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作 者:徐伶俐[1] 罗伟生[1] 谭宁[2] 徐庆[2] 徐宾[2] 诸葛福艳[2]
机构地区:[1]桂林医学院附属医院消化内科,广西壮族自治区桂林市541004 [2]桂林医学院科学实验中心,广西壮族自治区桂林市541004
出 处:《世界华人消化杂志》2015年第4期539-546,共8页World Chinese Journal of Digestology
基 金:国家自然科学基金资助项目;No.81360530~~
摘 要:目的:研究荔枝核总黄酮(total flavonoids of litchi,TFL)对人肝星状细胞LX2增殖的影响及其相关作用机制.方法:使用不同浓度(7.8125、15.6250、31.2500、62.5000、125.0000μg/m L)TFL处理LX2.采用CCK-8法检测细胞的增殖活力,通过流式细胞仪分析各组细胞周期的分布,使用RT-PCR和Western blot技术测定细胞中p27基因m RNA和蛋白的表达.结果:TFL作用48、72 h可抑制LX2细胞增殖,且随着时间延长,抑制效果更加明显.T F L处理72 h后可测得L X2细胞被阻滞在S期,且明显上调p27基因的m RNA和蛋白的表达.结论:TFL抑制人肝星状细胞增殖并将其阻滞在S期,该作用机制可能与p27表达上调相关.AIM: To investigate the effect of total flavonoids of litchi(TFL) on the proliferation of LX2 human hepatic stellate cells and to explore the underlying mechanism. METHODS: LX2 cells treated with different concentrations(7.8125, 15.6250, 31.2500, 62.5000, and 125.0000 μg/m L) of TFL were examined for cell growth inhibition using CCK-8. Flow cytometry was used to analyze the changes in cell cycle distribution of LX2 cells. The expression of p27 m RNA and protein in LX2 cells was determined by real-time quantitative PCR and Western blot, respectively. RESULTS: Exposure to TFL caused significant dose- and time-dependent inhibition of LX2 cell proliferation. TFL induced S-phase cell cycle arrest as shown by flow cytometric analysis. In addition, expression of p27 m RNA and protein in LX2 cells was upregulated in the treatment groups. CONCLUSION: TFL treatment inhibits LX2 cell proliferation and arrests cells at S phase, and the mechanism may be associated with the upregulation of p27 expression.
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