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作 者:巫世瑶[1] 黄建林[1] 谢宝钊[1] 王明霞[1] 古洁若[1]
机构地区:[1]中山大学附属第三医院风湿免疫科
出 处:《广东医学》2011年第3期277-280,共4页Guangdong Medical Journal
基 金:广东省科技计划项目(编号:2008B060600033)
摘 要:目的观察来氟米特活性代谢产物A771726对经PMA活化的THP-1细胞MMP-2及MMP-9表达的影响。方法 THP-1细胞悬浮生长于含10%胎牛血清的RPM I 1640培养液中。细胞密度达5×105.mL-1时用于实验。THP-1细胞经PMA刺激24 h(诱导THP-1细胞分化成巨噬细胞)后,细胞进行无血清化处理12 h,继而加入不同剂量的A771726(5、15、45μg/mL),干预24 h。实时荧光定量PCR检测细胞MMP-2、MMP-9mRNA的表达,明胶酶谱法检测细胞培养上清液中MMP-2、MMP-9的活性。结果细胞经不同浓度的A771726处理后,MMP-2、MMP-9 mRNA表达量均有下降(P<0.01)。中、高剂量的A771726(15、45μg/mL)可降低PMA活化的THP-1细胞培养上清液中MMP-2、MMP-9活性(P<0.01)。结论来氟米特活性代谢产物A771726可以降低经PMA活化的THP-1细胞MMP-2及MMP-9的表达。Objective To investigate the effects of leflunomide active metabolite (A771726) on the expression of MMP -2 and MMP -9 in PMA - activated THP - 1 cells. Methods THP - 1 cells were cultured in RPMI - 1640 medium supplemented with 10% fetal bovine serum. For all experiments, THP -1 cells were started with an initial density of 5 × 10^5 · mL^-1. Before A771726 treating, cells were cultured wifll serum - free RPMI - 1640 medium for 12h. PMA - activated THP - 1 cells ( THP - 1 cells were induced to differentiate into macrophages with PMA for 24 h ) were treated with different concentrations of A771726 (5, 15 and 45 μg/mL) for 24h. The mRNA expression and activity of MMP -2 and MMP - 9 was qualified by real - time PCR and gelatin zymography, respectively. Results The expression of MMP - 2 and MMP -9 mRNA was significantly inhibited by A771726 (5, 15 and 45 μg/mL, P 〈0. 01 ). The activity of MMP - 2 and MMP- 9 was inhibited by A771726( 15 and 45ug/mL)in the supernatant of PMA- activated THP- 1 cells (P 〈 0. 01 ). Conclusion Leflunomide active metabolite (A771726) can decrease the expression of MMP -2 and MMP -9 in PMA - activated THP - 1 cells.
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