Lee Kun Yeong, Jeon Young Jin
Department of Pharmacology, Chosun University College of Medicine, 375 Susukdong, Kwangju 501-709, South Korea.
Int Immunopharmacol. 2003 Oct;3(10-11):1353-62. doi: 10.1016/S1567-5769(03)00113-9.
We show that PCSC, a polysaccharide isolated from the sclerotium of Poria cocos with 1% sodium carbonate, 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 PCSC induced NO production by peritoneal macrophages of B6C3F1 mice. PCSC also dose-dependently induced the production of NO in isolated mouse peritoneal macrophages and RAW 264.7, a murine macrophage-like cell line. Moreover, iNOS protein and mRNA transcription were strongly induced by PCSC in RAW 264.7 cells. To further investigate the mechanism responsible for the induction of iNOS gene expression, we investigated the effect of PCSC 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 PCSC produced strong induction of NF-kappaB/Rel-dependent reporter gene expression, whereas Oct-dependent gene expression was not affected by PCSC. DNA binding activity of NF-kappaB/Rel was significantly induced by PCSC, and this effect was mediated through the degradation of IkappaBalpha. In conclusion, we demonstrate that PCSC stimulates macrophages to express iNOS gene through the activation of NF-kappaB/Rel.
我们发现,用1%碳酸钠从茯苓菌核中分离得到的多糖PCSC,通过激活核因子-κB/Rel(NF-κB/Rel),能显著诱导一氧化氮(NO)生成及诱导型NO合酶(iNOS)转录。给B6C3F1小鼠腹腔注射PCSC可诱导其腹腔巨噬细胞产生NO。PCSC还能剂量依赖性地诱导分离的小鼠腹腔巨噬细胞及鼠巨噬细胞样细胞系RAW 264.7产生NO。此外,PCSC能强烈诱导RAW 264.7细胞中iNOS蛋白及mRNA转录。为进一步研究iNOS基因表达诱导的机制,我们研究了PCSC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PCSC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PCSC影响。PCSC能显著诱导NF-κB/Rel的DNA结合活性,且这种作用是通过IκBα的降解介导的。总之,我们证明PCSC通过激活NF-κB/Rel刺激巨噬细胞表达iNOS基因。