LIPOPOLYSACCHARIDE INHIBITS ACTIVATION OF LATENT TRANSFORMING GROWTH-FACTOR-BETA IN BOVINE ENDOTHELIAL-CELLS

Citation
S. Kojima et al., LIPOPOLYSACCHARIDE INHIBITS ACTIVATION OF LATENT TRANSFORMING GROWTH-FACTOR-BETA IN BOVINE ENDOTHELIAL-CELLS, Journal of cellular physiology, 163(1), 1995, pp. 210-219
Citations number
51
Categorie Soggetti
Physiology,"Cell Biology
ISSN journal
00219541
Volume
163
Issue
1
Year of publication
1995
Pages
210 - 219
Database
ISI
SICI code
0021-9541(1995)163:1<210:LIAOLT>2.0.ZU;2-P
Abstract
The activation of latent transforming growth factor-beta (TGF-beta) by vascular endothelial cells (ECs) is regulated by cellular plasminogen activator (PA)/plasmin, transglutaminase (TGase), and latent TGF-beta levels. Because lipopolysaccharide (LPS) has been reported to reduce EC surface plasmin levels by increasing the production of the inhibito r of PA, PA inhibitor-1 (PAI-1), we have tested whether LPS might supp ress latent TGF-beta activation in ECs using two different systems, na mely, bovine aortic ECs (BAECs) cocultured with smooth muscle cells (S MCs) and BAECs treated with retinol. BAECs were either cocultured with SMCs after treatment with 15 ng/ml LPS or were treated with 2 mu M re tinol and/or 10 ng/ml LPS, and the expression of PA, surface plasmin, TGase, and the amounts of active and latent TGF-beta secreted into the culture medium were measured. The downregulation of surface PA/plasmi n levels with LPS was accompanied by a profound decline of both TGase and latent TGF-beta expression as well as the suppression of surface a ctivation of latent TGF-beta. The effect was dependent on the concentr ation of LPS and on treatment time. The formation of TGF-beta did not occur in cells maintained in LPS-contaminated culture medium. (C) 1995 Wiley-Liss, Inc.