Thromb Haemost 2000; 83(01): 93-101
DOI: 10.1055/s-0037-1613763
Commentary
Schattauer GmbH

Characterization of Transgenic Mice that Secrete Functional Human Protein C Inhibitor into the Circulation

Gerry T. M. Wagenaar
1   From the Thrombosis and Haemostasis Laboratory, Department of Haematology, Utrecht
3   Institute for Biomembranes, Utrecht University, The Netherlands
,
A. J. Hanneke van Vuuren5
1   From the Thrombosis and Haemostasis Laboratory, Department of Haematology, Utrecht
3   Institute for Biomembranes, Utrecht University, The Netherlands
,
Merone Girma
1   From the Thrombosis and Haemostasis Laboratory, Department of Haematology, Utrecht
,
Margriet J. Tiekstra
1   From the Thrombosis and Haemostasis Laboratory, Department of Haematology, Utrecht
,
Liane Kwast
1   From the Thrombosis and Haemostasis Laboratory, Department of Haematology, Utrecht
,
Johanna G. Koster
2   Department of Endocrinology, University Medical Center, Utrecht
,
Anita W. Rijneveld
4   Laboratory of Experimental Internal Medicine, Academic Medical Center, University of Amsterdam, The Netherlands
,
Marc G.L.M. Elisen6
1   From the Thrombosis and Haemostasis Laboratory, Department of Haematology, Utrecht
,
Tom van der Poll
4   Laboratory of Experimental Internal Medicine, Academic Medical Center, University of Amsterdam, The Netherlands
,
Joost C.M. Meijers
1   From the Thrombosis and Haemostasis Laboratory, Department of Haematology, Utrecht
3   Institute for Biomembranes, Utrecht University, The Netherlands
› Author Affiliations
Further Information

Publication History

Received 03 November 1998

Accepted after resubmission 29 June 1999

Publication Date:
06 December 2017 (online)

Summary

Protein C inhibitor (PCI) is a heparin binding serine protease inhibitor in plasma, which exerts procoagulant activity by inhibiting thrombomodulinbound thrombin or activated protein C (APC). Since the role of PCI in vivo is largely unknown we generated genetically modified mice with expression of human PCI mRNA in hepatocytes only. Three transgenic lines have been characterized. Transgenic mice did not show gross developmental abnormalities. Two lines showed a pericentral and one line showed a periportal expression pattern of human PCI mRNA in the liver. Genetically modified mice secreted a functional transgenic protein into the circulation (3-5 µg/ml plasma in heterozygous mice and 10 µg/ml in homozygous mice), which inhibited human APC activity in the presence of heparin. Interestingly, transgenic mice in which human PCI was expressed periportally in the liver had the highest specific activity. Endogenous mouse PCI mRNA could only be detected in the male and female reproductive system, but not in the liver, indicating that endogenous PCI levels in the circulation are low or even absent in mice. These results demonstrate that the human PCI transgenic mice are a suitable model for studying the in vivo role of PCI in blood coagulation.

5 Department of Immunology, University Medical Center, Utrecht, The Netherlands


6 Department of Clinical Chemistry, St. Franciscus Gasthuis, Rotterdam, The Netherlands


 
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