ATP-stimulated release of interleukin (IL)-1 beta and IL-18 requires priming by lipopolysaccharide and is independent of caspase-1 cleavage

Citation
Vb. Mehta et al., ATP-stimulated release of interleukin (IL)-1 beta and IL-18 requires priming by lipopolysaccharide and is independent of caspase-1 cleavage, J BIOL CHEM, 276(6), 2001, pp. 3820-3826
Citations number
42
Categorie Soggetti
Biochemistry & Biophysics
Journal title
JOURNAL OF BIOLOGICAL CHEMISTRY
ISSN journal
00219258 → ACNP
Volume
276
Issue
6
Year of publication
2001
Pages
3820 - 3826
Database
ISI
SICI code
0021-9258(20010209)276:6<3820:AROI(B>2.0.ZU;2-Q
Abstract
Interleukin (IL)-1 beta and IL-18 are structurally similar proteins that re quire caspase-1 processing for activation. Both proteins are released hom t he cytosol by unknown pathway(s). To better characterize the release pathwa y(s) for IL-1 beta and IL-18 we evaluated the role of lipopolysaccharide pr iming, of interleukin-1 beta -converting enzyme (ICE) inhibition, of human purinergic receptor (P2X(7) function, and of signaling pathways in human mo nocytes induced by ATP. Monocytes rapidly processed and released both IL-1 beta and IL-18 after exogenous ATP. Despite its constitutive cytosolic pres ence, IL-18 required lipopolysaccharide priming for the ATP-induced release . Neither IL-1 beta nor IL-18 release was prevented by ICE inhibition, and IL-18 release was not induced by ICE activation itself. Release of both cyt okines was blocked completely by a P2X7 receptor antagonist, oxidized ATP, and partially by an antibody to P2X(7), receptor. In evaluating the signali ng components involved in the ATP effect, we identified that the protein-ty rosine kinase inhibitor, AG126, produced a profound inhibition of both ICE activation as well as release of IG1 beta /IL-18 Taken together, these resu lts suggest that, although synthesis of IL-1 beta and IL-18 differ, ATP-med iated release of both cytokines requires a priming step but not proteolytic ally functional caspase-1.