Thromb Haemost 1986; 55(01): 065-069
DOI: 10.1055/s-0038-1661449
Original Article
Schattauer GmbH Stuttgart

The Fast-Acting Inhibitor of Tissue-Type Plasminogen Activator in Plasma Is also the Primary Plasma Inhibitor of Urokinase

Egbert K.O Kruithof
The Hematology Division, Department of Medicine, University Hospital Center, CHUV, Lausanne, Switzerland
,
Chiên Tran-Thang
The Hematology Division, Department of Medicine, University Hospital Center, CHUV, Lausanne, Switzerland
,
Fedor Bachmann
The Hematology Division, Department of Medicine, University Hospital Center, CHUV, Lausanne, Switzerland
› Author Affiliations
Further Information

Publication History

Received 09 August 1985

Accepted 31 October 1985

Publication Date:
19 July 2018 (online)

Summary

We have compared the ability of a plasminogen activator inhibitor (PA-inhibitor) in human plasma, to form complexes with radioiodinated tissue-type plasminogen activator (t-PA) and high molecular weight urokinase (HMr-UK). Addition of 125I-t-PA (final concentration 10 IU/ml) or of 125I-HMr-UK (2 IU/ml) to a plasma containing 33 U/ml of PA-inhibitor resulted in the rapid formation of a 110,000 Mr complex of 125I-t-PA or a 95,000 Mr complex of 125I-HMr-UK with PA-inhibitor. Upon prolonged incubation of the plasma with 125I-HMr-UK a secondary complex of a Mr of 88,000 was observed, which probably derives from limited degradation of the 95,000 complex. Preincubation of the plasma with unlabelled t-PA, HMr-UK or LMr-UK at higher concentrations prevented the subsequent formation of complexes between radiolabelled PAs and the PA-inhibitor. These results thus demonstrate that t-PA and UK form complexes with the same PA-inhibitor. The rate of complex formation of 125I-t-PA or of 125I-HMr-UK with the plasma PA-inhibitor was similar (second order rate constant of association with PA-inhibitor in the order of 107 M−1s−1).

 
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