gms | German Medical Science

102. Jahrestagung der DOG

Deutsche Ophthalmologische Gesellschaft e. V.

23. bis 26.09.2004, Berlin

Gene expression of components of the fibrinolytic system in serum-free cultured human keratocytes

Meeting Abstract

  • corresponding author M. W. Meyer - Augenklinik der Medizinischen Hochschule Hannover, Hannover
  • M. Depka - Hämatologie der Medizinischen Hochschule Hannover, Hannover
  • A. Meyer - Augenklinik der Medizinischen Hochschule Hannover, Hannover
  • A. Schröder - Augenklinik der Medizinischen Hochschule Hannover, Hannover
  • R. Winter - Augenklinik der Medizinischen Hochschule Hannover, Hannover
  • C. Erb - Augenklinik der Medizinischen Hochschule Hannover, Hannover

Evidenzbasierte Medizin - Anspruch und Wirklichkeit. 102. Jahrestagung der Deutschen Ophthalmologischen Gesellschaft. Berlin, 23.-26.09.2004. Düsseldorf, Köln: German Medical Science; 2004. Doc04dogDO.08.11

The electronic version of this article is the complete one and can be found online at: http://www.egms.de/en/meetings/dog2004/04dog078.shtml

Published: September 22, 2004

© 2004 Meyer et al.
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Outline

Text

Objective

To determine the gene expression encoding for important components of the fibrinolytic system in serum-free cultured human keratocytes.

Methods

Total mRNA of confluent primary cultures of human keratocytes was isolated after 48 hours of serum-free cultivation. For each component of the fibrinolytic system reverse transcribed mRNA was measured by real time polymerase chain reaction (TaqMan® PCR) with primers and probes deduced from the human genes.

Results

In cultured human keratocytes we detected mRNA expression of plasminogen activator inhibitor-1 (PAI-1), thrombin activatable fibrinolysis inhibitor (TAFI), tissue-type plasminogen activator (tPA), urokinase-type plasminogen activator (uPA), protein C and protein S.

Conclusions

We localized the gene expression of important components of the fibrinolytic system in cultured keratocytes of the human eye. PAI-1 and TAFI are main regulators of the fibrinolytic system. Both inhibitors reduce plasminogen activity and attenuate fibrinolysis and proteolysis. In addition, PAI-1 leads to decreased dissolution of extracellur matrix. Therefore, stimulation of PAI-1 and TAFI production may be involved in inflammation and wound healing processes of the cornea.

Supported by Deutsche Forschungsgemeinschaft (DFG), ER 259/1