as apoptosis progresses.

摘要

背景

微管(MT)是细胞骨架的重要组成部分,在细胞运动、有丝分裂和减数分裂中起关键作用。它们也是几种抗癌药物的作用靶点,这表明它们在维持细胞活力方面的重要性。在经历细胞毒性药物诱导凋亡的正常细胞和肿瘤细胞中,微管重组会导致凋亡形态的出现。本研究的目的是将微管的变化与凋亡细胞中γ-微管蛋白的行为相关联,并观察凋亡微管是否表现出稳定微管的生化特征。

方法

通过用1微摩尔全反式维甲酸处理人白血病细胞(HL-60)5天来诱导凋亡。使用流式细胞术、DNA片段化和免疫细胞化学对标记有α-微管蛋白、乙酰化α-微管蛋白和γ-微管蛋白的细胞评估变化的时间进程。

结果

结果表明,细胞经历凋亡后,γ-微管蛋白含量增加,呈弥漫性胞质模式。α-微管蛋白在凋亡细胞中未显示任何特定的聚合模式,与非凋亡细胞相比,乙酰化α-微管蛋白含量也降低。

结论

我们的结果支持微管重组是哺乳动物细胞对凋亡反应的重要因素这一观点,并且随着凋亡进展,微管性质的改变并未反映功能的变化。

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