Herbal Medicinal Product Technology Division Pharmacognosy Laboratory, Industrial Technology Research Institute, Hsinchu, 30011, Taiwan.
Chin Med. 2012 Aug 24;7(1):19. doi: 10.1186/1749-8546-7-19.
α-Mangostin (α-MG) is a main constituent of the fruit hull of the mangosteen. Previous studies have shown that α-MG has pharmacological activities such as antioxidant, antitumor, anti-inflammatory, antiallergic, antibacterial, antifungal and antiviral effects. This study aims to investigate the anti-inflammatory molecular action of α-MG on gene expression profiles.
U937 and EL4 cells were treated with different concentrations of α-MG in the presence of 0.1 ng/mL lipopolysaccharide (LPS) for 4 h. The anti-inflammatory effects of α-MG were measured by the levels of tumor necrosis factor (TNF)-α and interleukin (IL)-4 in cell culture media, which were determined with enzyme-linked immunosorbent assay kits. The gene expression profiles of all samples were analyzed with a whole human genome microarray, Illumina BeadChip WG-6 version 3, containing 48804 probes. The protein levels were determined by Western blotting analyses.
α-MG decreased the LPS induction of the inflammatory cytokines TNF-α (P = 0.038) and IL-4 (P = 0.04). α-MG decreased the gene expressions in oncostatin M signaling via mitogen-activated protein kinase (MAPK) pathways, including extracellular signal-regulated kinases (P = 0.016), c-Jun N-terminal kinase (P = 0.01) , and p38 (P = 0.008). α-MG treatment of U937 cells reduced the phosphorylation of MAPK kinase 3 / MAPK kinase 6 (P = 0.0441), MAPK-activated protein kinase-2 (P = 0.0453), signal transducers and activators of transcription-1 (STAT1) (P = 0.0012), c-Fos (P = 0.04), c-Jun (P = 0.019) and Ets-like molecule 1 (Elk-1) (P = 0.038).
This study demonstrates that α-MG attenuates LPS-mediated activation of MAPK, STAT1, c-Fos, c-Jun and EIK-1, inhibiting TNF-α and IL-4 production in U937 cells.
α-倒捻子素(α-MG)是山竹果皮的主要成分之一。先前的研究表明,α-MG 具有抗氧化、抗肿瘤、抗炎、抗过敏、抗菌、抗真菌和抗病毒等药理作用。本研究旨在探讨 α-MG 对基因表达谱的抗炎分子作用。
用不同浓度的 α-MG 处理 U937 和 EL4 细胞,同时加入 0.1ng/mL 脂多糖(LPS)孵育 4 小时。用酶联免疫吸附试验试剂盒检测细胞培养上清液中肿瘤坏死因子(TNF)-α和白细胞介素(IL)-4 的水平来评估 α-MG 的抗炎作用。用全人类基因组微阵列(Illumina BeadChip WG-6 version 3,包含 48804 个探针)分析所有样本的基因表达谱。用 Western 印迹分析测定蛋白水平。
α-MG 降低了 LPS 诱导的炎症细胞因子 TNF-α(P=0.038)和 IL-4(P=0.04)的产生。α-MG 通过丝裂原活化蛋白激酶(MAPK)途径降低了肿瘤坏死因子信号转导中的基因表达,包括细胞外信号调节激酶(P=0.016)、c-Jun N-末端激酶(P=0.01)和 p38(P=0.008)。α-MG 处理 U937 细胞后,MAPK 激酶 3/6(P=0.0441)、MAPK 激活蛋白激酶-2(P=0.0453)、信号转导和转录激活因子 1(STAT1)(P=0.0012)、c-Fos(P=0.04)、c-Jun(P=0.019)和 Ets 样分子 1(Elk-1)(P=0.038)的磷酸化减少。
本研究表明,α-MG 可减弱 LPS 介导的 MAPK、STAT1、c-Fos、c-Jun 和 EIK-1 的激活,抑制 U937 细胞 TNF-α和 IL-4 的产生。