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作 者:陈林华[1] 王教[1] 陈晓燕[1] 鹿润霞[1] 周翔天[1]
机构地区:[1]温州医学院附属眼视光医院,浙江温州325027
出 处:《中华眼视光学与视觉科学杂志》2010年第2期91-94,共4页Chinese Journal Of Optometry Ophthalmology And Visual Science
基 金:国家自然科学基金重点资助项目(30830107);国家自然科学基金资助项目(30973278)
摘 要:目的 研究外源性视黄酸(RA)对人巩膜成纤维细胞(HSF)生长的调控,以及对基质金属蛋白酶2(MMP-2)和基质金属蛋白酶2组织抑制剂(TIMP-2)mRNA水平的影响.方法 体外培养HSF,取第5~7代细胞,经10^-10、10^-9、10^-8、10^-7、10^-6mol/L浓度的RA作用6 d后,进行细胞计数,观察RA对HSF生长的调控情况;用Real-time PCR检测RA作用后HSF中MMP-2、TIMP-2的mRNA水平.对不同浓度组问比较采用单因素方差分析,两两比较采用t检验.结果 RA作用HSF 6 d后,浓度≥10^-9 mol/L RA组对细胞的生长抑制作用差异均有统计学意义(P〈0.05),随着RA浓度增高,细胞数量逐渐减少,抑制作用呈剂量效应.RA作用6 d后,RA≥10^-8 mol/L时,HSF中MMP-2 mRNA水平有升高趋势,但各组差异无统计学意义(P〉0.05);RA≥10^-9 mol/L时,TIMP-2 mRNA水平下降(P〈0.05).结论 RA能够抑制HSF的生长,并可能通过调控TIMP-2的mRNA水平,使巩膜主动重塑.Objective To study effects of exogenous retinoic acid (RA) on the growth of human scleral fibroblasts (HSF) and the mRNA level of matrix metalloproteinase-2 (MMP-2) and its tissue inhibitor (TIMP-2). Methods HSF of 5-7 passages were quantitated after being treated with RA at concentrations of 10^-10 mol/L, 10^-9 mol/L,10^-8 mol/L, 10^-7 mol/L, 10^-6 mol/L, respectively for 6 days. The mRNA level of MMP-2 and TIMP-2 was measured by Real-time PCR followd by analysis using one-way ANOVA. Results The growth of HSF was significantly inhibited after 6 days of treatment with at least 10^-9 mol/L of RA (P〈0.05). The reduction in number of HSF was positively correlated to the RA concentrations used. The mRNA level of MMP-2 was increased when the concentration of RA 〉 10^-8 mol/L. However, there was not significantly different between RA treated and non-RA treated HSF (P〉0.05). The mRNA level of TIMP-2 decreased (P〈0.05) in HSF treated with RA at concentration ≥10^-9 mol/L. Conclusion RA could inhibit the growth of HSF cells and downregulate the mRNA level of TIMP-2, probably resulting in scleral remodeling.
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