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Updated: Oct 7, 2026

Neisseria meningitidis Infection of Induced Pluripotent Stem-Cell Derived Brain Endothelial Cells
Published on: July 14, 2020
Outer membrane vesicles from Neisseria meningitidis: effects on tissue factor and plasminogen activator inhibitor-2
M R Mirlashari1, E A Høiby, J Holst
1Research Forum, Ullevaal University Hospital, Oslo, Norway. m.r.mirlashari@ioks.uio.no
Abstract:
Lipopolysaccharide-containing outer membrane vesicles (OMV-LPS) which are spontaneously released from Neisseria meningitidis during logarithmic growth were studied for their ability to induce procoagulant (tissue factor), profibrinolytic (urokinase-type plasminogen activator) and antifibrinolytic (plasminogen activator inhibitor-2) factors in purified human monocytes. Cell-associated tissue factor was 5.0-fold (n=5) increased, peaking after 8 h, in the presence of OMV-LPS (1 microg/ml, final concentration). Plasminogen activator inhibitor-2 release from monocytes was maximal after 24 h OMV-LPS (1 microg/ml) stimulation and 13.7-fold (n=5) increased compared to controls; whereas urokinase-type plasminogen activator antigen in culture medium remained uninfluenced by OMV-LPS. In conclusion, these OMV-induced imbalances favor fibrin deposition in the monocyte microenvironment and is probably of great importance in the development of disseminated intravascular coagulation, microthrombosis and organ dysfunction related to fulminant meningococcal septicemia.
Insights
Outer membrane vesicles (OMV-LPS) from Neisseria meningitidis increase procoagulant and antifibrinolytic factors in monocytes. This imbalance likely contributes to disseminated intravascular coagulation and organ dysfunction in meningococcal septicemia.
Area of Science:
- Microbiology
- Immunology
- Pathophysiology
Background:
- Neisseria meningitidis releases outer membrane vesicles (OMV-LPS) during growth.
- These vesicles play a role in bacterial pathogenesis.
Purpose of the Study:
- To investigate the effect of OMV-LPS on procoagulant, profibrinolytic, and antifibrinolytic factors in human monocytes.
- To understand the role of OMV-LPS in the development of severe meningococcal disease.
Main Methods:
- Purified human monocytes were stimulated with OMV-LPS.
- Levels of tissue factor, urokinase-type plasminogen activator, and plasminogen activator inhibitor-2 were measured.
Main Results:
- Cell-associated tissue factor increased 5.0-fold after 8 hours of OMV-LPS exposure.
- Plasminogen activator inhibitor-2 release increased 13.7-fold after 24 hours of OMV-LPS stimulation.
- Urokinase-type plasminogen activator levels remained unchanged.
Conclusions:
- OMV-LPS induces an imbalance favoring fibrin deposition in monocytes.
- This imbalance is significant in the pathogenesis of disseminated intravascular coagulation and organ dysfunction in meningococcal septicemia.
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