Yang G H, Li S, Pestka J J
National Food Safety and Toxicology Center, Michigan State University, East Lansing, Michigan, 48824, USA.
Toxicol Appl Pharmacol. 2000 Feb 1;162(3):207-17. doi: 10.1006/taap.1999.8842.
The mechanisms by which trichothecene mycotoxins cause immunological effects in leukocytes such as cytokine up-regulation, aberrant IgA production, or apoptotic cell death are not fully understood. In the present study, mRNA differential display analysis was used to evaluate changes in gene expression induced by the trichothecene vomitoxin (VT or deoxynivalenol) in a T-cell model, the murine EL-4 thymoma, that was stimulated with phorbol 12-myristate 13-acetate (PMA) and ionomycin (ION). Ten differentially expressed fragments of cDNA were isolated and sequenced and three of these were identified as the known genes GRP78/BiP, P58(IPK), and RAD17. Most notably, expression of GRP78/BiP (a 78-kDa glucose-regulated protein), a stress-response gene induced by agents or conditions that adversely affect endoplasmic reticulum (ER) function, was found to decrease in VT-exposed cells. Competitive RT-PCR analysis revealed that 250 ng/ml VT decreased GRP78/BiP mRNA expression in both unstimulated and PMA/ION-stimulated EL-4 cells at 6 and 24 h after VT treatment. Western blotting confirmed that VT (50 to 1000 ng/ml) also significantly diminished GRP/BiP protein levels in a dose-response manner in PMA/ION-stimulated cells. GRP78/BiP has been shown to play a role in regulation of protein folding and secretion, and to protect cells from apoptosis. When PMA/ION-stimulated cells were incubated with 50 to 1000 ng/ml VT for 24 h, 200-bp DNA laddering, a hallmark of apoptosis, increased in a dose-dependent manner. In addition to GRP78, mRNA expression of the cochaperone P58(IPK), which is the 58-kDa cellular inhibitor of the double-stranded RNA-regulated protein kinase (PKR), was also shown to be suppressed by VT-treatment. GRP78 and P58(IPK) are critical for maintenance of cell homeostasis and prevention of apoptosis. The down-regulation of these molecular chaperones by VT represent a novel observation and has the potential to impact immune function at multiple levels.
单端孢霉烯族霉菌毒素在白细胞中引发免疫效应(如细胞因子上调、异常IgA产生或凋亡性细胞死亡)的机制尚未完全明确。在本研究中,运用mRNA差异显示分析来评估在T细胞模型(即经佛波酯12 - 肉豆蔻酸酯13 - 乙酸酯(PMA)和离子霉素(ION)刺激的小鼠EL - 4胸腺瘤)中,单端孢霉烯族呕吐毒素(VT或脱氧雪腐镰刀菌烯醇)诱导的基因表达变化。分离并测序了10个差异表达的cDNA片段,其中3个被鉴定为已知基因GRP78/BiP、P58(IPK)和RAD17。最值得注意的是,GRP78/BiP(一种78 kDa的葡萄糖调节蛋白)的表达在暴露于VT的细胞中降低,GRP78/BiP是一种由对内质网(ER)功能产生不利影响的因素或条件所诱导的应激反应基因。竞争性RT - PCR分析显示,在VT处理后6小时和24小时,250 ng/ml的VT降低了未刺激的以及PMA/ION刺激的EL - 4细胞中GRP78/BiP mRNA的表达。蛋白质印迹法证实,在PMA/ION刺激的细胞中,VT(50至10化0 ng/ml)也以剂量反应方式显著降低了GRP/BiP蛋白水平。GRP78/BiP已被证明在蛋白质折叠和分泌的调节中发挥作用,并保护细胞免于凋亡。当用50至1000 ng/ml的VT处理PMA/ION刺激的细胞24小时时,凋亡的标志——200 bp的DNA梯状条带以剂量依赖方式增加。除了GRP78,共伴侣蛋白P58(IPK)(即双链RNA调节蛋白激酶(PKR)的58 kDa细胞抑制剂)的mRNA表达也显示受到VT处理的抑制。GRP78和P58(IPK)对于维持细胞内稳态和预防凋亡至关重要。VT对这些分子伴侣的下调代表了一种新的观察结果,并且有可能在多个层面影响免疫功能。