Interleukin-1β up-regulates the plasminogen activator/plasmin system in human mesangial cells

Heather M. Wilson*, Neva E. Haites, Fiona J. Reid, Nuala A. Booth

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

20 Citations (Scopus)


The plasminogen activators (PA), which are regulated by their specific inhibitor, PAI-1, convert the zymogen plasminogen to plasmin, a protease involved in fibrinolysis and extracellular matrix turnover. Interleukin 1β (IL-1) is a key cytokine released from infiltrating monocytes/macrophages during the initial stages of glomerular injury. We investigated the effects of IL-1 on the production of tissue-type plasminogen activator (t-PA), urokinase (u-PA) and PAI-1 by glomerular cells. IL-1 significantly increased the synthesis of t-PA by mesangial cells and glomerular epithelial cells (P < 0.005 for both cell types), while u-PA production was unaltered. PAI-1 in mesangial cell supernatants was significantly lower when cultured in the presence of IL-1 (P < 0.008), and the synthesis decreased in a time and dose dependent manner. The effects of IL-1 were elimininated by anti-IL-1 neutralizing antibodies. The PAI-1 sequestered in the extracellular matrix of mesangial cells was also decreased. No significant change in PAI-1 synthesis by epithelial cells was observed with exogenous IL-1. Northern blot analysis paralleled the protein results, demonstrating an increase in t-PA and a decrease in PAI-1 mRNA of mesangial cells after 6 and 24 hours stimulation with 10 U/ml IL-1. These studies suggest a role for IL-1 in regulating localized proteolysis by mesangial cells during acute inflammation.

Original languageEnglish
Pages (from-to)1097-1104
Number of pages8
JournalKidney International
Issue number4
Publication statusPublished - 30 Jan 1996

Bibliographical note

This study was supported by The Medical Research Council. The eDNAprobe for PAT-i was generously provided by Professor K Dano, Copen-hagen


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