Bimodal concentration-dependent effect of thrombin on endothelial cell proliferation and growth factor release in culture

Citation
V. Borrelli et al., Bimodal concentration-dependent effect of thrombin on endothelial cell proliferation and growth factor release in culture, J SURG RES, 100(2), 2001, pp. 154-160
Citations number
33
Categorie Soggetti
Surgery,"Medical Research Diagnosis & Treatment
Journal title
JOURNAL OF SURGICAL RESEARCH
ISSN journal
00224804 → ACNP
Volume
100
Issue
2
Year of publication
2001
Pages
154 - 160
Database
ISI
SICI code
0022-4804(200110)100:2<154:BCEOTO>2.0.ZU;2-B
Abstract
Background. The role of thrombin in the stimulation of endothelial cell (EC ) proliferation is controversial. The aim of this study was to investigate if thrombin regulates cell proliferation and production of platelet-derived growth factor (PDGF), bovine fibroblast growth factor (bFGF), and transfor ming growth factor beta (1) (TGF-beta (1)) by bovine aortic ECs. Methods. ECs, obtained from thoracic aortas of calves, were stimulated with thrombin at various concentrations (from 0.05 to 1.0 IU/ml) in serum free culture. Mitogenic activity of thrombin on ECs was determined by tritiated thymidine uptake. The release of PDGF, bFGF, and TGF-beta (1) was assessed by ELISA. PDGF release was confirmed by Western blot and bFGF and TGF-beta (1) mRNA expression was determined by polymerase chain reaction (PCR). Results. Thrombin at high concentrations did not cause any increase in EC p roliferation after 72 h of culture and induced inhibition of EC proliferati on after 96 h and 8 days of culture. It induced a decrease in PDGF release and an increase in TGF-beta (1) release. Thrombin at low concentrations ind uced a significant increase in EC proliferation at 72 h, 96 h, and 8 days o f culture. It induced an increase in PDGF release and a decrease in TGF-bet a (1) release. bFGF release was higher than control at all thrombin concent rations. These data were confirmed by Western blot and PCR studies. Conclusions. Thrombin regulates EC growth through the inhibition of EC prol iferation at high concentrations and through the stimulation of EC prolifer ation at low physiological concentrations. EC proliferation is partially me diated by autocrine production of PDGF, bFGF, and TGF-beta (1). (C) 2001 Ac ademic Press.