Lucidenic acids-rich extract from antlered form of Ganoderma lucidum enhances TNFα induction in THP-1 monocytic cells possibly via its modulation of MAP kinases p38 and JNK

p38丝裂原活化蛋白激酶 THP1细胞系 脂多糖 激酶 MAPK/ERK通路 肿瘤坏死因子α 丝裂原活化蛋白激酶 化学 蛋白激酶A 免疫系统 生物化学 药理学 生物 细胞培养 免疫学 遗传学
作者
Kenji Watanabe,Tsuyoshi Shuto,Miki Sato,Kouhei Onuki,Shota Mizunoe,Shingo Suzuki,Takashi Sato,Tomoaki Koga,Mary Ann Suico,Hirofumi Kai,Tsuyoshi Ikeda
出处
期刊:Biochemical and Biophysical Research Communications [Elsevier BV]
卷期号:408 (1): 18-24 被引量:15
标识
DOI:10.1016/j.bbrc.2011.03.108
摘要

The Ganoderma lucidum (G. lucidum) is one of the oriental fungi that has been reported to have immunomodulatory properties. Although effect of β-glucans from G. lucidum has been well documented, little is known about how other major bioactive components, the triterpenes, contribute to the immunomodulatory function of G. lucidum. Here, we showed that triterpenes-rich extract of antlered form of G. lucidum (G. lucidum AF) induces TNFα production in monocytic THP-1 cells. Furthermore, the extract also synergized with lipopolysaccharide (LPS) to induce TNFα production in THP-1 cells, suggesting an immunostimulatory role of triterpenes-rich extract of G. lucidum AF. Notably, the extract enhanced LPS-induced phosphorylation of p38 mitogen-activated protein kinase (MAPK), while it suppressed LPS-induced phosphorylation of c-Jun N-terminal kinase (JNK) MAPK. p38 Inhibitor suppressed TNFα production, while JNK inhibitor enhanced TNFα production, implying that synergistic effect of the extract may work by modulating p38 and JNK MAPKs. Moreover, we found that the triterpenes-rich extract of G. lucidum AF contains high amounts of lucidenic acids. Lucidenic acid-A, -F and -D2, which seem to dominantly exist in the extract, were purified from the triterpenes-rich extract. We also identified Lucidenic acid-A and -F as modulators of JNK and p38, respectively. Thus, our data demonstrate that lucidenic acids-rich extract from G. lucidum AF enhances LPS-induced immune responses in monocytic THP-1 cells possibly via the modulation of p38 and JNK MAPKs activation.
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