Boudjellab N, Chan-Tang H S, Li X, Zhao X
Department of Animal Science, McGill University, Ste-Anne-de-Bellevue, Québec, Canada.
Am J Vet Res. 1998 Dec;59(12):1563-7.
To determine whether an established bovine mammary epithelial cell line expresses interleukin 8 (IL-8) mRNA and synthesizes antigenic IL-8 in response to lipopolysaccharide (LPS) stimulation.
A bovine mammary epithelial cell line (MAC-T).
mRNA was isolated from cells stimulated with graded concentrations of LPS. The first strand of IL-8 cDNA was synthesized, using a reverse transcriptase (RT) reaction with a specific oligonucleotide. Amplification of IL-8 cDNA was obtained by use of polymerase chain reaction (PCR). The MAC-T-derived antigenic IL-8 was quantified by use of a commercial anti-human IL-8 kit in a sandwich ELISA.
RT-PCR revealed expression of MAC-T-derived mRNA within the first hour after stimulation with LPS. Expression of IL-8 mRNA was correlated to production of IL-8 protein detected in medium by use of the sandwich ELISA. Amounts of antigenic IL-8 increased in a dose- and time-dependent manner, and were maximal (57 pg/ml) at 48 hours after stimulation with 20 microg of LPS/ml.
MAC-T cells secrete IL-8 in response to stimulation with LPS in a dose- and time- dependent manner. The results were consistent with our hypothesis that mammary gland epithelial cells can be a source of IL-8 during the early stage of mastitis. Therefore, IL-8 may have a pivotal role in resolving bacterial infections.
确定一种已建立的牛乳腺上皮细胞系是否表达白细胞介素8(IL-8)mRNA,并在脂多糖(LPS)刺激下合成具有抗原性的IL-8。
一种牛乳腺上皮细胞系(MAC-T)。
从用不同浓度LPS刺激的细胞中分离mRNA。使用特异性寡核苷酸通过逆转录酶(RT)反应合成IL-8 cDNA的第一条链。通过聚合酶链反应(PCR)扩增IL-8 cDNA。使用商业抗人IL-8试剂盒通过夹心ELISA对MAC-T衍生的具有抗原性的IL-8进行定量。
RT-PCR显示在LPS刺激后的第一小时内MAC-T衍生的mRNA有表达。IL-8 mRNA的表达与通过夹心ELISA在培养基中检测到的IL-8蛋白的产生相关。具有抗原性的IL-8的量呈剂量和时间依赖性增加,在用20μg/ml LPS刺激后48小时达到最大值(57 pg/ml)。
MAC-T细胞在LPS刺激下以剂量和时间依赖性方式分泌IL-8。结果与我们的假设一致,即乳腺上皮细胞可能是乳腺炎早期IL-8的来源。因此,IL-8可能在解决细菌感染中起关键作用。