雌激素调节phorbol酯刺激的人单核THP-1细胞肿瘤坏死因子α mRNA的表达。

Lymphokine and cytokine research Pub Date : 1994-12-01
G Shanker, M Sorci-Thomas, M R Adams
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引用次数: 0

摘要

包括肿瘤坏死因子α (tnf - α)在内的单一因子与包括动脉粥样硬化在内的几种病理过程的发病机制有关。由于雌激素已被发现对动脉粥样硬化进程提供一定程度的保护,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。将细胞暴露于12- o -十四烷酚13-乙酸酯(TPA, 50 ng/ml)中48或96 h诱导分化。部分细胞在最后3小时用脂多糖(LPS, 10微克/毫升)处理,或在最后20小时用乙炔雌二醇(雌激素,10(-9)M)处理。分离细胞总RNA,合成cDNA,然后在两组(对)32p标记的引物存在下,用聚合酶链反应(PCR)进行共扩增,一组引物用于tnf - α(产物大小为325 bp),另一组引物用于内控甘油醛3-磷酸脱氢酶(G3PDH);983个基点)。通过琼脂糖凝胶电泳分离得到的PCR产物,并利用tnf - α PCR产物与G3PDH产物的放射性比值来评估不同物质对tnf - α mRNA丰度的相对变化。TPA处理48 h可诱导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刺激细胞96小时也得到了类似的结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Estrogen modulates the expression of tumor necrosis factor alpha mRNA in phorbol ester-stimulated human monocytic THP-1 cells.

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)

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