• Medientyp: E-Artikel
  • Titel: Human Vascular Smooth Muscle Cells Express Interleukin-1β–converting Enzyme (ICE), but Inhibit Processing of the Interleukin-1β Precursor by ICE
  • Beteiligte: Schönbeck, Uwe; Herzberg, Mona; Petersen, Arnd; Wohlenberg, Claudia; Gerdes, Johannes; Flad, Hans-Dieter; Loppnow, Harald
  • Erschienen: Rockefeller University Press, 1997
  • Erschienen in: The Journal of Experimental Medicine
  • Sprache: Englisch
  • DOI: 10.1084/jem.185.7.1287
  • ISSN: 0022-1007; 1540-9538
  • Schlagwörter: Immunology ; Immunology and Allergy
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  • Beschreibung: <jats:p>Local immunoregulatory processes during normal vascular biology or pathogenesis are mediated in part by the production of and response to cytokines by vessel wall cells. Among these cytokines interleukin (IL)-1 is considered to be of major importance. Although vascular smooth muscle (SMC) and endothelial cells (EC) expressed both IL-1α and IL-1β as cell-associated, 33-kilodalton (kD) precursors, SMC neither contained detectable mature IL-1β, nor processed recombinant IL-1β precursor into its mature 17-kD form. Thus, we investigated the expression and function of IL-1β–converting enzyme (ICE) in vascular cells. We demonstrate in processing experiments with recombinant IL-1 precursor molecules that EC processed IL-1β, in contrast to SMC. Despite the failure of SMC to process IL-1β, these cells expressed ICE mRNA, immunoreactive ICE protein, and the expected IL-1β nucleotide sequence. The lack of processing was explained by our finding that extracts of SMC specifically and concentration dependently blocked processing of IL-1β precursor by recombinant or native ICE. The initial biochemical characterization of the inhibitory activity showed that it is heat-labile, has a molecular size of 50–100 kD, and is associated to the cell membrane compartment. Inhibition of processing, i.e., activation of IL-1β precursor by SMC may constitute a novel regulatory mechanism during normal vascular biology or pathogenesis of vascular diseases.</jats:p>
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