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Article has an altmetric score of 3

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Referenced in 16 patents
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Research Article Free access | 10.1172/JCI118598

Activated transcription factor nuclear factor-kappa B is present in the atherosclerotic lesion.

K Brand, S Page, G Rogler, A Bartsch, R Brandl, R Knuechel, M Page, C Kaltschmidt, P A Baeuerle, and D Neumeier

Institute of Clinical Chemistry and Pathobiochemistry, Technical University Munich, Germany.

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Institute of Clinical Chemistry and Pathobiochemistry, Technical University Munich, Germany.

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Institute of Clinical Chemistry and Pathobiochemistry, Technical University Munich, Germany.

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Institute of Clinical Chemistry and Pathobiochemistry, Technical University Munich, Germany.

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Institute of Clinical Chemistry and Pathobiochemistry, Technical University Munich, Germany.

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Institute of Clinical Chemistry and Pathobiochemistry, Technical University Munich, Germany.

Find articles by Knuechel, R. in: JCI | PubMed | Google Scholar

Institute of Clinical Chemistry and Pathobiochemistry, Technical University Munich, Germany.

Find articles by Page, M. in: JCI | PubMed | Google Scholar

Institute of Clinical Chemistry and Pathobiochemistry, Technical University Munich, Germany.

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Institute of Clinical Chemistry and Pathobiochemistry, Technical University Munich, Germany.

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Institute of Clinical Chemistry and Pathobiochemistry, Technical University Munich, Germany.

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Published April 1, 1996 - More info

Published in Volume 97, Issue 7 on April 1, 1996
J Clin Invest. 1996;97(7):1715–1722. https://doi.org/10.1172/JCI118598.
© 1996 The American Society for Clinical Investigation
Published April 1, 1996 - Version history
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Abstract

Nuclear factor-kappa B (NF-kappaB)/Rel transcription factors play an important role in the inducible regulation of a variety of genes involved in the inflammatory and proliferative responses of cells. The present study was designed to elucidate the implication of NF-kappaB/Rel in the pathogenesis of atherosclerosis. Activation of the dimeric NF-kappaB complex is regulated at a posttranslational level and requires the release of the inhibitor protein IkappaB. The newly developed mAb alpha-p65mAb recognizes the IkappaB binding region on the p65 (RelA) DNA binding subunit and therefore selectively reacts with p65 in activated NF-kappaB. Using immunofluorescence and immunohistochemical techniques, activated NF-kappaB was detected in the fibrotic-thickened intima/media and atheromatous areas of the atherosclerotic lesion. Activation of NF-kappaB was identified in smooth muscle cells, macrophages, and endothelial cells. Little or no activated NF-kappaB was detected in vessels lacking atherosclerosis. Electrophoretic mobility shift assays and colocalization of activated NF-kappaB with NF-kappaB target gene expression suggest functional implications for this transcription factor in the atherosclerotic lesion. This study demonstrates the presence of activated NF-kappaB in human atherosclerotic tissue for the first time. Atherosclerosis, characterized by features of chronic inflammation and proliferative processes, may be a paradigm for the involvement of NF-kappaB/Rel in chronic inflammatory disease.

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Referenced in 16 patents
155 readers on Mendeley
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