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组蛋白去乙酰化酶抑制剂曲古抑菌素A诱导人白血病U937细胞凋亡并抑制端粒酶活性

Induction of apoptosis and inhibition of telomerase activity by trichostatin A, a histone deacetylase inhibitor, in human leukemic U937 cells.

作者信息

Woo Hyun Joo, Lee Su Jae, Choi Byung Tae, Park Yeong-Min, Choi Yung Hyun

机构信息

Department of Biochemistry, Dongeui University College of Oriental Medicine, Busan 614-052, South Korea.

出版信息

Exp Mol Pathol. 2007 Feb;82(1):77-84. doi: 10.1016/j.yexmp.2006.02.004. Epub 2006 Mar 30.

DOI:10.1016/j.yexmp.2006.02.004
PMID:16574101
Abstract

The objective of the present study was to investigate the effect of trichostatin A (TSA), a histone deacetylase (HDAC) inhibitor, on the cell growth and apoptosis and its effect on the telomerase activity in human leukemic cell line U937. Exposure of U937 cells to TSA resulted in growth inhibition and induction of apoptosis in a dose-dependent manner as measured by hemocytometer counts, fluorescence microscopy, agarose gel electrophoresis and flow cytometry analysis. The increase in apoptosis was associated with the up-regulation in proapoptotic Bax expression and down-regulation of antiapoptotic Bcl-2 and Bcl-X(L). TSA treatment inhibited the levels of cIAP family members and induced the proteolytic activation of caspase-3, which was associated with concomitant degradation of poly(ADP-ribose)-polymerase and beta-catenin protein. TSA treatment markedly inhibited the activity of telomerase in a dose-dependent fashion. Additionally, the expression of human telomerase reverse transcriptase (hTERT), a main determinant of the telomerase enzymatic activity, was progressively down-regulated by TSA treatment. We therefore conclude that TSA demonstrated antiproliferative and apoptosis-inducing effects on U937 cells in vitro, and that changes in Bcl-2 family protein levels as well as telomerase activity may play an important role in its mechanism of action.

摘要

本研究的目的是探讨组蛋白脱乙酰酶(HDAC)抑制剂曲古抑菌素A(TSA)对人白血病细胞系U937细胞生长、凋亡的影响及其对端粒酶活性的作用。通过血细胞计数器计数、荧光显微镜检查、琼脂糖凝胶电泳和流式细胞术分析测定,U937细胞暴露于TSA后导致生长抑制并呈剂量依赖性诱导凋亡。凋亡增加与促凋亡蛋白Bax表达上调以及抗凋亡蛋白Bcl-2和Bcl-X(L)表达下调有关。TSA处理抑制了细胞凋亡抑制蛋白(cIAP)家族成员的水平,并诱导了半胱天冬酶-3的蛋白水解激活,这与聚(ADP-核糖)聚合酶和β-连环蛋白的伴随降解有关。TSA处理以剂量依赖性方式显著抑制端粒酶活性。此外,作为端粒酶活性主要决定因素的人端粒酶逆转录酶(hTERT)的表达通过TSA处理逐渐下调。因此,我们得出结论,TSA在体外对U937细胞具有抗增殖和诱导凋亡的作用,并且Bcl-2家族蛋白水平以及端粒酶活性的变化可能在其作用机制中起重要作用

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