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Research Article Free access | 10.1172/JCI114645

Modulation of interleukin 1 beta gene expression by the immediate early genes of human cytomegalovirus.

G K Iwamoto, M M Monick, B D Clark, P E Auron, M F Stinski, and G W Hunninghake

Department of Medicine, University of Iowa College of Medicine, Iowa City 52242.

Find articles by Iwamoto, G. in: PubMed | Google Scholar

Department of Medicine, University of Iowa College of Medicine, Iowa City 52242.

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Department of Medicine, University of Iowa College of Medicine, Iowa City 52242.

Find articles by Clark, B. in: PubMed | Google Scholar

Department of Medicine, University of Iowa College of Medicine, Iowa City 52242.

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Department of Medicine, University of Iowa College of Medicine, Iowa City 52242.

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Department of Medicine, University of Iowa College of Medicine, Iowa City 52242.

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Published June 1, 1990 - More info

Published in Volume 85, Issue 6 on June 1, 1990
J Clin Invest. 1990;85(6):1853–1857. https://doi.org/10.1172/JCI114645.
© 1990 The American Society for Clinical Investigation
Published June 1, 1990 - Version history
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Abstract

The immediate early (IE) genes of human cytomegalovirus (HCMV) can be expressed in monocytes/macrophages and are known to regulate other viral genes. The purpose of these studies was to determine if HCMV IE gene products also modulate expression of a monocyte/macrophage-derived gene, interleukin 1 (IL-1) beta. Steady-state cell-derived IL-1 beta mRNA was increased in lipopolysaccharide (LPS)-stimulated THP-1 cells when transfected with the HCMV IE1 + 2 genes, when compared to cells transfected with a control DNA. LPS-stimulated THP-1 cells also exhibited approximately 30-fold higher IL-1 CAT activity when cotransfected with IE1 + 2 than was observed for the same cells cotransfected with IL-1 CAT and a control plasmid containing the IE promoter alone. LPS increased IL-1 CAT activity in the absence of HCMV genes only twofold. IE1, by itself, increased IL-1 CAT activity in LPS-stimulated cells, whereas, IE2, by itself, caused no change in IL-1 CAT activity. These studies show that the IE1 gene of HCMV can regulate IL-1 beta gene expression. The observations further suggest that some of the inflammatory processes associated with HCMV infection may be due to an effect of HCMV IE genes on cell-derived genes, such as the IL-1 beta gene.

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