Department of Food and Nutrition, Chungnam National University, Yuseong-gu, Daejeon 305-764, Republic of Korea.
Department of Bio-Environmental Chemistry, Chungnam National University, Yuseong-gu, Daejeon 305-764, Republic of Korea.
Int J Mol Med. 2014 Feb;33(2):469-77. doi: 10.3892/ijmm.2013.1590. Epub 2013 Dec 13.
In this study, we investigated the anti-allergic action of mulberry fruit extract (MFE) or MFE in combination with naringinase (MFEN) in IgE-activated RBL-2H3 cells, and investigated the mechanisms responsible for the anti-allergic effects of MFEN. β-hexosaminidase release assay was used to measure the amount of β-hexosaminidase released from the cells, and ELISA was used to measure the levels of tumor necrosis factor-α (TNF-α). We found that MFE significantly reduced the release of β-hexosaminidase (IC(50), 10.59 mg/ml) and TNF-α (IC(50), 4.87 mg/ml). Moreover, MFEN enhanced the inhibitory effects on the release of β-hexosaminidase (IC(50), 123.10 µg/ml) and TNF-α (IC(50), 65.01 µg/ml). Furthermore, MFEN had no cytotoxicity at the concentration range used to exert the anti-allergic effects. In addition, we evaluated the effects of MFEN on the formation of pro-inflammatory lipid mediators, such as prostaglandin D(2) (PGD(2)), leukotriene C(4) (LTC(4)) and leukotriene B(4) (LTB(4)) using enzyme immunoassay (EIA) kits. MFEN markedly reduced the formation of PGD(2) (IC(50), 6.47 µg/ml) and LTC(4) (IC(50), 0.31 µg/ml), but not LTB(4) (IC(50), 25.75 µg/ml). In mechanistic analyses, we measured the phosphorylation of Syk, Lyn and Fyn by immunoblot analysis. MFEN significantly inhibited the phosphorylation of Syk, but not that of Lyn or Fyn. MFEN also suppressed the phosphorylation of phospholipase C (PLC)γ1/2, protein kinase C (PKC)δ, linker for activation of T cells (LAT), extracellular signal-regulated protein kinase (ERK)1/2, JNK, GRB2-associated binding protein 2 (Gab2), phosphoinositide-3-kinase (PI3K), Akt, cytosolic phospholipase A2 and 5-lipoxygenase, as well as the expression of cyclooxygenase-2. In conclusion, these results suggest that MFEN exerts potent inhibitory effects on allergic response through the suppression of the activation of the FcεRI signaling cascade. Our data demonstrating the anti-allergic effects of MFEN may provide further insight into the therapeutic application of MFEN or its use as a functional food.
在这项研究中,我们研究了桑椹果提取物(MFE)或 MFE 与柚皮苷酶(MFEN)联合对 IgE 激活的 RBL-2H3 细胞的抗过敏作用,并研究了 MFEN 抗过敏作用的机制。β-己糖胺酶释放试验用于测量从细胞释放的β-己糖胺酶的量,ELISA 用于测量肿瘤坏死因子-α(TNF-α)的水平。我们发现 MFE 可显著减少β-己糖胺酶(IC(50),10.59mg/ml)和 TNF-α(IC(50),4.87mg/ml)的释放。此外,MFEN 增强了对β-己糖胺酶(IC(50),123.10μg/ml)和 TNF-α(IC(50),65.01μg/ml)释放的抑制作用。此外,MFEN 在发挥抗过敏作用的浓度范围内没有细胞毒性。此外,我们使用酶免疫分析(EIA)试剂盒评估了 MFEN 对形成促炎脂质介质(如前列腺素 D(2)(PGD(2)),白三烯 C(4)(LTC(4))和白三烯 B(4)(LTB(4))的影响。MFEN 显著减少 PGD(2)(IC(50),6.47μg/ml)和 LTC(4)(IC(50),0.31μg/ml)的形成,但不减少 LTB(4)(IC(50),25.75μg/ml)。在机制分析中,我们通过免疫印迹分析测量了 Syk、Lyn 和 Fyn 的磷酸化。MFEN 显著抑制了 Syk 的磷酸化,但不抑制 Lyn 或 Fyn 的磷酸化。MFEN 还抑制了磷脂酶 C(PLC)γ1/2、蛋白激酶 C(PKC)δ、T 细胞激活接头(LAT)、细胞外信号调节激酶(ERK)1/2、JNK、GRB2 相关结合蛋白 2(Gab2)、磷酸肌醇 3-激酶(PI3K)、Akt、细胞质磷脂酶 A2 和 5-脂氧合酶的磷酸化,以及环氧化酶-2 的表达。总之,这些结果表明 MFEN 通过抑制 FcεRI 信号级联的激活,对过敏反应发挥强大的抑制作用。我们的数据表明 MFEN 具有抗过敏作用,这可能为 MFEN 的治疗应用或作为功能性食品提供进一步的见解。