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莱菔硫烷诱导人肝细胞硫氧还蛋白还原酶表达 被引量:2

Induction of TR1 by sulforaphane in human immortalized hepatocytes
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摘要 目的探讨莱菔硫烷(sulforaphane,SFN)对人肝细胞系HHL-5细胞硫氧还蛋白还原酶-1(thioredoxin reductase1,TR1)的诱导作用及机制。方法采用WST试验观察SFN对HHL-5细胞24h的细胞毒作用,及TaqMan one-step RT-PCR测定对TR1mRNA的诱导,蛋白印迹法(Western blotting)测定核因子E2相关因子2(nuclear factor erythroid2-related factor2,Nrf2)的蛋白表达。结果5mol/LSFN处理HHL-5细胞24h促进细胞增殖,更高剂量表现生长抑制作用;SFN处理HHL-5细胞24h呈剂量依赖性诱导TR1转录,10mol/LSFN对TR1的诱导为对照组的4.6倍;20μmol/LSFN处理1h后明显诱导了胞浆和胞核Nrf2蛋白表达,并且这种诱导呈明显的时间依赖性。结论SFN可能通过诱导转录因子Nrf2介导的TR1转录,从而增强机体抗氧化防御系统机能。 Objective To study the effect of sulforphane(SFN) on TR1 mRNA expression in human immortalized hepatocytes(HHL-5 cells) and the potential mechanism involved.Methods WST assay was used to observe the cytotoxicity of SFN.TR1 mRNA induction was quantified by TaqMan one-step RT-PCR and Nrf 2 expression was detected by Western blot.Results SFN promoted HHL-5 cells growth at 5μM and inhibited cells growth at higher dose.TR1 mRNA was induced dose-dependently by SFN(2~10μM 24h),with the maximal induction of 4.6-fold with 10μM SFN treatment.Moreover,Nrf 2 protein was upregulated in a time-dependent manner both in cytoplasm and in nucleus after 20μM SFN exposure,and significant induction was shown at 1h.Conclusion SFN might increase antioxidative defense in cells through induction of TR1 via Nrf 2-mediated transcription.
出处 《中国公共卫生》 CAS CSCD 北大核心 2009年第2期189-191,共3页 Chinese Journal of Public Health
关键词 莱菔硫烷 异硫氰酸盐 硫氧还蛋白还原酶 核因子E2相关因子2 sulforaphane(SFN) isothiocyanates(ITCs) thioredoxin reductasel(TR1) nuclear factor erythroid 2-related factor 2(Nrf 2)
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