Peer Reviewed

1

Document Type

Article

Publication Date

19-12-2005

Keywords

Animals, Binding, Competitive, Blotting, Western, Cell Line, Cell Nucleus, Chromatin Immunoprecipitation, Cytokines, DNA, Electrophoretic Mobility Shift Assay, Enzyme-Linked Immunosorbent Assay, Lipopolysaccharides, Microscopy, Confocal, Monocytes, NF-kappa B, Oligonucleotides, Protein Transport, Proteinase Inhibitory Proteins, Secretory, Proteins, Rats, Secretory Leukocyte Peptidase Inhibitor, Transcription Factor RelA

Funder/Sponsor

We wish to acknowledge funding from the Alpha One Foundation (to C.C. Taggart), the Health Research Board of Ireland (RP/198/2002 to C.C. Taggart), Science Foundation Ireland (04/BR/B0640 to C.C. Taggart and SC/2004/B0419 to S.-A. Cryan), the Research Committee of the Royal College of Surgeons in Ireland (13/02 to C.C. Taggart), the Programme for Research in Third Level Institutes administered by Higher Education Authority of Ireland (to N.G. McElvaney), the Cystic Fibrosis Association of Ireland (to C.C. Taggart), the CF Research Trust, and the CF Hope Source.

Comments

This article is also available at http://jem.rupress.org/content/202/12/1659

Abstract

Secretory leucoprotease inhibitor (SLPI) is a nonglycosylated protein produced by epithelial cells. In addition to its antiprotease activity, SLPI has been shown to exhibit antiinflammatory properties, including down-regulation of tumor necrosis factor alpha expression by lipopolysaccharide (LPS) in macrophages and inhibition of nuclear factor (NF)-kappaB activation in a rat model of acute lung injury. We have previously shown that SLPI can inhibit LPS-induced NF-kappaB activation in monocytic cells by inhibiting degradation of IkappaBalpha without affecting the LPS-induced phosphorylation and ubiquitination of IkappaBalpha. Here, we present evidence to show that upon incubation with peripheral blood monocytes (PBMs) and the U937 monocytic cell line, SLPI enters the cells, becoming rapidly localized to the cytoplasm and nucleus, and affects NF-kappaB activation by binding directly to NF-kappaB binding sites in a site-specific manner. SLPI can also prevent p65 interaction with the NF-kappaB consensus region at concentrations commensurate with the physiological nuclear levels of SLPI and p65. We also demonstrate the presence of SLPI in nuclear fractions of PBMs and alveolar macrophages from individuals with cystic fibrosis and community-acquired pneumonia. Therefore, SLPI inhibition of NF-kappaB activation is mediated, in part, by competitive binding to the NF-kappaB consensus-binding site.

Disciplines

Medicine and Health Sciences

Citation

Taggart CC, Cryan SA, Weldon S, Gibbons A, Greene CM, Kelly E, Low TB, O'Neill SJ, McElvaney NG. Secretory leucoprotease inhibitor binds to NF-kappaB binding sites in monocytes and inhibits p65 binding. Journal of Experimental Medicine. 2005;202(12):1659-1668.

PubMed ID

16352738

DOI Link

10.1084/jem.20050768

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