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Inhibitive Effect of Proanthocyanidins on Cyclooxygenase-2 Expression in A549 Cells Induced by Cytokine Interleukin-1 Beta

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【作者】 卢婷婷梁统赵玉丛周克元

【Author】 LU Ting-ting 1,LIANG Tong 2,ZHAO Yu-cong 1,ZHOU Ke-yuan 2(1.Department of Pharmacy,Zhengzhou College of Animal Husbandry Engineering,Zhengzhou 450011,China;2.Department of Biochemistry and Molecular Biology,Guangdong Medical College,Zhanjiang 524023,Guangdong,China)

【机构】 Department of Pharmacy,Zhengzhou College of Animal Husbandry EngineeringDepartment of Biochemistry and Molecular Biology,Guangdong Medical College

【摘要】 Cyclooxygenase-2(COX-2),an important enzyme,plays a pathological role in diseases,which can be inhibited by proanthocyanidins(PCs) effectively.In this paper,we investigated the inhibitive mechanism of COX-2 performed by PCs.Reverse transcription-polymerase chain reaction(RT-PCR) was performed to identify the mRNA expression level of COX-2 in A549 cell,which was induced by interleukin-1 beta(IL-1β).The pGL3 luciferase reporter vector containing the COX-2 gene promoter fragment(pGL3/COX-2p) was transfected into A549 cell induced by IL-1β,the interference on the COX-2 promoter activity from PCs was analyzed using a dualluciferase reporter assay,and the expressions of the nuclear factor κB composed of subunit p65(NF-κB/p65) and the inhibitor-κB(I-κB) were measured by the Western blotting and immunocytochemistry.The results exhibited that PCs not only inhibited the transcript of COX-2 mRNA and the COX-2 promoter activity,but also suppressed the nuclear translocation of NF-κB/p65 protein and the degradation of I-κB protein.

【Abstract】 Cyclooxygenase-2(COX-2),an important enzyme,plays a pathological role in diseases,which can be inhibited by proanthocyanidins(PCs) effectively.In this paper,we investigated the inhibitive mechanism of COX-2 performed by PCs.Reverse transcription-polymerase chain reaction(RT-PCR) was performed to identify the mRNA expression level of COX-2 in A549 cell,which was induced by interleukin-1 beta(IL-1β).The pGL3 luciferase reporter vector containing the COX-2 gene promoter fragment(pGL3/COX-2p) was transfected into A549 cell induced by IL-1β,the interference on the COX-2 promoter activity from PCs was analyzed using a dualluciferase reporter assay,and the expressions of the nuclear factor κB composed of subunit p65(NF-κB/p65) and the inhibitor-κB(I-κB) were measured by the Western blotting and immunocytochemistry.The results exhibited that PCs not only inhibited the transcript of COX-2 mRNA and the COX-2 promoter activity,but also suppressed the nuclear translocation of NF-κB/p65 protein and the degradation of I-κB protein.

【基金】 the Special Supported by Guangdong Key Program (No.GX0307);the Guangdong Science and Technology Planning Project in the Field of Social Development (No.35025)
  • 【文献出处】 Journal of Shanghai Jiaotong University(Science) ,上海交通大学学报(英文版) , 编辑部邮箱 ,2012年04期
  • 【分类号】R285
  • 【下载频次】31
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