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Thromb Haemost 1995; 74(04): 1096-1102
DOI: 10.1055/s-0038-1649887
Original Article
Coagulation
Schattauer GmbH Stuttgart

Tissue Factor Expression on Mesothelial Cells is Induced during in vitro Culture – Manipulation of Culture Conditions Creates Perspectives for Mesothelial Cells as a Source for Cell Seeding Procedures on Vascular Grafts

Hence J M Verhagen
1   The Department of Surgery, University Hospital Utrecht, The Netherlands
2   The Department of Haematology, University Hospital Utrecht, The Netherlands
,
Glenda J Heijnen-Snyder
2   The Department of Haematology, University Hospital Utrecht, The Netherlands
,
Tom Vink
2   The Department of Haematology, University Hospital Utrecht, The Netherlands
,
Apollo Pronk
1   The Department of Surgery, University Hospital Utrecht, The Netherlands
,
Theo J M V van Vroonhoven
1   The Department of Surgery, University Hospital Utrecht, The Netherlands
,
Bert C Eikelboom
1   The Department of Surgery, University Hospital Utrecht, The Netherlands
,
Jan J Sixma
2   The Department of Haematology, University Hospital Utrecht, The Netherlands
,
Philip G de Groot
2   The Department of Haematology, University Hospital Utrecht, The Netherlands
› Author Affiliations
Further Information

Publication History

Received 16 January 1994

Accepted after resubmission 23 June 1995

Publication Date:
27 July 2018 (online)

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Summary

Lining the luminal surface of prosthetic small diameter bypasses with endothelial cells (EC) will lower its thrombogenicity. Unfortunately, human EC are only scarcely available. Mesotheliai cells (MC) have antithrombotic properties in vivo and can be harvested in large numbers, from the omentum. Recent work demonstrated that the expression of tissue factor (TF) is induced in MC after isolation and culture. Different culture conditions were studied to suppress TF-expression.

MC grown in pooled human serum (HS) are procoagulant (717 ± 119 pM factor Xa/min.105 cells). Replacing HS for fetal calf serum, precoating the surface with extracellular matrix and the addition of the xanthine-oxidase inhibitor allopurinol, inhibited TF expression by 90% (p <0.001). Allopurinol clearly reduced TF-mRNA levels.

TF expression on cultured MC is an in-vitro effect due to culture conditions and the formation of oxygen free radicals. By reducing TF expression by 90%, we have established conditions in which MC are a good alternative for EC for seeding on synthetic grafts.

 

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