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在 p53 抑制剂 pifithrin-α存在的情况下,研究 X 射线诱导的 G2 期人淋巴细胞凋亡和染色体损伤。

Study on X-ray-induced apoptosis and chromosomal damage in G2 human lymphocytes in the presence of pifithrin-α, an inhibitor of p53.

机构信息

Department of Ecology and Biology, University of Tuscia, Viterbo, Italy.

出版信息

Mutat Res. 2011 Nov 27;726(1):29-35. doi: 10.1016/j.mrgentox.2011.07.013. Epub 2011 Aug 26.

DOI:10.1016/j.mrgentox.2011.07.013
PMID:21889606
Abstract

The aim of this study is to investigate the role of the cell-cycle phase in cells exposed to radiation and chemicals in relation to the cellular response. The analysis was focused on the G2 cell-cycle phase, exploring the impact of p53 inhibition in human lymphocytes irradiated with X-rays in the presence or absence of pifithrin-α (PFT-α), a p53-specific inhibitor. Lymphocytes, 44h after stimulation to proliferate, were X-irradiated with 0.5Gy both in the presence or the absence of PFT-α and post-treated with a pulse of 5-bromodeoxyuridine (BrdUrd) to distinguish cells in the S- or G2-phase at the moment of irradiation. At early sampling times after X-ray exposure the following parameters were analysed: cellular proliferation, apoptosis, chromosomal aberrations and p53 expression. The results show an enhancement of apoptotic cells in G2 at early sampling times after irradiation and no differences in terms of chromosomal aberration induction both in cells treated with X-rays alone and in cells treated with X-rays plus PFT-α. Expression of p53 was not detectable at all recovery times. The results suggest a p53-independent apoptotic pathway acting at early times after X-ray exposure in G2 lymphocytes. Furthermore, the same yield of X-ray-induced chromatid breaks was observed both in the presence or absence of PFT-α implying that in G2 X-irradiated lymphocytes this inhibitor of the p53 protein does not affect DNA repair.

摘要

本研究旨在探讨细胞暴露于辐射和化学物质时细胞周期阶段与细胞反应的关系。分析集中在 G2 细胞周期阶段,探讨在存在或不存在 p53 特异性抑制剂 pifithrin-α(PFT-α)的情况下,X 射线照射人淋巴细胞时 p53 抑制对细胞的影响。刺激增殖 44 小时后,将淋巴细胞用 0.5Gy X 射线照射,同时存在或不存在 PFT-α,并在 X 射线照射时用 5-溴脱氧尿苷(BrdUrd)脉冲处理,以区分 S 期或 G2 期的细胞。在 X 射线暴露后的早期采样时间分析了以下参数:细胞增殖、细胞凋亡、染色体畸变和 p53 表达。结果显示,在 X 射线照射后的早期采样时间,G2 中的凋亡细胞增加,单独用 X 射线处理的细胞和用 X 射线加 PFT-α 处理的细胞之间,染色体畸变的诱导没有差异。在所有恢复时间都无法检测到 p53 的表达。结果表明,在 G2 淋巴细胞中,X 射线暴露后早期存在 p53 非依赖性凋亡途径。此外,在存在或不存在 PFT-α 的情况下,观察到相同的 X 射线诱导的染色单体断裂产量,这意味着在 G2 期 X 射线照射的淋巴细胞中,这种 p53 蛋白的抑制剂不影响 DNA 修复。

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