肉豆蔻酸酯(PMA)对奶牛凝集素基因表达的影响

B. Mulakala, M. Worku
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摘要

半乳糖凝集素(GAL)是一种β-半乳糖苷结合蛋白。本研究的目的是评估PMA对牛血和中性粒细胞中半乳糖凝集素基因表达的调节作用。从3头临床健康的荷斯坦奶牛身上采集血液。通过差速离心分离中性粒细胞。用10ng/ml的PMA处理血液和中性粒细胞,或在370℃下在磷酸盐缓冲盐水中维持30分钟。将汇集的总RNA转录成cDNA用于实时PCR。使用牛LGALS-1、-2、-3、-4、-7、-8、-9、-11、-12及其结合蛋白(bp)、T细胞免疫球蛋白和粘蛋白结构域3(TIM-3)的特异性引物。管家基因RPLP0和UCHL5作为内部对照。使用Livak方法计算褶皱变化。总蛋白浓度使用双宁可宁酸测定法进行评估。使用牛GAL特异性ELISA评估GAL-1、-2、-3、-4、-8、-9的分泌。所有测试的LGALS均被检测到。PMA的激活不同地调节血液和中性粒细胞中GAL的表达和分泌。LGALS-1和LGALS-3的表达水平没有受到影响。LGALS-7、-8、-9、-11、-12和TIM-3的表达受到差异调节。对PMA的反应使GAL-3的分泌显著增加。PMA对LGALS-9、TIM-3表达和GAL-3分泌的影响最为显著。因此,GAL可以作为具有功能后果的细胞活化的生物标志物,并值得进一步研究。
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Phorbol 12-myristate 13-acetate (PMA) Alters Galectin Gene Expression in Cows
Galectins (GAL) are β-galactoside binding proteins. The objective of this study was to assess the effect of PMA on the regulation of galectin gene expression in bovine blood and neutrophils. Blood was collected from 3 clinically healthy Holstein cows. Neutrophils were isolated by differential centrifugation. Blood and neutrophils were treated with 10ng/ml of PMA or maintained in phosphate-buffered saline for 30 minutes at 370 C. Pooled total RNA were transcribed to cDNA for real-time PCR. Specific primers for bovine LGALS -1, -2, -3, -4, -7, -8, -9, -11, -12, and their binding proteins (bp) LGALS3bp, T cell immunoglobulin and mucin domain 3 (TIM-3) were used. Housekeeping genes RPLP0 and UCHL5 served as internal controls. Fold changes were calculated using the Livak method. Total protein concentration was assessed using the Bicinchoninic acid assay. Secretion of GAL -1, -2, -3, -4, -8, -9 was assessed using bovine GAL specific ELISA. All tested LGALS were detected. Activation with PMA differentially modulated expression and secretion of GAL in blood and neutrophils. Expression levels of LGALS -1 and LGALS -3 was not affected. Expression of LGALS -7, -8, -9, -11, -12, and TIM-3 was differentially modulated. The secretion of GAL -3 was significantly increased in response to PMA. The most pronounced effect of PMA was observed on LGALS-9, TIM-3 expression, and the secretion of GAL -3. Thus, GAL may serve as biomarkers of cell activation with functional consequences and warrant further study.
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