Lee Kun Yeong, Jeon Young Jin
Department of Pharmacology, Chosun University College of Medicine, 375 Susukdong, Kwangju, 501-709, Republic of Korea.
Int Immunopharmacol. 2005 Jul;5(7-8):1225-33. doi: 10.1016/j.intimp.2005.02.020. Epub 2005 Apr 9.
We show that APS, a polysaccharide isolated from the roots of Astragalus membranaceus, significantly induces nitric oxide (NO) production and inducible NO synthase (iNOS) transcription through the activation of nuclear factor-kappaB/Rel (NF-kappaB/Rel). In vivo administration of APS induced NO production by peritoneal macrophages of B6C3F1 mice. APS also dose-dependently induced the production of NO in isolated mouse peritoneal macrophages and RAW 264.7, a mouse macrophage-like cell line. Moreover, iNOS protein and mRNA transcription were strongly induced by APS in RAW 264.7 cells. To further investigate the mechanism responsible for the induction of iNOS gene expression, we investigated the effect of APS on the activation of transcription factors including NF-kappaB/Rel and Oct, whose binding sites were located in the promoter of iNOS gene. Treatment of RAW 264.7 cells with APS produced strong induction of NF-kappaB/Rel-dependent reporter gene expression, whereas Oct-dependent gene expression was not affected by APS. Nuclear translocation and DNA binding activity of NF-kappaB/Rel was significantly induced by APS. The treatment with NF-kappaB SN50, an inhibitor of NF-kappaB/Rel nuclear translocation, effectively inhibited the activation of NF-kappaB/Rel binding complexes and NO production. In conclusion, we demonstrate that APS stimulates macrophages to express iNOS gene through the activation of NF-kappaB/Rel.
我们发现,从黄芪根部分离得到的多糖APS,通过激活核因子-κB/Rel(NF-κB/Rel),显著诱导一氧化氮(NO)生成以及诱导型NO合酶(iNOS)转录。在体内,给B6C3F1小鼠腹腔巨噬细胞注射APS可诱导NO生成。APS还能剂量依赖性地诱导分离的小鼠腹腔巨噬细胞以及小鼠巨噬细胞样细胞系RAW 264.7产生NO。此外,APS能在RAW 264.7细胞中强烈诱导iNOS蛋白和mRNA转录。为进一步研究诱导iNOS基因表达的机制,我们研究了APS对包括NF-κB/Rel和Oct在内的转录因子激活的影响,这些转录因子的结合位点位于iNOS基因启动子上。用APS处理RAW 264.7细胞可强烈诱导NF-κB/Rel依赖的报告基因表达,而Oct依赖的基因表达不受APS影响。APS显著诱导NF-κB/Rel的核转位和DNA结合活性。用NF-κB SN50(一种NF-κB/Rel核转位抑制剂)处理可有效抑制NF-κB/Rel结合复合物的激活和NO生成。总之,我们证明APS通过激活NF-κB/Rel刺激巨噬细胞表达iNOS基因。