Biological and Thrombolytic Properties of Proenzyme and Active Forms of Human Urokinase – II. Turnover of Natural and Recombinant Urokinase in Rabbits and Squirrel Monkeys

D Collen; F De Cock; H R Lijnen

doi:10.1055/s-0038-1661128

Thrombosis and Haemostasis, Table of Contents

Thromb Haemost 1984; 52(01): 024-026
DOI: 10.1055/s-0038-1661128

Original Article

Schattauer GmbH Stuttgart

Biological and Thrombolytic Properties of Proenzyme and Active Forms of Human Urokinase – II. Turnover of Natural and Recombinant Urokinase in Rabbits and Squirrel Monkeys

Authors

D Collen

The Center for Thrombosis and Vascular Research, Department of Medical Research, University of Leuven, Belgium
F De Cock

The Center for Thrombosis and Vascular Research, Department of Medical Research, University of Leuven, Belgium
H R Lijnen

The Center for Thrombosis and Vascular Research, Department of Medical Research, University of Leuven, Belgium

Abstract

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Summary

The turnover of recombinant pro-urokinase (Rec-pro-UK), recombinant urokinase (Rec-UK) and natural urinary urokinase (Nat-UK) was studied in rabbits and in squirrel monkeys (Samiri sciureus). Following intravenous injection, urokinase activity disappeared rapidly from the blood. The initial disappearance rate could be described by a single exponential term with a t½ of 3 to 6 min for each molecular form of urokinase in both species. Urokinase related antigen, measured with a radioimmunoassay in the plasma of the squirrel monkeys disappeared with a t½ of 3.5 min for Rec-pro-UK, 6.0 min for Rec-UK and 8.0 min for Nat-UK.

The clearance and organ distribution of Rec-pro-UK, Rec-UK and Nat-UK was studied with the use of ¹²⁵I-labeled preparations. In each case the radioactivity initially disappeared rapidly from the plasma, also with a t½ of a few min, but then the disappearance rate slowed down. Labeled Rec-UK in which the active site histidine was irreversibly blocked by alkylation, disappeared equally rapidly from the plasma. Measurement of the organ distribution of ¹²⁵I at different time intervals revealed that all three types of urokinase were rapidly accumulated in the liver, which was followed by release of degradation products in the blood. Experimental hepatectomy prolonged the t½ of each type of urokinase very markedly (t½ >30 min).

These findings indicate that urokinase is rapidly removed from the blood by clearance and degradation in the liver. Recognition by the liver does not require a functional active site and is not mediated via carbohydrate side chains. Inactivation by plasma protease inhibitors does not represent a significant pathway of urokinase inhibition in vivo.

Keywords

Recombinant urokinase - Recombinant pro-urokinase - Turnover in rabbits - Turnover in squirrel monkeys - Clearance mechanism - Inactivation

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References

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