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亚砷酸钠通过延迟白细胞介素-2的产生和分泌来抑制PHA激活的T细胞增殖。

Sodium arsenite retards proliferation of PHA-activated T cells by delaying the production and secretion of IL-2.

作者信息

Galicia Georgina, Leyva Rosario, Tenorio Eda Patricia, Ostrosky-Wegman Patricia, Saavedra Rafael

机构信息

Departamento de Inmunología y Enfermedades Infecciosas, Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México, Apartado Postal 70228, CU, Mexico City CP 04510, Mexico.

出版信息

Int Immunopharmacol. 2003 May;3(5):671-82. doi: 10.1016/S1567-5769(03)00049-3.

Abstract

Arsenic is a metalloid that commonly contaminates drinking water, and is a known human carcinogen. It has been shown that peripheral blood mononuclear cells (PBMCs) from healthy donors treated in vitro with NaAsO(2) and stimulated with phytohemagglutinin (PHA) show a lower proliferation than nontreated cells. We reported previously a reduction in the secretion of IL-2 in NaAsO(2)-treated PBMCs stimulated with PHA, an observation that might explain, in part, the reduction in proliferation. Since arsenic induces cytoskeleton alterations, which in turn may affect protein transport of the cell, we assumed that NaAsO(2) induced an accumulation of IL-2 inside the cells, and thus a reduction in the secretion of IL-2. In order to demonstrate this hypothesis, we assessed the intracellular IL-2 at the single cell level by flow cytometry, and unexpectedly found a reduction in the percentage of IL-2 producing T cells in the presence of NaAsO(2). We tracked the proliferation of T cells by using the 5,6-carboxyfluorescein diacetate succinimidyl ester (CFSE) dye and found that NaAsO(2) slows down the entrance to cell division and delays the proliferation of cells that have already entered the cell cycle. Nevertheless, the expression of the activation molecules, CD25 and CD69, was unaltered. Assessment of the intracellular and secreted IL-2 in kinetic experiments showed that in fact, NaAsO(2) delays the production of IL-2, given that a recovery of both intracellular and secreted IL-2 was detected at 72 h. Evaluation of the cell cycle showed a higher proportion of cells in G(0)/G(1) and a lower proportion in G(2)/M in the presence of NaAsO(2). We thus conclude that NaAsO(2) reduces proliferation of T cells by delaying the production and secretion of IL-2, thus blocking T cells in G(1); as a consequence, the entry to cell cycle and the rounds of cell division are retarded, and a lower proliferation of T cells is hence observed.

摘要

砷是一种准金属,常污染饮用水,是一种已知的人类致癌物。研究表明,来自健康供体的外周血单个核细胞(PBMCs)在体外经亚砷酸钠(NaAsO₂)处理并用植物血凝素(PHA)刺激后,其增殖能力低于未处理的细胞。我们之前报道过,在经PHA刺激的NaAsO₂处理的PBMCs中,白细胞介素-2(IL-2)的分泌减少,这一观察结果可能部分解释了增殖的减少。由于砷会诱导细胞骨架改变,进而可能影响细胞的蛋白质运输,我们推测NaAsO₂会导致IL-2在细胞内积累,从而使IL-2的分泌减少。为了验证这一假设,我们通过流式细胞术在单细胞水平评估细胞内IL-2,意外地发现,在存在NaAsO₂的情况下,产生IL-2的T细胞百分比降低。我们使用5,6-羧基荧光素二乙酸琥珀酰亚胺酯(CFSE)染料追踪T细胞的增殖,发现NaAsO₂减缓了细胞进入分裂的进程,并延迟了已经进入细胞周期的细胞的增殖。然而,活化分子CD25和CD69的表达未改变。动力学实验中对细胞内和分泌的IL-2的评估表明,事实上,NaAsO₂延迟了IL-2的产生,因为在72小时时检测到细胞内和分泌的IL-2均有所恢复。细胞周期评估显示,在存在NaAsO₂的情况下,处于G(0)/G(1)期的细胞比例更高,而处于G(2)/M期的细胞比例更低。因此,我们得出结论,NaAsO₂通过延迟IL-2的产生和分泌来降低T细胞的增殖,从而将T细胞阻滞在G(1)期;结果,细胞进入细胞周期和细胞分裂轮次均受到阻碍,因此观察到T细胞的增殖较低。

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