cDNA cloning of an intracellular form of the human interleukin 1 receptor antagonist associated with epithelium.

Stephen Haskill(University of North Carolina at Chapel Hill), George A. Martin(University of North Carolina at Chapel Hill), Linda Van Le(University of North Carolina at Chapel Hill), Joan K. Morris(University of North Carolina at Chapel Hill), A Peace(University of North Carolina at Chapel Hill), Carl F. Bigler(University of North Carolina at Chapel Hill), G. J. Jaffe(University of North Carolina at Chapel Hill), Craig Hammerberg(University of North Carolina at Chapel Hill), S A Sporn(University of North Carolina at Chapel Hill), Susan Fong(University of North Carolina at Chapel Hill)
Proceedings of the National Academy of Sciences
May 1, 1991
Cited by 324Open Access

Abstract

A cDNA encoding a receptor antagonist of interleukin 1 (IL-1ra), secreted from human monocytes, has recently been isolated and sequenced [Eisenberg, S. P., Evans, R. J., Arend, W. P., Verderber, E., Brewer, M. T., Hannum, C. H. & Thompson, R. C. (1990) Nature (London) 343, 341-346]. We have identified another version of this IL-1ra, which is predominantly expressed in epithelial cells. This IL-1ra lacks a leader sequence and, thus, is probably intracellular. Both proteins are derived from the same gene through use of an alternative transcriptional start site and internal splice-acceptor site. Expression of intracellular IL-1ra cDNA in COS cells demonstrated that the intracellular product specifically inhibited exogenous interleukin 1-dependent responses. Keratinocytes were shown to contain significant amounts of nonsecreted IL-1ra protein. Constitutive expression of the intracellular IL-1ra may be an intracellular defensive mechanism in exposed epithelial cells and/or may serve to regulate autocrine interleukin 1-mediated pathways of differentiation.


Related Papers

No related papers found

Powered by citation graph analysis