INTERFERON-ALPHA-2 COUNTERACTS INTERLEUKIN-1-ALPHA-STIMULATED EXPRESSION OF UROKINASE-TYPE PLASMINOGEN-ACTIVATOR IN HUMAN FORESKIN MICROVASCULAR ENDOTHELIAL-CELLS IN-VITRO

Citation
J. Wojta et al., INTERFERON-ALPHA-2 COUNTERACTS INTERLEUKIN-1-ALPHA-STIMULATED EXPRESSION OF UROKINASE-TYPE PLASMINOGEN-ACTIVATOR IN HUMAN FORESKIN MICROVASCULAR ENDOTHELIAL-CELLS IN-VITRO, Lymphokine and cytokine research, 13(2), 1994, pp. 133-138
Citations number
22
Categorie Soggetti
Immunology,Biology
ISSN journal
10565477
Volume
13
Issue
2
Year of publication
1994
Pages
133 - 138
Database
ISI
SICI code
1056-5477(1994)13:2<133:ICIE>2.0.ZU;2-K
Abstract
We investigated the effect of interferon-alpha 2 (IFN-alpha 2) on inte rleukin-1 alpha (IL-1 alpha)-induced up-regulation of urokinase type p lasminogen activator (u-PA) expression in human foreskin microvascular endothelial cells (HFMEC) and human umbilical vein endothelial cells (HUVEC) in vitro. When IFN-alpha 2 and IL-1 alpha were added to the ce lls simultaneously, IFN-alpha 2 inhibited IL-la-induced up-regulation of u-PA antigen in a dose- and time-dependent fashion in HFMEC, wherea s in HUVEC no effect of IFN-alpha 2 on IL-1 alpha-induced u-PA was see n. IL-1 alpha-induced up-regulation of PAI-1 antigen in HFMEC was not counteracted by IFN-alpha 2. When IFN-alpha 2 was added to HFMEC 1 or 2 h after IL-1 alpha a significant inhibition in u-PA synthesis was se en, whereas when IFN-alpha 2 was added to the cells 8 h after IL-1 alp ha no effect on the induction of u-PA synthesis by IL-1 alpha was seen . IFN-alpha 2 also inhibited significantly the IL-1 alpha stimulated u p-regulation of specific u-PA mRNA expression. In conclusion, our data show that IFN-alpha 2 can counteract the IL-1 alpha-induced up-regula tion of u-PA in a similar way as IFN-gamma. This effect, which seems t o be specific for microvascular endothelial cells, could contribute to the modulation of endothelial cell-mediated extravascular proteolysis in processes such as wound healing, neovascularisation, and endotheli al cell migration.