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肿瘤坏死因子α对黏膜血管地址素细胞黏附分子1编码基因的诱导作用是由核因子κB蛋白介导的。

Induction of the gene encoding mucosal vascular addressin cell adhesion molecule 1 by tumor necrosis factor alpha is mediated by NF-kappa B proteins.

作者信息

Takeuchi M, Baichwal V R

机构信息

Yamanouchi Pharmaceutical Co., Ltd., Ibaraki, Japan.

出版信息

Proc Natl Acad Sci U S A. 1995 Apr 11;92(8):3561-5. doi: 10.1073/pnas.92.8.3561.

DOI:10.1073/pnas.92.8.3561
PMID:7724598
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC42207/
Abstract

Mucosal vascular addressin cell adhesion molecule 1 (MAdCAM-1) is involved in trafficking of lymphocytes to mucosal endothelium. Expression of MAdCAM-1 is induced in the murine endothelial cell line bEnd.3 by tumor necrosis factor alpha (TNF-alpha), interleukin 1, and bacterial lipopolysaccharide. Here we show that TNF-alpha enhances expression of a firefly luciferase reporter directed by the MAdCAM-1 promoter, confirming transcriptional regulation of MAdCAM-1. Mutational analysis of the promoter indicates that a DNA fragment extending from nt -132 to nt +6 of the gene is sufficient for TNF-alpha inducibility. Two regulatory sites critical for TNF-alpha induction were identified in this region. DNA-binding experiments demonstrate that NF-kappa B proteins from nuclear extracts of TNF-alpha-stimulated bEnd.3 cells bind to these sites, and transfection assays with promoter mutants of the MAdCAM-1 gene indicate that occupancy of both sites is essential for promoter function. The predominant NF-kappa B binding activity detected with these nuclear extracts is a p65 homodimer. These findings establish that, as with other endothelial cell adhesion molecules, transcriptional induction of MAdCAM-1 by TNF-alpha requires activated NF-kappa B proteins.

摘要

黏膜血管定居素细胞黏附分子1(MAdCAM-1)参与淋巴细胞向黏膜内皮的转运。肿瘤坏死因子α(TNF-α)、白细胞介素1和细菌脂多糖可诱导小鼠内皮细胞系bEnd.3中MAdCAM-1的表达。在此我们表明,TNF-α增强了由MAdCAM-1启动子指导的萤火虫荧光素酶报告基因的表达,证实了MAdCAM-1的转录调控。对该启动子的突变分析表明,从基因的nt -132到nt +6延伸的DNA片段足以实现TNF-α诱导。在该区域鉴定出了两个对TNF-α诱导至关重要的调控位点。DNA结合实验表明,来自TNF-α刺激的bEnd.3细胞核提取物中的NF-κB蛋白与这些位点结合,并且用MAdCAM-1基因启动子突变体进行的转染实验表明,两个位点的占据对于启动子功能至关重要。用这些核提取物检测到的主要NF-κB结合活性是p65同二聚体。这些发现表明,与其他内皮细胞黏附分子一样,TNF-α对MAdCAM-1的转录诱导需要激活的NF-κB蛋白。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54b4/42207/2edd99390d44/pnas01492-0498-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54b4/42207/d64fc4e9c558/pnas01492-0495-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54b4/42207/3032ee67fbcb/pnas01492-0497-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54b4/42207/bce7bb3e0d93/pnas01492-0497-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54b4/42207/2edd99390d44/pnas01492-0498-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54b4/42207/d64fc4e9c558/pnas01492-0495-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54b4/42207/3032ee67fbcb/pnas01492-0497-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54b4/42207/bce7bb3e0d93/pnas01492-0497-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54b4/42207/2edd99390d44/pnas01492-0498-a.jpg

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