| Literature DB >> 10092080 |
M Muzio1, N Polentarutti, F Facchetti, G Peri, A Doni, M Sironi, P Transidico, M Salmona, M Introna, A Mantovani.
Abstract
Three molecular forms of the IL-1 receptor antagonist (IL-1ra) have been identified and cloned. Secreted IL-1ra (sIL-1ra or IL-1ra1) contains a classical leader peptide giving a released mature protein. Two intracellular isoforms, icIL-1ra type I (IL-1ra2) and icIL-1ra type II (IL-1ra3), have no leader sequence, thus predicting that these proteins remain intracellular. In an effort to define its biological role, we structurally and functionally characterized IL-1ra3. Endogenous immunoreactive IL-1ra3 was detected in a variety of inflammatory cells and tissues. We used a gene transfer strategy to explore the possible intracellular functions of IL-1ra3 (and IL-1ra2) and the cell-associated agonist IL-1alpha. The intracellular IL-1ra3 isoform, as well as IL-1ra2, does not block the action of exogenous and endogenous IL-1 under these conditions. Intact IL-1ra3 was released from the cells killed by NK effectors. The intracellular isoforms may represent a reservoir of IL-1ra, released upon cell death, whose function is to limit the pro-inflammatory action of cell debris.Entities:
Mesh:
Substances:
Year: 1999 PMID: 10092080 DOI: 10.1002/(SICI)1521-4141(199903)29:03<781::AID-IMMU781>3.0.CO;2-0
Source DB: PubMed Journal: Eur J Immunol ISSN: 0014-2980 Impact factor: 5.532