Shanker G, Sorci-Thomas M, Adams M R
Department of Comparative Medicine, Bowman Gray School of Medicine, Wake Forest University, Winston-Salem, North Carolina.
Lymphokine Cytokine Res. 1994 Dec;13(6):377-82.
Monokines, including tumor necrosis factor alpha (TNF-alpha), have been implicated in the pathogenesis of several pathologic processes, including atherosclerosis. Because estrogen has been found to offer a certain degree of protection against atherosclerotic progression, we examined the effect of estrogen on the expression of TNF-alpha mRNA in a monocyte-macrophage cell line, THP-1. Cells were exposed to 12-O-tetradecanoylphorbol 13-acetate (TPA, 50 ng/ml) for 48 or 96 h to induce differentiation. Some of the cells were treated with lipopolysaccharide (LPS, 10 micrograms/ml) in the last 3 h and/or ethinyl estradiol (estrogen, 10(-9) M) in the last 20 h. Total cellular RNA was isolated and cDNA synthesized and than coamplified using the polymerase chain reaction (PCR) in the presence of two sets (pairs) of 32P-labeled primers, one for TNF-alpha (product size 325 bp) and the second for the internal control, glyceraldehyde 3-phosphate dehydrogenase (G3PDH; 983 bp). The resultant PCR products were separated by agarose gel electrophoresis, and the ratios of radioactivity incorporated into TNF-alpha PCR products to G3PDH products were used to assess the relative changes in the levels of TNF-alpha mRNA abundance in response to various substances. Treatment with TPA for 48 h induced the expression of TNF-alpha mRNA. Treatment of these TPA-stimulated cells with estrogen caused a 62% decrease in TNF-alpha message abundance (p < 0.01). Similar results were obtained with cells stimulated with TPA for 96 h.(ABSTRACT TRUNCATED AT 250 WORDS)
包括肿瘤坏死因子α(TNF-α)在内的单核因子与包括动脉粥样硬化在内的多种病理过程的发病机制有关。由于已发现雌激素对动脉粥样硬化进展具有一定程度的保护作用,我们研究了雌激素对单核巨噬细胞系THP-1中TNF-α mRNA表达的影响。细胞用12-O-十四酰佛波醇-13-乙酸酯(TPA,50 ng/ml)处理48或96小时以诱导分化。部分细胞在最后3小时用脂多糖(LPS,10微克/毫升)和/或在最后20小时用乙炔雌二醇(雌激素,10^(-9) M)处理。分离总细胞RNA并合成cDNA,然后在两组(对)32P标记引物存在下使用聚合酶链反应(PCR)进行共扩增,一组用于TNF-α(产物大小325 bp),另一组用于内对照甘油醛-3-磷酸脱氢酶(G3PDH;983 bp)。将所得PCR产物通过琼脂糖凝胶电泳分离,将掺入TNF-α PCR产物与G3PDH产物中的放射性比率用于评估TNF-α mRNA丰度水平对各种物质反应的相对变化。用TPA处理48小时诱导了TNF-α mRNA的表达。用雌激素处理这些TPA刺激的细胞导致TNF-α信息丰度降低62%(p < 0.01)。用TPA刺激96小时的细胞也得到了类似结果。(摘要截短于250字)