首页> 外文期刊>Frontiers in Microbiology >Lipoteichoic Acid of Probiotic Lactobacillus plantarum Attenuates Poly I:C-Induced IL-8 Production in Porcine Intestinal Epithelial Cells
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Lipoteichoic Acid of Probiotic Lactobacillus plantarum Attenuates Poly I:C-Induced IL-8 Production in Porcine Intestinal Epithelial Cells

机译:益生菌植物乳杆菌的脂磷壁酸可减轻猪肠上皮细胞中Poly I:C诱导的IL-8产生。

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FIGURE 1. TLR3 ligand poly I:C induces IL-8 production in IPEC-J2 cells. IPEC-J2 cells (5 × 105 cells/ml) were plated in 96-well plates and treated with 1 or 10 μg/ml poly I:C (A) for 24 h in serum-free medium. Then, the supernatants were collected and IL-8 secretion was determined by ELISA. IPEC-J2 cells (5 × 105 cells/ml) were plated in 12-well plates and treated with 0.1, 1, or 10 μg/ml poly I:C for 3 h (B), or 1 μg/ml poly I:C for 0, 1, 3, 6, or 12 h in serum-free medium (C). After treatment, total RNA was extracted and IL-8 mRNA expression was determined by real-time PCR. Data are mean ± standard deviation of triplicate samples. (D) IPEC-J2 cells (5 × 105 cells/ml) were plated in 96-well culture plates and treated with 1 μg/ml poly I:C for 1, 3, 6, 12 and 24 h, and IL-8 secretion was determined by ELISA. Data are expressed as mean value ± standard deviation of triplicate samples. Asterisk (?) indicates significant difference compared with the non-treatment control group (P < 0.05).
机译:图1. TLR3配体poly I:C在IPEC-J2细胞中诱导IL-8的产生。将IPEC-J2细胞(5×105细胞/ ml)铺在96孔板中,并在无血清培养基中用1或10μg/ ml聚I:C(A)处理24小时。然后,收集上清液并通过ELISA确定IL-8分泌。将IPEC-J2细胞(5×105细胞/ ml)铺在12孔板中,并用0.1、1或10μg/ ml聚I:C处理3小时(B)或1μg/ ml聚I: C在无血清培养基(C)中放置0、1、3、6或12小时。处理后,提取总RNA,并通过实时PCR测定IL-8 mRNA表达。数据为三次样品的平均值±标准偏差。 (D)将IPEC-J2细胞(5×105细胞/ ml)铺在96孔培养板中,并用1μg/ ml聚I:C处理1、3、6、12和24小时以及IL-8通过ELISA确定分泌。数据表示为平均值±一式三份样品的标准偏差。星号(?)表示与非治疗对照组相比有显着差异(P <0.05)。

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