首页 | 本学科首页   官方微博 | 高级检索  
检索        

扇贝多肽对UVB照射HaCaT细胞后NO释放及热休克蛋白70表达的影响
引用本文:王春波,李金莲,张正洋,陈雪红,韩彦弢.扇贝多肽对UVB照射HaCaT细胞后NO释放及热休克蛋白70表达的影响[J].中国药理学通报,2011,27(3):334-337.
作者姓名:王春波  李金莲  张正洋  陈雪红  韩彦弢
作者单位:1. 青岛大学医学院药理学教研室,山东,青岛,266071
2. 滨州医学院机能学实验室,山东,烟台,264003
基金项目:国家自然科学基金资助项目
摘    要:目的观察UVB诱导的HaCaT细胞一氧化氮(nitricoxide,NO)释放及诱导型一氧化氮合酶(iNOS)表达的动态变化,探究扇贝多肽(polypeptide from Chlamys farreri,PCF)对UVB照射后NO释放、热休克蛋白70(heat shock protein70,HSP70)表达的影响。方法以电子自旋共振(electronspin resonance,ESR)技术检测NO的释放量;蛋白质印迹法检测iNOS、HSP70蛋白表达。结果 20 mJ.cm-2 UVB照射HaCaT细胞后NO释放明显增多,有3、24 h两个释放高峰期;PCF对各时间点NO的释放均有抑制作用;iNOS蛋白表达在UVB照射后6 h开始逐渐升高,18~24 h达到高峰;iN-OS抑制剂可抑制UVB照射后24 h时NO的释放,对3 h时NO的释放无影响;PCF可剂量依赖性增强UVB照射后HSP70的蛋白表达。结论 UVB照射HaCaT细胞诱导iNOS高表达从而引起NO产生增加,但在照射前期也可通过非iNOS途径生成NO;PCF可能通过增强UVB照射后HSP70的表达,进而抑制iNOS蛋白表达、减少NO的生成而保护HaCaT细胞免受UVB辐射损伤。

关 键 词:UVB  HaCaT细胞  扇贝多肽  一氧化氮  热休克蛋白70  诱导型一氧化氮合酶

Effect of polypeptide from Chlamys farreri on UVB-induced NO release and HSP70 expression in HaCaT cells
WANG Chun-bo,LI Jin-lian,ZHANG Zheng-yang,CHEN Xue-hong,HAN Yan-tao.Effect of polypeptide from Chlamys farreri on UVB-induced NO release and HSP70 expression in HaCaT cells[J].Chinese Pharmacological Bulletin,2011,27(3):334-337.
Authors:WANG Chun-bo  LI Jin-lian  ZHANG Zheng-yang  CHEN Xue-hong  HAN Yan-tao
Institution:WANG Chun-bo1,LI Jin-lian2,ZHANG Zheng-yang1,CHEN Xue-hong1,HAN Yan-tao1(1.Dept of Pharmacology,Medical College,Qingdao University,Qingdao Shandong 266071,China,2.Binzhou Medical College,Yantai Shandong 264003,China)
Abstract:Aim To observe dynamic changes of nitric oxide(NO)release and inducible nitric oxide synthase(iNOS)expression in HaCaT cells after UVB radiation,and to investigate the effect of Polypeptide from Chlamys farreri(PCF)on UVB-induced NO release and heat shock protein 70(HSP70)expression.Methods The release of NO was assayed by electron spin resonance(ESR).Western blot analysis was used to determine the protein levels of iNOS and HSP70.Results NO release was significantly increased after 20 mJ·cm-2 UVB radiation and there were two peaks at 3 h and 24 h respectively.PCF inhibited the release of NO at each time point.iNOS protein expressed six hours after UVB radiation and increased gradually,then reached to peak 18~24 h later.iNOS inhibitor reduced the release of NO at 24 h after UVB radiation,but had no effect at 3 h.PCF enhanced HSP70 expression in a dose-dependent manner.Conclusions UVB exposure to HaCaT cells induced expression of iNOS and then the release of NO increased,but in early stages of exposure,NO can also be generated by non-iNOS pathway.PCF may enhance the expression of HSP70,thereby inhibit iNOS expression and reduce the generation of NO,thus protect HaCaT cells against UVB radiation.
Keywords:UVB
本文献已被 CNKI 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号