Sakai Shota, Sugawara Tatsuya, Matsubara Kiminori, Hirata Takashi
Division of Applied Biosciences, Graduate School of Agriculture, Kyoto University, Kyoto 606-8502.
Division of Applied Biosciences, Graduate School of Agriculture, Kyoto University, Kyoto 606-8502.
J Biol Chem. 2009 Oct 9;284(41):28172-28179. doi: 10.1074/jbc.M109.001099. Epub 2009 Aug 21.
Carotenoids have been demonstrated to possess antioxidative and anti-inflammatory effects. However, there is no report that the effects of carotenoids on degranulation of mast cell is critical for type I allergy. In this study, we focused on the effect of carotenoids on antigen-induced degranulation of mast cells. Fucoxanthin, astaxanthin, zeaxanthin, and beta-carotene significantly inhibited the antigen-induced release of beta-hexosaminidase in rat basophilic leukemia 2H3 cells and mouse bone marrow-derived mast cells. Those carotenoids also inhibited antigen-induced aggregation of the high affinity IgE receptor (Fc epsilonRI), which is the most upstream of the degranulating signals of mast cells. Furthermore, carotenoids inhibited Fc epsilonRI-mediated intracellular signaling, such as phosphorylation of Lyn kinase and Fyn kinase. It suggests that the inhibitory effect of carotenoids on the degranulation of mast cells were mainly due to suppressing the aggregation of Fc epsilonRI followed by intracellular signaling. In addition, those carotenoids inhibited antigen-induced translocation of Fc epsilonRI to lipid rafts, which are known as platforms of the aggregation of Fc epsilonRI. We assume that carotenoids may modulate the function of lipid rafts and inhibit the translocation of Fc epsilonRI to lipid rafts. This is the first report that focused on the aggregation of Fc epsilonRI to investigate the mechanism of the inhibitory effects on the degranulation of mast cells and evaluated the functional activity of carotenoids associated with lipid rafts.
类胡萝卜素已被证明具有抗氧化和抗炎作用。然而,尚无关于类胡萝卜素对肥大细胞脱颗粒的影响对I型过敏至关重要的报道。在本研究中,我们重点关注类胡萝卜素对抗原诱导的肥大细胞脱颗粒的影响。岩藻黄质、虾青素、玉米黄质和β-胡萝卜素显著抑制大鼠嗜碱性白血病2H3细胞和小鼠骨髓来源肥大细胞中抗原诱导的β-己糖胺酶释放。这些类胡萝卜素还抑制抗原诱导的高亲和力IgE受体(FcεRI)聚集,FcεRI是肥大细胞脱颗粒信号的最上游。此外,类胡萝卜素抑制FcεRI介导的细胞内信号传导,如Lyn激酶和Fyn激酶的磷酸化。这表明类胡萝卜素对肥大细胞脱颗粒的抑制作用主要是由于抑制FcεRI聚集,随后抑制细胞内信号传导。此外,这些类胡萝卜素抑制抗原诱导的FcεRI向脂筏的转位,脂筏是已知的FcεRI聚集平台。我们推测类胡萝卜素可能调节脂筏的功能并抑制FcεRI向脂筏的转位。这是第一篇聚焦于FcεRI聚集以研究对肥大细胞脱颗粒抑制作用机制并评估与脂筏相关的类胡萝卜素功能活性的报道。