Yang Gabsik, Kyoung Seo Eun, Lee Je-Hyun, Young Lee Joo
Integrated Research Institute of Pharmaceutical Sciences, College of Pharmacy, The Catholic University of Korea, Bucheon 420-743, Korea, (phone: +82-2-21644095; fax: +82-2-21644059).
Chem Biodivers. 2015 Apr;12(4):538-46. doi: 10.1002/cbdv.201400376.
We investigated the modulation of innate and adaptive immune cell activation by Eucommia ulmoides Oliver extract (EUE) and its ingredient genipin. As an innate immunity indicator, the phagocytic activity of macrophages was determined by measuring engulfed, fluorescently labeled Escherichia coli. As a surrogate marker for the respective activation of cellular and humoral adaptive immunity, concanavalin A (Con A) and lipopolysaccharide (LPS) induction of primary splenocyte proliferation was assayed in in vitro and ex vivo systems. EUE and genipin suppressed the proliferation of primary splenic lymphocytes induced by Con A or LPS, but not macrophage phagocytosis. Oral administration of EUE and genipin to mice decreased splenic lymphocyte proliferation induced by Con A or LPS. These results revealed that E. ulmoides and genipin suppressed cellular and humoral adaptive immunity, and they suggest that E. ulmoides and genipin are promising candidates for immunosuppressive drugs that target diseases that involve excessive activation of adaptive immunity.
我们研究了杜仲提取物(EUE)及其成分京尼平对先天性和适应性免疫细胞激活的调节作用。作为先天性免疫指标,通过测量吞噬的荧光标记大肠杆菌来确定巨噬细胞的吞噬活性。作为细胞和体液适应性免疫各自激活的替代标志物,在体外和体内系统中检测了伴刀豆球蛋白A(Con A)和脂多糖(LPS)诱导的原代脾细胞增殖。EUE和京尼平抑制了Con A或LPS诱导的原代脾淋巴细胞增殖,但不影响巨噬细胞吞噬作用。给小鼠口服EUE和京尼平可降低Con A或LPS诱导的脾淋巴细胞增殖。这些结果表明,杜仲和京尼平抑制了细胞和体液适应性免疫,提示杜仲和京尼平有望成为针对涉及适应性免疫过度激活疾病的免疫抑制药物候选物。