A novel function of serum amyloid A: A potent stimulus for the release of tumor necrosis factor-alpha, interleukin-1 beta, and interleukin-8 by humanblood neutrophil

Citation
Cj. Furlaneto et A. Campa, A novel function of serum amyloid A: A potent stimulus for the release of tumor necrosis factor-alpha, interleukin-1 beta, and interleukin-8 by humanblood neutrophil, BIOC BIOP R, 268(2), 2000, pp. 405-408
Citations number
24
Categorie Soggetti
Biochemistry & Biophysics
Journal title
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
ISSN journal
0006291X → ACNP
Volume
268
Issue
2
Year of publication
2000
Pages
405 - 408
Database
ISI
SICI code
0006-291X(20000216)268:2<405:ANFOSA>2.0.ZU;2-M
Abstract
High density lipoprotein (HDL) and its main apolipoproteins, AI and serum a myloid A (SAA), present in physiological and acute phase response condition s, respectively, affect the inflammatory process. This study focuses on the effect of AI, SAA, and HDL from healthy (N-HDL) and acute phase individual s (AP-HDL) on the release of TNF-alpha, IL-1 beta, and IL-8 by human blood neutrophils, It was observed that SAA (100 mu g/mL) causes a dramatic incre ase (75-400 times) in the basal liberation of the three cytokines assayed. This effect is not triggered by AP-HDL, Although Al (100 mu g/ml) increases the release of IL-1 beta and IL-8 modestly, N-HDL does not. Both HDLs (0.1 6-0.32 mg of protein/mL) had an anti-inflammatory action, decreasing the ba sal and LPS-stimulated cytokine release. Given that the biological role of SAA is still uncertain, the present study adds an important finding potenti ally pertinent to the biological role of this acute phase protein. (C) 2000 Academic Press.