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作 者:邓法明[1] 肖志平[1] 粟娟[1] 龙娟[1] 陈明亮[1]
机构地区:[1]中南大学湘雅医院皮肤科,湖南长沙410008
出 处:《中国现代医学杂志》2013年第22期1-5,共5页China Journal of Modern Medicine
基 金:湖南省自然科学基金(No:07JJ3059);湖南省卫生厅科研基金(No:B2006021)
摘 要:目的探讨褪黑素对人黑色素瘤细胞A375 VEGF表达的影响及其可能涉及的信号转导通路。方法用褪黑素、褪黑素受体拮抗剂、forskolin+褪黑素、8-brom-camp+褪黑素处理A375细胞,Real-time PCR、Western blot、ELISA等检测VEGF mRNA、蛋白表达的变化。结果 10μmol/L褪黑素处理A375细胞24 h后,VEGF mRNA的表达水平下降了48.7%(P<0.01)、细胞培养上清中VEGF蛋白表达水平下降了24.3%(P<0.01);10μmol/L褪黑素处理A375细胞6、12和24 h后,胞浆中VEGF蛋白的表达水平分别下降了14.2%、27.3%和41.8%(P<0.01);10μmol/L褪黑素受体拮抗剂处理A375细胞24 h后,胞浆、细胞培养上清中VEGF蛋白表达水平与对照组相比分别下降了32.3%和20.1%(P<0.01);30μmol/L PKA激动剂(8-brom-camp)、500μmol/L腺苷酸环化酶激动剂(forskolin)处理A375细胞24 h后,胞浆VEGF的表达水平分别是对照组的1.58和2.24倍,细胞培养上清中VEGF的表达水平分别为对照组的1.65和2.39,与褪黑素组相比均差异有显著性(P<0.01)。结论褪黑素可下调A375细胞VEGF的表达,其作用机制可能是通过褪黑素受体阻断cAMP-PKA信号转导通路所致。[ Objective ] To explore the effect of melatonin on VEGF expression in human melanoma cells A375 and the possible mechanisms of signal transduction pathways. [Methods] A375 cells were treated with melatonin, melatonin receptor inhibitors, forskolin+MT, 8-brom-camp+PGE2. VEGF mRNA and protein expression were exam- ined by Real-time PCR, Western blot and ELISA in A375 cells. [ Results ] The expression of VEGF mRNA in A375 cells were decreased by 48.7% (P 〈0.01), and the expression of VEGF in culture supernatant of A375 cells were de- creased by 24.0% (P 〈0.01) after treated with MT (10/xmol//L) for 24 h. The expression of VEGF in cytoplasm of A375 cells were decreased by 14.2%,27.3%,41.8% (P 〈0.01) after treated with MT (10lxmol/L) for 6 h, 12 h, 24 h respectively. The expression of VEGF in cytoplasm and culture supernatant of A375 cells were decreased by 32.3%, 20.1% (P 〈0.01) after treated with melatonin receptor inhibitors(101xmol/L) for 24 h respectively. After the treatment of 8-brom-camp (301xmol/L) and forskolin (5001xmol/L) for 24 h, the expression of VEGF in cytoplasm of A375 cells was increased by 58.0% and 24.0%, and the expression of VEGF in culture supernatant of A375 cells was increased by 65% and 39%, respectively, vs MT (P 〈0.01). [ Conclusion] It suggested that MT might down-regulate the ex- pression of VEGF through MT receptor of A375 cells, which could be partly related to the cAMP-PKA signal con-duction pathway.
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