Peer Reviewed

1

Document Type

Article

Publication Date

13-9-2002

Keywords

Cysteine Endopeptidases, DNA-Binding Proteins, Humans, I-kappa B Proteins, Interleukin-1 Receptor-Associated Kinases, Lipopolysaccharides, Multienzyme Complexes, NF-KappaB Inhibitor alpha, Phosphorylation, Proteasome Endopeptidase Complex, Protein Kinases, Proteinase Inhibitory Proteins, Secretory, Proteins, Secretory Leukocyte Peptidase Inhibitor, U937 Cells, Ubiquitin

Funder/Sponsor

Health Research Board of Ireland. Higher Education Authority of Ireland. Charitable Infirmary Charitable Trust. Royal College of Surgeons in Ireland.

Comments

The original article is available at www.jbc.org

Abstract

Secretory leucoprotease inhibitor (SLPI) is a non-glycosylated protein produced by epithelial cells, macrophages, and neutrophils and was initially identified as a serine protease inhibitor of the neutrophil proteases elastase and cathepsin G. In addition to its antiprotease activity, SLPI has been shown to exhibit anti-inflammatory properties including down-regulation of tumor necrosis factor-alpha expression by lipopolysaccharide (LPS) in monocytes, inhibition of NF-kappaB activation by IgG immune complexes in a rat model of acute lung injury, and prevention of human immunodeficiency virus infectivity in monocytic cells via as yet unidentified mechanisms. In this report we have shown that SLPI prevents LPS-induced NF-kappaB activation by inhibiting degradation of IkappaBalpha without affecting the LPS-induced phosphorylation and ubiquitination of IkappaBalpha. We have also demonstrated that SLPI prevents LPS-induced interleukin-1 receptor-associated kinase and IkappaBbeta degradation. In addition, we have demonstrated that oxidized SLPI, a variant of SLPI that has diminished antiprotease activity, cannot prevent LPS-induced NF-kappaB activation or Inhibitor kappaB alpha/beta degradation indicating that the anti-inflammatory effect of SLPI on the LPS-signaling pathway is dependent on its antiprotease activity. These results suggest that SLPI may be inhibiting proteasomal degradation of NF-kappaB regulatory proteins, an effect that is dependent on the antiprotease activity of SLPI.

Disciplines

Medicine and Health Sciences

Citation

Taggart CC, Greene CM, McElvaney NG, O'Neill S. Secretory leucoprotease inhibitor prevents lipopolysaccharide-induced IkappaBalpha degradation without affecting phosphorylation or ubiquitination. Journal of Biological Chemistry. 2002;277(37):33648-53.

PubMed ID

12084717

DOI Link

10.1074/jbc.M203710200

Creative Commons License

Creative Commons License
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