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作 者:王燕燕[1] 周政涛[1] 崔向军[1] 黄骥[1]
机构地区:[1]三峡大学第三临床医学院、宜昌市中心人民医院,宜昌市443003
出 处:《中国药房》2010年第25期2336-2339,共4页China Pharmacy
基 金:湖北省卫生厅科研基金资助项目(JX2B89)
摘 要:目的:探讨蛋白激酶C(PKC)抑制剂星形孢菌素(STS)对肺腺癌A549细胞侵袭移动的影响及作用机制。方法:取A549细胞加入不同浓度STS(1、10、100 nmol.L-1)处理后,应用Transwell小室检测A549细胞移动抑制率和侵袭抑制率;免疫荧光染色法检测细胞内蛋白水解酶基质金属蛋白水解酶-9(MMP-9)和尿激酶型纤溶酶原激活剂(uPA)蛋白表达;激光共聚焦法观测细胞内骨架蛋白微管蛋白α-tubulin的分布,Western blot法检测胞膜和胞浆内PKC-α活性。同时设立不加STS处理的对照组进行比较。结果:与对照组比较,A549细胞的移动抑制率、侵袭抑制率、MMP-9和uPA蛋白表达量均明显下降(P<0.05或P<0.01);胞浆内α-tubulin蛋白分布不均;胞膜内PKC-α蛋白含量减少,而胞浆内PKC-α蛋白含量无明显变化。结论:PKC抑制剂STS能抑制A549细胞移动和侵袭;其机制可能与抑制PKC-α的活性,减弱肿瘤细胞中MMP-9、uPA表达,诱导肿瘤细胞骨架变化相关。OBJECTIVE:To evaluate the effects of protein kinase C(PKC) inhibitor staurosporine(STS) on cell invasion ability of lung adenocarcinoma cell line A549 cells and its mechanism.METHODS:Transwell assay was applied to observe the motility inhibition rate and invasion inhibition rate of A549 cells after A549 cells were treated with STS at different concentrations(1,10,100 nmol·L^-1).Protein expression of matrix metalloproteinase-9(MMP-9) and urokinase-type plasminogen activator(uPA) were detected by immunofluoresence stain assay.Laser confocal scanning microscopy was used to observe the distribution of α-tubulin.Western blot was used to determine the activity of PKC-α in membrane and endochylema.Control group were not treated with STS.RESULTS:Compared with control group,motility inhibition rate and invasion inhibition rate of A549 cells and protein expression of MMP-9 and uPA were decreased significantly(P〈0.05 or P〈0.01).The distribution of α-tubulin in endochylema showed uneven situation.The content of PKC-α in the membrane was decreased while that in endochylema had no obvious change.CONCLUSION:PKC inhibitor STS could inhibit the motility and invasion of A549 cells.The inhibition effect may be associated with inhibiting the activity of PKC-α,decreasing protein expression of MMP-9 and uPA and inducing cytoskeleton change.
关 键 词:蛋白激酶C抑制剂 星形孢菌素 肺腺癌A549细胞 侵袭 移动 基质金属蛋白水解酶-9 尿激酶型纤溶酶原激活剂 微管蛋白
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