Journal
INTERNATIONAL JOURNAL OF IMMUNOPATHOLOGY AND PHARMACOLOGY
Volume 17, Issue 2, Pages 145-155Publisher
SAGE PUBLICATIONS INC
DOI: 10.1177/039463200401700206
Keywords
inflammation; lipid mediators; acute-phase reactants; cytokines; transcription factors
Categories
Funding
- NIAMS NIH HHS [AR-45931] Funding Source: Medline
Ask authors/readers for more resources
Lipoxin A(4) (LXA(4)) is a potent eicosanoid that inhibits IL-1beta-induced activation of human fibroblast-like synoviocytes (FLS) via the LXA(4) receptor (ALXR). Serum amyloid A (SAA) is an acute phase reactant with cytokine-like properties. SAA has been shown to bind the same seven transmembrane G protein-coupled receptor ligated by LXA(4). Here we compared the inflammatory responses of lipid (LXA(4)) and peptide (SAA) ligands in human FLS via the shared ALX and characterized their downstream signaling. LXA(4) induced stimulation of tissue inhibitors of metalloproteinase-2, whereas SAA induced interleukin-8 and matrix metalloproteinase-3 production. SAA up-regulated NF-kB and AP-1 DNA binding activity, while LXA(4) markedly inhibited these responses after IL-1beta stimulation. A human IL-8 promoter luciferase construct was transfected into CHO cells stably expressing ALXR in order to determine the role of NF-kB and/or AP-1 in the regulation of IL-8 gene expression. The NF-kB pathway proved to be the preeminent for the biological responses elicited by both ligands. These findings suggest that two endogenous molecules, targeting a common receptor, could participate in the pathogenesis of inflammatory arthritis by differentially regulating inflammatory responses in tissues expressing the ALXR.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available