Thromb Haemost 1993; 70(03): 481-485
DOI: 10.1055/s-0038-1649609
Original Article
Fibrinolysis
Schattauer GmbH Stuttgart

Comparison of the In Vitro Fibrinolytic Activities of Low and High Molecular Weight Single-Chain Urokinase-Type Plasminogen Activator

Gerard A W de Munk
IVVO-TNO Gaubius Laboratory Leiden, The Netherlands
,
Eleonore Groeneveld
IVVO-TNO Gaubius Laboratory Leiden, The Netherlands
,
Dingeman C Rijken
IVVO-TNO Gaubius Laboratory Leiden, The Netherlands
› Author Affiliations
Further Information

Publication History

Received 19 November 1992

Accepted after revision 05 April 1993

Publication Date:
05 July 2018 (online)

Summary

The fibrinolytic activity of low molecular weight (LMW) single-chain urokinase-type plasminogen activator (scu-PA) lacking the epidermal growth factor domain and the kringle domain was compared with the activity of high molecular weight (HMW) scu-PA. LMW scu-PA was 1-5 times less active than HMW scu-PA in a fibrin plate method, in a purified fibrin clot lysis assay and in a plasma clot lysis assay. Time course experiments in a chromogenic plasminogen activator assay suggested that LMW scu-PA was less sensitive to activation by plasmin than HMW scu-PA. This was confirmed in a scu-PA activation test, which showed that at a concentration of 40 IU/ml LMW scu-PA required a three-fold higher plasmin concentration for 50% activation in 20 min than did HMW scu-PA. Kinetic experiments in the presence of 0.1 M NaCl showed non-standard Michaelis-Menten kinetics for the activation by plasmin of both HMW and LMW scu-PA. In contrast, standard kinetics was observed at 0.15 M NaCl, showing a 2.6-fold lower catalytic efficiency for LMW scu-PA than for HMW scu-PA. It is concluded that the plasmin activation of LMW scu-PA is about three times slower than the activation of HMW scu-PA. This explains, at least partially, the lower fibrinolytic activity of LMW scu-PA in comparison with HMW scu-PA.

 
  • References

  • 1 Gurewich V. Experiences with pro-urokinase and potentiation of its fibrinolytic effect by urokinase and by tissue plasminogen activator. J Am Coll Cardiol 1987; 10: 16B-21B
  • 2 Lijnen HR, Stump DC, Collen D. Single-chain urokinase-type plasminogen activator: Mechanism of action and thrombolytic properties. Semin Thromb Hemostas 1987; 13: 152-159
  • 3 De Munk GAW, Rijken DC. Fibrinolytic properties of single-chain urokinasetype plasminogen activator (pro-urokinase). Fibrinolysis 1990; 4: 1-9
  • 4 Wijngaards G, Rijken DC, Van Wezel AL, Groeneveld E, Van der velden CAM. Characterization and fibrin-binding properties of different molecular forms of pro-urokinase from a monkey kidney cell culture. Thromb Res 1986; 42: 749-760
  • 5 Stump DC, Lijnen HR, Collen D. Purification of a novel low molecular weight form of single-chain urokinase-type plasminogen activator. J Biol Chem 1986; 261: 17120-17126
  • 6 Marcotte PA, Dudlak D, Leski ML, Ryan J, Henkin J. Characterization of a metalloprotease which cleaves with high site specificity the Glu (143)-Leu (144) bond of urokinase. Fibrinolysis 1992; 6 (Suppl. 01) 57-62
  • 7 Marcotte PA, Kozan IM, Dorwin SA, Ryan JM. The matrix metalloproteinase pump-1 catalyzes formation of low molecular weight (pro)urokinase in cultures of normal human kidney cells. J Biol Chem 1992; 267: 13803-13806
  • 8 Lijnen HR, Nelles L, Holmes WE, Collen D. Biochemical and thrombolytic properties of a low molecular weight form (comprising Leu144 through Leu411) of recombinant single-chain urokinase-type plasminogen activator. J Biol Chem 1988; 263: 5594-5598
  • 9 Orsini G, Brandazza A, Sarmientos P, Molinari A, Lansen J, Cauet G. Efficient renaturation and fibrinolytic properties of prourokinase and a deletion mutant expressed in Escherichia coli as inclusion bodies. Eur J Biochem 1991; 195: 691-697
  • 10 Appella E, Robinson EA, Ullrich SJ, Stoppelli MP, Corti A, Casani G, Blasi F. The receptor binding sequence of urokinase. A biological function for the growth-factor module of proteases. J Biol Chem 1987; 262: 4437-4440
  • 11 Dumler I, Petri T, Schmidt D, Schleuning WD. Interaction of the urokinase-type plasminogen activator with its cellular receptor induces tyrosine phosphoryla tion. Fibrinolysis. 1992 (6 suppl. 2) 13. (abstract 30)
  • 12 Rabbani SA, Mazar A, Bemier SM, Haq M, Bolivar I, Henkin J, Golzman D. Structural requirements for the growth factor activity of the amino-terminal domain of urokinase. J Biol Chem 1992; 267: 14151-14156
  • 13 Nusrath AR, Chapman HA. An autocrine role for urokinase in phorbol ester-mediated differentiation of myeloid cell lines. J Clin Invest 1991; 87: 1091-1097
  • 14 Mazar AP, Buko A, Petros AM, Barnathan ES, Henkin J. Domain analysis of urokinase plasminogen activator (u-PA): preparation and characterization of intact A-chain molecules. Fibrinolysis 1992; 6 (Suppl. 01) 49-55
  • 15 Rijken D, Binnema DJ, Los P. Specific fibrinolytic properties of different molecular forms of pro-urokinase from a monkey kidney cell culture. Thromb Res 1986; 42: 761-768
  • 16 Spriggs DJ, Stassen JM, Hashimoto Y, Collen D. Thrombolytic properties of human tissue-type plasminogen activator, single-chain urokinase-type plasmino-gen activator, and synergistic combinations in venous thrombosis models in dogs and rabbits. Blood 1989; 73: 1207-1212
  • 17 Stump DC, Stassen JM, Demarsin E, Collen D. Comparative thrombolytic properties of single-chain forms of urokinase-type plasminogen activator. Blood 1987; 68: 592-596
  • 18 Scully MF, Ellis V, Watahiki Y, Kakkar W. Activation of pro-urokinase by plasmin: non-Michaelian kinetics indicates a mechanism of negative cooperativ-ity. Arch Biochem Biophys 1989; 268: 438-446
  • 19 Longstaff C, Clough AM, Gaffney P. Kinetics of plasmin activation of single chain urinary-tpe plasminogen activator (scu-PA) and demonstration of a high affinity interaction between scu-PA and plasminogen. J Biol Chem 1992; 267: 173-179
  • 20 Badylak SF, Voytik S, Klabunde RE, Henkin J, Leski M. Bolus dose response characteristics of single-chain urokinase-type plasminogen activator in a dog model of arterial thrombosis. Thromb Res 1988; 52: 569-577
  • 21 De Munk GAW, Groeneveld E, Rijken DC. Acceleration of the thrombin inactivation of single-chain urokinase-type plasminogen activator (pro-urokin-ase) by thrombomodulin. J Clin Invest 1991; 88: 1680-1686
  • 22 Nelles L, Lijnen HR, Collen D, Holmes WE. Characterization of recombinant human single-chain urokinase-type plasminogen activator mutants produced by site specific mutagenesis of lysine 158. J Biol Chem 1987; 262: 5682-5689
  • 23 Brakman P. A Standardized Fibrin Plate Method and a Fibrinolytic Assay of Plasminogen. Fibrinolysis. Scheltema & Holkema, Amsterdam. 1967
  • 24 Haverkate F, Brakman P. Fibrin plate assay. In Progress in Chemical Fibrinolysis and Thrombolysis. Davidson JF, Samama MM, Desnoyers PC. (eds) Raven Press; New York: 1975. 34: 151-159
  • 25 Urano S, Metzger AR, Castellino FJ. Plasmin-mediated fibrinolysis by variant recombinant tissue plasminogen activators. Proc Natl Acad Sci USA 1989; 86: 2568-2571
  • 26 Gurewich V, Pannell R. Inactivation of single-chain urokinase (pro-urokinase) by thrombin and thrombin-like enzymes: relevance of the findings to the interpretation of fibrin-binding experiments. Blood 1987; 69: 679-772
  • 27 Drapier JC, Tenu JP, Lemaire G, Petit JF. Regulation of plasminogen activator secretion in mouse peritoneal macrophages. I. - Role of serum studied by a new spectrometric assay for plasminogen activators. Biochimie 1979; 61: 463-471
  • 28 Lenich C, Pannell R, Henkin J, Gurewich V. The influence of glycosylation on the catalytic and fibrinolytic properties of pro-urokinase. Thromb Haemostas 1992; 68: 539-544
  • 29 Collen D, Zamarron C, Lijnen HR, Hoylaerts M. Activation of plasminogen by pro-urokinase. II. Kinetics. J Biol Chem 1986; 261: 1259-1266
  • 30 Molinari A, Giorgetti C, Lansen J, Vaghi F, Orsini G, Faioni EM, Mannucci PM. Thrombomodulin is a cofactor for thrombin degradation of recombinant single-chain urokinase plasminogen activator "in vitro" and in a perfused rabbit heart model. Thromb Haemostas 1992; 67: 226-232
  • 31 De Munk GAW, Molinari A, Rijken DC. Inactivation of high and low molecular weight single-chain urokinase-type plasminogen activator (pro-urokinase) by thrombin in the presence of thrombomodulin. Thromb Haemostas 1993; 69: 88
  • 32 Pannell R, Gurewich V. Pro-urokinase: a study of its stability in plasma and of a mechanism for its selective fibrinolytic effect. Blood 1986; 67: 1215-1233
  • 33 Gurewich V, Pannell R, Louie S, Kelley P, Suddith L, Greenlee R. Effective and fibrin-specific clot lysis by a zymogen precursor form of urokinase (pro-urokinase). A study in vitro and in two animal species. J Clin Invest 1984; 73: 1731-1739
  • 34 Declerck PJ, Lijnen HR, Vestreken M, Collen D. Role of α2-antiplasmin in fibrin-specific clot lysis with single-chain urokinase-type plasminogen activator in human plasma. Thromb Haemostas 1991; 65: 394-398