Inactivation of single-chain urokinase-type plasminogen activator by thrombin in human subjects

Citation
Eam. Braat et al., Inactivation of single-chain urokinase-type plasminogen activator by thrombin in human subjects, J LA CL MED, 134(2), 1999, pp. 161-167
Citations number
35
Categorie Soggetti
Research/Laboratory Medicine & Medical Tecnology","Medical Research General Topics
Journal title
JOURNAL OF LABORATORY AND CLINICAL MEDICINE
ISSN journal
00222143 → ACNP
Volume
134
Issue
2
Year of publication
1999
Pages
161 - 167
Database
ISI
SICI code
0022-2143(199908)134:2<161:IOSUPA>2.0.ZU;2-J
Abstract
Thrombin cleaves single-chain urokinase-type plasminogen activator (scu-PA) into a virtually inactive two-chain form (tcu-PA/T), a process that may pr otect a blood clot from early fibrinolysis. It is not known under what circ umstances tcu-PA/T can be generated in vivo. We have studied the occurrence of tcu-PA/T in human subjects with a varying degree of hypercoagulability, tcu-PA/T was assessed in the plasma of patients with disseminated intravas cular coagulation (DIC), endotoxin-treated volunteers, patients with unstab le angina pectoris, and patients selected for hip replacement, Relationship s between tcu-PA/T and several markers reflecting thrombin generation were examined, tcu-PA/T was observed only in the plasma of patients with DIC and was associated with all thrombin markers and with scu-PA and urokinase ant igen. Prothrombin fragment 1 + 2 and urokinase antigen were independent pre dictors of tcu-PA/T, The fact that tcu-PA/T could not be detected in the ot her three groups was explained by a lower extent of thrombin generation, a greater inhibition of thrombin by antithrombin, or less available urokinase antigen in these groups, The contribution of scu-PA to total urokinase ant igen was decreased in the patients with DIC because of inactivation by thro mbin, which may be an additional explanation for the inadequate fibrinolysi s observed in these patients. These findings show that scu-PA can be inacti vated in the circulation under severe pathophysiologic circumstances and th at the process of inactivation depends not only on the generation of thromb in but also on the control of thrombin activity by its inhibitor antithromb in.