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作 者:邢凌霄[1] 张祥宏[1] 李月红[1] 左连富[2] 严霞[1] 王俊灵[1] 王凤荣[1]
机构地区:[1]河北医科大学病理研究室,石家庄市050017 [2]河北省肿瘤研究所细胞室,石家庄市050511
出 处:《细胞生物学杂志》2007年第4期609-612,共4页Chinese Journal of Cell Biology
基 金:河北省自然科学基金资助项目(No.C2004000613)~~
摘 要:探讨伏马菌素B1(FB1)对体外培养的人外周血单个核细胞(hPBMC)抗原加工相关转运子(TAP-1)表达的影响。采用流式细胞定量检测(FCM)、免疫印迹(Western印迹)及半定量RT-PCR方法,研究不同浓度FB1(0,10和50μmol/L)处理后人外周血单个核细胞TAP-1在mRNA和蛋白质水平表达的影响。RT-PCR检测结果表明,10和50μmol/L FB1处理24h后,处理组细胞TAP-1mRNA明显低于对照组。在蛋白质水平,FCM定量分析表明,两个处理组细胞表面TAP1的平均荧光强度均较对照组降低,以50μmol/LFB1处理组降低显著(P<0.05)。免疫印迹结果亦表明,FB1处理组TAP-1的表达均较对照组降低。10和50μmol/LFB1可抑制体外培养的hPBMCTAP-1mRNA和蛋白质表达。To explore the effects of fumonisin (FB 1) on TAP- 1 (transporter associated with antigen processing) expression of human peripheral blood mononuclear cells (hPBMC) in vitro. The expression of TAP- 1 of hPBMC by FB1 pretreatment at three different dosages (0, 10 and 50 μmol/L) were detected with flow cytometry (FCM), Western blot and semi-RT-PCR respectively. TAP- 1 mRNA was decreased in 10 and 50 μmol/L FB 1 treated groups than that in control group. FCM quantitative analysis showed that at protein level, TAP- 1 expression (as expressed by FI) of hPBMC at FB1 treated groups were lower than that of control, especially in 50 μmol/L FB1 treated groups (P〈0.05). Western blot results further confirmed the above results. 10 and 50 μmol/L FB 1 treatment could inhibit the expression of TAP- 1 at mRNA and protein level.
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