Division of Gastrointestinal Pathophysiology, Department of Bioscience, Institute of Natural Medicine, University of Toyama, Toyama, Japan.
FEBS Lett. 2010 Jan 4;584(1):111-8. doi: 10.1016/j.febslet.2009.11.007.
Mast cell activation by immunoglobulin E (IgE)-mediated stimuli is a central event in the pathogenesis of allergic disorders. The present report shows that treatment with pentagalloylglucose (PGG) resulted in a down-regulation of FcepsilonRI surface expression on mucosal-type murine bone marrow-derived mast cells (mBMMCs), which correlated with a reduction in IgE-mediated activation of mBMMCs. Furthermore, PGG prevented development of allergic diarrhea in a food-allergy mouse model and suppressed the up-regulated FcepsilonRI surface expression on mast cells derived from the food-allergy mouse colon. These findings on PGG suggest its therapeutic potential for allergic diseases through suppressing the FcepsilonRI surface expression.
免疫球蛋白 E (IgE)-介导的刺激引起的肥大细胞激活是过敏疾病发病机制中的一个核心事件。本报告显示,五倍子酰葡萄糖 (PGG) 的治疗导致黏膜型鼠骨髓来源的肥大细胞 (mBMMC) 表面 FcepsilonRI 的表达下调,这与 IgE 介导的 mBMMC 激活减少相关。此外,PGG 可预防食物过敏小鼠模型中过敏性腹泻的发生,并抑制来自食物过敏小鼠结肠的肥大细胞中上调的 FcepsilonRI 表面表达。这些关于 PGG 的发现表明,通过抑制 FcepsilonRI 表面表达,它可能具有治疗过敏疾病的潜力。