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过氧化氢和肿瘤坏死因子-α在内皮细胞和上皮细胞中诱导氧化还原反应性转录因子AP-1和核因子-κB与白细胞介素-8启动子的差异性结合。

H2O2 and tumor necrosis factor-alpha induce differential binding of the redox-responsive transcription factors AP-1 and NF-kappaB to the interleukin-8 promoter in endothelial and epithelial cells.

作者信息

Lakshminarayanan V, Drab-Weiss E A, Roebuck K A

机构信息

Department of Immunology/Microbiology, Rush-Presbyterian, St. Luke's Medical Center, Chicago, Illinois 60612, USA.

出版信息

J Biol Chem. 1998 Dec 4;273(49):32670-8. doi: 10.1074/jbc.273.49.32670.

Abstract

We previously demonstrated that tumor necrosis factor-alpha (TNFalpha) and H2O2 differentially regulate interleukin-8 (IL-8) and intercellular adhesion molecule (ICAM-1) gene expression in endothelial and epithelial cells. H2O2 induced IL-8 expression in the A549 and BEAS-2B epithelial cell lines, but not in the human microvessel endothelial cell line, HMEC-1 or human umbilical vein endothelial cells. In contrast, H2O2 induced ICAM-1 only in endothelial cells. Unlike H2O2, the proinflammatory cytokine TNFalpha induced IL-8 and ICAM-1 in both cell types. In this study, we examine the role of the redox-responsive transcription factors AP-1 and nuclear factor-kappaB (NF-kappaB) in the differential expression of IL-8. DNA binding studies using nuclear protein extracts from HMEC-1 and A549 cells stimulated with H2O2 or TNFalpha demonstrated differential activation and promoter binding of AP-1 and NF-kappaB. H2O2 activated AP-1 but not NF-kappaB in A549, whereas TNFalpha activated AP-1 as well as NF-kappaB. In HMEC-1, TNFalpha activated NF-kappaB but not AP-1, while H2O2 did not activate either transcription factor. The differential activation of the factors was also reflected in their differential binding to the IL-8 promoter. Moreover, the H2O2 concentration dependent increase in epithelial IL-8 mRNA expression directly corresponded to the H2O2 concentration dependent binding of AP-1 to the IL-8 promoter. Supershift analysis revealed H2O2 as well as TNFalpha induced AP-1 complexes containing c-Fos and JunD. TNFalpha induced NF-kappaB complexes containing Rel A (p65). Immunohistochemical staining of HMEC-1 and A549 cells revealed TNFalpha stimulated nuclear localization of Rel A, whereas no translocation of Rel A was detected in either cell type stimulated by H2O2. These data indicate that the cell type-specific induction of IL-8 gene expression by H2O2 and TNFalpha in HMEC-1 and A549 cells can be explained by the differential binding of AP-1 and NF-kappaB to the IL-8 promoter.

摘要

我们先前证明,肿瘤坏死因子-α(TNFα)和过氧化氢(H2O2)对内皮细胞和上皮细胞中白细胞介素-8(IL-8)和细胞间黏附分子(ICAM-1)基因表达的调节存在差异。H2O2可诱导A549和BEAS-2B上皮细胞系中IL-8的表达,但在人微血管内皮细胞系HMEC-1或人脐静脉内皮细胞中则不然。相反,H2O2仅在内皮细胞中诱导ICAM-1的表达。与H2O2不同,促炎细胞因子TNFα在两种细胞类型中均能诱导IL-8和ICAM-1的表达。在本研究中,我们探讨了氧化还原反应性转录因子AP-1和核因子-κB(NF-κB)在IL-8差异表达中的作用。使用经H2O2或TNFα刺激的HMEC-1和A549细胞核蛋白提取物进行的DNA结合研究表明,AP-1和NF-κB存在差异激活及与启动子的结合。H2O2在A549细胞中激活AP-1但不激活NF-κB,而TNFα则同时激活AP-1和NF-κB。在HMEC-1中,TNFα激活NF-κB但不激活AP-1,而H2O2则不激活任何一种转录因子。这些因子的差异激活也反映在它们与IL-8启动子的差异结合上。此外,上皮细胞中IL-8 mRNA表达随H2O2浓度的增加直接对应于AP-1与IL-8启动子的结合随H2O2浓度的增加。超迁移分析显示,H2O2以及TNFα均可诱导包含c-Fos和JunD的AP-1复合物形成。TNFα可诱导包含Rel A(p65)的NF-κB复合物形成。对HMEC-1和A549细胞进行的免疫组织化学染色显示,TNFα可刺激Rel A的核定位,而在H₂O₂刺激的两种细胞类型中均未检测到Rel A的转位。这些数据表明,H2O2和TNFα在HMEC-1和A549细胞中对IL-8基因表达的细胞类型特异性诱导可通过AP-1和NF-κB与IL-8启动子的差异结合来解释。

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